Neurofibromatosis type I (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Neurofibromatosis type I" in English language version.

refsWebsite

Global rank English rank

61nih.gov

4^th place

46doi.org

2^nd place

13semanticscholar.org

11^th place

8^th place

7web.archive.org

1^st place

6worldcat.org

5^th place

4fda.gov

447^th place

338^th place

2ctf.org

low place

2mostgene.org

low place

2wiley.com

222^nd place

297^th place

1mayoclinic.org

1,610^th place

1,279^th place

1wikimedia.org

low place

1uchospitals.edu

low place

1nwhealth.edu

low place

1medlineplus.gov

1,581^st place

1,299^th place

1cancer.gov

1,684^th place

1,350^th place

1harvard.edu

18^th place

17^th place

1genecards.org

low place

1ucsc.edu

3,619^th place

2,621^st place

1handle.net

102^nd place

76^th place

1omim.org

4,380^th place

4,305^th place

1bionews.org.uk

low place

1genome.gov

9,308^th place

8,899^th place

1sagepub.com

731^st place

638^th place

1nervetumours.org.uk

low place

bionews.org.uk

Blackburn-Starzan A (9 June 2008). "British couple successfully screens out genetic disorder using NHS-funded PGD". BioNews. Archived from the original on March 30, 2016. Retrieved May 16, 2011.

cancer.gov

seer.cancer.gov

"Cancer Statistics Review, 1975-2012". SEER Cancer Statistics Review. Retrieved 2023-11-15.

ctf.org

"NF1 | Children's Tumor Foundation". Archived from the original on 2021-10-21. Retrieved 2016-10-25.
Children’s Tumor Foundation (November 2023). "Learning Disabilities in Children with NF1" (PDF). ctf.org. Retrieved 12 October 2024.

