(Q21203049)

Armas Ralph Gustaf Gräsbeck

inferred from title

author

1

Ralph Gräsbeck

Ralph

Gräsbeck

1 reference

Dimensions Publication ID

Dimensions

1032271409

Orphanet Journal of Rare Diseases

17 August 2022

language of work or name

English

0 references

publication date

19 May 2006

9 references

6 March 2019

14 March 2019

19 March 2019

24 March 2019

30 June 2019

29 May 2020

3 July 2020

1 September 2020

2 October 2020

9 references

6 March 2019

14 March 2019

19 March 2019

24 March 2019

30 June 2019

29 May 2020

3 July 2020

1 September 2020

2 October 2020

1

0 references

issue

1

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page(s)

17

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copyright license

Creative Commons Attribution 2.0 Generic

9 references

6 March 2019

14 March 2019

19 March 2019

24 March 2019

30 June 2019

29 May 2020

3 July 2020

1 September 2020

on focus list of Wikimedia project

2 October 2020

copyright status

copyrighted

0 references

ScienceSource

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/1750-1172-1-17

0 references

cites work

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=1513194

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Update on cobalamin, folate, and homocysteine

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Transfer of cobalamin from intrinsic factor to transcobalamin II

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Megaloblastic Anaemia (MA).

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Cobalamin transport proteins and their cell-surface receptors

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Proteinuria in cubilin-deficient patients with selective vitamin B12 malabsorption

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domain

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Laboratory diagnosis of vitamin B12 and folate deficiency: a guide for the primary care physician

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Why has cyanocobalamin not been withdrawn?

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Congenital and selective malabsorption of vitamin B12 with proteinuria

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Homocysteine and vitamin B12 status relate to bone turnover markers, broadband ultrasound attenuation, and fractures in healthy elderly people.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Homocysteine and disability in hospitalized geriatric patients.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Canine Imerslund-Gräsbeck syndrome maps to a region orthologous to HSA14q.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Idiopathic chronic megaloblastic anemia in children

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

Selective vitamin B12 malabsorption and proteinuria in young people. A syndrome.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513194

A urinary radioisotope-binding assay to diagnose Gräsbeck-Imerslund disease

29 November 2018

1 reference

12 December 2020

Congenital specific vitamin B 12 malabsorption syndrome with proteinuria

1 reference

12 December 2020

1 reference

12 December 2020

Intrinsic factor studies II. The effect of gastric juice on the urinary excretion of radioactivity after the oral administration of radioactive vitamin B12

1 reference

12 December 2020

Neurologic findings of vitamin B12 deficiency: presentation of 7 cases

1 reference

12 December 2020

Imerslund-Gräsbeck anemia. A long-term follow-up study

1 reference

12 December 2020

Nonradioactive vitamin B12 absorption test evaluated in controls and in patients with inherited malabsorption of vitamin B12

1 reference

12 December 2020

Selective cobalamin malabsorption and the cobalamin-intrinsic factor receptor

1 reference

12 December 2020

FAMILIAL VITAMIN B12 MALABSORPTION

1 reference

12 December 2020

Identifiers

DOI

10.1186/1750-1172-1-17

1 reference

Dimensions Publication ID

2411564

1032271409

0 references

2411564

1 reference

1 reference

1 reference