Results 241 to 250 of about 171,735 (299)

Neurodevelopmental assessment at 24 months in infants with esophageal atresia: A prospective cohort study

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objective To evaluate neurodevelopment at 24 months in infants surgically treated for esophageal atresia (EA), using the ages and stages questionnaire (ASQ), and identify perinatal and early‐life factors associated with developmental delay. Methods Infants with EA were prospectively enrolled in a structured multidisciplinary follow‐up program.
Julia Tagmouti, Manon Midavaine, Victor Sartorius, Nicolas Vinit, Elise Leroy‐Terquem, Sylvie Beaudoin, Elsa Kermorvant‐Duchemin, Véronique Rousseau, Alexandre Lapillonne   +8 more
wiley   +1 more source

Abortions and Congenital Malformations in Small Ruminants Associated with Toxic Plant Consumption in the Brazilian Semi-Arid Region. [PDF]

Animals (Basel)
Rocha VC, Santos Filho GJ, de Souza MF, Assis EB, da Silva MA, Sousa MS, Sousa ESS, Simões SVD, Lucena RB.   +8 more
europepmc   +1 more source

Diagnostic dilemma of cystic biliary atresia: A series of two cases and brief review of the diagnostic modalities

JPGN Reports, EarlyView.
Abstract Cystic biliary atresia (CBA) is a rare variant of biliary atresia that closely resembles choledochal cyst (CC), complicating diagnosis and potentially delaying critical surgical intervention. We report two cases of CBA that were difficult to diagnose.
Hamza Hassan Khan, Leslie Hirsig Spence, Nagraj Kasi   +2 more
wiley   +1 more source

'We are the engine': a focus group study on clinical practice guideline development with European patient advocates for rare congenital malformations and/or intellectual disability. [PDF]

Orphanet J Rare Dis
Klein Haneveld MJ, de Mortier CA, Hugon A, Cornel MC, Gaasterland CMW, van Eeghen AM.   +5 more
europepmc   +1 more source

PERCC1‐associated enteropathy: Diagnostic challenges and enteral autonomy achieved with teduglutide

JPGN Reports, EarlyView.
Abstract Congenital diarrheas and enteropathies (CODE) are rare inherited disorders characterized by early‐onset intractable diarrhea. Though progress has been made in elucidating the genetic basis of CODE, much remains to be discovered. Another challenge is the lack of curative therapies—treatment is primarily supportive including enteral and ...
Angela Tran, Vivien Nguyen, Phuong Huynh
wiley   +1 more source

Mortality in Stray Kittens under Eight Weeks Old: Focusing on Congenital Malformations. [PDF]

Vet Sci
Contreras G, Viegas C, Gama A, Silva F, Pires I.   +4 more
europepmc   +1 more source

Amniotic fluid-derived stem cells: potential factories of natural and mimetic strategies for congenital malformations. [PDF]

Stem Cell Res Ther
Fonteles CSR, Enterria-Rosales J, Lin Y, Steele JW, Villarreal-Leal RA, Xiao J, Idowu DI, Burgelin B, Wlodarczyk BJ, Finnell RH, Corradetti B.   +10 more
europepmc   +1 more source

First Trimester Tetracycline Exposure and Risk of Major Congenital Malformations.

JAMA Netw Open
Nakitanda AO, Odsbu I, Cesta CE, Pazzagli L, Pasternak B.   +4 more
europepmc   +1 more source

Hydroxychloroquine in lupus or rheumatoid arthritis pregnancy and risk of major congenital malformations: a population-based cohort study. [PDF]

Rheumatology (Oxford)
Nguyen NV, Svenungsson E, Dominicus A, Altman M, Hellgren K, Simard JF, Arkema EV.   +6 more
europepmc   +1 more source

Assessing Differential Transfusion Requirements for Children with Congenital Malformations vs. Pediatric Acute Abdomen Emergencies. [PDF]

Diagnostics (Basel)
Ionescu A, Mihăilescu A, Chiriță-Emandi A, Munagala N, David VL, Dumache R, Săndesc D, Bedreag O, Folescu R, Bratosin F, Barata PI, Cristescu DM, Săndesc MA.   +12 more
europepmc   +1 more source