神经发育障碍 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "神经发育障碍" in Chinese language version.

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36doi.org

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34nih.gov

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13web.archive.org

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8semanticscholar.org

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6archive.org

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4worldcat.org

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1neuroci.com

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1nads.org

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archive.org

Reynolds CR, Goldstein S. Handbook of neurodevelopmental and genetic disorders in children. New York: The Guilford Press. 1999: 3–8. ISBN 978-1-57230-448-2.
Merla G, Howald C, Henrichsen CN, Lyle R, Wyss C, Zabot MT, et al. Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes. American Journal of Human Genetics. August 2006, 79 (2): 332–41. PMC 1559497 . PMID 16826523. doi:10.1086/506371.
Brown AS. Prenatal infection as a risk factor for schizophrenia. Schizophrenia Bulletin. April 2006, 32 (2): 200–202. PMC 2632220 . PMID 16469941. doi:10.1093/schbul/sbj052.
Northam EA, Anderson PJ, Jacobs R, Hughes M, Warne GL, Werther GA. Neuropsychological profiles of children with type 1 diabetes 6 years after disease onset. Diabetes Care. September 2001, 24 (9): 1541–6. PMID 11522696. doi:10.2337/diacare.24.9.1541 .
Olsson GM, Hulting AL, Montgomery SM. Cognitive function in children and subsequent type 2 diabetes. Diabetes Care. March 2008, 31 (3): 514–6. PMC 2453642 . PMID 18083794. doi:10.2337/dc07-1399. ^{[永久失效連結]}
Lee PJ, Ridout D, Walter JH, Cockburn F. Maternal phenylketonuria: report from the United Kingdom Registry 1978-97. Archives of Disease in Childhood. February 2005, 90 (2): 143–6. PMC 1720245 . PMID 15665165. doi:10.1136/adc.2003.037762.

archive.today

ICD-11 for Mortality and Morbidity Statistics - Neurodevelopmental disorders. WHO. [2023-04-18]. （原始内容存档于2018-08-01）（英语）.

cdc.gov

Folic scid: topic home. Centers for Disease Control and Prevention. U.S. Department of Health and Human Services. [2008-08-02]. （原始内容存档于2021-08-26）.
The basics about spina bifida. Centers for Disease Control and Prevention. U.S. Department of Health and Human Services. [2008-08-02]. （原始内容存档于2021-08-26）.
Fetal alcohol syndrome: guidelines for referral and diagnosis (PDF). 互联网档案馆的存檔，存档日期2009-04-23. CDC (July 2004). Retrieved on 2007-04-11
Facts About TBI (PDF). U.S. Centers for Disease Control and Prevention. [2008-08-06]. （原始内容存档于2021-08-26）.

