(Q53905200)

22 May 2018

title

Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up. (English)

1 reference

22 May 2018

author name string

F Sicurelli

1

1 reference

22 May 2018

M A Carluccio

2

1 reference

22 May 2018

F Toraldo

3

1 reference

22 May 2018

M Tozzi

4

1 reference

22 May 2018

A Bucalossi

5

1 reference

22 May 2018

M Lenoci

6

1 reference

22 May 2018

G Jacomelli

7

1 reference

22 May 2018

V Micheli

8

1 reference

22 May 2018

E Cardaioli

9

1 reference

22 May 2018

M Mondelli

10

1 reference

22 May 2018

A Federico

11

1 reference

22 May 2018

G Marotta

12

1 reference

22 May 2018

M T Dotti

13

1 reference

22 May 2018

publication date

25 April 2012

1 reference

22 May 2018

published in

Journal of Neurology

1 reference

22 May 2018

volume

259

1 reference

22 May 2018

issue

9

1 reference

22 May 2018

page(s)

1985-1987

1 reference

22 May 2018

https://scigraph.springernature.com/pub.10.1007/s00415-012-6500-z

exact match

0 references

cites work

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6500-Z

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6500-Z

Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6500-Z

Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6500-Z

Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22532170

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22532170

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00415-012-6500-Z

1 reference

22 May 2018

1 reference

22 May 2018