(Q35133264)

6 August 2017

title

Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE (English)

1 reference

6 August 2017

author

Maria Lucia Valentino

8

object named as

M L Valentino

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6 August 2017

M Hirano

1

1 reference

6 August 2017

R Martí

2

1 reference

6 August 2017

C Casali

3

1 reference

6 August 2017

S Tadesse

4

1 reference

6 August 2017

T Uldrick

5

1 reference

6 August 2017

B Fine

6

1 reference

6 August 2017

D M Escolar

7

1 reference

6 August 2017

I Nishino

9

1 reference

6 August 2017

C Hesdorffer

10

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6 August 2017

J Schwartz

11

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6 August 2017

R G Hawks

12

1 reference

6 August 2017

D L Martone

13

1 reference

6 August 2017

M S Cairo

14

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6 August 2017

S DiMauro

15

1 reference

6 August 2017

M Stanzani

16

1 reference

6 August 2017

J H Garvin

17

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6 August 2017

D G Savage

18

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6 August 2017

language of work or name

English

0 references

publication date

13 September 2006

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6 August 2017

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6 August 2017

volume

67

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6 August 2017

issue

8

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6 August 2017

page(s)

1458-1460

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A pilot study of reduced intensity conditioning and allogeneic stem cell transplantation from unrelated cord blood and matched family donors in children and adolescent recipients

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

Origins of mitochondrial thymidine triphosphate: Dynamic relations to cytosolic pools

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

Altered thymidine metabolism due to defects of thymidine phosphorylase

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

Late-onset MNGIE due to partial loss of thymidine phosphorylase activity.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

Elevated plasma deoxyuridine in patients with thymidine phosphorylase deficiency

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4345106

Infusion of platelets transiently reduces nucleoside overload in MNGIE

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16971696

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/01.WNL.0000240853.97716.24

1 reference

6 August 2017

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6 August 2017

1 reference