Results 31 to 40 of about 12,209 (257)

Endocrine cells in atresic chick embryo intestine: histochemical and immunohistochemical study

European Journal of Histochemistry, 2009
Intestinal motility disorders are an important problem in the postoperative management of patients with intestinal atresia. Intestinal motility could be initiated by luminal factors that activate intrinsic and extrinsic primary afferent nerves involved ...
R. Vaccaro, E. Parisi Salvi, I. Nofroni, I. D’Este, S.M. Baglaj, T. Renda   +5 more
doaj   +3 more sources

Evaluation of intestinal damage biomarkers in calves with atresia coli

Journal of Veterinary Research, 2018
Intestinal obstruction such as atresia coli causes pathophysiological changes in gastrointestinal tissue due to the rise of intra-abdominal pressure. The aim of this study is to determine the intestinal damage with intestinal biomarkers in calves with ...
Yildiz Ramazan, Ok Mahmut, Ider Merve, Aydogdu Ugur, Naseri Amir, Parlak Kurtulus, Gulersoy Erdem   +6 more
doaj   +1 more source

Ileocecal valve atresia with volvulus

Journal of Pediatric Surgery Case Reports, 2022
Atresia of the ileocecal valve is a very rare etiology of neonatal intestinal obstruction. We report the case of a newborn who presents a neonatal occlusion in whom the exploration has found a volvulus of the last intestinal loop and the cecum which were
Hicham Ajdar, Abdelhalim Mahmoudi, Othmane Alaoui, Khalid Khattala, Youssef Bouabdallah   +4 more
doaj   +1 more source

Delayed diagnosis of Hirschsprung's disease associated with colonic atresia and multiple anomalies: Report of a case and review of the literature

Journal of Pediatric Surgery Case Reports, 2016
The co-occurrence of colonic atresia and Hirschsprung's disease is extremely rare and presents a diagnostic and therapeutic challenge. Although colonic atresia is usually recognized shortly after birth, the diagnosis of co-existent Hirschsprung's disease
Jinyoung Park
doaj   +1 more source

Real‐Time and High‐Resolution NIR‐II‐L Imaging of Netrin‐1‐Mediated Neurovascular Coupling Driven by Dose‐Dependent Electroacupuncture

Advanced Science, EarlyView.
Disrupted neurovascular coupling contributes to ovarian dysfunction in polycystic ovary syndrome. Using near‑infrared II long‑wavelength imaging, this study visualizes how electroacupuncture dynamically regulates ovarian blood vessels in vivo. Immediate and cumulative stimulation elicit distinct vascular responses via a Netrin‐1 dependent mechanism ...
Yicong Wang, Zi‐Han Chen, Jiajia Li, Wei Hu, Ying Cao, Yu Wang, Xiaoyu Tong, Wenhan Lu, Yuze Yang, Yuehao Wang, Yan Xiao, Wenhao Gao, Yuning Chen, Yuyan Hou, Fan Zhang, Yi Feng   +15 more
wiley   +1 more source

CURRENT ISSUES OF NEWBORN CARE IN SURGICAL DISEASES

Медицинский вестник Юга России, 2015
Purpose: to identify the trigger group nosology in newborns, acting on which it is possible to reduce infant mortality and to assess the links between the development of complications and the period from birth to transfer to the surgical ward in ...
T. U. Bykovskaya, M. A. Shishov
doaj   +1 more source

Ileal atresia concurrent with agenesis of the ileocaecal valve and intestinal volvulus in a goat kid [PDF]

Bulgarian Journal of Veterinary Medicine, 2017
Atresia of the distal ileum concurrent with ileocaecal valve agenesis is one of the rare types of intestinal atresia with very few reports in the literature. We herein present a case of type II distal ileal atresia, ileocaecal valve agenesis and volvulus
R. Kheirandish, J. Tajik
doaj   +1 more source

Annual Report of the 2022 National Clinical Database: Decade‐Long Trends and Current Status of Gastroenterological Surgery in Japan

Annals of Gastroenterological Surgery, EarlyView.
ABSTRACT Aim The National Clinical Database (NCD) of Japan is the largest nationwide registry, covering over 95% of surgeries in the country. This 2022 annual report summarizes the short‐term outcomes of gastroenterological surgeries and discusses trends and insights over the past decade.
Koshi Kumagai, Arata Takahashi, Hideki Ueno, Naoki Hiki, Yoshiki Kajiwara, Tomoki Ebata, Takao Otsuka, Taro Oshikiri, Yoshihiro Kakeji, Takanori Goi, Akio Saiura, Hiroshi Saeki, Chie Tanaka, Masanori Tokunaga, Tsutomu Fujii, Satoru Matsuda, Tsunekazu Mizushima, Hiroyuki Yamamoto, Yuko Kitagawa, Ken Shirabe   +19 more
wiley   +1 more source

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss, Amanda V. Karam, Julia Shalen, David E. Tunkel, Belina Y. Yi, Kelsey S. Guthrie, Emily M. Kudalkar, Anna E. Patrick, Sonja A. Rasmussen   +8 more
wiley   +1 more source

Complicated Intestinal Atresias

Annals of Surgery, 1979
In this group of 45 intestinal atresia patients (duodenum, 16; jejunum, 24; ileum five) at the University of Mississippi Medical Center, individual hospitalizations ranged up to 245 days. Twelve patients required multiple operations, and the overall mortality rate was 22% (ten patients).
openaire   +3 more sources