Hurler syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hurler syndrome" in English language version.

refsWebsite

Global rank English rank

12nih.gov

4^th place

7doi.org

2^nd place

2semanticscholar.org

11^th place

8^th place

1medscape.com

719^th place

636^th place

1clinicaltrials.gov

5,225^th place

4,062^nd place

1whonamedit.com

2,888^th place

2,730^th place

1zenodo.org

621^st place

380^th place

clinicaltrials.gov

"Ascending Dose Study of Genome Editing by the Zinc Finger Nuclease (ZFN) Therapeutic SB-318 in Subjects With MPS I". clinicaltrials.gov. U.S. National Library of Medicine. Retrieved 7 February 2019.

doi.org

Myer CM (July 1991). "Airway obstruction in Hurler's syndrome--radiographic features". International Journal of Pediatric Otorhinolaryngology. 22 (1): 91–6. doi:10.1016/0165-5876(91)90101-g. PMID 1917344.
Moore D, Connock MJ, Wraith E, Lavery C (September 2008). "The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK". Orphanet Journal of Rare Diseases. 3: 24. doi:10.1186/1750-1172-3-24. PMC 2553763. PMID 18796143.
Chkioua L, Boudabous H, Jaballi I, Grissa O, Turkia HB, Tebib N, Laradi S (May 2018). "Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome". Diagnostic Pathology. 13 (1). BioMed Central: 35. doi:10.1186/s13000-018-0710-3. PMC 5975427. PMID 29843745.
Peters C, Shapiro EG, Anderson J, Henslee-Downey PJ, Klemperer MR, Cowan MJ, et al. (April 1998). "Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group". Blood. 91 (7): 2601–8. doi:10.1182/blood.V91.7.2601. PMID 9516162.
Staba SL, Escolar ML, Poe M, Kim Y, Martin PL, Szabolcs P, et al. (May 2004). "Cord-blood transplants from unrelated donors in patients with Hurler's syndrome". The New England Journal of Medicine. 350 (19): 1960–9. doi:10.1056/NEJMoa032613. PMID 15128896. S2CID 43572313.
Ponder KP, Haskins ME (September 2007). "Gene therapy for mucopolysaccharidosis". Expert Opinion on Biological Therapy. 7 (9): 1333–45. doi:10.1517/14712598.7.9.1333. PMC 3340574. PMID 17727324.
Hurler, G. (1919). "Über einen Typ multipler Abartungen, vorwiegend am Skelettsystem". Zeitschrift für Kinderheilkunde. 24 (5–6): 220–234. doi:10.1007/BF02222956. S2CID 34471544.

medscape.com

emedicine.medscape.com

Banikazemi M (12 Oct 2014). "Hurler syndrome, Hurler-Scheie Syndrome, and Scheie Syndrome (Mucopolysaccharidosis Type I)". Medscape. Retrieved 10 May 2018.

nih.gov

pubmed.ncbi.nlm.nih.gov

Myer CM (July 1991). "Airway obstruction in Hurler's syndrome--radiographic features". International Journal of Pediatric Otorhinolaryngology. 22 (1): 91–6. doi:10.1016/0165-5876(91)90101-g. PMID 1917344.
Moore D, Connock MJ, Wraith E, Lavery C (September 2008). "The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK". Orphanet Journal of Rare Diseases. 3: 24. doi:10.1186/1750-1172-3-24. PMC 2553763. PMID 18796143.
Chkioua L, Boudabous H, Jaballi I, Grissa O, Turkia HB, Tebib N, Laradi S (May 2018). "Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome". Diagnostic Pathology. 13 (1). BioMed Central: 35. doi:10.1186/s13000-018-0710-3. PMC 5975427. PMID 29843745.
Peters C, Shapiro EG, Anderson J, Henslee-Downey PJ, Klemperer MR, Cowan MJ, et al. (April 1998). "Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group". Blood. 91 (7): 2601–8. doi:10.1182/blood.V91.7.2601. PMID 9516162.
Staba SL, Escolar ML, Poe M, Kim Y, Martin PL, Szabolcs P, et al. (May 2004). "Cord-blood transplants from unrelated donors in patients with Hurler's syndrome". The New England Journal of Medicine. 350 (19): 1960–9. doi:10.1056/NEJMoa032613. PMID 15128896. S2CID 43572313.
Ponder KP, Haskins ME (September 2007). "Gene therapy for mucopolysaccharidosis". Expert Opinion on Biological Therapy. 7 (9): 1333–45. doi:10.1517/14712598.7.9.1333. PMC 3340574. PMID 17727324.

ncbi.nlm.nih.gov

Moore D, Connock MJ, Wraith E, Lavery C (September 2008). "The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK". Orphanet Journal of Rare Diseases. 3: 24. doi:10.1186/1750-1172-3-24. PMC 2553763. PMID 18796143.
Chkioua L, Boudabous H, Jaballi I, Grissa O, Turkia HB, Tebib N, Laradi S (May 2018). "Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome". Diagnostic Pathology. 13 (1). BioMed Central: 35. doi:10.1186/s13000-018-0710-3. PMC 5975427. PMID 29843745.
Ponder KP, Haskins ME (September 2007). "Gene therapy for mucopolysaccharidosis". Expert Opinion on Biological Therapy. 7 (9): 1333–45. doi:10.1517/14712598.7.9.1333. PMC 3340574. PMID 17727324.

ghr.nlm.nih.gov

"IDUA gene". Genetics Home Reference. 11 June 2019. Retrieved 18 June 2019.
"Mucopolysaccharidosis type I". Genetics Home Reference. Retrieved 10 May 2018.

ninds.nih.gov

"Mucopolysaccharidoses Fact Sheet". National Institute of Neurological Disorders and Stroke. 15 Nov 2017. Retrieved 11 May 2018.

semanticscholar.org

api.semanticscholar.org

Staba SL, Escolar ML, Poe M, Kim Y, Martin PL, Szabolcs P, et al. (May 2004). "Cord-blood transplants from unrelated donors in patients with Hurler's syndrome". The New England Journal of Medicine. 350 (19): 1960–9. doi:10.1056/NEJMoa032613. PMID 15128896. S2CID 43572313.
Hurler, G. (1919). "Über einen Typ multipler Abartungen, vorwiegend am Skelettsystem". Zeitschrift für Kinderheilkunde. 24 (5–6): 220–234. doi:10.1007/BF02222956. S2CID 34471544.

whonamedit.com

Hurler's syndrome at Who Named It?

zenodo.org

Hurler, G. (1919). "Über einen Typ multipler Abartungen, vorwiegend am Skelettsystem". Zeitschrift für Kinderheilkunde. 24 (5–6): 220–234. doi:10.1007/BF02222956. S2CID 34471544.