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Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type

Known as: HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE, Vitamin B12-Responsive Homocystinuria, CblE Type, Methylcobalamin Deficiency, CblE Type 
National Institutes of Health

Related topics

Related topics

9 relations
Anemia, MegaloblasticAutosomal recessive inheritanceCerebral atrophyFailure to Thrive

Papers overview

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2012
2012
Late Onset Cobalamin C Disease: A Case Report of an Adolescent Presenting with Peripheral Neuropathy (P03.189)
Objective: To describe a case of late onset Cobalamin C disease presenting with peripheral neuropathy. Background Cobalamin C… 
2011
2011
Option Pricing Models with HF Data - A Comparative Study - The Properties of the Black Model with Different Volatility Measures
This paper compares option pricing models, based on Black model notion (Black, 1976), especially focusing on the volatility… 
1994
1994
제1주제: 미국 Cble TV의 Public Access Channel과 수용자 참여
1970
1970
Absorption and metabolism of 1-14C-hydroxy octadecadienoate in the rat
The metabolism of 1-14C-9(13)-hydroxy octadecadienoic acid methyl ester (1-14C-HAME) by the rat was investigated in vivo and in… 
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