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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 11462735)

  • 41. A case of methylmalonic and propionic acidemia due to methulmalonyl-CoA carbonylmutase apoenzyme deficiency.
    van den Berg H; Boelkens MT; Hommes FA
    Acta Paediatr Scand; 1976 Jan; 65(1):113-8. PubMed ID: 3087
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Mutations in mut methylmalonic acidemia: clinical and enzymatic correlations.
    Ledley FD; Rosenblatt DS
    Hum Mutat; 1997; 9(1):1-6. PubMed ID: 8990001
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency.
    Packman S; Mahoney MJ; Tanaka K; Hsia YE
    J Pediatr; 1978 May; 92(5):769-71. PubMed ID: 25314
    [No Abstract]   [Full Text] [Related]  

  • 44. [Methylmalonic acid].
    Tanaka A; Yamaoka S
    Nihon Rinsho; 2004 Nov; 62 Suppl 11():696-9. PubMed ID: 15628513
    [No Abstract]   [Full Text] [Related]  

  • 45. Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.
    Morel CF; Watkins D; Scott P; Rinaldo P; Rosenblatt DS
    Mol Genet Metab; 2005; 86(1-2):160-71. PubMed ID: 16150626
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Neurological dysfunction in methylmalonic acidaemia is probably related to the inhibitory effect of methylmalonate on brain energy production.
    Wajner M; Coelho JC
    J Inherit Metab Dis; 1997 Nov; 20(6):761-8. PubMed ID: 9427143
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Growth hormone deficiency associated with methylmalonic acidemia.
    Al-Owain M; Freehauf C; Bernstein L; Kappy M; Thomas J
    J Pediatr Endocrinol Metab; 2004 Feb; 17(2):239-43. PubMed ID: 15055362
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Inhibition by methylmalonate of glycine uptake by synaptosomes from rat spinal cord.
    Lopez-Lahoya J; García ML; Benavides J; Ugarte M
    J Neurochem; 1981 Jan; 36(1):325-7. PubMed ID: 6109757
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Methylmalonic acidemia and kidney transplantation.
    Lubrano R; Perez B; Elli M
    Pediatr Nephrol; 2013 Oct; 28(10):2067-8. PubMed ID: 23793882
    [No Abstract]   [Full Text] [Related]  

  • 50. Liver transplantation for methylmalonic acidaemia.
    van't Hoff W; McKiernan PJ; Surtees RA; Leonard JV
    Eur J Pediatr; 1999 Dec; 158 Suppl 2():S70-4. PubMed ID: 10603103
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Metabolic stroke in methylmalonic acidemia five years after liver transplantation.
    Chakrapani A; Sivakumar P; McKiernan PJ; Leonard JV
    J Pediatr; 2002 Feb; 140(2):261-3. PubMed ID: 11865284
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Novel mutations found in two genes of thai patients with isolated methylmalonic acidemia.
    Keeratichamroen S; Cairns JR; Sawangareetrakul P; Liammongkolkul S; Champattanachai V; Srisomsap C; Kamolsilp M; Wasant P; Svasti J
    Biochem Genet; 2007 Jun; 45(5-6):421-30. PubMed ID: 17410422
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study.
    Larnaout A; Mongalgi MA; Kaabachi N; Khiari D; Debbabi A; Mebazza A; Ben Hamida M; Hentati F
    J Inherit Metab Dis; 1998 Aug; 21(6):639-44. PubMed ID: 9762599
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Detection of errors in methylmalonyl-CoA metabolism by using amniotic fluid.
    Morrow G; Revsin B; Lebowitz J; Britt W; Giles H
    Clin Chem; 1977 May; 23(5):791-5. PubMed ID: 15739
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A radio-HPLC assay for the measurement of methylmalonyl-CoA mutase.
    Causey AG; Bartlett K
    Clin Chim Acta; 1984 May; 139(2):179-86. PubMed ID: 6145531
    [No Abstract]   [Full Text] [Related]  

  • 56. Methylmalonic aciduria: follow-up and enzymology on the original case after 36 years.
    Bain MD; Till J; Jones MG; Besley GT; Lee P; Oliveira D; Chalmers RA
    J Inherit Metab Dis; 2005; 28(6):1179-80. PubMed ID: 16435224
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Case of methylmalonic acidemia presenting clinically Leigh encephalopathy].
    Ito H; Mori K; Ito M; Naito E; Yokota I; Kuroda Y
    No To Hattatsu; 2004 Jul; 36(4):324-9. PubMed ID: 15272617
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Methylmalonic acidemia presenting with an ichthyosis vulgaris-like aspect.
    Boggio P; Machado MC; De Oliveira ZN; Sotto MN
    Pediatr Dermatol; 2007; 24(4):455-6. PubMed ID: 17845195
    [No Abstract]   [Full Text] [Related]  

  • 59. Renal transplant in methylmalonic acidemia: could it be the best option? Report on a case at 10 years and review of the literature.
    Lubrano R; Elli M; Rossi M; Travasso E; Raggi C; Barsotti P; Carducci C; Berloco P
    Pediatr Nephrol; 2007 Aug; 22(8):1209-14. PubMed ID: 17401587
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mutation and biochemical analysis of 19 probands with mut0 and 13 with mut- methylmalonic aciduria: identification of seven novel mutations.
    Lempp TJ; Suormala T; Siegenthaler R; Baumgartner ER; Fowler B; Steinmann B; Baumgartner MR
    Mol Genet Metab; 2007 Mar; 90(3):284-90. PubMed ID: 17113806
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.