(Q43711275)

26 November 2017

Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance. (English)

1 reference

26 November 2017

1 reference

V Humbertclaude

1

1 reference

26 November 2017

F Rivier

2

1 reference

26 November 2017

A Roubertie

3

1 reference

26 November 2017

B Echenne

4

1 reference

26 November 2017

H Bellet

5

1 reference

26 November 2017

C Vallat

6

1 reference

26 November 2017

D Morin

7

1 reference

26 November 2017

language of work or name

1 reference

1 August 2001

1 reference

Journal of Child Neurology

26 November 2017

1 reference

26 November 2017

16

1 reference

26 November 2017

8

1 reference

26 November 2017

622-623

1 reference

Hyperprolinaemia type I and white matter disease: coincidence or causal relationship?

26 November 2017

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600820

Type II hyperprolinaemia with renal involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600820

Association of hyperprolinaemia type I and heparin cofactor II deficiency with CATCH 22 syndrome: evidence for a contiguous gene syndrome locating the proline oxidase gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600820

A human homologue of the Drosophila melanogaster sluggish-A (proline oxidase) gene maps to 22q11.2, and is a candidate gene for type-I hyperprolinaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600820

Proline-induced inhibition of glutamate release in hippocampal area CA1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600820

10.1177/088307380101600820

21 January 2018

Identifiers

DOI

1 reference

26 November 2017

1 reference