doi.org

Kunc V, Venkatramani H, Sabapathy SR (May 2019). "Neurofibromatosis 1 Diagnosed in Mother Only after a Follow-up of Her Daughter". Indian Journal of Plastic Surgery. 52 (2): 260. doi:10.1055/s-0039-1693503. PMC 6785427. PMID 31602150.
Costa RM, Silva AJ (August 2002). "Molecular and cellular mechanisms underlying the cognitive deficits associated with neurofibromatosis 1". Journal of Child Neurology. 17 (8): 622–626, discussion 626–9, 626–51. doi:10.1177/088307380201700813. PMID 12403561. S2CID 20385802.
Graphical abstract from: Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, et al. (August 2021). "Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation". Genetics in Medicine. 23 (8): 1506–1513. doi:10.1038/s41436-021-01170-5. PMC 8354850. PMID 34012067.
- "User License: Creative Commons Attribution (CC BY 4.0)"
Evans DG, Baser ME, McGaughran J, Sharif S, Howard E, Moran A (May 2002). "Malignant peripheral nerve sheath tumours in neurofibromatosis 1". Journal of Medical Genetics. 39 (5): 311–314. doi:10.1136/jmg.39.5.311. PMC 1735122. PMID 12011145.
Mutua V, Mong'are N, Bundi B, von Csefalvay C, Oriko D, Kitunguu P (September 2021). "Sudden bilateral lower limb paralysis with dural ectasia in Neurofibromatosis type 1: A case report". Medicine: Case Reports and Study Protocols. 2 (9): e0165. doi:10.1097/MD9.0000000000000165. ISSN 2691-3895.
Cornett KM, North KN, Rose KJ, Burns J (August 2015). "Muscle weakness in children with neurofibromatosis type 1". Developmental Medicine and Child Neurology. 57 (8): 733–736. doi:10.1111/dmcn.12777. PMID 25913846. S2CID 38835893.
Sullivan K, El-Hoss J, Quinlan KG, Deo N, Garton F, Seto JT, et al. (March 2014). "NF1 is a critical regulator of muscle development and metabolism". Human Molecular Genetics. 23 (5): 1250–1259. doi:10.1093/hmg/ddt515. PMC 3954124. PMID 24163128.
Stevenson DA, Allen S, Tidyman WE, Carey JC, Viskochil DH, Stevens A, et al. (September 2012). "Peripheral muscle weakness in RASopathies". Muscle & Nerve. 46 (3): 394–399. doi:10.1002/mus.23324. PMID 22907230. S2CID 21120799.
Lakshmanan A, Bubna A, Sankarasubramaniam A, Veeraraghavan M, Rangarajan S, Sundaram M (2016). "A clinical study of neurofibromatosis-1 at a tertiary health care centre in south India". Pigment International. 3 (2): 102. doi:10.4103/2349-5847.196302.
Hyman SL, Shores A, North KN (October 2005). "The nature and frequency of cognitive deficits in children with neurofibromatosis type 1". Neurology. 65 (7): 1037–1044. doi:10.1212/01.wnl.0000179303.72345.ce. PMID 16217056. S2CID 10198510.
Hyman SL, Gill DS, Shores EA, Steinberg A, Joy P, Gibikote SV, et al. (April 2003). "Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1". Neurology. 60 (7): 1139–1145. doi:10.1212/01.WNL.0000055090.78351.C1. PMID 12682321. S2CID 26812237.
Garg S, Lehtonen A, Huson SM, Emsley R, Trump D, Evans DG, et al. (February 2013). "Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based study". Developmental Medicine and Child Neurology. 55 (2): 139–145. doi:10.1111/dmcn.12043. PMID 23163236. S2CID 11781870.
Thompson HL, Viskochil DH, Stevenson DA, Chapman KL (February 2010). "Speech-language characteristics of children with neurofibromatosis type 1". American Journal of Medical Genetics. Part A. 152A (2): 284–290. doi:10.1002/ajmg.a.33235. PMID 20101681. S2CID 26650152.
van der Vaart T, van Woerden GM, Elgersma Y, de Zeeuw CI, Schonewille M (June 2011). "Motor deficits in neurofibromatosis type 1 mice: the role of the cerebellum". Genes, Brain and Behavior. 10 (4): 404–409. doi:10.1111/j.1601-183X.2011.00685.x. PMID 21352477. S2CID 19609654.
Vivarelli R, Grosso S, Calabrese F, Farnetani M, Di Bartolo R, Morgese G, et al. (May 2003). "Epilepsy in neurofibromatosis 1". Journal of Child Neurology. 18 (5): 338–342. doi:10.1177/08830738030180050501. PMID 12822818. S2CID 39229702.
Listernick R, Charrow J, Gutmann DH (March 1999). "Intracranial gliomas in neurofibromatosis type 1". American Journal of Medical Genetics. 89 (1): 38–44. doi:10.1002/(sici)1096-8628(19990326)89:1<38::aid-ajmg8>3.0.co;2-m. PMID 10469435.
Polster SP, Dougherty MC, Zeineddine HA, Lyne SB, Smith HL, MacKenzie C, et al. (May 2020). "Dural Ectasia in Neurofibromatosis 1: Case Series, Management, and Review". Neurosurgery. 86 (5): 646–655. doi:10.1093/neuros/nyz244. PMID 31350851.
Cohen JS, Levy HP, Sloan J, Dariotis J, Biesecker BB (November 2015). "Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life". Clinical Genetics. 88 (5): 425–430. doi:10.1111/cge.12551. PMC 4573679. PMID 25534182.
Berardelli I, Maraone A, Belvisi D, Pasquini M, Giustini S, Miraglia E, et al. (November 2021). "The importance of suicide risk assessment in patients affected by neurofibromatosis". International Journal of Psychiatry in Clinical Practice. 25 (4): 350–355. doi:10.1080/13651501.2021.1921217. PMID 34270353. S2CID 235999769.
Brar KS, Trivedi C, Kaur N, Adnan M, Patel H, Beg U, et al. (October 2023). "Prevalence of Psychiatric Comorbidities in Patients With Neurofibromatosis". The Primary Care Companion for CNS Disorders. 25 (5): 49254. doi:10.4088/PCC.23m03514. PMID 37816254. S2CID 263240202.
Miguel CS, Chaim-Avancini TM, Silva MA, Louzã MR (2015-03-25). "Neurofibromatosis type 1 and attention deficit hyperactivity disorder: a case study and literature review". Neuropsychiatric Disease and Treatment. 11: 815–821. doi:10.2147/NDT.S75038. PMC 4378869. PMID 25848279.
Chisholm AK, Haebich KM, Pride NA, Walsh KS, Lami F, Ure A, et al. (January 2022). "Delineating the autistic phenotype in children with neurofibromatosis type 1". Molecular Autism. 13 (1): 3. doi:10.1186/s13229-021-00481-3. PMC 8729013. PMID 34983638.
Korf BR (March 1999). "Plexiform neurofibromas". American Journal of Medical Genetics. 89 (1): 31–37. doi:10.1002/(sici)1096-8628(19990326)89:1<31::aid-ajmg7>3.0.co;2-w. PMID 10469434.
Matsui I, Tanimura M, Kobayashi N, Sawada T, Nagahara N, Akatsuka J (November 1993). "Neurofibromatosis type 1 and childhood cancer". Cancer. 72 (9): 2746–2754. doi:10.1002/1097-0142(19931101)72:9<2746::AID-CNCR2820720936>3.0.CO;2-W. PMID 8402499.
Duong TA, Sbidian E, Valeyrie-Allanore L, Vialette C, Ferkal S, Hadj-Rabia S, et al. (May 2011). "Mortality associated with neurofibromatosis 1: a cohort study of 1895 patients in 1980-2006 in France". Orphanet Journal of Rare Diseases. 6: 18. doi:10.1186/1750-1172-6-18. PMC 3095535. PMID 21542925.
Suarez-Kelly LP, Yu L, Kline D, Schneider EB, Agnese DM, Carson WE (2019-03-25). "Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literature". Hereditary Cancer in Clinical Practice. 17 (1): 12. doi:10.1186/s13053-019-0110-z. PMC 6434896. PMID 30962859.
Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, et al. (July 1990). "Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients". Science. 249 (4965): 181–186. Bibcode:1990Sci...249..181W. doi:10.1126/science.2134734. PMID 2134734.
Goldberg NS, Collins FS (November 1991). "The hunt for the neurofibromatosis gene". Archives of Dermatology. 127 (11): 1705–1707. doi:10.1001/archderm.1991.01680100105014. PMID 1952978.
Pasmant E, Sabbagh A, Spurlock G, Laurendeau I, Grillo E, Hamel MJ, et al. (June 2010). "NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype". Human Mutation. 31 (6): E1506 – E1518. doi:10.1002/humu.21271. PMID 20513137. S2CID 24525378.
Marchuk DA, Saulino AM, Tavakkol R, Swaroop M, Wallace MR, Andersen LB, et al. (December 1991). "cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product". Genomics. 11 (4): 931–940. doi:10.1016/0888-7543(91)90017-9. hdl:2027.42/29018. PMID 1783401.
Gutmann DH, Giovannini M (2002). "Mouse models of neurofibromatosis 1 and 2". Neoplasia. 4 (4): 279–290. doi:10.1038/sj.neo.7900249. PMC 1531708. PMID 12082543.
Feldkamp MM, Angelov L, Guha A (February 1999). "Neurofibromatosis type 1 peripheral nerve tumors: aberrant activation of the Ras pathway". Surgical Neurology. 51 (2): 211–218. doi:10.1016/S0090-3019(97)00356-X. PMID 10029430.
Hannan F, Ho I, Tong JJ, Zhu Y, Nurnberg P, Zhong Y (April 2006). "Effect of neurofibromatosis type I mutations on a novel pathway for adenylyl cyclase activation requiring neurofibromin and Ras". Human Molecular Genetics. 15 (7): 1087–1098. doi:10.1093/hmg/ddl023. PMC 1866217. PMID 16513807.
Ozawa T, Araki N, Yunoue S, Tokuo H, Feng L, Patrakitkomjorn S, et al. (November 2005). "The neurofibromatosis type 1 gene product neurofibromin enhances cell motility by regulating actin filament dynamics via the Rho-ROCK-LIMK2-cofilin pathway". The Journal of Biological Chemistry. 280 (47): 39524–39533. doi:10.1074/jbc.M503707200. PMID 16169856.
Le LQ, Parada LF (July 2007). "Tumor microenvironment and neurofibromatosis type I: connecting the GAPs". Oncogene. 26 (32): 4609–4616. doi:10.1038/sj.onc.1210261. PMC 2760340. PMID 17297459.
"Neurofibromatosis: Conference Statement". Archives of Neurology. 45 (5): 575. 1 May 1988. doi:10.1001/archneur.1988.00520290115023.
Rodrigues LO, Batista PB, Goloni-Bertollo EM, de Souza-Costa D, Eliam L, Eliam M, et al. (March 2014). "Neurofibromatoses: part 1 - diagnosis and differential diagnosis". Arquivos de Neuro-Psiquiatria. 72 (3): 241–250. doi:10.1590/0004-282X20130241. PMID 24676443.
Vogel AC, Gutmann DH, Morris SM (November 2017). "Neurodevelopmental disorders in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 59 (11): 1112–1116. doi:10.1111/dmcn.13526. ISSN 0012-1622. PMID 28845518. Retrieved 2024-10-12.
Garg S, Plasschaert E, Descheemaeker MJ, Huson S, Borghgraef M, Vogels A, et al. (2015-06-01). "Autism Spectrum Disorder Profile in Neurofibromatosis Type I". Journal of Autism and Developmental Disorders. 45 (6): 1649–1657. doi:10.1007/s10803-014-2321-5. ISSN 1573-3432. PMID 25475362. Retrieved 2024-07-23.
Lubbers K, Stijl EM, Dierckx B, Hagenaar DA, ten Hoopen LW, Legerstee JS, et al. (2022-05-16). "Autism Symptoms in Children and Young Adults With Fragile X Syndrome, Angelman Syndrome, Tuberous Sclerosis Complex, and Neurofibromatosis Type 1: A Cross-Syndrome Comparison". Frontiers in Psychiatry. 13. doi:10.3389/fpsyt.2022.852208. ISSN 1664-0640. PMC 9149157. PMID 35651825.
Morotti H, Mastel S, Keller K, Barnard RA, Hall T, O'Roak BJ, et al. (2021). "Autism and attention-deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 63 (2): 226–232. doi:10.1111/dmcn.14558. ISSN 1469-8749. PMID 32406525.
Lion-François L, Herbillon V, Peyric E, Mercier C, Gérard D, Ginhoux T, et al. (November 2020). "Attention and Executive Disorders in Neurofibromatosis 1: Comparison Between NF1 With ADHD Symptomatology (NF-1 + ADHD) and ADHD Per Se". Journal of Attention Disorders. 24 (13): 1807–1823. doi:10.1177/1087054717707579. ISSN 1087-0547. PMID 28587546. Retrieved 2024-10-24.
Coltin H, Perreault S, Larouche V, Black K, Wilson B, Vanan MI, et al. (August 2022). "Selumetinib for symptomatic, inoperable plexiform neurofibromas in children with neurofibromatosis type 1: A national real-world case series". Pediatric Blood & Cancer. 69 (8): e29633. doi:10.1002/pbc.29633. PMID 35289492. S2CID 247453317.
Armstrong AE, Belzberg AJ, Crawford JR, Hirbe AC, Wang ZJ (June 2023). "Treatment decisions and the use of MEK inhibitors for children with neurofibromatosis type 1-related plexiform neurofibromas". BMC Cancer. 23 (1): 553. doi:10.1186/s12885-023-10996-y. PMC 10273716. PMID 37328781.
Valeyrie-Allanore L, Roujeau JC, Revuz J (2005). "Neurofibromatosis type 1: From diagnosis to therapeutic challenges". American Journal of Medical Genetics Part A. 137A (1): 12–23. doi:10.1002/ajmg.a.38486. PMID 29388340.
Legendre CM, Charpentier-Côté C, Drouin R, Bouffard C (2011-01-01). "Neurofibromatosis type 1: persisting misidentification of the "elephant man" disease". Journal of the American Board of Family Medicine. 24 (1): 112–114. doi:10.3122/jabfm.2011.01.100219. PMID 21209351.

