Results 101 to 110 of about 19,416 (274)

Distribution of carbon monoxide-producing neurons in human colon and in Hirschsprung's disease patients [PDF]

, 2002
Hirschsprung's disease (HSCR) is characterized by the absence of ganglion cells and impaired relaxation of the gut. Nitric oxide (NO) and, more recently, carbon monoxide (CO) have been identified as inhibitory neurotransmitters causing relaxation.
Chen, Y, Lui, VCH, Sham, MH, Tam, PKH
core   +1 more source

Estenose hipertrófica congênita do piloto: estudo de 10 casos. [PDF]

, 1982
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Miranda, Gisele Faraco
core  

Capsule endoscopy assisted by traditional upper endoscopy [PDF]

, 2008
BACKGROUND AND AIMS: Capsule endoscopy (CE) can be prevented by difficulties in swallowing the device and/or its gastric retention. In such cases, endoscopic delivery of the capsule to duodenum is very useful.
Almeida, N, Figueiredo, P, Freire, P, Gouveia, H, Leitão, M, Lopes, S, Lérias, C   +6 more
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Stomach and First Part of Duodenum from Case of Hypertrophic Pyloric Stenosis Removed Seventeen Days after Rammstedt's Operation [PDF]

, 1924
C. Max Page
openalex   +1 more source

Incomplete Annular Pancreas with Ectopic Opening of the Pancreatic and Bile Ducts into the Pyloric Ring: First Report of a Rare Anomaly

Case Reports in Gastroenterology, 2016
The patient was a 56-year-old woman who had experienced epigastralgia and dorsal pain several times over the last 20 years. She was admitted for a diagnosis of acute cholecystitis, and severe intra- and extrahepatic bile duct dilatation with inner air ...
Shinjiro Kobayashi, Horoyuki Hoshino, Kouhei Segami, Satoshi Koizumi, Nobuyuki Ooike, Takehito Otsubo   +5 more
doaj   +1 more source

Wolff-Parkinson-White syndrome in an adolescent with depression [PDF]

, 2016
Wolff-Parkinson-White (WPW) syndrome is a congenital disorder characterised by a macro-reentrant arrhythmia caused by preexcitation of the ventricles.
Chen, Fei, D'Andrea, Géraldine, Eap Chin, B., Grandjean, Christophe, Richard, Sandra   +4 more
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Comprehensive clinical and molecular analysis of 12 families with type 1 recessive cutis laxa. [PDF]

, 2013
Autosomal recessive cutis laxa type I (ARCL type I) is characterized by generalized cutis laxa with pulmonary emphysema and/or vascular complications. Rarely, mutations can be identified in FBLN4 or FBLN5.
Bresson, J.L., Callewaert, B., Coucke, P.J., Davis, E.C., De Almeida, S., De Paepe, A., Gaspar, H., Gosendi, M.E., Heimdal, K., Kornak, U., Lee, J.G., Mac Neal, M., Madan-Khetarpal, S., Malfait, F., Mansour, S., Piérard, G.E., Prescott, K., Salhi, A., Schulz, B., Sciurba, F.C., Su, C.T., Symoens, S., Unger, S., Urban, Z., Van Damme, T., Van Maldergem, L., Vanakker, O., Vlummens, P.   +27 more
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CONGENITAL HYPERTROPHIC PYLORIC STENOSIS AND ITS TREATMENT BY ATROPIN [PDF]

, 1922
Sidney V. Haas
openalex   +1 more source

Late-Onset Hypertrophic Pyloric Stenosis in a 14-Weeks-Old Full Term Male Infant

Acta Medica, 2019
Background: Hypertrophic pyloric stenosis is the most common cause of gastric outlet obstruction in infants, and classically presents at 2 to 6 weeks of age. Delayed presentation is an extremely rare occurrence after early infancy.
Zenon Pogorelić, Ivana Čulo Čagalj, Vanda Žitko, Ana Nevešćanin, Vjekoslav Krželj   +4 more
doaj   +1 more source

Fetuses with right aortic arch Multicentre cohort study and meta-analysis. [PDF]

, 2016
OBJECTIVES: Recent antenatal screening guidelines for cardiac abnormalities has increased fetal diagnosis of right aortic arch (RAA). We aimed to establish outcome of fetal RAA without intra-cardiac abnormalities (ICA) to guide postnatal management ...
Carvalho, JS, D'Antonio, F, Khalil, A, Zidere, V   +3 more
core   +1 more source