doi.org

Rutter, Michael; Cooper, Miriam; Thapar, Anita. Neurodevelopmental disorders. The Lancet Psychiatry. 2017-04-01, 4 (4): 339–346. ISSN 2215-0366. PMID 27979720. doi:10.1016/S2215-0366(16)30376-5 （英语）.
Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. March 2020, 22 (1): 65–72. ISSN 1294-8322. PMC 7365295 . PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. March 2020, 22 (1): 65–72. ISSN 1294-8322. PMC 7365295 . PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
Murray RM, Lewis SW. Is schizophrenia a neurodevelopmental disorder?. British Medical Journal. September 1987, 295 (6600): 681–2. PMC 1247717 . PMID 3117295. doi:10.1136/bmj.295.6600.681.
May, Philip A.; Chambers, Christina D.; Kalburg, Wendy O. Prevalence of Fetal Alcohol Spectrum Disorders in 4 US Communities. JAMA. 2018, 319 (5): 474–482 [28 January 2021]. PMC 5839298 . PMID 29411031. doi:10.1001/jama.2017.21896. （原始内容存档于25 January 2021）.
Mammarella IC, Cornoldi C. Nonverbal learning disability (developmental visuospatial disorder). Handbook of Clinical Neurology. 2020, 174: 83–91. ISBN 9780444641489. PMID 32977898. S2CID 221939377. doi:10.1016/B978-0-444-64148-9.00007-7.
Incháustegui MV. Nonverbal Learning Disabilities (Nld) – Clinical Description about Neurodevelopmental Disabilities. Archives in Neurology & Neuroscience. 2019-06-18, 4 (1). doi:10.33552/ANN.2019.04.000579 .
Mammarella IC, Cornoldi C. Nonverbal learning disability (developmental visuospatial disorder). Neurocognitive Development: Disorders and Disabilities. Handbook of Clinical Neurology 174. Elsevier. 2020: 83–91. ISBN 978-0-444-64148-9. PMID 32977898. S2CID 221939377. doi:10.1016/b978-0-444-64148-9.00007-7 （英语）.
Spreen, Otfried. Nonverbal learning disabilities: A critical review. Child Neuropsychology. September 2011, 17 (5): 418–443 [2021-04-29]. ISSN 0929-7049. PMID 21462003. S2CID 31974898. doi:10.1080/09297049.2010.546778. （原始内容存档于2021-07-20）（英语）.
Mammarella IC, Cornoldi C. An analysis of the criteria used to diagnose children with Nonverbal Learning Disability (NLD). Child Neuropsychology. 2014-05-04, 20 (3): 255–80,256. PMID 23705673. S2CID 34107811. doi:10.1080/09297049.2013.796920. hdl:11577/2668053.
Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. 31 March 2020, 22 (1): 65–72. PMC 7365295 . PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
Pletikos M, Sousa AM, Sedmak G, Meyer KA, Zhu Y, Cheng F, et al. Temporal specification and bilaterality of human neocortical topographic gene expression. Neuron. January 2014, 81 (2): 321–32. PMC 3931000 . PMID 24373884. doi:10.1016/j.neuron.2013.11.018.
Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. February 2005, 14 (4): 483–92. PMC 1224722 . PMID 15615769. doi:10.1093/hmg/ddi045.
van IJzendoorn MH, Palacios J, Sonuga-Barke EJ, Gunnar MR, Vorria P, McCall RB, et al. Children in Institutional Care: Delayed Development and Resilience. Monographs of the Society for Research in Child Development. December 2011, 76 (4): 8–30. PMC 4130248 . PMID 25125707. doi:10.1111/j.1540-5834.2011.00626.x.
Nelson CA, Zeanah CH, Fox NA, Marshall PJ, Smyke AT, Guthrie D. Cognitive recovery in socially deprived young children: the Bucharest Early Intervention Project. Science. December 2007, 318 (5858): 1937–40. Bibcode:2007Sci...318.1937N. PMID 18096809. S2CID 1460630. doi:10.1126/science.1143921. ^{[永久失效連結]}
Diamandopoulos K, Green J. Down syndrome: An integrative review. Journal of Neonatal Nursing. October 2018, 24 (5): 235–241. S2CID 57620027. doi:10.1016/j.jnn.2018.01.001.
Martin JP, Bell J. A pedigree of mental defect showing sex-linkage. Journal of Neurology and Psychiatry. July 1943, 6 (3–4): 154–7. PMC 1090429 . PMID 21611430. doi:10.1136/jnnp.6.3-4.154.
Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. October 1999, 23 (2): 185–8. PMID 10508514. S2CID 3350350. doi:10.1038/13810.
Merla G, Howald C, Henrichsen CN, Lyle R, Wyss C, Zabot MT, et al. Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes. American Journal of Human Genetics. August 2006, 79 (2): 332–41. PMC 1559497 . PMID 16826523. doi:10.1086/506371.