fda.gov

accessdata.fda.gov

"GOMEKLI (mirdametinib) capsules, for oral use" (PDF). SpringWorks Therapeutics, Inc. U.S. Food and Drug Administration. February 2025.
AstraZeneca Pharmaceuticals LP. Koselugo(Selumetinib)[package insert]. U.S. Food and Drug Administration website.https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/213756s000lbl.pdf. Accessed June 21, 2020.

fda.gov

"FDA approves mirdametinib for adult and pediatric patients with neurofibromatosis type 1 who have symptomatic plexiform neurofibromas not amenable to complete resection". U.S. Food and Drug Administration (FDA). 11 February 2025. Archived from the original on 13 February 2025. Retrieved 16 February 2025. This article incorporates text from this source, which is in the public domain.
Office of the Commissioner (2020-04-10). "FDA Approves First Therapy for Children with Debilitating and Disfiguring Rare Disease". FDA. Retrieved 2020-06-21.

genecards.org

"neurofibromin 1" GeneCards

genome.gov

"About Neurofibromatosis". Genome.gov. Retrieved 2020-03-05.

handle.net

hdl.handle.net

Marchuk DA, Saulino AM, Tavakkol R, Swaroop M, Wallace MR, Andersen LB, et al. (December 1991). "cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product". Genomics. 11 (4): 931–940. doi:10.1016/0888-7543(91)90017-9. hdl:2027.42/29018. PMID 1783401.

harvard.edu

ui.adsabs.harvard.edu

Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, et al. (July 1990). "Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients". Science. 249 (4965): 181–186. Bibcode:1990Sci...249..181W. doi:10.1126/science.2134734. PMID 2134734.

mayoclinic.org

- Source for main symptoms: "Neurofibromatosis". Mayo Clinic. 2021-01-21.
- Image by Mikael Häggström, MD, using source images by various authors.

