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La ricerca find articoli where authors phrase all words ' Hagenfeldt, L' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 28 riferimenti
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    1. Fugelseth, D; Guthenberg, C; Hagenfeldt, L; Liestol, K; Hallerud, M; Lindemann, R
      Patent ductus venosus does not lead to alimentary galactosaemia in preterminfants

      ACTA PAEDIATRICA
    2. Nordenstrom, A; Wedell, A; Hagenfeldt, L; Marcus, C; Larsson, A
      Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants

      PEDIATRICS
    3. Flyckt, L; Venizelos, N; Edman, G; Bjerkenstedt, L; Hagenfeldt, L; Wiesel, FA
      Aberrant tyrosine transport across the cell membrane in patients with schizophrenia

      ARCHIVES OF GENERAL PSYCHIATRY
    4. Eeg-Olofsson, O; Zhang, WW; Olsson, Y; Jagell, S; Hagenfeldt, L
      D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boy

      JOURNAL OF CHILD NEUROLOGY
    5. Wiesel, FA; Andersson, JLR; Westerberg, G; Wieselgren, IM; Bjerkenstedt, L; Hagenfeldt, L; Langstrom, B
      Tyrosine transport is regulated differently in patients with schizophrenia

      SCHIZOPHRENIA RESEARCH
    6. Johansson, A; Guthenberg, C; Ahlman, H; Von Dobeln, U; Hagenfeldt, L
      Prevalence of the 985A > G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Sweden

      SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
    7. Appelkvist, EL; Venizelos, N; Zhang, YY; Parmryd, I; Hagenfeldt, L; Dallner, G
      Synthesis of mevalonate pathway lipids in fibroblasts from Zellweger and X-linked ALD patients

      PEDIATRIC RESEARCH
    8. Nordenstrom, A; Thilen, A; Hagenfeldt, L; Larsson, A; Wedell, A
      Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    9. Solders, G; Celsing, G; Hagenfeldt, L; Ljungman, P; Isberg, B; Ringden, O
      Improved peripheral nerve conduction, EEG and verbal IQ after bone marrow transplantation for adult metachromatic leukodystrophy

      BONE MARROW TRANSPLANTATION
    10. HAGENFELDT L
      COMPROMISED FATTY-ACID OXIDATION IN MITOCHONDRIAL DISORDERS

      Journal of inherited metabolic disease
    11. VENIZELOS N; VONDOBELN U; HAGENFELDT L
      FATTY-ACID OXIDATION IN FIBROBLASTS FROM PATIENTS WITH DEFECTS IN BETA-OXIDATION AND IN THE RESPIRATORY-CHAIN

      Journal of inherited metabolic disease
    12. THILEN A; NORDENSTROM A; HAGENFELDT L; VONDOBELN U; GUTHENBERG C; LARSSON A
      BENEFITS OF NEONATAL SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) IN SWEDEN

      Pediatrics
    13. KOSTULAS K; CRISBY M; HUANG WX; LANNFELT L; HAGENFELDT L; EGGERTSEN G; KOSTULAS V; HILLERT J
      A METHYLENETETRAHYDROFOLATE REDUCTASE GENE POLYMORPHISM IN ISCHEMIC STROKE AND IN CAROTID-ARTERY STENOSIS

      European journal of clinical investigation
    14. MALM G; RINGDEN O; ANVRET W; VONDOBELN U; HAGENFELDT L; ISBERG B; KNUUTILA S; NENNESMO I; WINIARSKI J; MARCUS C
      TREATMENT OF ADRENOLEUKODYSTROPHY WITH BONE-MARROW TRANSPLANTATION

      Brain pathology
    15. MALM G; RINGDEN O; ANVRET M; VONDOBELN U; HAGENFELDT L; ISBERG B; KNUUTILA S; NENNESMO I; WINIARSKI J; MARCUS C
      TREATMENT OF ADRENOLEUKODYSTROPHY WITH BONE-MARROW TRANSPLANTATION

      Acta paediatrica
    16. BJERKENSTEDT L; WIESEL FA; HAGENFELDT L
      REDUCED TYROSINE TRANSPORT IN SCHIZOPHRENIA

      Schizophrenia research
    17. WIESEL FA; ANDERSSON J; WIESELGREN IM; BLOMQVIST G; BJERKENSTEDT L; HAGENFELDT L
      TYROSINE TRANSPORT IN SCHIZOPHRENIA

      Schizophrenia research
    18. GIBSON KM; JAKOBS C; OGIER H; HAGENFELDT L; EEGOLOFSSON KE; EEGOLOFSSON O; AKSU F; WEBER HP; ROSSIER E; VOLLMER B; LEHNERT W
      VIGABATRIN THERAPY IN 6 PATIENTS WITH SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY

      Journal of inherited metabolic disease
    19. HAGENFELDT L; VENIZELOS N; VONDOBELN U
      CLINICAL AND BIOCHEMICAL PRESENTATION OF LONG-CHAIN 3-HYDROXYACYL-COADEHYDROGENASE-DEFICIENCY

      Journal of inherited metabolic disease
    20. WIESEL FA; VENIZELOS N; BJERKENSTEDT L; HAGENFELDT L
      TYROSINE TRANSPORT IN SCHIZOPHRENIA

      Schizophrenia research
    21. HAGENFELDT L; VONDOBELN U; SOLDERS G; KAIJSER L
      CREATINE TREATMENT IN MELAS

      Muscle & nerve
    22. VONDOBELN U; VENIZELOS N; WESTGREN M; HAGENFELDT L
      LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE IN CHORIONIC VILLI, FETAL LIVER AND FIBROBLASTS AND PRENATAL-DIAGNOSIS OF 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY

      Journal of inherited metabolic disease
    23. SVENSSON E; ISELIUS L; HAGENFELDT L
      SEVERITY OF MUTATION IN THE PHENYLALANINE-HYDROXYLASE GENE INFLUENCESPHENYLALANINE METABOLISM IN PHENYLKETONURIA AND HYPERPHENYLALANINEMIAHETEROZYGOTES

      Journal of inherited metabolic disease
    24. HAVERKORN C; BLOMQUIST HK; SNELLMAN K; AHLMAN H; VONDOBELN U; HAGENFELDT L
      THYMINE-URACILURIA - A DISEASE OR A FORTUITOUS FINDING

      Pediatric research
    25. VENIZELOS N; IJLST L; WANDERS RJA; HAGENFELDT L
      BETA-OXIDATION ENZYMES IN FIBROBLASTS FROM PATIENTS WITH 3-HYDROXYDICARBOXYLIC ACIDURIA

      Pediatric research
    26. GIESECKE K; KLINGSTEDT C; LJUNGQVIST O; HAGENFELDT L
      THE MODIFYING INFLUENCE OF ANESTHESIA ON POSTOPERATIVE PROTEIN CATABOLISM

      British Journal of Anaesthesia
    27. WESTGREN M; EK S; BUI TH; HAGENFELDT L; MARKLING L; PSCHERA H; SEIGER A; SUNDSTROM E; RINGDEN O
      ESTABLISHMENT OF A TISSUE-BANK FOR FETAL STEM-CELL TRANSPLANTATION

      Acta obstetricia et gynecologica Scandinavica
    28. VONDOBELN U; WIBOM R; AHLMAN H; NENNESMO I; NYCTELIUS H; HULTMAN E; HAGENFELDT L
      FATAL NEONATAL LACTIC-ACIDOSIS WITH RESPIRATORY INSUFFICIENCY DUE TO COMPLEX-I AND COMPLEX-IV DEFICIENCY

      Acta paediatrica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 08/08/20 alle ore 15:27:48