Martin CL, Ledbetter DH. Chromosomal Microarray Testing for Children With Unexplained Neurodevelopmental Disorders. JAMA. June 2017, 317 (24): 2545–2546. PMC 7058144 . PMID 28654998. doi:10.1001/jama.2017.7272.
Dale RC, Heyman I, Giovannoni G, Church AW. Incidence of anti-brain antibodies in children with obsessive-compulsive disorder. The British Journal of Psychiatry. October 2005, 187 (4): 314–9. PMID 16199788. doi:10.1192/bjp.187.4.314 .
Pavone P, Bianchini R, Parano E, Incorpora G, Rizzo R, Mazzone L, Trifiletti RR. Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection. Pediatric Neurology. February 2004, 30 (2): 107–10. PMID 14984902. doi:10.1016/S0887-8994(03)00413-2. hdl:2108/194065 .
Dale RC, Heyman I, Giovannoni G, Church AW. Incidence of anti-brain antibodies in children with obsessive-compulsive disorder. The British Journal of Psychiatry. October 2005, 187 (4): 314–9. PMID 16199788. doi:10.1192/bjp.187.4.314 .
Swedo SE. Genetics of childhood disorders: XXXIII. Autoimmunity, part 6: poststreptococcal autoimmunity.. Journal of the American Academy of Child & Adolescent Psychiatry. December 2001, 40 (12): 1479–82 [2008-08-17]. PMID 11765296. doi:10.1097/00004583-200112000-00021. （原始内容存档于2021-07-20）.
Boivin MJ, Kakooza AM, Warf BC, Davidson LL, Grigorenko EL. Reducing neurodevelopmental disorders and disability through research and interventions. Nature. November 2015, 527 (7578): S155–60. Bibcode:2015Natur.527S.155B. PMID 26580321. doi:10.1038/nature16029 .
Brown AS. Prenatal infection as a risk factor for schizophrenia. Schizophrenia Bulletin. April 2006, 32 (2): 200–202. PMC 2632220 . PMID 16469941. doi:10.1093/schbul/sbj052.
Richardson AJ, Ross MA. Fatty acid metabolism in neurodevelopmental disorder: a new perspective on associations between attention-deficit/hyperactivity disorder, dyslexia, dyspraxia and the autistic spectrum. Prostaglandins, Leukotrienes, and Essential Fatty Acids. July 2000, 63 (1–2): 1–9. PMID 10970706. doi:10.1054/plef.2000.0184.
Northam EA, Anderson PJ, Jacobs R, Hughes M, Warne GL, Werther GA. Neuropsychological profiles of children with type 1 diabetes 6 years after disease onset. Diabetes Care. September 2001, 24 (9): 1541–6. PMID 11522696. doi:10.2337/diacare.24.9.1541 .
Olsson GM, Hulting AL, Montgomery SM. Cognitive function in children and subsequent type 2 diabetes. Diabetes Care. March 2008, 31 (3): 514–6. PMC 2453642 . PMID 18083794. doi:10.2337/dc07-1399. ^{[永久失效連結]}
Ornoy A, Wolf A, Ratzon N, Greenbaum C, Dulitzky M. Neurodevelopmental outcome at early school age of children born to mothers with gestational diabetes. Archives of Disease in Childhood. Fetal and Neonatal Edition. July 1999, 81 (1): F10–4. PMC 1720965 . PMID 10375355. doi:10.1136/fn.81.1.F10.
Lee PJ, Ridout D, Walter JH, Cockburn F. Maternal phenylketonuria: report from the United Kingdom Registry 1978-97. Archives of Disease in Childhood. February 2005, 90 (2): 143–6. PMC 1720245 . PMID 15665165. doi:10.1136/adc.2003.037762.
Rouse B, Azen C, Koch R, Matalon R, Hanley W, de la Cruz F, et al. Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelae. American Journal of Medical Genetics. March 1997, 69 (1): 89–95. PMID 9066890. doi:10.1002/(SICI)1096-8628(19970303)69:1<89::AID-AJMG17>3.0.CO;2-K.
Skeaff, Sheila. Iodine Deficiency in Pregnancy: The Effect on Neurodevelopment in the Child (PDF). Nutrients. 18 February 2011, 3 (2): 265–273 [1 July 2022]. PMC 3257674 . PMID 22254096. doi:10.3390/nu3020265 . （原始内容存档 (PDF)于2022-06-15）.
Collins, Kim A.; Popek, Edwina. Birth Injury: Birth Asphyxia and Birth Trauma. Academic Forensic Pathology. December 2018, 8 (4): 788–864. PMC 6491540 . PMID 31240076. doi:10.1177/1925362118821468.
Kratimenos P, Penn AA. Placental programming of neuropsychiatric disease. Pediatric Research. August 2019, 86 (2): 157–164. PMID 31003234. S2CID 124094051. doi:10.1038/s41390-019-0405-9 .
Martin CL, Ledbetter DH. Chromosomal Microarray Testing for Children With Unexplained Neurodevelopmental Disorders. JAMA. June 2017, 317 (24): 2545–2546. PMC 7058144 . PMID 28654998. doi:10.1001/jama.2017.7272.

