ABERRANT COBALAMIN METABOLISM WITH HOMOCYSTINURIA AND METHYMALONIC ACIDURIA
نویسندگان
چکیده
منابع مشابه
Maculopathy and retinal degeneration in cobalamin C methylmalonic aciduria and homocystinuria.
1. George F, Brisson C, Poncelet P, et al. Rapid isolation of human endothelial cells from whole blood using S-Endo1 monoclonal antibody coupled with immunomagnetic beads: demonstration of endothelial injury after angioplasty. Thromb Haemost. 1992;67:147-153. 2. Rambaud JC, Galian A, Touchard G, et al. Digestive tract and renal small vessel hyalinosis, idiopathic nonarteriosclerotic intracerebr...
متن کاملAbnormal Deoxyuridine Suppression Test in Congenital Methylmalonic Aciduria-Homocystinuria Without Megaloblastic Anemia: Divergent Biochemical and Morphological Bone Marrow Manifestations of Disordered Cobalamin Metabolism in Man
We studied two brothers (J.R. and M.R.) with the cobalamin D variant of congenital methylmalonic aciduria-homocystinuria. whose previously reported lack of megaloblastic anemia conflicted with current concepts of cobalamin’s role in DNA synthesis and the “methyltetrahydrofolate (MTHF) trapS’ hypothesis. Both subjects were indeed hematologically normal. although JR. had a mean corpuscular volume...
متن کاملAbnormal Deoxyuridine Suppression Test in Congenital Methylmalonic Aciduria-Homocystinuria Without Megaloblastic Anemia: Divergent Biochemical and Morphological Bone Marrow Manifestations of Disordered Cobalamin Metabolism in Man
We studied two brothers (J.R. and M.R.) with the cobalamin D variant of congenital methylmalonic aciduria-homocystinuria. whose previously reported lack of megaloblastic anemia conflicted with current concepts of cobalamin’s role in DNA synthesis and the “methyltetrahydrofolate (MTHF) trapS’ hypothesis. Both subjects were indeed hematologically normal. although JR. had a mean corpuscular volume...
متن کاملcobalamin metabolism in man biochemical and morphological bone marrow manifestations of disordered aciduria-homocystinuria without megaloblastic anemia: divergent Abnormal deoxyuridine suppression test in congenital methylmalonic
http://bloodjournal.hematologylibrary.org/site/misc/rights.xhtml#repub_requests Information about reproducing this article in parts or in its entirety may be found online at: http://bloodjournal.hematologylibrary.org/site/misc/rights.xhtml#reprints Information about ordering reprints may be found online at: http://bloodjournal.hematologylibrary.org/site/subscriptions/index.xhtml Information abo...
متن کاملAbnormal Deoxyuridine Suppression Test in Congenital Methylmalonic Aciduria-Homocystinuria Without Megaloblastic Anemia: Divergent Biochemical and Morphological Bone Marrow Manifestations of Disordered Cobalamin Metabolism in Man
We studied two brothers (J.R. and M.R.) with the cobalamin D variant of congenital methylmalonic aciduria-homocystinuria. whose previously reported lack of megaloblastic anemia conflicted with current concepts of cobalamin’s role in DNA synthesis and the “methyltetrahydrofolate (MTHF) trapS’ hypothesis. Both subjects were indeed hematologically normal. although JR. had a mean corpuscular volume...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Pediatric Research
سال: 1984
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-198404001-00780