(Q38005286)

English

A novel mtDNA large-scale mutation clinically exclusively presenting with refractory anemia: is there a chance to predict disease progression?

scientific article published on May 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

A novel mtDNA large-scale mutation clinically exclusively presenting with refractory anemia: is there a chance to predict disease progression? (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

refractory anemia

1 reference

based on heuristic

inferred from title

Arndt Borkhardt

5

object named as

Arndt Borkhardt

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

author name string

Vera Binder

1

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Laura Steenpass

2

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Hans-Juergen Laws

3

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Jochen Ruebo

4

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

publication date

1 May 2012

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Journal of Pediatric Hematology/Oncology

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

283-292

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

B12 deficient megaloblastic anemia in a toddler with a history of gastroschisis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Gastrointestinal abnormalities in vitamin B12 deficient patients with megaloblastic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Cutaneous lesions and vitamin B12 deficiency: an often-forgotten link

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Acquired and inherited disorders of cobalamin and folate in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Imerslund-Gräsbeck syndrome (selective vitamin B(12) malabsorption with proteinuria)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

A child with vitamin B12 deficiency presenting with pancytopenia and hyperpigmentation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Improved outcomes in the treatment of gastroschisis using a preformed silo and delayed repair approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Persistence of neutrophil hypersegmentation during recovery from megaloblastic granulopoiesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302209

1 October 2018

Generalized hyperpigmentation of the skin due to vitamin B12 deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22082743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gastric emptying in patients with vitamin B(12) deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22082743

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/MPH.0B013E3182288249

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

release_lghz6wudtneyza2o3ppjb7hgsa

1 reference

https://api.fatcat.wiki/v0/release/lghz6wudtneyza2o3ppjb7hgsa

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

0 references

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