(Q35738984)

10 August 2017

1 reference

title

New insights into human enteric neuropathies (English)

1 reference

10 August 2017

De Giorgio R

1

1 reference

10 August 2017

Guerrini S

2

1 reference

10 August 2017

Barbara G

3

1 reference

10 August 2017

Cremon C

4

1 reference

10 August 2017

Stanghellini V

5

1 reference

10 August 2017

Corinaldesi R

6

1 reference

10 August 2017

1 April 2004

1 reference

Neurogastroenterology and Motility

10 August 2017

1 reference

10 August 2017

16 Suppl 1

1 reference

10 August 2017

143-147

1 reference

Primary enteric neuropathies underlying gastrointestinal motor dysfunction

10 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Integrity of cholinergic innervation to the lower esophageal sphincter in achalasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Antineuronal antibodies in idiopathic achalasia and gastro-oesophageal reflux disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Mutant WD-repeat protein in triple-A syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Enteric nervous system disorders: genetic and molecular insights for the neurogastroenterologist

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Special basic science review

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Clinical features of a form of Hirschsprung's disease caused by a novel genetic abnormality

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease [published erratum appears in Hum Mol Genet 1998 Oct;7(11):1831]

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1743-3150.2004.00491.X

10.1111/J.1743-3150.2004.00491.X

21 January 2018

Identifiers

DOI

1 reference

10 August 2017

1 reference