Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity. - Wikidata - wikimedia - TriplyDB

Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity.

Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity.

http://www.wikidata.org/entity/Q38862309

about

Influenza-associated thrombotic microangiopathies.Late Onset Cobalamin Disorder and Hemolytic Uremic Syndrome: A Rare Cause of Nephrotic Syndrome.Complement C5-inhibiting therapy for the thrombotic microangiopathies: accumulating evidence, but not a panacea.Combined methylmalonic acidemia and homocysteinemia presenting predominantly with late-onset diffuse lung disease: a case series of four patients.Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review.Diseases of complement dysregulation-an overview.Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic uremic syndrome.A child presenting with severe hypertension and circulatory failure-a diagnostic conundrum: Answers.Thrombotic Microangiopathy and the Kidney.Renal thrombotic microangiopathy and pulmonary arterial hypertension in a patient with late-onset cobalamin C deficiency.Favorable course of previously undiagnosed Methylmalonic Aciduria with Homocystinuria (cblC type) presenting with pulmonary hypertension and aHUS in a young child: a case report

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P2860

Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity.

http://www.wikidata.org/entity/Q38862309

description

2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

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2016年學術文章

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2016年學術文章

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name

Renal thrombotic microangiopat ...... of an under-recognized entity.

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Renal thrombotic microangiopat ...... of an under-recognized entity.

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Renal thrombotic microangiopat ...... of an under-recognized entity.

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Renal thrombotic microangiopat ...... of an under-recognized entity.

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Arjan Diepstra

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Bodo B Beck

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FrancJan van Spronsen

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Rolf M F Berger

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P2860

Decyanation of vitamin B12 by a trafficking chaperone

Antioxidants, inflammation and cardiovascular disease

Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancy

Novel inborn error of folate metabolism: identification by exome capture and sequencing of mutations in the MTHFD1 gene in a single proband

Thrombotic microangiopathy: new insights

Genetic disorders of vitamin B12 metabolism: eight complementation groups – eight genes

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

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

[Hemolytic-uremic syndrome: bilateral necrosis of the renal cortex in acute acquired hemolytic anemia].

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

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