PF Nichol, JD Tyrrell… - Journal of Surgical Research, 2011 - Elsevier Homozygous null mutation of fibroblast growth factor receptor 2 (Fgfr2IIIb) or its ligand fibroblast growth factor 10 (Fgf10) results in duodenal atresia in mice. Mutations of either of these genes in humans cause Matthew-Wood syndrome and associated duodenal stenosis. Recently, ... Related articles - All 3 versions
FS Alatas, K Masumoto, G Esumi… - Journal of Pediatric …, 2011 - journals.lww.com Background/purpose: Duodenal atresia (DA) is a well-known neonatal intestinal disease. Even after surgery, the proximal segment can continue to be severely dilated with hypoperistalsis, resulting in intestinal dysmotility problems in later life. However, no data have yet been ...
SL Castle, BJ Naik-Mathuria… - Journal of Pediatric Surgery, 2011 - Elsevier A 3010 g male infant was born at 39 weeks gestational age to a gravida 1, para 0 mother via emergency C-section because of placental abruption. Prenatal ultrasound had demonstrated evidence of duodenal obstruction and polyhydramnios at 24 weeks gestational age but ...
H Lehnen, G Schwennicke, W Rommen… - … fur Geburtshilfe und …, 2011 - ncbi.nlm.nih.gov A double-bubble sign was detected by ultrasonography in a GII, PII, who suffers from Ehlers-Danlos syndrome type II. The delivery was done by Caesarean section based on the suspicion of premature placental separation. Postnatally, the child was found to have ...
C Keys, N Makkar, T Clarnette… - Journal of pediatric …, 2011 - ncbi.nlm.nih.gov ... Double duodenalatresia with perforation: a case report. Keys C, Makkar N, Clarnette T, Muthucumaru M, Cheng W. Duodenalatresia is a common cause of neonatal bowel obstruction. Double duodenalatresia has been reported as a rare variation of duodenalatresia. ... All 4 versions
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