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    1. GELLERA C; BOTTI S; CASTELLOTTI B; RIGGIO MC; MAZZUCCHELLI F; DIDONATO S; TARONI F
      FRATAXIN GENE-MUTATIONS IN FRIEDREICHS ATAXIA ALLELES NOT CARRYING THE GAA EXPANSION

      Neurology
    2. CAVALIER L; OUAHCHI K; KAYDEN HJ; DIDONATO S; REUTENAUER L; MANDEL JL; KOENIG M
      ATAXIA WITH ISOLATED VITAMIN-E-DEFICIENCY - HETEROGENEITY OF MUTATIONS AND PHENOTYPIC VARIABILITY IN A LARGE NUMBER OF FAMILIES

      American journal of human genetics
    3. BENEDETTI S; DIMECO F; POLLO B; CIRENEI N; COLOMBO BM; BRUZZONE MG; CATTANEO E; VESCOVI A; DIDONATO S; COLOMBO MP; FINOCCHIARO G
      LIMITED EFFICACY OF THE HSV-TK GCV SYSTEM FOR GENE-THERAPY OF MALIGNANT GLIOMAS AND PERSPECTIVES FOR THE COMBINED TRANSDUCTION OF THE INTERLEUKIN-4 GENE/

      Human gene therapy
    4. MONTERMINI L; RICHTER A; MORGAN K; JUSTICE CM; JULIEN D; CASTELLOTTI B; MERCIER J; POIRIER J; CAPOZZOLI F; BOUCHARD JP; LEMIEUX B; MATHIEU J; VANASSE M; SENI MH; GRAHAM G; ANDERMANN F; ANDERMANN E; MELANCON SB; KEATS BJB; DIDONATO S; PANDOLFO M
      PHENOTYPIC VARIABILITY IN FRIEDREICH-ATAXIA - ROLE OF THE ASSOCIATED GAA TRIPLET REPEAT EXPANSION

      Annals of neurology
    5. GELLERA C; PAREYSON D; CASTELLOTTI B; MAZZUCCHELLI F; ZAPPACOSTA B; PANDOLFO M; DIDONATO S
      VERY LATE-ONSET FRIEDREICHS ATAXIA WITHOUT CARDIOMYOPATHY IS ASSOCIATED WITH LIMITED GAA EXPANSION IN THE X25 GENE

      Neurology
    6. ZAPPACOSTA B; GELLERA C; MAZZUCCHELLI F; CASTELLOTTI B; RIGGIO MC; PAREYSON D; DIDONATO S
      CLINICAL AND GENETIC-STUDIES IN ITALIAN AUTOSOMAL-DOMINANT CEREBELLARATAXIAS

      Neurology
    7. PAREYSON D; GELLERA C; CASTELLOTTI B; ZAPPACOSTA B; MAZZUCCHELLI F; RIGGIO MC; TARONI F; PANDOLFO M; DIDONATO S
      FRIEDREICHS ATAXIA IN NORTHERN ITALY - DNA EXPANSION AND GENOTYPE-PHENOTYPE CORRELATIONS

      Neurology
    8. ANTOZZI C; CONFALONIERI P; MANTEGAZZA R; DIDONATO S
      EMERGING TREATMENTS IN MYOPATHIES

      European neurology
    9. CAVADINI P; DIBLASI C; PRINCIVALLE A; BARATTA S; DIDONATO S; BATTAGLIA G; MORA M; TARONI F
      EVIDENCES THAT HUMAN FRATAXIN LOCALIZES IN THE MITOCHONDRIA AND IS EXPRESSED IN NEURAL TISSUES SELECTIVELY AFFECTED IN FRIEDREICHS ATAXIA

      American journal of human genetics
    10. BOTTI S; CASTELLOTTI B; RIGGIO MC; BARATTA S; DIDONATO S; CAVADINI P; GELLERA C; TARONI F
      GENE MICROMUTATIONS IN FRIEDREICHS ATAXIA ALLELES NOT CARRYING THE GAA EXPANSION

      American journal of human genetics
    11. DIDONATO S
      CELLULAR-MODELS FOR PATHOGENESIS IN MITOCHONDRIAL DISEASES