medlineplus.gov

MedlinePlus Encyclopedia: Optic glioma

mostgene.org

Viskochil D (2010). "Neurofibromatosis 1: Current Issues in Diagnosis, Therapy, and Patient Management" (PDF). Mountain States Genetic Foundation. Denver. Archived from the original (PDF) on 2015-11-06. Retrieved 2011-05-15.
Klesse L (2010). "Current Therapies for Neurofibromatosis Type 1" (PDF). Mountain States Genetic Foundation. Denver. Archived from the original (PDF) on 2012-03-09. Retrieved 2011-05-15.

nervetumours.org.uk

Ashton R, Crawford H, Morrison P, McKee S, Huson S (2012). "Neurofibromatosis Type 1 (NF1) a Guide for Adults and Families" (PDF). Nerve Tumours UK. Retrieved 2021-04-27.

nih.gov

pubmed.ncbi.nlm.nih.gov

Kunc V, Venkatramani H, Sabapathy SR (May 2019). "Neurofibromatosis 1 Diagnosed in Mother Only after a Follow-up of Her Daughter". Indian Journal of Plastic Surgery. 52 (2): 260. doi:10.1055/s-0039-1693503. PMC 6785427. PMID 31602150.
Costa RM, Silva AJ (August 2002). "Molecular and cellular mechanisms underlying the cognitive deficits associated with neurofibromatosis 1". Journal of Child Neurology. 17 (8): 622–626, discussion 626–9, 626–51. doi:10.1177/088307380201700813. PMID 12403561. S2CID 20385802.
Graphical abstract from: Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, et al. (August 2021). "Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation". Genetics in Medicine. 23 (8): 1506–1513. doi:10.1038/s41436-021-01170-5. PMC 8354850. PMID 34012067.
- "User License: Creative Commons Attribution (CC BY 4.0)"
Evans DG, Baser ME, McGaughran J, Sharif S, Howard E, Moran A (May 2002). "Malignant peripheral nerve sheath tumours in neurofibromatosis 1". Journal of Medical Genetics. 39 (5): 311–314. doi:10.1136/jmg.39.5.311. PMC 1735122. PMID 12011145.
Summers MA, Quinlan KG, Payne JM, Little DG, North KN, Schindeler A (June 2015). "Skeletal muscle and motor deficits in Neurofibromatosis Type 1". Journal of Musculoskeletal & Neuronal Interactions. 15 (2): 161–170. PMC 5133719. PMID 26032208.
Cornett KM, North KN, Rose KJ, Burns J (August 2015). "Muscle weakness in children with neurofibromatosis type 1". Developmental Medicine and Child Neurology. 57 (8): 733–736. doi:10.1111/dmcn.12777. PMID 25913846. S2CID 38835893.
Sullivan K, El-Hoss J, Quinlan KG, Deo N, Garton F, Seto JT, et al. (March 2014). "NF1 is a critical regulator of muscle development and metabolism". Human Molecular Genetics. 23 (5): 1250–1259. doi:10.1093/hmg/ddt515. PMC 3954124. PMID 24163128.
Stevenson DA, Allen S, Tidyman WE, Carey JC, Viskochil DH, Stevens A, et al. (September 2012). "Peripheral muscle weakness in RASopathies". Muscle & Nerve. 46 (3): 394–399. doi:10.1002/mus.23324. PMID 22907230. S2CID 21120799.
Hyman SL, Shores A, North KN (October 2005). "The nature and frequency of cognitive deficits in children with neurofibromatosis type 1". Neurology. 65 (7): 1037–1044. doi:10.1212/01.wnl.0000179303.72345.ce. PMID 16217056. S2CID 10198510.
Hyman SL, Gill DS, Shores EA, Steinberg A, Joy P, Gibikote SV, et al. (April 2003). "Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1". Neurology. 60 (7): 1139–1145. doi:10.1212/01.WNL.0000055090.78351.C1. PMID 12682321. S2CID 26812237.
Garg S, Lehtonen A, Huson SM, Emsley R, Trump D, Evans DG, et al. (February 2013). "Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based study". Developmental Medicine and Child Neurology. 55 (2): 139–145. doi:10.1111/dmcn.12043. PMID 23163236. S2CID 11781870.
Thompson HL, Viskochil DH, Stevenson DA, Chapman KL (February 2010). "Speech-language characteristics of children with neurofibromatosis type 1". American Journal of Medical Genetics. Part A. 152A (2): 284–290. doi:10.1002/ajmg.a.33235. PMID 20101681. S2CID 26650152.
van der Vaart T, van Woerden GM, Elgersma Y, de Zeeuw CI, Schonewille M (June 2011). "Motor deficits in neurofibromatosis type 1 mice: the role of the cerebellum". Genes, Brain and Behavior. 10 (4): 404–409. doi:10.1111/j.1601-183X.2011.00685.x. PMID 21352477. S2CID 19609654.
Vivarelli R, Grosso S, Calabrese F, Farnetani M, Di Bartolo R, Morgese G, et al. (May 2003). "Epilepsy in neurofibromatosis 1". Journal of Child Neurology. 18 (5): 338–342. doi:10.1177/08830738030180050501. PMID 12822818. S2CID 39229702.
Listernick R, Charrow J, Gutmann DH (March 1999). "Intracranial gliomas in neurofibromatosis type 1". American Journal of Medical Genetics. 89 (1): 38–44. doi:10.1002/(sici)1096-8628(19990326)89:1<38::aid-ajmg8>3.0.co;2-m. PMID 10469435.
Polster SP, Dougherty MC, Zeineddine HA, Lyne SB, Smith HL, MacKenzie C, et al. (May 2020). "Dural Ectasia in Neurofibromatosis 1: Case Series, Management, and Review". Neurosurgery. 86 (5): 646–655. doi:10.1093/neuros/nyz244. PMID 31350851.
Cohen JS, Levy HP, Sloan J, Dariotis J, Biesecker BB (November 2015). "Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life". Clinical Genetics. 88 (5): 425–430. doi:10.1111/cge.12551. PMC 4573679. PMID 25534182.
Berardelli I, Maraone A, Belvisi D, Pasquini M, Giustini S, Miraglia E, et al. (November 2021). "The importance of suicide risk assessment in patients affected by neurofibromatosis". International Journal of Psychiatry in Clinical Practice. 25 (4): 350–355. doi:10.1080/13651501.2021.1921217. PMID 34270353. S2CID 235999769.
Brar KS, Trivedi C, Kaur N, Adnan M, Patel H, Beg U, et al. (October 2023). "Prevalence of Psychiatric Comorbidities in Patients With Neurofibromatosis". The Primary Care Companion for CNS Disorders. 25 (5): 49254. doi:10.4088/PCC.23m03514. PMID 37816254. S2CID 263240202.
Miguel CS, Chaim-Avancini TM, Silva MA, Louzã MR (2015-03-25). "Neurofibromatosis type 1 and attention deficit hyperactivity disorder: a case study and literature review". Neuropsychiatric Disease and Treatment. 11: 815–821. doi:10.2147/NDT.S75038. PMC 4378869. PMID 25848279.
Chisholm AK, Haebich KM, Pride NA, Walsh KS, Lami F, Ure A, et al. (January 2022). "Delineating the autistic phenotype in children with neurofibromatosis type 1". Molecular Autism. 13 (1): 3. doi:10.1186/s13229-021-00481-3. PMC 8729013. PMID 34983638.
