Results 121 to 130 of about 9,070 (214)

Omphalocele [PDF]

, 2020
openaire   +2 more sources

Morbimortality of Newborns with Omphalocele in a Level III Neonatal Intensive Care Unit [PDF]

, 2014
Sofia Madureira Vasconcelos Lopes
core  

A novel maternally inherited CDKN1C variant in a familial beckwith-wiedemann syndrome case: expanding the genotype-phenotype spectrum. [PDF]

BMC Med Genomics
Wu S, Zhang Y, Zhang H, Yan X, Pi Y.
europepmc   +1 more source

Early postnatal C-reactive protein elevation during initial hospitalization in neonates with giant omphalocele undergoing delayed repair. [PDF]

Front Pediatr
Huang Z, Peng Y, Lv J, Zhong W, He Q.
europepmc   +1 more source

Fostering continuous quality improvement in a European rare disease network: Where are we now? [PDF]

Orphanet J Rare Dis
van der Kamp LM, Galdrán SR, Irvine WFE, Rossi D, van Steekelenburg R, ERNICA Representatives, Wijnen RMH, Ista E, Spivack OKC.   +8 more
europepmc   +1 more source

Pentalogy of Cantrell: two patients and a review to determine prognostic factors for optimal approach [PDF]

Jeroen H. L. van Hoorn, Rob M. J. Moonen, Clément J. R. Huysentruyt, L. W. Ernest van Heurn, Jos P. M. Offermans, A. L. M. Twan Mulder, HI Abdallah, A Alayunt, E Araujo Junior, A Aslan, ME Baker, RY Bhat, D Bick, S Bittmann, AJ Bogers, JR Cantrell, R Carmi, CP Chen, Y Chen, MS Correa-Rivas, FM Denath, JF Egan, JE Fox, EJ Grethel, FJ Halbertsma, LK Hornberger, YY Hsieh, W Knirsch, P Laloyaux, RI Liang, E Marijon, RA Martin, JM Morales, S Nanda, T Oka, L Onderoglu, EK Pivnick, I Polat, RM Rashid, C Siles, A Song, SP Soper, R Spencer, WM Toyama, D Uygur, JF Vazquez-Jimenez   +45 more
core   +1 more source

Proxy-reported health-related quality of life in children with omphalocele: a cross-sectional study in China. [PDF]

Transl Pediatr
Wang P, Jin H, Guan L, Gao M, Shao Y, Faizan A, Sun L, Pan T, Tou J, Bai G.   +9 more
europepmc   +1 more source

Twin paradox: Monoamniotic twin pregnancy discordant for limb body wall complex: Presentation of a rare syndrome with a review of embryology. [PDF]

Ultrasound
Varghese TA, Agarwal I, Prabhu A, Mohan V, Chandra S, Kaul A.   +5 more
europepmc   +1 more source

Prenatal detection of Gorlin-Goltz syndrome: a case report and focused review of the literature. [PDF]

Front Med (Lausanne)
Oelmeier K, Horváth J, Vogtmann R, Meyer-Wittkopf M, Möllers M, Schmitz R, Oberste KM, Willy D.   +7 more
europepmc   +1 more source

Long-term follow-up of scar quality and satisfaction after surgical closure of congenital abdominal wall defects: a single center perspective. [PDF]

Pediatr Surg Int
Reindl N, Seitz S, Schleier M, Besendörfer M, Diez S.   +4 more
europepmc   +1 more source