Results 31 to 40 of about 9,792 (217)

Multiple Roles of Ret Signalling During Enteric Neurogenesis

open access: yesFrontiers in Molecular Neuroscience, 2022
The majority of the enteric nervous system is formed by vagal neural crest cells which enter the foregut and migrate rostrocaudally to colonise the entire length of the gastrointestinal tract.
Dipa Natarajan   +9 more
doaj   +1 more source

Different Fecal Microbiota in Hirschsprung's Patients With and Without Associated Enterocolitis

open access: yesFrontiers in Microbiology, 2022
Background and ObjectivesPatients with Hirschsprung's disease are at risk of developing Hirschsprung-associated enterocolitis, especially in the first 2 years of life.
Alexis P. Arnaud   +17 more
doaj   +1 more source

Les échanges culturels de la France et de l'Espagne avec la Colombie (1900-1930)

open access: yes, 1992
Hirschsprung Nathalie. Les échanges culturels de la France et de l'Espagne avec la Colombie (1900-1930). In: Matériaux pour l'histoire de notre temps, n°27, 1992.
Hirschsprung, Nathalie
core   +1 more source

The use of carglumic acid in hyperammonemia secondary to bacterial overgrowth in lately diagnosed Hirschsprung disease

open access: yesJournal of Pediatric Surgery Case Reports, 2022
Hirschsprung disease is associated with significant bacterial proliferation and colonic dysbiosis leading to life threating hyperammonemia. In this report, we highlight the use of carglumic acid; a synthetic ammonia scavenger in hyperammonemia secondary ...
Tala Shalakhti   +6 more
doaj   +1 more source

Hirschsprung disease

open access: yes, 2016
© Springer International Publishing AG 2011, 2017. Hirschsprung disease refers to congenital aganglionosis of some or all of the colon. Patients typically present with constipation early in life.
Jeffrey R. Avansino   +3 more
core   +1 more source

Concurrent hirschsprung disease and esophageal atresia with tracheoesophageal fistula in a preterm neonate

open access: yesJournal of Pediatric Surgery Case Reports, 2018
We describe a preterm neonate with concomitant Hirschsprung disease (HD) and esophageal atresia (EA) with tracheoesophageal fistula (TEF). This is the first report to identify the coexistence of these distinct malformations in a preterm infant. Keywords:
Rashmi Gulati, MD   +2 more
doaj   +1 more source

Role of SoxE transcription factors in development and disease

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Sox8, Sox9, and Sox10 arose by multiple rounds of genome duplications from a single SoxE gene in ancestral vertebrates. In this review, we will briefly discuss the molecular structure and function of SoxE transcription factors and their evolutionary origin. We will then discuss their expression, function, and developmental disorders.
Merin Lawrence, Gerhard Schlosser
wiley   +1 more source

Parenteral nutrition and hospital outcomes in Australian adults: A descriptive cohort study

open access: yesJournal of Parenteral and Enteral Nutrition, EarlyView.
Abstract Background There is limited information regarding real‐world use of parenteral nutrition in hospitals. The objective of the study was to provide a real‐world description of parenteral nutrition administration in hospitalized patients. Methods This was a descriptive cohort study in 507 hospitalized adults who received parenteral nutrition at ...
Frank M. P. van Haren   +16 more
wiley   +1 more source

Enterocolitis asociada a enfermedad de Hirschsprung: estudio observacional sobre clínica y manejo en un servicio de urgencias hospitalarias

open access: yesAnales de Pediatría, 2018
Resumen: Introducción: La enterocolitis asociada a la enfermedad de Hirschsprung es su complicación más grave y conlleva una importante morbimortalidad. Se presenta con síntomas inespecíficos que dificultan el diagnóstico.
Margarita Sellers   +6 more
doaj   +1 more source

Congenital short bowel syndrome: Clinical aspects by systematic review

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund   +2 more
wiley   +1 more source

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