393 related articles for article (PubMed ID: 43301)
1. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations.
Baumgartner ER; Wick H; Linnell JC; Gaull GE; Bachmann C; Steinmann B
Helv Paediatr Acta; 1979; 34(5):483-96. PubMed ID: 43301
[TBL] [Abstract][Full Text] [Related]
2. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology.
Baumgartner ER; Wick H; Maurer R; Egli N; Steinmann B
Helv Paediatr Acta; 1979; 34(5):465-82. PubMed ID: 528229
[TBL] [Abstract][Full Text] [Related]
3. A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.
Mamlok RJ; Isenberg JN; Rassin DK; Norcross K; Tallan HH
Neuropediatrics; 1986 May; 17(2):94-9. PubMed ID: 2873525
[TBL] [Abstract][Full Text] [Related]
4. Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts.
Mellman I; Willard HF; Rosenberg LE
J Clin Invest; 1978 Nov; 62(5):952-60. PubMed ID: 30783
[TBL] [Abstract][Full Text] [Related]
5. Enhanced levels of biochemical markers for cobalamin deficiency in totally gastrectomized rats: uncoupling of the enhancement from the severity of spongy vacuolation in spinal cord.
Scalabrino G; Buccellato FR; Tredici G; Morabito A; Lorenzini EC; Allen RH; Lindenbaum J
Exp Neurol; 1997 Apr; 144(2):258-65. PubMed ID: 9168827
[TBL] [Abstract][Full Text] [Related]
6. Vitamin B12 in health and disease: part I--inherited disorders of function, absorption, and transport.
Kapadia CR
Gastroenterologist; 1995 Dec; 3(4):329-44. PubMed ID: 8775094
[TBL] [Abstract][Full Text] [Related]
7. Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.
Rosenblatt DS; Cooper BA; Pottier A; Lue-Shing H; Matiaszuk N; Grauer K
J Clin Invest; 1984 Dec; 74(6):2149-56. PubMed ID: 6511919
[TBL] [Abstract][Full Text] [Related]
8. Identification of ABC transporters acting in vitamin B
McDonald MK; Fritz JA; Jia D; Scheuchner D; Snyder FF; Stanislaus A; Curle J; Li L; Stabler SP; Allen RH; Mains PE; Gravel RA
Mol Genet Metab; 2017 Dec; 122(4):160-171. PubMed ID: 29153845
[TBL] [Abstract][Full Text] [Related]
9. Cobalamin metabolism in cultured human chorionic villus cells.
Begley JA; Colligan PD; Chu RC; Hall CA
J Cell Physiol; 1993 Jul; 156(1):43-7. PubMed ID: 8100234
[TBL] [Abstract][Full Text] [Related]
10. Cobalt: its role in health and disease.
Yamada K
Met Ions Life Sci; 2013; 13():295-320. PubMed ID: 24470095
[TBL] [Abstract][Full Text] [Related]
11. Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood.
Carmel R; Watkins D; Goodman SI; Rosenblatt DS
N Engl J Med; 1988 Jun; 318(26):1738-41. PubMed ID: 2897628
[No Abstract] [Full Text] [Related]
12. Renal involvement in a patient with cobalamin A type (cblA) methylmalonic aciduria: a 42-year follow-up.
Haarmann A; Mayr M; Kölker S; Baumgartner ER; Schnierda J; Hopfer H; Devuyst O; Baumgartner MR
Mol Genet Metab; 2013 Dec; 110(4):472-6. PubMed ID: 24095221
[TBL] [Abstract][Full Text] [Related]
13. Recognition of two intracellular cobalamin binding proteins and their identification as methylmalonyl-CoA mutase and methionine synthetase.
Kolhouse JF; Allen RH
Proc Natl Acad Sci U S A; 1977 Mar; 74(3):921-5. PubMed ID: 15259
[TBL] [Abstract][Full Text] [Related]
14. Gene identification for the cblD defect of vitamin B12 metabolism.
Coelho D; Suormala T; Stucki M; Lerner-Ellis JP; Rosenblatt DS; Newbold RF; Baumgartner MR; Fowler B
N Engl J Med; 2008 Apr; 358(14):1454-64. PubMed ID: 18385497
[TBL] [Abstract][Full Text] [Related]
15. Inherited defects of cobalamin metabolism.
Watkins D; Rosenblatt DS
Vitam Horm; 2022; 119():355-376. PubMed ID: 35337626
[TBL] [Abstract][Full Text] [Related]
16. Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver.
Mellman IS; Youngdahl-Turner P; Willard HF; Rosenberg LE
Proc Natl Acad Sci U S A; 1977 Mar; 74(3):916-20. PubMed ID: 15258
[TBL] [Abstract][Full Text] [Related]
17. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
Schuh S; Rosenblatt DS; Cooper BA; Schroeder ML; Bishop AJ; Seargeant LE; Haworth JC
N Engl J Med; 1984 Mar; 310(11):686-90. PubMed ID: 6700644
[TBL] [Abstract][Full Text] [Related]
18. Inherited disorders of cobalamin metabolism.
Qureshi AA; Rosenblatt DS; Cooper BA
Crit Rev Oncol Hematol; 1994 Oct; 17(2):133-51. PubMed ID: 7818787
[No Abstract] [Full Text] [Related]
19. New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.
Rosenblatt DS; Laframboise R; Pichette J; Langevin P; Cooper BA; Costa T
Pediatrics; 1986 Jul; 78(1):51-4. PubMed ID: 3725502
[TBL] [Abstract][Full Text] [Related]
20. [Neonatal onset methylmalonic aciduria and homocystinuria:Biochemical and clinical improvement with betaine therapy].
Urbón Artero A; Aldana Gómez J; Reig Del Moral C; Nieto Conde C; Merinero Cortés B
An Esp Pediatr; 2002 Apr; 56(4):337-41. PubMed ID: 11927078
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]