Results 11 to 20 of about 4,891,717 (200)

Texas Preventable Disease News [PDF]

, 1989
Newsletter of the Texas Bureau of Disease Control and Epidemiology discussing the news, activities, and events of the organization and other information related to health in ...
Texas. Bureau of Disease Control and Epidemiology.
core   +19 more sources

Texas Preventable Disease News [PDF]

, 1988
Newsletter of the Texas Bureau of Disease Control and Epidemiology discussing the news, activities, and events of the organization and other information related to health in ...
Texas. Bureau of Disease Control and Epidemiology.
core   +12 more sources

The Correlation of Post Definitive Surgery and Quality of Life on Patient with Hirschsprung’s Disease: A Literature Review [PDF]

, 2022
Hirschsprungs disease is a congenital malformation of parasympathetic ganglion in colon with the result of interfering defecation process. Since Hirschsprungs disease usually diagnoses in the early life of the patients, complain of defecation problem ...
Alpha Fardah Athiyah, -, I Gusti Bagus Adria Hariastawa, -, Ailsa Reina Faradiba, -   +2 more
core   +1 more source

Hirschsprung's disease [PDF]

Seminars in Pediatric Surgery, 2010
Hirschsprung's disease (HSCR) is characterized by absence of the enteric nervous system in a variable portion of the distal gut. Affected infants usually present in the days after birth with bowel obstruction. Despite surgical advances, long-term outcomes remain variable.
GarciaBarcelo, M, Tam, PKH, Kenny, SE
openaire   +4 more sources

Extended long-segment Hirschsprungs’ disease in the Waardenburg–Shah syndrome [PDF]

, 2015
Hypopigmentation, either a white forelock or changes in the eyebrows and/or isochromia irides, associated with signs of bowel obstruction should alert the paediatrician and paediatric surgeons to the possibility of aganglionosis.
Setra, AE, Ambi, U, Hatti, RB, Yelamali, BC   +3 more
core   +1 more source

Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. [PDF]

, 2010
The unparalleled collection of clinical data and biomaterials within the EHDN's REGISTRY can expedite the search for disease modifiers (genetic and environmental) of age at onset and disease progression that could be harnessed for the development of ...
Handley, Olivia J, Landwehrmeyer, G Bernhard, Aileen K Ho, Bisson, Jonathan Ian, Schwenke C, David Craufurd, Dunnett, Stephen B., Handley, Olivia, Investigators of the European Huntington's Disease Network, The, DI MARIA, EMILIO, Craufurd D, Dunnett, SB, Carsten Schwenke, the investigators of the European Huntington's Disease Network, Craufurd, David, Edward Wild, Landwehrmeyer, GB, Busse, Monica, Rosser, Anne Elizabeth, Olivia J Handley, Romano Silvia., Tabrizi SJ, Ho, Aileen K., Wild, E, Landwehrmeyer GB, Craufurd, D, Tabrizi, SJ, Tabrizi, Sarah J., Handley, OJ, Rickards, Hugh, Dunnett, Stephen, Ho, Aileen K, Orth, Michael, Ho, AK, Wild, Edward, Stephen B. Dunnett, Sarah J Tabrizi, Wild, EJ, Landwehrmeyer, G. Bernhard, Naji, Jenny, Landwehrmeyer, G. Bernhard, Wild E, Investigators of the European Huntington's Disease Network, Handley, Olivia J., Orth, M, Ellison-Rose, Lynda, Tabrizi, Sarah J, Price, Kathleen, Ho AK, ABBRUZZESE, GIOVANNI, Schwenke, C, Ho, A, Orth M, Handley OJ, Schwenke, Carsten, Dunnett SB, Dunnett, Stephen B, Michael Orth, G. Bernhard Landwehrmeyer   +59 more
core   +1 more source

HIRSCHSPRUNG'S DISEASE − EARLY AND LATE COMPLICATIONS

Slovenska pediatrija, 2020
Hirschsprung’s disease is a congenital disruption of bowel motility, which occurs in approximately 1 / 5000 births. Timely recognition and treatment of the disease are of utmost importance in enabling the affected children to have good functional ...
Jože Maučec, Julija Pavčnik, Diana Gvardijančič   +2 more
doaj   +1 more source

Specific serum microRNA profile in the molecular diagnosis of Hirschsprungs disease. [PDF]

, 2014
Hirschsprungs disease (HSCR), a congenital gastrointestinal disorder, is one of the most common causes of neonatal bowel obstruction. Without an early screening and diagnosis, some patients develop serious complications, such as toxic megacolon or acute ...
Qin, Jingjing, Li, Hongxing, Lei, Hao, Wu, Wei, Xu, Xiaoqun, Cai, Peng, Li, Bo, Tang, Weibing, Huo, Weiwei, Rehan, Virender, Tang, Junwei, Geng, Qiming, Zhang, Hongwei, Xia, Yankai   +13 more
core   +1 more source

Late diagnosis of Hirschsprung's disease

Journal of Coloproctology, 2015
Hirschsprung's disease is a condition characterized by the absence of ganglion cells in a variable segment of the large intestine, mainly producing the symptom of constipation and being usually diagnosed in the first year of life. With diagnostic methods
Marielle Rodrigues Martins, Carlos Henrique Marques dos Santos, Gustavo Ribeiro Falcão   +2 more
doaj   +1 more source

Hirschsprung's Disease - Review of Clinical Features, Diagnosis and Treatment

Journal of Education, Health and Sport, 2023
Introduction and purpose: Hirschsprung's disease, also known as congenital aganglionic megacolon, is a rare congenital disorder that affects the large intestine.
Rafał Tkaczyk, Gabriela Świątek, Jakub Tomczyk, Weronika Sosnowska, Maria Tomkiewicz, Kalina Taracha, Maciej Tomkiewicz, Aleksandra Brzozowska, Kornelia Trusz, Iwona Wanat   +9 more
doaj   +1 more source