Advances in understanding functional variations in the Hirschsprung disease spectrum (variant Hirschsprung disease)

No abstract is available for this paper.

• Publication year

  2017

• Venue

  Pediatric surgery international (Print)

• Publication date

  2017-03-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00383-016-4038-3PMID 27988850
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2002cited by this paper
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  2002cited by this paper
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  2002cited by this paper
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• Analysis of the RET,GDNF, EDN3, andEDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease

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  2001cited by this paper
• Mutational Analysis of the RET and GDNF Gene in Children with Hypoganglionosis

  2001cited by this paper
• Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation

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• Peripheral neuropathy with hypomyelination, chronic intestinal pseudo‐obstruction and deafness: A developmental “neural crest syndrome” related to a SOX10 mutation

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  1999cited by this paper
• Specific polymorphisms in the RETproto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression

  1999cited by this paper
• Congenital Colonic Hypoganglionosis in Murine Trisomy 16 - An Animal Model for Down's Syndrome

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• Morphometric aspects of the submucous plexus in whole-mount preparations of normal human distal colon.

  1998cited by this paper
• Increased submucosal nerve trunk caliber in aganglionosis: a "positive" and objective finding in suction biopsies and segmental resections in Hirschsprung's disease.

  1998cited by this paper
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  1998cited by this paper
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  1997cited by this paper
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  1997cited by this paper
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• Neuronal Intestinal Malformations: A Retro- and Prospective Study on 203 Patients

  1994cited by this paper
• A histological grading system for the evaluation of co-existing NID with Hirschsprung's disease.

  1994cited by this paper
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  1994cited by this paper
• Hirschsprung's Disease and Allied Disorders - A Review

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  1991cited by this paper
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  1990cited by this paper
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• Enfermedad de Hirschsprung, un enfoque practico.

  2022cites this paper
• Diagnostic utility of Bcl-2 immunohistochemical expression in pediatric functional bowel obstruction cases with ganglionated specimens

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• RET compound inheritance in Chinese patients with Hirschsprung disease: lack of penetrance from insufficient gene dysfunction

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• RET somatic mutations are underrecognized in Hirschsprung disease

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• Cell therapy for GI motility disorders: comparison of cell sources and proposed steps for treating Hirschsprung disease.

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