      Current opinion in neurology
    12. BENEDETTI S; DIMECO F; CIRENEI N; POLLO B; BRUZZONE MG; COLOMBO BM; VESCOVI A; COLOMBO M; DIDONATO S; FINOCCHIARO G
      EFFECTS OF HSV-TK AND IL-4 GENE-TRANSFER IN EXPERIMENTAL GLIOMAS

      Cancer gene therapy
    13. DIDONATO S; FEDERICO A
      TRIBUTE TO HARDING,ANITA (1952-1995) - OBITUARY

      Italian journal of neurological sciences
    14. CAMPUZANO V; MONTERMINI L; MOLTO MD; PIANESE L; COSSEE M; CAVALCANTI F; MONROS E; RODIUS F; DUCLOS F; MONTICELLI A; ZARA F; CANIZARES J; KOUTNIKOVA H; BIDICHANDANI SI; GELLERA C; BRICE A; TROUILLAS P; DEMICHELE G; FILLA A; DEFRUTOS R; PALAU F; PATEL PI; DIDONATO S; MANDEL JL; COCOZZA S; KOENIG M; PANDOLFO M
      FRIEDREICHS-ATAXIA - AUTOSOMAL RECESSIVE DISEASE CAUSED BY AN INTRONIC GAA TRIPLET REPEAT EXPANSION

      Science
    15. MONTERMINI L; ZARA F; BIDICHANDANI S; PATEL PI; PANDOLFO M; CAMPUZANO V; COSSEE M; RODIUS F; DUCLOS F; KOUTNIKOVA H; MANDEL JL; KOENIG M; PIANESE FL; MONTICELLI A; CAVALCANTI F; COCOZZA S; DEMICHELE G; FILLA A; BRICE A; TROUILLAS P; MONROS E; PALAU F; CANIZARES J; DEFRUTOS R; GELLERA C; DIDONATO S
      FRIEDREICH ATAXIA - AUTOSOMAL RECESSIVE DISEASE CAUSED BY AN INTRONICGAA TRIPLET REPEAT EXPANSION

      Neurology
    16. TARONI F; BOTTI S; SGHIRLANZONI A; SCAIOLI V; DIDONATO S; PAREYSON D
      HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - A NONSENSEMUTATION IN THE PMP22 GENE IN A FAMILY NOT CARRYING THE COMMON 17P11.2-12 DELETION

      Neurology
    17. GELLERA C; MEONI C; CASTELLOTTI B; ZAPPACOSTA B; GIROTTI F; TARONI F; DIDONATO S
      ERRORS IN HUNTINGTON DISEASE DIAGNOSTIC-TEST CAUSED BY TRINUCLEOTIDE DELETION IN THE IT15 GENE

      American journal of human genetics
    18. ALBAROSA R; COLOMBO BM; ROZ L; MAGNANI I; POLLO B; CIRENEI N; GIANI C; CONTI AMF; DIDONATO S; FINOCCHIARO G
      DELETION MAPPING OF GLIOMAS SUGGESTS THE PRESENCE OF 2 SMALL REGIONS FOR CANDIDATE TUMOR-SUPPRESSOR GENES IN A 17-CM INTERVAL ON CHROMOSOME-10Q

      American journal of human genetics
    19. DIDONATO S
      CAN WE AVOID AVED

      Nature genetics
    20. EOLI M; PANDOLFO M; AMOROSO A; SALMAGGI A; ZAFFARONI M; GASPARINI P; DIDONATO S; MILANESE C; ZEVIANI M
      EVIDENCE OF LINKAGE BETWEEN SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS AND HLA-CLASS-II LOCI IN ITALIAN MULTIPLEX FAMILIES

      European journal of human genetics
    21. ZARA F; BIANCHI A; AVANZINI G; DIDONATO S; CASTELLOTTI B; PATEL PI; PANDOLFO M
      MAPPING OF GENES PREDISPOSING TO IDIOPATHIC GENERALIZED EPILEPSY

      Human molecular genetics
    22. TIRANTI V; MUNARO M; SANDONA D; LAMANTEA E; RIMOLDI M; DIDONATO S; BISSON R; ZEVIANI M
      NUCLEAR-DNA ORIGIN OF CYTOCHROME-C-OXIDASE DEFICIENCY IN LEIGHS SYNDROME - GENETIC-EVIDENCE BASED ON PATIENTS-DERIVED RHO-DEGREES TRANSFORMANTS

