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 *

251 related articles for article (PubMed ID: 9350306)

  • 61. Sudden and unexpected neonatal death: a protocol for the postmortem diagnosis of fatty acid oxidation disorders.
    Rinaldo P; Yoon HR; Yu C; Raymond K; Tiozzo C; Giordano G
    Semin Perinatol; 1999 Apr; 23(2):204-10. PubMed ID: 10331471
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Medium chain acyl-coenzyme A dehydrogenase deficiency.
    Bennett MJ; Hale DE
    N J Med; 1992 Sep; 89(9):675-8. PubMed ID: 1436730
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation.
    Saudubray JM; Coudé FX; Demaugre F; Johnson C; Gibson KM; Nyhan WL
    Pediatr Res; 1982 Oct; 16(10):877-81. PubMed ID: 7145511
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Medium-chain acyl-CoA dehydrogenase defect. Acute cerebral episodes and nonketotic hypoglycemia in children].
    von Mühlendahl KE; Lehnert W; Mönch E
    Dtsch Med Wochenschr; 1990 Aug; 115(33):1235-8. PubMed ID: 2387217
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Sudden unexpected infant death (SUDI) in a newborn due to medium chain acyl CoA dehydrogenase (MCAD) deficiency with an unusual severe genotype.
    Lovera C; Porta F; Caciotti A; Catarzi S; Cassanello M; Caruso U; Gallina MR; Morrone A; Spada M
    Ital J Pediatr; 2012 Oct; 38():59. PubMed ID: 23095120
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype.
    Roe DS; Vianey-Saban C; Sharma S; Zabot MT; Roe CR
    Clin Chim Acta; 2001 Oct; 312(1-2):55-67. PubMed ID: 11580910
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Rapid diagnosis of long chain and medium chain fatty acid oxidation disorders using lymphocytes.
    Brivet M; Slama A; Saudubray JM; Legrand A; Lemonnier A
    Ann Clin Biochem; 1995 Mar; 32 ( Pt 2)():154-9. PubMed ID: 7785942
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings.
    Catzeflis C; Bachmann C; Hale DE; Coates PM; Wiesmann U; Colombo JP; Joris F; Délèze G
    Eur J Pediatr; 1990 May; 149(8):577-81. PubMed ID: 2347356
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Neonatal multiple acyl-CoA dehydrogenase deficiency: essentially absent fatty acid oxidation activity in proband but normal activity in parental cultured skin fibroblasts.
    Ip WC; Hammond JW; Wilcken B
    J Inherit Metab Dis; 1996; 19(3):379-80. PubMed ID: 8803790
    [No Abstract]   [Full Text] [Related]  

  • 70. Fatty acid beta-oxidation in leukocytes from control subjects and medium-chain acyl-CoA dehydrogenase deficient patients.
    Wanders RJ; Ijlst L
    Biochim Biophys Acta; 1992 Jan; 1138(1):80-4. PubMed ID: 1737072
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Retrospective study of the medium-chain acyl-CoA dehydrogenase deficiency in Portugal.
    Ventura FV; Leandro P; Luz A; Rivera IA; Silva MF; Ramos R; Rocha H; Lopes A; Fonseca H; Gaspar A; Diogo L; Martins E; Leão-Teles E; Vilarinho L; Tavares de Almeida I
    Clin Genet; 2014 Jun; 85(6):555-61. PubMed ID: 23829193
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Treem WR; Rinaldo P; Hale DE; Stanley CA; Millington DS; Hyams JS; Jackson S; Turnbull DM
    Hepatology; 1994 Feb; 19(2):339-45. PubMed ID: 8294091
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Mitochondrial fatty acid oxidation disorders and cyclic vomiting syndrome.
    Rinaldo P
    Dig Dis Sci; 1999 Aug; 44(8 Suppl):97S-102S. PubMed ID: 10490047
    [TBL] [Abstract][Full Text] [Related]  

  • 74. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.
    Sims HF; Brackett JC; Powell CK; Treem WR; Hale DE; Bennett MJ; Gibson B; Shapiro S; Strauss AW
    Proc Natl Acad Sci U S A; 1995 Jan; 92(3):841-5. PubMed ID: 7846063
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected children.
    Iafolla AK; Thompson RJ; Roe CR
    J Pediatr; 1994 Mar; 124(3):409-15. PubMed ID: 8120710
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Screening of the most common medium-chain acyl CoA dehydrogenase (MCAD) deficiency mutation (K329E) in the Czech newborn population.
    Kozàk L; Hrabincovà E; Rudolfoà J; Vràbelovà S; Freiberger T
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():49-50. PubMed ID: 11400780
    [TBL] [Abstract][Full Text] [Related]  

  • 77. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
    Stanley CA
    Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Post-mortem analysis for two prevalent beta-oxidation mutations in sudden infant death.
    Yang Z; Lantz PE; Ibdah JA
    Pediatr Int; 2007 Dec; 49(6):883-7. PubMed ID: 18045290
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Fatty acid oxidation defects.
    von Döbeln U
    Acta Paediatr Suppl; 1993 Jun; 82 Suppl 389():88-90. PubMed ID: 8374203
    [No Abstract]   [Full Text] [Related]  

  • 80. Genetics of the sudden infant death syndrome.
    Courts C; Madea B
    Forensic Sci Int; 2010 Dec; 203(1-3):25-33. PubMed ID: 20674198
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.