Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder (Q33376703)

26 July 2017

Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder (English)

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26 July 2017

Ajay P Sharma

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26 July 2017

Cheryl R Greenberg

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2

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26 July 2017

Asuri N Prasad

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3

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26 July 2017

Chitra Prasad

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4

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26 July 2017

14 September 2007

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26 July 2017

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26 July 2017

22

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26 July 2017

2097-2103

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26 July 2017

12

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https://scigraph.springernature.com/pub.10.1007/s00467-007-0604-1

26 July 2017

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cites work

Long-term outcome in treated combined methylmalonic acidemia and homocystinemia

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00467-007-0604-1

Optic atrophy in association with cobalamin C (cblC) disease

21 January 2018

1 reference

12 December 2020

Experimental production of renal glycosuria, phosphaturia, and aminoaciduria by injection of maleic acid

1 reference

12 December 2020

Binding of copper is a mechanism of homocysteine toxicity leading to COX deficiency and apoptosis in primary neurons, PC12 and SHSY-5Y cells.

1 reference

12 December 2020

Methylmalonic acidemia: 6 years' clinical experience with two variants unresponsive to vitamin B12 therapy

1 reference

12 December 2020

Homocysteine-induced modulation of tissue plasminogen activator binding to its endothelial cell membrane receptor

1 reference

12 December 2020

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

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12 December 2020

Cobalamin C defect associated with hemolytic-uremic syndrome

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12 December 2020

Cobalamin and folate deficiency: acquired and hereditary disorders in children

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12 December 2020

Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations

1 reference

12 December 2020

Adverse vascular effects of homocysteine are modulated by endothelium-derived relaxing factor and related oxides of nitrogen

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12 December 2020

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

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12 December 2020

Prenatal and postnatal treatment in cobalamin C defect

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12 December 2020

Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy

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12 December 2020

Thrombotic Microangiopathies

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12 December 2020

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

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12 December 2020

Atypical (non-diarrhea-associated) hemolytic-uremic syndrome in childhood

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

Activation of endogenous factor V by a homocysteine-induced vascular endothelial cell activator

1 reference

12 December 2020

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

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12 December 2020

Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndrome

1 reference

12 December 2020

Hyperhomocysteinemia and cobalamin disorders.

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12 December 2020

Epigenetics and human disease

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12 December 2020

Tubulointerstitial nephritis in methylmalonic acidemia

1 reference

12 December 2020

Heterogeneity of atypical haemolytic uraemic syndromes

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12 December 2020

Chemical pathology of homocysteine. I. Atherogenesis

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12 December 2020

Update on cobalamin, folate, and homocysteine

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12 December 2020

Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period

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12 December 2020

The many faces of vitamin B12: catalysis by cobalamin-dependent enzymes

1 reference

12 December 2020

Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria

1 reference

12 December 2020

Neonatal hemolytic-uremic syndrome, methylmalonic aciduria and homocystinuria caused by intracellular vitamin B 12 deficiency. Value of etiological diagnosis

1 reference

12 December 2020

Cobalamin C deficiency complicated by an atypical glomerulopathy

1 reference

12 December 2020

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation

1 reference

12 December 2020

10.1007/S00467-007-0604-1

Identifiers

DOI

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Dimensions Publication ID

26 July 2017

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