Virdis R, Street ME, Bandello MA, Tripodi C, Donadio A, Villani AR, et al. (March 2003). "Growth and pubertal disorders in neurofibromatosis type 1". Journal of Pediatric Endocrinology & Metabolism. 16 (Suppl 2): 289–292. PMID 12729406.
Korf BR (March 1999). "Plexiform neurofibromas". American Journal of Medical Genetics. 89 (1): 31–37. doi:10.1002/(sici)1096-8628(19990326)89:1<31::aid-ajmg7>3.0.co;2-w. PMID 10469434.
Matsui I, Tanimura M, Kobayashi N, Sawada T, Nagahara N, Akatsuka J (November 1993). "Neurofibromatosis type 1 and childhood cancer". Cancer. 72 (9): 2746–2754. doi:10.1002/1097-0142(19931101)72:9<2746::AID-CNCR2820720936>3.0.CO;2-W. PMID 8402499.
Duong TA, Sbidian E, Valeyrie-Allanore L, Vialette C, Ferkal S, Hadj-Rabia S, et al. (May 2011). "Mortality associated with neurofibromatosis 1: a cohort study of 1895 patients in 1980-2006 in France". Orphanet Journal of Rare Diseases. 6: 18. doi:10.1186/1750-1172-6-18. PMC 3095535. PMID 21542925.
Suarez-Kelly LP, Yu L, Kline D, Schneider EB, Agnese DM, Carson WE (2019-03-25). "Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literature". Hereditary Cancer in Clinical Practice. 17 (1): 12. doi:10.1186/s13053-019-0110-z. PMC 6434896. PMID 30962859.
Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, et al. (July 1990). "Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients". Science. 249 (4965): 181–186. Bibcode:1990Sci...249..181W. doi:10.1126/science.2134734. PMID 2134734.
Goldberg NS, Collins FS (November 1991). "The hunt for the neurofibromatosis gene". Archives of Dermatology. 127 (11): 1705–1707. doi:10.1001/archderm.1991.01680100105014. PMID 1952978.
Pasmant E, Sabbagh A, Spurlock G, Laurendeau I, Grillo E, Hamel MJ, et al. (June 2010). "NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype". Human Mutation. 31 (6): E1506 – E1518. doi:10.1002/humu.21271. PMID 20513137. S2CID 24525378.
Marchuk DA, Saulino AM, Tavakkol R, Swaroop M, Wallace MR, Andersen LB, et al. (December 1991). "cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product". Genomics. 11 (4): 931–940. doi:10.1016/0888-7543(91)90017-9. hdl:2027.42/29018. PMID 1783401.
Gutmann DH, Giovannini M (2002). "Mouse models of neurofibromatosis 1 and 2". Neoplasia. 4 (4): 279–290. doi:10.1038/sj.neo.7900249. PMC 1531708. PMID 12082543.
Feldkamp MM, Angelov L, Guha A (February 1999). "Neurofibromatosis type 1 peripheral nerve tumors: aberrant activation of the Ras pathway". Surgical Neurology. 51 (2): 211–218. doi:10.1016/S0090-3019(97)00356-X. PMID 10029430.
Hannan F, Ho I, Tong JJ, Zhu Y, Nurnberg P, Zhong Y (April 2006). "Effect of neurofibromatosis type I mutations on a novel pathway for adenylyl cyclase activation requiring neurofibromin and Ras". Human Molecular Genetics. 15 (7): 1087–1098. doi:10.1093/hmg/ddl023. PMC 1866217. PMID 16513807.
Ozawa T, Araki N, Yunoue S, Tokuo H, Feng L, Patrakitkomjorn S, et al. (November 2005). "The neurofibromatosis type 1 gene product neurofibromin enhances cell motility by regulating actin filament dynamics via the Rho-ROCK-LIMK2-cofilin pathway". The Journal of Biological Chemistry. 280 (47): 39524–39533. doi:10.1074/jbc.M503707200. PMID 16169856.
Le LQ, Parada LF (July 2007). "Tumor microenvironment and neurofibromatosis type I: connecting the GAPs". Oncogene. 26 (32): 4609–4616. doi:10.1038/sj.onc.1210261. PMC 2760340. PMID 17297459.
Rodrigues LO, Batista PB, Goloni-Bertollo EM, de Souza-Costa D, Eliam L, Eliam M, et al. (March 2014). "Neurofibromatoses: part 1 - diagnosis and differential diagnosis". Arquivos de Neuro-Psiquiatria. 72 (3): 241–250. doi:10.1590/0004-282X20130241. PMID 24676443.
Vogel AC, Gutmann DH, Morris SM (November 2017). "Neurodevelopmental disorders in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 59 (11): 1112–1116. doi:10.1111/dmcn.13526. ISSN 0012-1622. PMID 28845518. Retrieved 2024-10-12.
Garg S, Plasschaert E, Descheemaeker MJ, Huson S, Borghgraef M, Vogels A, et al. (2015-06-01). "Autism Spectrum Disorder Profile in Neurofibromatosis Type I". Journal of Autism and Developmental Disorders. 45 (6): 1649–1657. doi:10.1007/s10803-014-2321-5. ISSN 1573-3432. PMID 25475362. Retrieved 2024-07-23.
Lubbers K, Stijl EM, Dierckx B, Hagenaar DA, ten Hoopen LW, Legerstee JS, et al. (2022-05-16). "Autism Symptoms in Children and Young Adults With Fragile X Syndrome, Angelman Syndrome, Tuberous Sclerosis Complex, and Neurofibromatosis Type 1: A Cross-Syndrome Comparison". Frontiers in Psychiatry. 13. doi:10.3389/fpsyt.2022.852208. ISSN 1664-0640. PMC 9149157. PMID 35651825.
Morotti H, Mastel S, Keller K, Barnard RA, Hall T, O'Roak BJ, et al. (2021). "Autism and attention-deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 63 (2): 226–232. doi:10.1111/dmcn.14558. ISSN 1469-8749. PMID 32406525.
Lion-François L, Herbillon V, Peyric E, Mercier C, Gérard D, Ginhoux T, et al. (November 2020). "Attention and Executive Disorders in Neurofibromatosis 1: Comparison Between NF1 With ADHD Symptomatology (NF-1 + ADHD) and ADHD Per Se". Journal of Attention Disorders. 24 (13): 1807–1823. doi:10.1177/1087054717707579. ISSN 1087-0547. PMID 28587546. Retrieved 2024-10-24.
Coltin H, Perreault S, Larouche V, Black K, Wilson B, Vanan MI, et al. (August 2022). "Selumetinib for symptomatic, inoperable plexiform neurofibromas in children with neurofibromatosis type 1: A national real-world case series". Pediatric Blood & Cancer. 69 (8): e29633. doi:10.1002/pbc.29633. PMID 35289492. S2CID 247453317.
Armstrong AE, Belzberg AJ, Crawford JR, Hirbe AC, Wang ZJ (June 2023). "Treatment decisions and the use of MEK inhibitors for children with neurofibromatosis type 1-related plexiform neurofibromas". BMC Cancer. 23 (1): 553. doi:10.1186/s12885-023-10996-y. PMC 10273716. PMID 37328781.
Valeyrie-Allanore L, Roujeau JC, Revuz J (2005). "Neurofibromatosis type 1: From diagnosis to therapeutic challenges". American Journal of Medical Genetics Part A. 137A (1): 12–23. doi:10.1002/ajmg.a.38486. PMID 29388340.
Legendre CM, Charpentier-Côté C, Drouin R, Bouffard C (2011-01-01). "Neurofibromatosis type 1: persisting misidentification of the "elephant man" disease". Journal of the American Board of Family Medicine. 24 (1): 112–114. doi:10.3122/jabfm.2011.01.100219. PMID 21209351.