      Human molecular genetics
    23. VERDERIO E; CAVADINI P; MONTERMINI L; WANG HW; LAMANTEA E; FINOCCHIARO G; DIDONATO S; GELLERA C; TARONI F
      CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY - STRUCTURE OF THE GENE AND CHARACTERIZATION OF 2 NOVEL DISEASE-CAUSING MUTATIONS

      Human molecular genetics
    24. TIRANTI V; ROSSI E; ROCCHI M; DIDONATO S; ZUFFARDI O; ZEVIANI M
      THE GENE (NFE2L1) FOR HUMAN NRF-1, AN ACTIVATOR INVOLVED IN NUCLEAR-MITOCHONDRIAL INTERACTIONS, MAPS TO 7Q32

      Genomics
    25. TIRANTI V; ROSSI E; RUIZCARRILLO A; ROSSI G; ROCCHI M; DIDONATO S; ZUFFARDI O; ZEVIANI M
      CHROMOSOMAL LOCALIZATION OF MITOCHONDRIAL TRANSCRIPTION FACTOR-A (TCF6), SINGLE-STRANDED DNA-BINDING PROTEIN (SSBP), AND ENDONUCLEASE-G (ENDOC), 3 HUMAN HOUSEKEEPING GENES INVOLVED IN MITOCHONDRIAL BIOGENESIS

      Genomics
    26. ANDRIA G; GATTI R; BALLABIO A; MASTROIACOVO P; BURGIO R; RUBINO A; CAO A; SABETTA G; DALLAPICCOLA B; DIDONATO S
      TREATMENT OF INTRATHECAL INFUSION OF WHIT E BLOOD-CELLS IN GENETIC-DISEASES

      Rivista italiana di pediatria
    27. DIONISIVICI C; GARAVAGLIA B; BURLINA A; BERTINI E; WANDERS RJA; HASHIMOTO T; SABETTA G; INVERNIZZI F; TARONI F; DIDONATO S
      MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - CLINICAL AND BIOCHEMICAL FINDINGS IN POUR PATIENTS

      Annals of neurology
    28. PALAU F; DEMICHELE G; VILCHEZ JJ; PANDOLFO M; MONROS E; COCOZZA S; SMEYERS P; LOPEZARLANDIS J; CAMPANELLA G; DIDONATO S; FILLA A
      EARLY-ONSET ATAXIA WITH CARDIOMYOPATHY AND RETAINED TENDON REFLEXES MAPS TO THE FRIEDREICHS ATAXIA LOCUS ON CHROMOSOME 9Q

      Annals of neurology
    29. ALBAROSA R; DIDONATO S; FINOCCHIARO G
      REDEFINITION OF THE CODING SEQUENCE OF THE MXI1 GENE AND IDENTIFICATION OF A POLYMORPHIC REPEAT IN THE 3' NONCODING REGION THAT ALLOWS THE DETECTION OF LOSS OF HETEROZYGOSITY OF CHROMOSOME 10Q25 IN GLIOBLASTOMAS

      Human genetics
    30. MARIOTTI C; UZIEL G; CARRARA F; MORA M; PRELLE A; TIRANTI V; DIDONATO S; ZEVIANI M
      EARLY-ONSET ENCEPHALOMYOPATHY ASSOCIATED WITH TISSUE-SPECIFIC MITOCHONDRIAL-DNA DEPLETION - A MORPHOLOGICAL, BIOCHEMICAL AND MOLECULAR-GENETIC STUDY

      Journal of neurology
    31. FABRIZI GM; TIRANTI V; MARIOTTI C; GUAZZI GC; MALANDRINI A; DIDONATO S; ZEVIANI M
      SEQUENCE-ANALYSIS OF MITOCHONDRIAL-DNA IN A NEW MATERNALLY INHERITED ENCEPHALOMYOPATHY

      Journal of neurology
    32. MARIOTTI C; SAVARESE N; SUOMALAINEN A; RIMOLDI M; COMI G; PRELLE A; ANTOZZI C; SERVIDEI S; JARRE L; DIDONATO S; ZEVIANI M
      GENOTYPE TO PHENOTYPE CORRELATIONS IN MITOCHONDRIAL ENCEPHALOMYOPATHIES ASSOCIATED WITH THE A3243G MUTATION OF MITOCHONDRIAL-DNA

