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La ricerca find articoli where soggetti phrase all words 'CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 28 riferimenti
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    1. Infante, JP; Huszagh, VA
      Impaired arachidonic (20 : 4n-6) and docosahexaenoic (22 : 6n-3) acid synthesis by phenylalanine metabolites as etiological factors in the neuropathology of phenylketonuria

      MOLECULAR GENETICS AND METABOLISM
    2. Gregersen, N; Andresen, BS; Corydon, M; Corydon, TJ; Olsen, RKJ; Bolund, L; Bross, P
      Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship

      HUMAN MUTATION
    3. Rinaldo, P
      Fatty acid transport and mitochondrial oxidation disorders

      SEMINARS IN LIVER DISEASE
    4. Ibdah, JA; Zhao, YW; Viola, J; Gibson, B; Bennett, MJ; Strauss, AW
      Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutations

      JOURNAL OF PEDIATRICS
    5. Ibdah, JA; Paul, H; Zhao, Y; Binford, S; Salleng, K; Cline, M; Matern, D; Bennett, MJ; Rinaldo, P; Strauss, AW
      Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death

      JOURNAL OF CLINICAL INVESTIGATION
    6. Lund, AM; Leonard, JV
      Feeding difficulties in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

      ARCHIVES OF DISEASE IN CHILDHOOD
    7. Ibdah, JA; Yang, Z; Bennett, MJ
      Liver disease in pregnancy and fetal fatty acid oxidation defects

      MOLECULAR GENETICS AND METABOLISM
    8. Bennett, MJ; Rinaldo, P; Strauss, AW
      Inborn errors of mitochondrial fatty acid oxidation

      CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES
    9. Guertl, B; Noehammer, C; Hoefler, G
      Metabolic cardiomyopathies

      INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY
    10. Ozand, PT
      Hypoglycemia in association with various organic and amino acid disorders

      SEMINARS IN PERINATOLOGY
    11. Towbin, JA; Lipshultz, SE
      Genetics of neonatal cardiomyopathy

      CURRENT OPINION IN CARDIOLOGY
    12. Wanders, RJA; Vreken, P; den Boer, MEJ; Wijburg, FA; van Gennip, AH; IJlst, L
      Disorders of mitochondrial fatty acyl-CoA beta-oxidation

      JOURNAL OF INHERITED METABOLIC DISEASE
    13. Ibdah, JA; Bennett, MJ; Rinaldo, P; Zhao, YW; Gibson, B; Sims, HF; Strauss, AW
      A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

      NEW ENGLAND JOURNAL OF MEDICINE
    14. IBDAH JA; TEIN I; DIONISIVICI C; BENNETT MJ; IJLST L; GIBSON B; WANDERS RJA; STRAUSS AW
      MILD TRIFUNCTIONAL PROTEIN-DEFICIENCY IS ASSOCIATED WITH PROGRESSIVE NEUROPATHY AND MYOPATHY AND SUGGESTS A NOVEL GENOTYPE-PHENOTYPE CORRELATION

      The Journal of clinical investigation
    15. MURPHY VJ; MANTAMADIOTIS T; BALDWIN GS
      GASTRIN AND GASTRIN RECEPTOR ANTAGONISTS BIND TO BOTH N-TERMINAL AND C-TERMINAL HALVES OF THE 78KDA GASTRIN-BINDING PROTEIN

      International journal of biochemistry & cell biology
    16. DING JH; YANG BZ; NADA MA; ROE CR
      IMPROVED DETECTION OF THE G1528C MUTATION IN LCHAD DEFICIENCY

      Biochemical and molecular medicine
    17. STRAUSS AW
      DEFECTS OF MITOCHONDRIAL PROTEINS AND PEDIATRIC HEART-DISEASE

      Progress in pediatric cardiology
    18. SCHAEFER J; JACKSON S; DICK DJ; TURNBULL DM
      TRIFUNCTIONAL ENZYME DEFICIENCY - ADULT PRESENTATION OF A USUALLY FATAL BETA-OXIDATION DEFECT

      Annals of neurology
    19. USHIKUBO S; AOYAMA T; KAMIJO T; WANDERS RJA; RINALDO P; VOCKLEY J; HASHIMOTO T
      MOLECULAR CHARACTERIZATION OF MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - FORMATION OF THE ENZYME COMPLEX IS IMPORTANT FOR STABILIZATION OF BOTH ALPHA-SUBUNIT AND BETA-SUBUNIT

      American journal of human genetics
    20. LEHOTAY DC; CLARKE JTR
      ORGANIC ACIDURIAS AND RELATED ABNORMAL

      Critical reviews in clinical laboratory sciences
    21. PLEET AB
      FUNNY SPELLS IN NEUROENDOCRINE DISORDERS

      Seminars in neurology
    22. WEINBERGER MJ; RINALDO P; STRAUSS AW; BENNETT MJ
      INTACT ALPHA-SUBUNIT IS REQUIRED FOR MEMBRANE-BINDING OF HUMAN MITOCHONDRIAL TRIFUNCTIONAL BETA-OXIDATION PROTEIN, BUT IS NOT NECESSARY FORCONFERRING 3-KETOACYL-COA THIOLASE ACTIVITY TO THE BETA-SUBUNIT

      Biochemical and biophysical research communications
    23. YANG SY
      THE LARGE SUBUNIT OF THE PIG-HEART MITOCHONDRIAL MEMBRANE-BOUND BETA-OXIDATION COMPLEX IS A LONG-CHAIN ENOYL-COA HYDRATASE - 3-HYDROXYACYL-COA DEHYDROGENASE BIFUNCTIONAL ENZYME

      Comparative biochemistry and physiology. B. Comparative biochemistry
    24. VENIZELOS N; IJLST L; WANDERS RJA; HAGENFELDT L
      BETA-OXIDATION ENZYMES IN FIBROBLASTS FROM PATIENTS WITH 3-HYDROXYDICARBOXYLIC ACIDURIA

      Pediatric research
    25. VOCKLEY J
      THE CHANGING FACE OF DISORDERS OF FATTY-ACID OXIDATION

      Mayo Clinic proceedings
    26. KAMIJO T; WANDERS RJA; SAUDUBRAY JM; AOYAMA T; KOMIYAMA A; HASHIMOTO T
      MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - CATALYTIC HETEROGENEITY OF THE MUTANT ENZYME IN 2 PATIENTS

      The Journal of clinical investigation
    27. BARTLETT K
      METHODS FOR THE INVESTIGATION OF HYPOGLYCEMIA WITH PARTICULAR REFERENCE TO INHERITED DISORDERS OF MITOCHONDRIAL BETA-OXIDATION

      Bailliere's clinical endocrinology and metabolism
    28. PEREZCERDA C; MERINERO B; JIMENEZ A; GARCIA MJ; SANZ P; IJLST L; WANDERS RJA; UGARTE M
      1ST REPORT OF PRENATAL-DIAGNOSIS OF LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY IN A PREGNANCY AT RISK

      Prenatal diagnosis


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 10/08/20 alle ore 09:20:03