ncbi.nlm.nih.gov

Kunc V, Venkatramani H, Sabapathy SR (May 2019). "Neurofibromatosis 1 Diagnosed in Mother Only after a Follow-up of Her Daughter". Indian Journal of Plastic Surgery. 52 (2): 260. doi:10.1055/s-0039-1693503. PMC 6785427. PMID 31602150.
Graphical abstract from: Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, et al. (August 2021). "Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation". Genetics in Medicine. 23 (8): 1506–1513. doi:10.1038/s41436-021-01170-5. PMC 8354850. PMID 34012067.
- "User License: Creative Commons Attribution (CC BY 4.0)"
Evans DG, Baser ME, McGaughran J, Sharif S, Howard E, Moran A (May 2002). "Malignant peripheral nerve sheath tumours in neurofibromatosis 1". Journal of Medical Genetics. 39 (5): 311–314. doi:10.1136/jmg.39.5.311. PMC 1735122. PMID 12011145.
Summers MA, Quinlan KG, Payne JM, Little DG, North KN, Schindeler A (June 2015). "Skeletal muscle and motor deficits in Neurofibromatosis Type 1". Journal of Musculoskeletal & Neuronal Interactions. 15 (2): 161–170. PMC 5133719. PMID 26032208.
Sullivan K, El-Hoss J, Quinlan KG, Deo N, Garton F, Seto JT, et al. (March 2014). "NF1 is a critical regulator of muscle development and metabolism". Human Molecular Genetics. 23 (5): 1250–1259. doi:10.1093/hmg/ddt515. PMC 3954124. PMID 24163128.
Cohen JS, Levy HP, Sloan J, Dariotis J, Biesecker BB (November 2015). "Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life". Clinical Genetics. 88 (5): 425–430. doi:10.1111/cge.12551. PMC 4573679. PMID 25534182.
Miguel CS, Chaim-Avancini TM, Silva MA, Louzã MR (2015-03-25). "Neurofibromatosis type 1 and attention deficit hyperactivity disorder: a case study and literature review". Neuropsychiatric Disease and Treatment. 11: 815–821. doi:10.2147/NDT.S75038. PMC 4378869. PMID 25848279.
Chisholm AK, Haebich KM, Pride NA, Walsh KS, Lami F, Ure A, et al. (January 2022). "Delineating the autistic phenotype in children with neurofibromatosis type 1". Molecular Autism. 13 (1): 3. doi:10.1186/s13229-021-00481-3. PMC 8729013. PMID 34983638.
Duong TA, Sbidian E, Valeyrie-Allanore L, Vialette C, Ferkal S, Hadj-Rabia S, et al. (May 2011). "Mortality associated with neurofibromatosis 1: a cohort study of 1895 patients in 1980-2006 in France". Orphanet Journal of Rare Diseases. 6: 18. doi:10.1186/1750-1172-6-18. PMC 3095535. PMID 21542925.
Suarez-Kelly LP, Yu L, Kline D, Schneider EB, Agnese DM, Carson WE (2019-03-25). "Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literature". Hereditary Cancer in Clinical Practice. 17 (1): 12. doi:10.1186/s13053-019-0110-z. PMC 6434896. PMID 30962859.
Gutmann DH, Giovannini M (2002). "Mouse models of neurofibromatosis 1 and 2". Neoplasia. 4 (4): 279–290. doi:10.1038/sj.neo.7900249. PMC 1531708. PMID 12082543.
Hannan F, Ho I, Tong JJ, Zhu Y, Nurnberg P, Zhong Y (April 2006). "Effect of neurofibromatosis type I mutations on a novel pathway for adenylyl cyclase activation requiring neurofibromin and Ras". Human Molecular Genetics. 15 (7): 1087–1098. doi:10.1093/hmg/ddl023. PMC 1866217. PMID 16513807.
Le LQ, Parada LF (July 2007). "Tumor microenvironment and neurofibromatosis type I: connecting the GAPs". Oncogene. 26 (32): 4609–4616. doi:10.1038/sj.onc.1210261. PMC 2760340. PMID 17297459.
Lubbers K, Stijl EM, Dierckx B, Hagenaar DA, ten Hoopen LW, Legerstee JS, et al. (2022-05-16). "Autism Symptoms in Children and Young Adults With Fragile X Syndrome, Angelman Syndrome, Tuberous Sclerosis Complex, and Neurofibromatosis Type 1: A Cross-Syndrome Comparison". Frontiers in Psychiatry. 13. doi:10.3389/fpsyt.2022.852208. ISSN 1664-0640. PMC 9149157. PMID 35651825.
Armstrong AE, Belzberg AJ, Crawford JR, Hirbe AC, Wang ZJ (June 2023). "Treatment decisions and the use of MEK inhibitors for children with neurofibromatosis type 1-related plexiform neurofibromas". BMC Cancer. 23 (1): 553. doi:10.1186/s12885-023-10996-y. PMC 10273716. PMID 37328781.

