(Q34306368)

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

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

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

1 reference

Europe PubMed Central

1 August 2017

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Albert de la Chapelle

14

object named as

Albert de la Chapelle

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object named as

Willy Lissens

10

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author name string

Stephan M Tanner

1

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Europe PubMed Central

1 August 2017

Zhongyuan Li

2

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Europe PubMed Central

1 August 2017

Ryan Bisson

3

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Europe PubMed Central

1 August 2017

Ceren Acar

4

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Europe PubMed Central

1 August 2017

Cihan Oner

5

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Europe PubMed Central

1 August 2017

Reyhan Oner

6

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Europe PubMed Central

1 August 2017

Mualla Cetin

7

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Europe PubMed Central

1 August 2017

Mohamed A Abdelaal

8

1 reference

Europe PubMed Central

1 August 2017

Essam A Ismail

9

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Europe PubMed Central

1 August 2017

Ralf Krahe

11

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Europe PubMed Central

1 August 2017

Harald Broch

12

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Europe PubMed Central

1 August 2017

Ralph Gräsbeck

13

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1 August 2017

publication date

1 April 2004

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Europe PubMed Central

1 August 2017

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Europe PubMed Central

1 August 2017

23

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1 August 2017

327-333

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4

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1 August 2017

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

21 January 2018

A cluster of autosomal recessive spondylocostal dysostosis caused by three newly identified DLL3 mutations segregating in a small village

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

21 January 2018

Familial selective vitamin B 12 malabsorption

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

21 January 2018

Reversal of severe neurological abnormalities after vitamin B12 replacement in the Imerslund-Grasbeck syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

21 January 2018

Imerslund-Gräsbeck Syndrome in a Saudi Family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome) in a pool of Turkish patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

A case report of 46,XX,del(21)(q22) de novo deletion associated with Imerslund-Grasbeck syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Megalin and cubilin: multifunctional endocytic receptors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Urinary excretion of intrinsic factor and the receptor for its cobalamin complex in Gräsbeck-Imerslund patients: the disease may have subsets

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

[Imerslund's disease. Clinical and biological aspects. Apropos of 6 cases]

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Inheritance of selective malabsorption of vitamin B12

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Genotypic/phenotypic heterogeneity of selective vitamin B12 malabsorption (Grasbeck-Imerslund syndrome) in two Bedouin families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Imerslund-Grasbeck syndrome in a Chinese family with distinct skin lesions refractory to vitamin B12.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Ileal Mucosa in Familial Selective Vitamin B12Malabsorption

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

The Finnish Disease Heritage III: the individual diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Imerslund-Gräsbeck syndrome in an African patient

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Confirmation of prenatal diagnosis results of X-linked recessive myotubular myopathy by mutational screening, and description of three new mutations in the MTM1 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteinuria in cubilin-deficient patients with selective vitamin B12 malabsorption

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20014

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20014

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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