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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1989 3
1990 2
1991 1
1992 1
1993 3
1994 2
1995 2
1996 1
1997 1
1999 5
2000 4
2001 3
2002 3
2003 3
2004 5
2005 3
2006 5
2007 10
2008 6
2009 6
2010 10
2011 11
2012 13
2013 21
2014 27
2015 21
2016 30
2017 28
2018 38
2019 36
2020 53
2021 59
2022 77
2023 82
2024 26

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503 results

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Page 1
Vitamin B12 deficiency: case report and review of literature.
Hasbaoui BE, Mebrouk N, Saghir S, Yajouri AE, Abilkassem R, Agadr A. Hasbaoui BE, et al. Pan Afr Med J. 2021 Mar 4;38:237. doi: 10.11604/pamj.2021.38.237.20967. eCollection 2021. Pan Afr Med J. 2021. PMID: 34046142 Free PMC article. Review.
Vitamin B12 deficiency in early childhood is an important cause of neurodevelopmental delay and regression. Most of these cases occur in exclusively breast-fed infants of deficient mothers. ...
Vitamin B12 deficiency in early childhood is an important cause of neurodevelopmental delay and regression. Most of these case …
Necrotizing Enterocolitis: Long Term Complications.
Bazacliu C, Neu J. Bazacliu C, et al. Curr Pediatr Rev. 2019;15(2):115-124. doi: 10.2174/1573396315666190312093119. Curr Pediatr Rev. 2019. PMID: 30864508 Review.
Necrotizing enterocolitis (NEC) remains the most threatening gastrointestinal complication of prematurity leading to high mortality, morbidity and cost. Common complications of NEC include neurodevelopmental delay, failure to thrive, gastrointestinal problems includ …
Necrotizing enterocolitis (NEC) remains the most threatening gastrointestinal complication of prematurity leading to high mortality, morbidi …
Epidemiology of bronchopulmonary dysplasia.
Jensen EA, Schmidt B. Jensen EA, et al. Birth Defects Res A Clin Mol Teratol. 2014 Mar;100(3):145-57. doi: 10.1002/bdra.23235. Epub 2014 Mar 17. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24639412 Free PMC article. Review.
The diagnosis of BPD predicts multiple adverse outcomes including chronic respiratory impairment and neurodevelopmental delay. This review summarizes the diagnostic criteria, incidence, risk factors, and long-term outcomes of BPD....
The diagnosis of BPD predicts multiple adverse outcomes including chronic respiratory impairment and neurodevelopmental delay. …
Neonatal Hypernatremic Dehydration.
Sarin A, Thill A, Yaklin CW. Sarin A, et al. Pediatr Ann. 2019 May 1;48(5):e197-e200. doi: 10.3928/19382359-20190424-01. Pediatr Ann. 2019. PMID: 31067335 Review.
Several small studies have documented varying degrees of neurodevelopmental delay on long-term follow-up of patients admitted for hypernatremic dehydration treatment as a neonate. ...
Several small studies have documented varying degrees of neurodevelopmental delay on long-term follow-up of patients admitted …
A developmental and genetic classification for malformations of cortical development: update 2012.
Barkovich AJ, Guerrini R, Kuzniecky RI, Jackson GD, Dobyns WB. Barkovich AJ, et al. Brain. 2012 May;135(Pt 5):1348-69. doi: 10.1093/brain/aws019. Epub 2012 Mar 16. Brain. 2012. PMID: 22427329 Free PMC article. Review.
Malformations of cerebral cortical development include a wide range of developmental disorders that are common causes of neurodevelopmental delay and epilepsy. In addition, study of these disorders contributes greatly to the understanding of normal brain development …
Malformations of cerebral cortical development include a wide range of developmental disorders that are common causes of neurodevelopment …
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.