dailymed.nlm.nih.gov

"KOSELUGO- selumetinib capsule". DailyMed. U.S. National Library of Medicine. Retrieved 2023-11-15.

nwhealth.edu

"Northwestern Health Sciences University ~ Diagnosis and Discussion". www.nwhealth.edu. Archived from the original on 2016-03-04. Retrieved 2015-10-27.

omim.org

Online Mendelian Inheritance in Man (OMIM): NEUROFIBROMATOSIS, TYPE I; NF1 - 162200

sagepub.com

journals.sagepub.com

Lion-François L, Herbillon V, Peyric E, Mercier C, Gérard D, Ginhoux T, et al. (November 2020). "Attention and Executive Disorders in Neurofibromatosis 1: Comparison Between NF1 With ADHD Symptomatology (NF-1 + ADHD) and ADHD Per Se". Journal of Attention Disorders. 24 (13): 1807–1823. doi:10.1177/1087054717707579. ISSN 1087-0547. PMID 28587546. Retrieved 2024-10-24.

semanticscholar.org

api.semanticscholar.org

Costa RM, Silva AJ (August 2002). "Molecular and cellular mechanisms underlying the cognitive deficits associated with neurofibromatosis 1". Journal of Child Neurology. 17 (8): 622–626, discussion 626–9, 626–51. doi:10.1177/088307380201700813. PMID 12403561. S2CID 20385802.
Cornett KM, North KN, Rose KJ, Burns J (August 2015). "Muscle weakness in children with neurofibromatosis type 1". Developmental Medicine and Child Neurology. 57 (8): 733–736. doi:10.1111/dmcn.12777. PMID 25913846. S2CID 38835893.
Stevenson DA, Allen S, Tidyman WE, Carey JC, Viskochil DH, Stevens A, et al. (September 2012). "Peripheral muscle weakness in RASopathies". Muscle & Nerve. 46 (3): 394–399. doi:10.1002/mus.23324. PMID 22907230. S2CID 21120799.
Hyman SL, Shores A, North KN (October 2005). "The nature and frequency of cognitive deficits in children with neurofibromatosis type 1". Neurology. 65 (7): 1037–1044. doi:10.1212/01.wnl.0000179303.72345.ce. PMID 16217056. S2CID 10198510.
Hyman SL, Gill DS, Shores EA, Steinberg A, Joy P, Gibikote SV, et al. (April 2003). "Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1". Neurology. 60 (7): 1139–1145. doi:10.1212/01.WNL.0000055090.78351.C1. PMID 12682321. S2CID 26812237.
Garg S, Lehtonen A, Huson SM, Emsley R, Trump D, Evans DG, et al. (February 2013). "Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based study". Developmental Medicine and Child Neurology. 55 (2): 139–145. doi:10.1111/dmcn.12043. PMID 23163236. S2CID 11781870.
Thompson HL, Viskochil DH, Stevenson DA, Chapman KL (February 2010). "Speech-language characteristics of children with neurofibromatosis type 1". American Journal of Medical Genetics. Part A. 152A (2): 284–290. doi:10.1002/ajmg.a.33235. PMID 20101681. S2CID 26650152.
van der Vaart T, van Woerden GM, Elgersma Y, de Zeeuw CI, Schonewille M (June 2011). "Motor deficits in neurofibromatosis type 1 mice: the role of the cerebellum". Genes, Brain and Behavior. 10 (4): 404–409. doi:10.1111/j.1601-183X.2011.00685.x. PMID 21352477. S2CID 19609654.
Vivarelli R, Grosso S, Calabrese F, Farnetani M, Di Bartolo R, Morgese G, et al. (May 2003). "Epilepsy in neurofibromatosis 1". Journal of Child Neurology. 18 (5): 338–342. doi:10.1177/08830738030180050501. PMID 12822818. S2CID 39229702.
Berardelli I, Maraone A, Belvisi D, Pasquini M, Giustini S, Miraglia E, et al. (November 2021). "The importance of suicide risk assessment in patients affected by neurofibromatosis". International Journal of Psychiatry in Clinical Practice. 25 (4): 350–355. doi:10.1080/13651501.2021.1921217. PMID 34270353. S2CID 235999769.
Brar KS, Trivedi C, Kaur N, Adnan M, Patel H, Beg U, et al. (October 2023). "Prevalence of Psychiatric Comorbidities in Patients With Neurofibromatosis". The Primary Care Companion for CNS Disorders. 25 (5): 49254. doi:10.4088/PCC.23m03514. PMID 37816254. S2CID 263240202.
Pasmant E, Sabbagh A, Spurlock G, Laurendeau I, Grillo E, Hamel MJ, et al. (June 2010). "NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype". Human Mutation. 31 (6): E1506 – E1518. doi:10.1002/humu.21271. PMID 20513137. S2CID 24525378.
Coltin H, Perreault S, Larouche V, Black K, Wilson B, Vanan MI, et al. (August 2022). "Selumetinib for symptomatic, inoperable plexiform neurofibromas in children with neurofibromatosis type 1: A national real-world case series". Pediatric Blood & Cancer. 69 (8): e29633. doi:10.1002/pbc.29633. PMID 35289492. S2CID 247453317.

