Methylmalonic aciduria and homocystinuria, cobalamin C type (cblC), constitute the most common inborn error of intracellular cobalamin metabolism. Here, we report the case of a 6-month-old child, presenting severe subacute neurological decline associated
Etienne Mondesert +8 more
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Assay of methylmalonic acid in the serum of patients with cobalamin deficiency using capillary gas chromatography-mass spectrometry. [PDF]
S P Stabler +4 more
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Inhibition of cobalamin-dependent enzymes by cobalamin analogues in rats. [PDF]
S P Stabler +3 more
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Methylmalonic Acid and Homocysteine in Plasma as Indicators of Functional Cobalamin Deficiency in Infants on Macrobiotic Diets [PDF]
Jørn Schneede +5 more
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Studies on Vitamin B<SUB>12</SUB>. I. : Thiamine as a Degradafion Factor of Cobalamins
Kiyoshi Harada +4 more
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Identification of cobalamin binding protein synthesized de novo by gastric cancer cells.
Yoshio Wakatsuki +5 more
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Purification by cobalamin-Sepharose affinity chromatography and intrinsic factor-binding activity of an extramembrane proteolytic product from pig ileal mucosa [PDF]
Yerima Alibada +5 more
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Serum levels of folate, 25‐hydroxyvitamin D3 and cobalamin during
Benedikt Weber +3 more
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