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

Year Number of Results
1984 1
1989 3
1990 2
1991 1
1992 2
1993 2
1994 2
1995 2
1996 2
1997 3
1999 1
2000 1
2002 3
2003 3
2004 7
2005 2
2006 5
2007 7
2008 3
2009 3
2010 11
2011 12
2012 14
2013 16
2014 18
2015 14
2016 18
2017 19
2018 18
2019 22
2020 28
2021 36
2022 37
2023 37
2024 13

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306 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.
The early diagnosis and treatment of vitamin B12 deficiency is crucial for significant neurological impairment and long-term prognosis. Treatment with vitamin B12 corrects these metabolic abnormalities very rapidly (within a few days). ...
The early diagnosis and treatment of vitamin B12 deficiency is crucial for significant neurological impairment and long-term prognosis …
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.
Additional important risk factors include intrauterine growth restriction, sepsis, and prolonged exposure to mechanical ventilation and supplemental oxygen. The diagnosis of BPD predicts multiple adverse outcomes including chronic respiratory impairment and neurodevelopmen …
Additional important risk factors include intrauterine growth restriction, sepsis, and prolonged exposure to mechanical ventilation and supp …
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.
Those who present with severe complications such as intestinal failure benefit from a multidisciplinary approach involving careful assessment and treatment. Studies done so far are limited in providing a long-term prognosis. Here we review some of these complications. More …
Those who present with severe complications such as intestinal failure benefit from a multidisciplinary approach involving careful assessmen …
Evaluation of Long-term Outcomes Associated With Preterm Exposure to Antenatal Corticosteroids: A Systematic Review and Meta-analysis.
Ninan K, Liyanage SK, Murphy KE, Asztalos EV, McDonald SD. Ninan K, et al. JAMA Pediatr. 2022 Jun 1;176(6):e220483. doi: 10.1001/jamapediatrics.2022.0483. Epub 2022 Jun 6. JAMA Pediatr. 2022. PMID: 35404395 Free PMC article.
RESULTS: A total of 30 studies met the inclusion criteria, and involved more than 1.25 million children who were at least 1 year of age when the outcomes were assessed. Exposure to a single course of antenatal corticosteroids for children with extremely preterm birth was a …
RESULTS: A total of 30 studies met the inclusion criteria, and involved more than 1.25 million children who were at least 1 year of age when …
Nonsyndromic Craniosynostosis.
Dempsey RF, Monson LA, Maricevich RS, Truong TA, Olarunnipa S, Lam SK, Dauser RC, Hollier LH Jr, Buchanan EP. Dempsey RF, et al. Clin Plast Surg. 2019 Apr;46(2):123-139. doi: 10.1016/j.cps.2018.11.001. Epub 2019 Jan 30. Clin Plast Surg. 2019. PMID: 30851746 Review.
Nonsyndromic craniosynostosis is most frequently associated with only 1 fused suture, creating a predictable head shape. Repair of craniosynostosis is recommended to avoid potential neurodevelopmental delay. ...
Nonsyndromic craniosynostosis is most frequently associated with only 1 fused suture, creating a predictable head shape. Repair of cr …
Fragile X Syndrome in children.
Acero-Garcés DO, Saldarriaga W, Cabal-Herrera AM, Rojas CA, Hagerman RJ. Acero-Garcés DO, et al. Colomb Med (Cali). 2023 May 20;54(2):e4005089. doi: 10.25100/cm.v54i2.5089. eCollection 2023 Apr-Jun. Colomb Med (Cali). 2023. PMID: 37664646 Free PMC article. Review.