uchospitals.edu

"About Neurofibromatosis – The University of Chicago Medicine". www.uchospitals.edu. Archived from the original on 2015-09-07. Retrieved 2015-10-27.

ucsc.edu

genome.ucsc.edu

"Human Gene NF1 (uc002hgf.1) Description and Page Index"

web.archive.org

"About Neurofibromatosis – The University of Chicago Medicine". www.uchospitals.edu. Archived from the original on 2015-09-07. Retrieved 2015-10-27.
"NF1 | Children's Tumor Foundation". Archived from the original on 2021-10-21. Retrieved 2016-10-25.
Viskochil D (2010). "Neurofibromatosis 1: Current Issues in Diagnosis, Therapy, and Patient Management" (PDF). Mountain States Genetic Foundation. Denver. Archived from the original (PDF) on 2015-11-06. Retrieved 2011-05-15.
Klesse L (2010). "Current Therapies for Neurofibromatosis Type 1" (PDF). Mountain States Genetic Foundation. Denver. Archived from the original (PDF) on 2012-03-09. Retrieved 2011-05-15.
"Northwestern Health Sciences University ~ Diagnosis and Discussion". www.nwhealth.edu. Archived from the original on 2016-03-04. Retrieved 2015-10-27.
Blackburn-Starzan A (9 June 2008). "British couple successfully screens out genetic disorder using NHS-funded PGD". BioNews. Archived from the original on March 30, 2016. Retrieved May 16, 2011.
"FDA approves mirdametinib for adult and pediatric patients with neurofibromatosis type 1 who have symptomatic plexiform neurofibromas not amenable to complete resection". U.S. Food and Drug Administration (FDA). 11 February 2025. Archived from the original on 13 February 2025. Retrieved 16 February 2025. This article incorporates text from this source, which is in the public domain.

wikimedia.org

commons.wikimedia.org

- Source for main symptoms: "Neurofibromatosis". Mayo Clinic. 2021-01-21.
- Image by Mikael Häggström, MD, using source images by various authors.

wiley.com

onlinelibrary.wiley.com

Vogel AC, Gutmann DH, Morris SM (November 2017). "Neurodevelopmental disorders in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 59 (11): 1112–1116. doi:10.1111/dmcn.13526. ISSN 0012-1622. PMID 28845518. Retrieved 2024-10-12.
Morotti H, Mastel S, Keller K, Barnard RA, Hall T, O'Roak BJ, et al. (2021). "Autism and attention-deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 63 (2): 226–232. doi:10.1111/dmcn.14558. ISSN 1469-8749. PMID 32406525.

worldcat.org

search.worldcat.org

Mutua V, Mong'are N, Bundi B, von Csefalvay C, Oriko D, Kitunguu P (September 2021). "Sudden bilateral lower limb paralysis with dural ectasia in Neurofibromatosis type 1: A case report". Medicine: Case Reports and Study Protocols. 2 (9): e0165. doi:10.1097/MD9.0000000000000165. ISSN 2691-3895.
Vogel AC, Gutmann DH, Morris SM (November 2017). "Neurodevelopmental disorders in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 59 (11): 1112–1116. doi:10.1111/dmcn.13526. ISSN 0012-1622. PMID 28845518. Retrieved 2024-10-12.
Garg S, Plasschaert E, Descheemaeker MJ, Huson S, Borghgraef M, Vogels A, et al. (2015-06-01). "Autism Spectrum Disorder Profile in Neurofibromatosis Type I". Journal of Autism and Developmental Disorders. 45 (6): 1649–1657. doi:10.1007/s10803-014-2321-5. ISSN 1573-3432. PMID 25475362. Retrieved 2024-07-23.
Lubbers K, Stijl EM, Dierckx B, Hagenaar DA, ten Hoopen LW, Legerstee JS, et al. (2022-05-16). "Autism Symptoms in Children and Young Adults With Fragile X Syndrome, Angelman Syndrome, Tuberous Sclerosis Complex, and Neurofibromatosis Type 1: A Cross-Syndrome Comparison". Frontiers in Psychiatry. 13. doi:10.3389/fpsyt.2022.852208. ISSN 1664-0640. PMC 9149157. PMID 35651825.
Morotti H, Mastel S, Keller K, Barnard RA, Hall T, O'Roak BJ, et al. (2021). "Autism and attention-deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1". Developmental Medicine & Child Neurology. 63 (2): 226–232. doi:10.1111/dmcn.14558. ISSN 1469-8749. PMID 32406525.
Lion-François L, Herbillon V, Peyric E, Mercier C, Gérard D, Ginhoux T, et al. (November 2020). "Attention and Executive Disorders in Neurofibromatosis 1: Comparison Between NF1 With ADHD Symptomatology (NF-1 + ADHD) and ADHD Per Se". Journal of Attention Disorders. 24 (13): 1807–1823. doi:10.1177/1087054717707579. ISSN 1087-0547. PMID 28587546. Retrieved 2024-10-24.