epa.gov

Neurodevelopmental Disorders (PDF), America's Children and the Environment 3, EPA: 12, August 2017 [2019-07-10], （原始内容存档 (PDF)于2021-07-20）

handle.net

hdl.handle.net

Mammarella IC, Cornoldi C. An analysis of the criteria used to diagnose children with Nonverbal Learning Disability (NLD). Child Neuropsychology. 2014-05-04, 20 (3): 255–80,256. PMID 23705673. S2CID 34107811. doi:10.1080/09297049.2013.796920. hdl:11577/2668053.
Pavone P, Bianchini R, Parano E, Incorpora G, Rizzo R, Mazzone L, Trifiletti RR. Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection. Pediatric Neurology. February 2004, 30 (2): 107–10. PMID 14984902. doi:10.1016/S0887-8994(03)00413-2. hdl:2108/194065 .

harvard.edu

ui.adsabs.harvard.edu

Nelson CA, Zeanah CH, Fox NA, Marshall PJ, Smyke AT, Guthrie D. Cognitive recovery in socially deprived young children: the Bucharest Early Intervention Project. Science. December 2007, 318 (5858): 1937–40. Bibcode:2007Sci...318.1937N. PMID 18096809. S2CID 1460630. doi:10.1126/science.1143921. ^{[永久失效連結]}
Boivin MJ, Kakooza AM, Warf BC, Davidson LL, Grigorenko EL. Reducing neurodevelopmental disorders and disability through research and interventions. Nature. November 2015, 527 (7578): S155–60. Bibcode:2015Natur.527S.155B. PMID 26580321. doi:10.1038/nature16029 .

jamanetwork.com

May, Philip A.; Chambers, Christina D.; Kalburg, Wendy O. Prevalence of Fetal Alcohol Spectrum Disorders in 4 US Communities. JAMA. 2018, 319 (5): 474–482 [28 January 2021]. PMC 5839298 . PMID 29411031. doi:10.1001/jama.2017.21896. （原始内容存档于25 January 2021）.

marchofdimes.org

Folic Acid. March of Dimes. [2014-11-10]. （原始内容存档于2021-08-26）.

mdpi-res.com

Skeaff, Sheila. Iodine Deficiency in Pregnancy: The Effect on Neurodevelopment in the Child (PDF). Nutrients. 18 February 2011, 3 (2): 265–273 [1 July 2022]. PMC 3257674 . PMID 22254096. doi:10.3390/nu3020265 . （原始内容存档 (PDF)于2022-06-15）.

msdmanuals.com

SULKES.STEPHEN. Definition of Developmental Disorders - Children's Health Issues. MSD Manual Consumer Version. 2019-08-22 [2019-08-23].

nads.org

Facts about down syndrome. National Association of Down Syndrome. （原始内容存档于2012-04-03）.

neuroci.com

Alzheimer's, ADHD, Autism, Brain Injury Treatment, Mood Disorders New Jersey: The NeuroCognitive and Behavioral Institute » Neurodevelopmental Disorders. [2022-04-25]. （原始内容存档于2022-03-08）（美国英语）.

