Results 91 to 100 of about 4,863,546 (170)

RET single nucleotide polymorphism in Indonesians with sporadic Hirschsprung’s disease

, 2016
The tyrosine kinase receptor RET, which is the protein product of the RET gene, is involved in the development of the mammalian nervous system that causes Hirschsprung’s disease (HSCR).
Wayan T Artama, Saryono Saryono, Wiryatun Lestariana, Ahmad Hamim Sadewa, Rochadi Rochadi   +4 more
core   +1 more source

Genetics of gastrointestinal disease: dismotility disorders, intestinal polyposis and gene therapy [PDF]

, 2008
Auricchio, Renata
core   +1 more source

Hirschsprung’s Disease

, 2016
Hirschsprung’s disease (HD) or “congenital megacolon” is a congenital developmental disorder characterized by the absence of ganglion cells in the distal intestine with variable proximal extension.
Teitelbaum, Daniel H., Ralls, Matthew W., Francesca Destro, Mario Lima, Arnold G. Coran, Daniel H. Teitelbaum, Destro, Francesca, Matthew W. Ralls, Coran, Arnold G., Lima, Mario   +9 more
core   +1 more source

Investigating the Diagnostic and Risk Factors for Enterocolitis in Children with Hirschsprung’s Disease

This study aimed to identify the clinical risk factors associated with Hirschsprung-associated enterocolitis (HAEC) in children with Hirschsprung’s disease (HD)
Peyvasteh M., Askarpour S., Javaherizadeh H., Mohammadi A., Soma Seyedsalehi S.   +4 more
core   +1 more source

Technical Modification of the Georgeson Procedure for Hirschsprung’s Disease: a 12 Years Experience with the Laparoscopic-Assisted Mesocolon Dissection

, 2014
Introduction: Actually the primary laparoscopic endorectal colon pull-through, reported by Georgeson, is the gold standard in the treatment of Hirschsprung’s disease.
GARGANO, TOMMASO, Randi, Beatrice, RUGGERI, GIOVANNI, Libri, Michele, Maffi, Michela, LIMA, MARIO   +5 more
core   +1 more source

Congenital central hypoventilation syndrome with hirschsprung's disease due to PHOX2B gene mutation in a Turkish infant

The Turkish Journal of Pediatrics, 2012
The association of congenital central hypoventilation syndrome (also known as Ondine's curse) and Hirschsprung's disease is termed Haddad syndrome, which is an extremely rare disorder.
Aytekin Kaymakçi, Fatma Narter, Ahmet Sami Yazar, Müberra Seğmen Yilmaz   +3 more
doaj  

Chinese expert consensus statement on the diagnosis and treatment of Hirschsprung disease

Chinese Medical Journal
Tianqi Zhu, Weibing Tang, Jiexiong Feng, the Chinese Research Group of Hirschsprung Disease, Jing Ni   +4 more
doaj   +1 more source

DIAGNOSTIC METHOD OF HIRSCPRUNG’S DISEASE

e-Jurnal Medika Udayana, 2013
Hirschsprung’s disease (congenital megacolon) is caused by the failed migration of colonic ganglion cells during gestation. Hirschsprung’s disease most commonly involves the rectosigmoid region of the colon but can affect the entire colon and, rarely ...
I Putu Trisnawan, I Made Darmajaya
doaj  

Growth and dietary effects on gastrointestinal symptoms in children with Hirschsprung's disease. [PDF]

Pediatr Surg Int
Telborn L, Axelsson I, Granéli C, Stenström P.   +3 more
europepmc   +1 more source

A Rare Case Report of Hirschsprung’s Disease-simulating Volvulus on Plain Radiography

Hirschsprung’s disease (HD) is a congenital disorder characterized by the absence of ganglion cells in the distal bowel, leading to functional intestinal obstruction. Radiological features often aid early diagnosis.
Nuraddeen Rabiu Mukhtar, Nasiru Musa Tahir, Adamu Saidu Muhammad   +2 more
core   +1 more source