Results 111 to 120 of about 9,336,073 (253)

L1cam acts as a modifier gene during enteric nervous system development

Neurobiology of Disease, 2010
The enteric nervous system is derived from neural crest cells that migrate from the caudal hindbrain and colonise the gut. Failure of neural crest cells to fully colonise the gut results in an “aganglionic zone” that lacks a functional enteric nervous ...
Adam S. Wallace, Claudia Schmidt, Melitta Schachner, Michael Wegner, Richard B. Anderson   +4 more
doaj   +1 more source

PHOX2B polymorphisms as Hirschsprung's Disease diagnostic markers and methods based thereon [PDF]

, 2003
The invention relates generally to polymorphisms or mutations of the PHOX2B gene. More particularly, the invention relates to polymorphisms or mutations of the PHOX2B gene that are responsible for the disease Hirschsprung's disease (HSCR), which is a ...

core  

Hirschsprung's disease: the "Swiss roll” technique revisited [PDF]

, 2018
Purpose: During pull-through for Hirschsprung's disease (HSCR), the assessment of innervation is mainly based on the presence of ganglion cells when conventional Hematoxylin and Eosin (HE) staining is used.
Ciola, Ana, Martin, Patricia, Meagher-Villemure, Kathleen, Meyrat, Blaise, Osterheld, Maria-Chiara, Vilas, Daniel   +5 more
core  

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  

Comparing surface electroenterography measurements between patients suffering from Hirschsprung’s disease and controls: a feasibility study

Scientific Reports
Current diagnostics in Hirschsprung’s disease are often challenging and invasive. This study aims to investigate whether surface electroenterography can non-invasively discern healthy subjects from subjects suffering from Hirschsprung’s disease.
Nick Rolleman, Willemijn Klein, Iris Nagtegaal, Michel van Putten, Ivo de Blaauw, Sanne Botden   +5 more
doaj   +1 more source

Effects of intraduodenally applied bile salts on pancreatic secretion [PDF]

, 1993
Lehnert, Peter, Riepl, Rudolf L.
core   +1 more source

Volume Four Subject Index [PDF]

, 1968
Subject index for MCV/Q, Medical College of Virginia Quarterly, Volume ...

core   +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  

Japanese clinical practice guidelines for allied disorders of Hirschsprung's disease, 2017

Pediatrics International, 2018
M. Muto, H. Matsufuji, T. Taguchi, T. Tomomasa, M. Nio, H. Tamai, M. Tamura, H. Sago, A. Toki, S. Nosaka, T. Kuroda, Masahiro Yoshida, A. Nakajima, Hiroyuki Kobayashi, H. Sou, K. Masumoto, Yoshio Watanabe, Y. Kanamori, Y. Hamada, A. Yamataka, N. Shimojima, A. Kubota, Kosuke Ushijima, K. Haruma, S. Fukudo, Y. Araki, T. Kudo, S. Obata, W. Sumita, Toshihiko Watanabe, S. Fukahori, Yoshimitsu Fujii, Yoshiyuki Yamada, Keisuke Jimbo, Fujimi Kawai, Tomoya Fukuoka, Shinsuke Onuma, T. Morizane, S. Ieiri, Genshiro Esumi, Takahiro Jimbo, T. Yamasaki   +41 more
semanticscholar   +1 more source

Perlecan, CollagenXVIII, and Agrin Expression in Normo-, Hypo-, and Aganglionic Segments in Hirschsprung's Disease. [PDF]

Neurogastroenterol Motil
van den Beld N, Fischer M, Scharr M, Scherer S, Beschorner R, Hirt B, Neckel PH.   +6 more
europepmc   +1 more source