nih.gov

ncbi.nlm.nih.gov

Rutter, Michael; Cooper, Miriam; Thapar, Anita. Neurodevelopmental disorders. The Lancet Psychiatry. 2017-04-01, 4 (4): 339–346. ISSN 2215-0366. PMID 27979720. doi:10.1016/S2215-0366(16)30376-5 （英语）.
Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. March 2020, 22 (1): 65–72. ISSN 1294-8322. PMC 7365295 . PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. March 2020, 22 (1): 65–72. ISSN 1294-8322. PMC 7365295 . PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
Murray RM, Lewis SW. Is schizophrenia a neurodevelopmental disorder?. British Medical Journal. September 1987, 295 (6600): 681–2. PMC 1247717 . PMID 3117295. doi:10.1136/bmj.295.6600.681.
May, Philip A.; Chambers, Christina D.; Kalburg, Wendy O. Prevalence of Fetal Alcohol Spectrum Disorders in 4 US Communities. JAMA. 2018, 319 (5): 474–482 [28 January 2021]. PMC 5839298 . PMID 29411031. doi:10.1001/jama.2017.21896. （原始内容存档于25 January 2021）.
Mammarella IC, Cornoldi C. Nonverbal learning disability (developmental visuospatial disorder). Handbook of Clinical Neurology. 2020, 174: 83–91. ISBN 9780444641489. PMID 32977898. S2CID 221939377. doi:10.1016/B978-0-444-64148-9.00007-7.
Mammarella IC, Cornoldi C. Nonverbal learning disability (developmental visuospatial disorder). Neurocognitive Development: Disorders and Disabilities. Handbook of Clinical Neurology 174. Elsevier. 2020: 83–91. ISBN 978-0-444-64148-9. PMID 32977898. S2CID 221939377. doi:10.1016/b978-0-444-64148-9.00007-7 （英语）.
Spreen, Otfried. Nonverbal learning disabilities: A critical review. Child Neuropsychology. September 2011, 17 (5): 418–443 [2021-04-29]. ISSN 0929-7049. PMID 21462003. S2CID 31974898. doi:10.1080/09297049.2010.546778. （原始内容存档于2021-07-20）（英语）.
Mammarella IC, Cornoldi C. An analysis of the criteria used to diagnose children with Nonverbal Learning Disability (NLD). Child Neuropsychology. 2014-05-04, 20 (3): 255–80,256. PMID 23705673. S2CID 34107811. doi:10.1080/09297049.2013.796920. hdl:11577/2668053.
Morris-Rosendahl, Deborah J.; Crocq, Marc-Antoine. Neurodevelopmental disorders—the history and future of a diagnostic concept. Dialogues in Clinical Neuroscience. 31 March 2020, 22 (1): 65–72. PMC 7365295 . PMID 32699506. doi:10.31887/DCNS.2020.22.1/macrocq.
Pletikos M, Sousa AM, Sedmak G, Meyer KA, Zhu Y, Cheng F, et al. Temporal specification and bilaterality of human neocortical topographic gene expression. Neuron. January 2014, 81 (2): 321–32. PMC 3931000 . PMID 24373884. doi:10.1016/j.neuron.2013.11.018.
Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. February 2005, 14 (4): 483–92. PMC 1224722 . PMID 15615769. doi:10.1093/hmg/ddi045.
van IJzendoorn MH, Palacios J, Sonuga-Barke EJ, Gunnar MR, Vorria P, McCall RB, et al. Children in Institutional Care: Delayed Development and Resilience. Monographs of the Society for Research in Child Development. December 2011, 76 (4): 8–30. PMC 4130248 . PMID 25125707. doi:10.1111/j.1540-5834.2011.00626.x.
Nelson CA, Zeanah CH, Fox NA, Marshall PJ, Smyke AT, Guthrie D. Cognitive recovery in socially deprived young children: the Bucharest Early Intervention Project. Science. December 2007, 318 (5858): 1937–40. Bibcode:2007Sci...318.1937N. PMID 18096809. S2CID 1460630. doi:10.1126/science.1143921. ^{[永久失效連結]}
Martin JP, Bell J. A pedigree of mental defect showing sex-linkage. Journal of Neurology and Psychiatry. July 1943, 6 (3–4): 154–7. PMC 1090429 . PMID 21611430. doi:10.1136/jnnp.6.3-4.154.
Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. October 1999, 23 (2): 185–8. PMID 10508514. S2CID 3350350. doi:10.1038/13810.
