Results 61 to 70 of about 12,267 (205)

Intestinale neuronale Dysplasie TypB: Wie verstehen wir sie heute? [PDF]

open access: yes, 2018
Zusammenfassung: Die intestinale neuronale Dysplasie TypB (INDB) stellt eine Anomalie des Plexus submucosus dar, die sich in einer sichtbaren Vermehrung von Riesenganglien äußert und mit einer typischerweise milden chronischen Obstipationssymptomatik ...
Bruder, E., Meier-Ruge, W.A.
core  

Konventionelle histologische Diagnostik in der Koloproktologie [PDF]

open access: yes, 2018
Zusammenfassung: Die histologische Diagnostik mit formalinfixiertem und in Paraffin eingebettetem Gewebe hat mit der Einführung immunhistochemischer Methoden in der Koloproktologie große Fortschritte gebracht.
Bruder, E., Meier-Ruge, W.A.
core  

Retinoblastoma protein prevents enteric nervous system defects and intestinal pseudo-obstruction [PDF]

open access: yes, 2013
The retinoblastoma 1 (RB1) tumor suppressor is a critical regulator of cell cycle progression and development. To investigate the role of RB1 in neural crest–derived melanocytes, we bred mice with a floxed Rb1 allele with mice expressing Cre from the ...
Carreira   +10 more
core   +2 more sources

Educational Case: Hirschsprung Disease

open access: yesAcademic Pathology, 2019
The following fictional case is intended as a learning tool within the Pathology Competencies for Medical Education (PCME), a set of national standards for teaching pathology.
Lauren Kroll-Wheeler MD   +1 more
doaj   +1 more source

Effects of potato-derived protease inhibitors on perianal dermatitis after colon resection for long-segment Hirschsprung's disease [PDF]

open access: yes, 2018
Background: After resection of long-segment Hirschsprung's disease, severe perianal dermatitis (SPAD) may occur because of high stool frequency and elevated concentrations of fecal pancreatic proteases.
Berger, Steffen   +4 more
core  

Variants of Hirschsprung disease

open access: yesSeminars in Pediatric Surgery, 2012
Variants of Hirschsprung disease are conditions that clinically resemble Hirschsprung disease, despite the presence of ganglion cells in rectal suction biopsies. The characterization and differentiation of various entities are mainly based on histologic, immunohistochemical, and electron microscopy findings of biopsies from patients with functional ...
Prem, Puri, Jan-Hendrik, Gosemann
openaire   +2 more sources

Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population [9] [PDF]

open access: yes, 2007
published_or_final_versio
Chan, EKW   +10 more
core   +1 more source

Hirschsprung disease [PDF]

open access: yesANZ Journal of Surgery, 2017
King, SK, Karpelowsky, J
openaire   +3 more sources

Prevalensi Bayi Lahir Cacat (Malformasi Kongenital) Di Rumah Sakit Pendidikan Fakultas Kedokteran Universitas YARSI [PDF]

open access: yes, 2009
Congenital Malformations was instrumental in perinatal morbidity and infant mortality. Patients with severe disorders are classified to be affected physically, mentally, and socially and require special attention.
Mustofa, S. (Samsul)   +2 more
core  

Hirschsprung disease in the U.S. associated Pacific Islands: more common than expected. [PDF]

open access: yes, 2005
INTRODUCTION: Tripler Army Medical Center (TAMC) in Honolulu, Hawaii, is uniquely situated to serve patients from the United States Associated Pacific Islands (USAPIs) through the congressionally funded Pacific Island Health Care Project (PIHCP). Because
de Lorimier, Arthur J   +2 more
core  

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