Results 121 to 130 of about 6,343 (196)

A case of mosaic Goltz syndrome in a male baby: Where persistence pays off. [PDF]

JAAD Case Rep
Gillespie Y, Colao B, Boothe M, Ahmad A, Motaparthi K, Joseph Lavery M.   +5 more
europepmc   +1 more source

Patient-Reported Long-Term Gastrointestinal Outcomes in Children with Omphalocele and Gastroschisis: A PedsQL GI Module Study. [PDF]

Eur J Pediatr Surg
Hogerwerf M, Pijpers AGH, Gorter RR, Koot BGP, Koppen IJN, Tabbers MM, Derikx JPM.   +6 more
europepmc   +1 more source

ERNICA evidence based guideline on omphalocele. [PDF]

Orphanet J Rare Dis
Irvine W, Kamp LMV, Spivack O, Wijnen R, Sgrò A, Brendel J, Zahn K, Matthyssens L, Gustafson E, Røkkum H, Migliazza L, Sfeir R, Mutanen A, Rolle U, Dariel A, Miserez M, Lukosiute-Urboniene A, Vivanti A, Peters N, Conner P, Machtejevienė E, Russo F, Torres AS, Kokešová A, Stensvold HJ, Kipfmueller F, Boukhris MR, Tognon C, Eaton S, den Uijl I, Benachi A, Burgos CM.   +31 more
europepmc   +1 more source

Case Report: Staged surgical repair and negative pressure wound therapy in congenital omphalocele. [PDF]

Front Pediatr
Misticoni F, Chiavaroli V, Cauzzo C, Scarponcini Fornaro D, Miscia ME, Fusillo M, Lisi G, Chiarelli F, Di Valerio S.   +8 more
europepmc   +1 more source

Enhancing rare disease guideline development with real-world data: a method evaluation. [PDF]

BMC Med Res Methodol
Irvine W, van der Kamp LM, Spivack O, Benachi A, Mesas Burgos C, Bakx R, Gaasterland C, Wijnen R.   +7 more
europepmc   +1 more source

Omphalocele

, 2017
openaire   +2 more sources

Prenatal Ultrasound Diagnosis of Complete Pentalogy of Cantrell: A Case Report. [PDF]

Cureus
Jain D, Mundada SM, Mundada M, Bandreddi LSG, Barre T.   +4 more
europepmc   +1 more source

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