Merla G, Howald C, Henrichsen CN, Lyle R, Wyss C, Zabot MT, et al. Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes. American Journal of Human Genetics. August 2006, 79 (2): 332–41. PMC 1559497 . PMID 16826523. doi:10.1086/506371.
Martin CL, Ledbetter DH. Chromosomal Microarray Testing for Children With Unexplained Neurodevelopmental Disorders. JAMA. June 2017, 317 (24): 2545–2546. PMC 7058144 . PMID 28654998. doi:10.1001/jama.2017.7272.
Dale RC, Heyman I, Giovannoni G, Church AW. Incidence of anti-brain antibodies in children with obsessive-compulsive disorder. The British Journal of Psychiatry. October 2005, 187 (4): 314–9. PMID 16199788. doi:10.1192/bjp.187.4.314 .
Pavone P, Bianchini R, Parano E, Incorpora G, Rizzo R, Mazzone L, Trifiletti RR. Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection. Pediatric Neurology. February 2004, 30 (2): 107–10. PMID 14984902. doi:10.1016/S0887-8994(03)00413-2. hdl:2108/194065 .
Dale RC, Heyman I, Giovannoni G, Church AW. Incidence of anti-brain antibodies in children with obsessive-compulsive disorder. The British Journal of Psychiatry. October 2005, 187 (4): 314–9. PMID 16199788. doi:10.1192/bjp.187.4.314 .
Swedo SE. Genetics of childhood disorders: XXXIII. Autoimmunity, part 6: poststreptococcal autoimmunity.. Journal of the American Academy of Child & Adolescent Psychiatry. December 2001, 40 (12): 1479–82 [2008-08-17]. PMID 11765296. doi:10.1097/00004583-200112000-00021. （原始内容存档于2021-07-20）.
Boivin MJ, Kakooza AM, Warf BC, Davidson LL, Grigorenko EL. Reducing neurodevelopmental disorders and disability through research and interventions. Nature. November 2015, 527 (7578): S155–60. Bibcode:2015Natur.527S.155B. PMID 26580321. doi:10.1038/nature16029 .
Brown AS. Prenatal infection as a risk factor for schizophrenia. Schizophrenia Bulletin. April 2006, 32 (2): 200–202. PMC 2632220 . PMID 16469941. doi:10.1093/schbul/sbj052.
Richardson AJ, Ross MA. Fatty acid metabolism in neurodevelopmental disorder: a new perspective on associations between attention-deficit/hyperactivity disorder, dyslexia, dyspraxia and the autistic spectrum. Prostaglandins, Leukotrienes, and Essential Fatty Acids. July 2000, 63 (1–2): 1–9. PMID 10970706. doi:10.1054/plef.2000.0184.
Northam EA, Anderson PJ, Jacobs R, Hughes M, Warne GL, Werther GA. Neuropsychological profiles of children with type 1 diabetes 6 years after disease onset. Diabetes Care. September 2001, 24 (9): 1541–6. PMID 11522696. doi:10.2337/diacare.24.9.1541 .
Olsson GM, Hulting AL, Montgomery SM. Cognitive function in children and subsequent type 2 diabetes. Diabetes Care. March 2008, 31 (3): 514–6. PMC 2453642 . PMID 18083794. doi:10.2337/dc07-1399. ^{[永久失效連結]}
Ornoy A, Wolf A, Ratzon N, Greenbaum C, Dulitzky M. Neurodevelopmental outcome at early school age of children born to mothers with gestational diabetes. Archives of Disease in Childhood. Fetal and Neonatal Edition. July 1999, 81 (1): F10–4. PMC 1720965 . PMID 10375355. doi:10.1136/fn.81.1.F10.
Lee PJ, Ridout D, Walter JH, Cockburn F. Maternal phenylketonuria: report from the United Kingdom Registry 1978-97. Archives of Disease in Childhood. February 2005, 90 (2): 143–6. PMC 1720245 . PMID 15665165. doi:10.1136/adc.2003.037762.
Rouse B, Azen C, Koch R, Matalon R, Hanley W, de la Cruz F, et al. Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelae. American Journal of Medical Genetics. March 1997, 69 (1): 89–95. PMID 9066890. doi:10.1002/(SICI)1096-8628(19970303)69:1<89::AID-AJMG17>3.0.CO;2-K.
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