(Q33344059)

26 July 2017

Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy (English)

1 reference

26 July 2017

Ron Wevers

8

0 references

Jean-Pierre Fryns

6

object named as

Jean-Pierre Fryns

1 reference

26 July 2017

Johan L K Van Hove

1

1 reference

26 July 2017

Rita Van Damme-Lombaerts

2

1 reference

26 July 2017

Stephanie Grünewald

3

1 reference

26 July 2017

Heidi Peters

4

1 reference

26 July 2017

Boudewijn Van Damme

5

1 reference

26 July 2017

Jozef Arnout

7

1 reference

26 July 2017

E Regula Baumgartner

9

1 reference

26 July 2017

Brian Fowler

10

1 reference

26 July 2017

1 August 2002

1 reference

American Journal of Medical Genetics Part A

26 July 2017

1 reference

26 July 2017

111

1 reference

26 July 2017

2

1 reference

26 July 2017

195-201

1 reference

Biochemical and clinical response to hydroxocobalamin versus cyanocobalamin treatment in patients with methylmalonic acidemia and homocystinuria (cblC).

26 July 2017

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Hyperhomocysteinemia in end-stage renal disease: prevalence, etiology, and potential relationship to arteriosclerotic outcomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Cor pulmonale as a complication of methylmalonic acidemia and homocystinuria (Cbl-C type).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalamin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Post- and prenatal diagnostic methods for the homocystinurias

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Cobalamin C defect associated with hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Methionine synthase deficiency without megaloblastic anaemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Heterogeneity of atypical haemolytic uraemic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

A congenital anomaly of vitamin B12 metabolism: a study of three cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

The haemolytic-uraemic syndrome in childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10499

21 January 2018

Identifiers

DOI

10.1002/AJMG.10499

1 reference

26 July 2017

1 reference