Le Duc D, Giulivi C, Hiatt SM, Napoli E, Panoutsopoulos A, Harlan De Crescenzo A, Kotzaeridou U, Syrbe S, Anagnostou E, Azage M, Bend R, Begtrup A, Brown NJ, Büttner B, Cho MT, Cooper GM, Doering JH, Dubourg C, Everman DB, Hildebrand MS, Santos FJR, Kellam B, Keller-Ramey J, Lemke JR, Liu S, Niyazov D, Payne K, Person R, Quélin C, Schnur RE, Smith BT, Strober J, Walker S, Wallis M, Walsh L, Yang S, Yuen RKC, Ziegler A, Sticht H, Pride MC, Orosco L, Martínez-Cerdeño V, Silverman JL, Crawley JN, Scherer SW, Zarbalis KS, Jamra R. Le Duc D, et al. Brain. 2019 Sep 1;142(9):2617-2630. doi: 10.1093/brain/awz198. Brain. 2019. PMID: 31327001 Free PMC article.
The underpinnings of mild to moderate neurodevelopmental delay remain elusive, often leading to late diagnosis and interventions. ...Overlapping symptoms included neurodevelopmental delay, intellectual disability, macrocephaly, and psychiatric disorder …
The underpinnings of mild to moderate neurodevelopmental delay remain elusive, often leading to late diagnosis and interventio …
Zika virus infection in pregnant women and their children: A review.
Marbán-Castro E, Goncé A, Fumadó V, Romero-Acevedo L, Bardají A. Marbán-Castro E, et al. Eur J Obstet Gynecol Reprod Biol. 2021 Oct;265:162-168. doi: 10.1016/j.ejogrb.2021.07.012. Epub 2021 Jul 9. Eur J Obstet Gynecol Reprod Biol. 2021. PMID: 34508989 Free article. Review.
Normocephalic children born to mothers with ZIKV infection in pregnancy, and with no observable Zika-associated birth defects, may also present with later neurodevelopmental delay or post-natal microcephaly. Screening and detection of ZIKV infection in pregnancy is …
Normocephalic children born to mothers with ZIKV infection in pregnancy, and with no observable Zika-associated birth defects, may also pres …
Mitochondrial encephalomyopathy.
Ng YS, McFarland R. Ng YS, et al. Handb Clin Neurol. 2023;195:563-585. doi: 10.1016/B978-0-323-98818-6.00025-X. Handb Clin Neurol. 2023. PMID: 37562887 Review.
Patients with mitochondrial disease can present at any age, ranging from neonatal onset to late adult life, with variable organ involvement and neurological manifestations including neurodevelopmental delay, seizures, stroke-like episodes, movement disorders, optic …
Patients with mitochondrial disease can present at any age, ranging from neonatal onset to late adult life, with variable organ involvement …
O'Donnell-Luria-Rodan syndrome: description of a second multinational cohort and refinement of the phenotypic spectrum.
Velmans C, O'Donnell-Luria AH, Argilli E, Tran Mau-Them F, Vitobello A, Chan MC, Fung JL, Rech M, Abicht A, Aubert Mucca M, Carmichael J, Chassaing N, Clark R, Coubes C, Denommé-Pichon AS, de Dios JK, England E, Funalot B, Gerard M, Joseph M, Kennedy C, Kumps C, Willems M, van de Laar IMBH, Aarts-Tesselaar C, van Slegtenhorst M, Lehalle D, Leppig K, Lessmeier L, Pais LS, Paterson H, Ramanathan S, Rodan LH, Superti-Furga A, Chung BHY, Sherr E, Netzer C, Schaaf CP, Erger F. Velmans C, et al. J Med Genet. 2022 Jul;59(7):697-705. doi: 10.1136/jmedgenet-2020-107470. Epub 2021 Jul 28. J Med Genet. 2022. PMID: 34321323 Free PMC article.
It seems likely that ODLURO, although just recently described, is among the more common single-gene aetiologies of neurodevelopmental delay and ASD. We present the second systematic case series of patients with ODLURO, further refining the mutational and phenotypic …
It seems likely that ODLURO, although just recently described, is among the more common single-gene aetiologies of neurodevelopmental …
Benign paroxysmal torticollis.
Yates T. Yates T. Handb Clin Neurol. 2023;198:241-247. doi: 10.1016/B978-0-12-823356-6.00013-5. Handb Clin Neurol. 2023. PMID: 38043967
503 results