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Abnormal propionic-methylmalonic-succinic acid metabolism in vitamin B12 deficiency and its possible relationship to the neurologic syndrome of pernicious anemia.

作者信息

Vivacqua R J, Myerson R M, Prescott D J, Rabinowitz J L

出版信息

Am J Med Sci. 1966 May;251(5):507-15. doi: 10.1097/00000441-196605000-00002.

DOI:10.1097/00000441-196605000-00002
PMID:5949008
Abstract
摘要

相似文献

1
Abnormal propionic-methylmalonic-succinic acid metabolism in vitamin B12 deficiency and its possible relationship to the neurologic syndrome of pernicious anemia.
Am J Med Sci. 1966 May;251(5):507-15. doi: 10.1097/00000441-196605000-00002.
2
The role of propionic acid as a precursor of methylmalonic acid in normal and vitamin B12-deficient man.
J Lab Clin Med. 1969 Jun;73(6):917-23.
3
METHYLMALONIC ACID EXCRETION AND VITAMIN B12 DEFICIENCY IN THE HUMAN.人体内甲基丙二酸排泄与维生素B₁₂缺乏症
Ann N Y Acad Sci. 1964 Apr 24;112:915-21. doi: 10.1111/j.1749-6632.1964.tb45066.x.
4
Possible interrelationship between vitamins E and b12 in the disturbance in methylmalonate metabolism in vitamin E deficiency.维生素E缺乏时维生素E与维生素B12在甲基丙二酸代谢紊乱中可能存在的相互关系。
Biochem J. 1978 Apr 15;172(1):115-21. doi: 10.1042/bj1720115.
5
Vitamin B12 dependent methylmalonicaciduria: defective B12 metabolism in cultured fibroblasts.维生素B12依赖型甲基丙二酸尿症：培养的成纤维细胞中维生素B12代谢缺陷
Biochem Biophys Res Commun. 1969 Nov 6;37(4):607-14. doi: 10.1016/0006-291x(69)90853-5.
6
The excretion of methylmalonic acid and succinic acid in vitamin B 12 and folate deficiency.维生素B12和叶酸缺乏时甲基丙二酸和琥珀酸的排泄情况。
Br J Haematol. 1967 Nov;13(6):1021-32. doi: 10.1111/j.1365-2141.1967.tb08871.x.
7
Identification of propionate as an endogenous CO2 acceptor in Rhodospirillum rubrum and properties of purified propionyl-coenzyme A carboxylase.红螺菌中丙酸作为内源性二氧化碳受体的鉴定及纯化的丙酰辅酶A羧化酶的性质
J Bacteriol. 1968 May;95(5):1774-8. doi: 10.1128/jb.95.5.1774-1778.1968.
8
[Provocation of methylmalonic acid excretion during vitamin B 12 deficiency].
Wien Z Inn Med. 1971 Sep;52(9):441-5.
9
Defective leukocyte metabolism in human cobalamin deficiency: impaired propionate oxidation and serine biosynthesis reversible by cyanocobalamin therapy.人类钴胺素缺乏时白细胞代谢缺陷：丙酸盐氧化受损和丝氨酸生物合成受损，氰钴胺治疗可使其逆转。
J Lab Clin Med. 1976 Jan;87(1):89-97.
10
Metabolism of propionic acid in animal tissues. IV. Further studies on the enzymatic isomerization of methylmalonyl coenzyme A.动物组织中丙酸的代谢。IV. 甲基丙二酰辅酶A酶促异构化的进一步研究。
J Biol Chem. 1958 Jun;232(2):931-8.

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1
Biochemical pathogenesis of subacute combined degeneration of the spinal cord and brain.脊髓和脑亚急性联合变性的生化发病机制
J Inherit Metab Dis. 1993;16(4):762-70. doi: 10.1007/BF00711908.
2
Neurological involvement in hereditary transcobalamin II deficiency.遗传性转钴胺素II缺乏症的神经系统受累情况。
J Neurol Neurosurg Psychiatry. 1982 Jan;45(1):74-7. doi: 10.1136/jnnp.45.1.74.
3
Assay of methylmalonic acid in the serum of patients with cobalamin deficiency using capillary gas chromatography-mass spectrometry.使用毛细管气相色谱-质谱联用技术测定钴胺素缺乏患者血清中的甲基丙二酸。
J Clin Invest. 1986 May;77(5):1606-12. doi: 10.1172/JCI112476.
4
Possible interrelationship between vitamins E and b12 in the disturbance in methylmalonate metabolism in vitamin E deficiency.维生素E缺乏时维生素E与维生素B12在甲基丙二酸代谢紊乱中可能存在的相互关系。
Biochem J. 1978 Apr 15;172(1):115-21. doi: 10.1042/bj1720115.