Fragile X syndrome is the most common monogenic cause of intellectual disability and autism spectrum disorder; the diagnosis should be suspected in every patient with neurodevelopmental delay. Early interventions could improve the functional prognosis of patients with Frag …
Fragile X syndrome is the most common monogenic cause of intellectual disability and autism spectrum disorder; the diagnosis should be suspe …
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
Hiatt SM, Trajkova S, Sebastiano MR, Partridge EC, Abidi FE, Anderson A, Ansar M, Antonarakis SE, Azadi A, Bachmann-Gagescu R, Bartuli A, Benech C, Berkowitz JL, Betti MJ, Brusco A, Cannon A, Caron G, Chen Y, Cochran ME, Coleman TF, Crenshaw MM, Cuisset L, Curry CJ, Darvish H, Demirdas S, Descartes M, Douglas J, Dyment DA, Elloumi HZ, Ermondi G, Faoucher M, Farrow EG, Felker SA, Fisher H, Hurst ACE, Joset P, Kelly MA, Kmoch S, Leadem BR, Lyons MJ, Macchiaiolo M, Magner M, Mandrile G, Mattioli F, McEown M, Meadows SK, Medne L, Meeks NJL, Montgomery S, Napier MP, Natowicz M, Newberry KM, Niceta M, Noskova L, Nowak CB, Noyes AG, Osmond M, Prijoles EJ, Pugh J, Pullano V, Quélin C, Rahimi-Aliabadi S, Rauch A, Redon S, Reymond A, Schwager CR, Sellars EA, Scheuerle AE, Shukarova-Angelovska E, Skraban C, Stolerman E, Sullivan BR, Tartaglia M, Thiffault I, Uguen K, Umaña LA, van Bever Y, van der Crabben SN, van Slegtenhorst MA, Waisfisz Q, Washington C, Rodan LH, Myers RM, Cooper GM. Hiatt SM, et al. Am J Hum Genet. 2023 Feb 2;110(2):215-227. doi: 10.1016/j.ajhg.2022.12.007. Epub 2022 Dec 30. Am J Hum Genet. 2023. PMID: 36586412 Free PMC article.
All variants affect evolutionarily conserved sites, and most are predicted to damage protein structure or function. ZMYM3 is relatively intolerant to variation in the general population, is widely expressed across human tissues, and encodes a component of the KDM1A-RCOR1 c …
All variants affect evolutionarily conserved sites, and most are predicted to damage protein structure or function. ZMYM3 is relative …
Neurological Phenotype of Mowat-Wilson Syndrome.
Cordelli DM, Di Pisa V, Fetta A, Garavelli L, Maltoni L, Soliani L, Ricci E. Cordelli DM, et al. Genes (Basel). 2021 Jun 27;12(7):982. doi: 10.3390/genes12070982. Genes (Basel). 2021. PMID: 34199024 Free PMC article. Review.
The nervous system involvement is extensive and constitutes one of the main features in MWS, heavily affecting prognosis and life quality of affected individuals. This review aims to comprehensively organize and discuss the neurological and neurodevelopmental phenotype of …
The nervous system involvement is extensive and constitutes one of the main features in MWS, heavily affecting prognosis and life qua …
Newborn cytomegalovirus screening: is this the new standard?
Gantt S. Gantt S. Curr Opin Otolaryngol Head Neck Surg. 2023 Dec 1;31(6):382-387. doi: 10.1097/MOO.0000000000000925. Epub 2023 Oct 11. Curr Opin Otolaryngol Head Neck Surg. 2023. PMID: 37820202 Review.
RECENT FINDINGS: Both universal screening (testing all newborns) and targeted screening (testing triggered by failed hearing screening) for cCMV appear valuable, feasible and cost-effective, though universal screening is predicted to have greatest potential overall benefit …
RECENT FINDINGS: Both universal screening (testing all newborns) and targeted screening (testing triggered by failed hearing screening) for …
Neurodevelopment after fetal growth restriction.
Baschat AA. Baschat AA. Fetal Diagn Ther. 2014;36(2):136-42. doi: 10.1159/000353631. Epub 2013 Jul 23. Fetal Diagn Ther. 2014. PMID: 23886893 Free article. Review.
Nutritional deficiency manifested in lagging head growth is the most powerful predictor of developmental delay in all forms of FGR. Extremes of blood flow resistance and cardiovascular deterioration, prematurity and intracranial hemorrhage increase the risks for psychomoto …
Nutritional deficiency manifested in lagging head growth is the most powerful predictor of developmental delay in all forms of FGR. E …
306 results