These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

391 related items for 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
    [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
    [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
    [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
    [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
    [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
    [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
    [Abstract] [Full Text] [Related]

  • 8. Identification of ABC transporters acting in vitamin B12 metabolism in Caenorhabditis elegans.
    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
    [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
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No 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
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Inherited defects of cobalamin metabolism.
    Watkins D, Rosenblatt DS.
    Vitam Horm; 2022 Mar; 119():355-376. PubMed ID: 35337626
    [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
    [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 15; 310(11):686-90. PubMed ID: 6700644
    [Abstract] [Full Text] [Related]

  • 18. Inherited disorders of cobalamin metabolism.
    Qureshi AA, Rosenblatt DS, Cooper BA.
    Crit Rev Oncol Hematol; 1994 Oct 15; 17(2):133-51. PubMed ID: 7818787
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No 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 15; 56(4):337-41. PubMed ID: 11927078
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.