      Journal of neurology
    33. DIONISIVICI C; SAPONARA I; BURLINA AB; GARAVAGLIA B; DIDONATO S; PICCA S; BERTINI E; SABETTA G
      MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY AND HYPOPARATHYROIDISM

      Pediatric research
    34. DIONSIVICI C; GARAVAGLIA B; BARTULI A; INVERNIZZI F; DIDONATO S; SABETTA G; KAHLER SG; MILLINGTON DS
      CARNITINE ACYLCARNITINE TRANSLOCASE DEFICIENCY - BENIGN COURSE WITHOUT CARDIAC INVOLVEMENT

      Pediatric research
    35. PAREYSON D; SCAIOLI V; LORENZETTI D; BOTTI S; SOLARI A; LUPSKI JR; DIDONATO S; TARONI F; SGHIRLANZONI A
      PHENOTYPIC HETEROGENEITY IN HNPP PATIENTS WITH THE 17P11.2-12 DELETION

      Neurology
    36. TENAN M; CARRARA F; DIDONATO S; FINOCCHIARO G
      ABSENCE OF MUTATIONS AND IDENTIFICATION OF 2 POLYMORPHISMS IN THE SSCP AND SEQUENCE-ANALYSIS OF P21(CKI) GENE IN MALIGNANT GLIOMAS

      International journal of cancer
    37. ZEVIANI M; TIRANTI V; MUNARO M; SANDONA D; LAMANTEA E; DIDONATO S; BISSON R
      USE OF PATIENT-DERIVED RHO-DEGREES CELLS TO ASSIGN THE NUCLEAR OR MITOCHONDRIAL ORIGIN OF DEFECTS OF THE RESPIRATORY-CHAIN COMPLEXES

      American journal of human genetics
    38. TARONI F; BOTTI S; SGHIRLANZONI A; BOTTEON G; DIDONATO S; PAREYSON D
      A NONSENSE MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) NOT ASSOCIATED WITH THE 17P11.2 DELETION

      American journal of human genetics
    39. GELLERA C; ZAPPACOSTA MB; GIROTTI F; MEONI C; CASTELLOTTI B; TARONI F; DIDONATO S
      UNUSUAL ATAXIC PHENOTYPE IN A PATIENT WITH ABNORMAL (GAG)(N) EXPANSION AT THE HD LOCUS

      American journal of human genetics
    40. DOERFLINGER N; LINDER C; OUAHCHI K; GYAPAY G; WEISSENBACH J; LEPASLIER D; RIGAULT P; BELAL S; BENHAMIDA C; HENTATI F; BENHAMIDA M; PANDOLFO M; DIDONATO S; SOKOL R; KAYDEN H; LANDRIEU P; DURR A; BRICE A; GOUTIERES F; KOHLSCHUTTER A; SABOURAUD P; BENOMAR A; YAHYAOUI M; MANDEL JL; KOENIG M
      ATAXIA WITH VITAMIN-E-DEFICIENCY - REFINEMENT OF GENETIC LOCALIZATIONAND ANALYSIS OF LINKAGE DISEQUILIBRIUM BY USING NEW MARKERS IN 14 FAMILIES

      American journal of human genetics
    41. LORENZETTI D; PAREYSON D; SGHIRLANZONI A; ROA BB; ABBAS NE; PANDOLFO M; DIDONATO S; LUPSKI JR
      A 1.5-MB DELETION IN 17P11.2-P12 IS FREQUENTLY OBSERVED IN ITALIAN FAMILIES WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      American journal of human genetics
    42. COLOMBO I; FINOCCHIARO G; GARAVAGLIA B; GARBUGLIO N; YAMAGUCHI S; FRERMAN FE; BERRA B; DIDONATO S
      MUTATIONS AND POLYMORPHISMS OF THE GENE ENCODING THE BETA-SUBUNIT OF THE ELECTRON-TRANSFER FLAVOPROTEIN IN 3 PATIENTS WITH GLUTARIC ACIDEMIA TYPE-II

      Human molecular genetics
    43. MINOLETTI F; COLOMBO I; MARTIN AL; DIDONATO S; TARONI F; FINOCCHIARO G; PANDOLFO M
      LOCALIZATION OF THE HUMAN GENE FOR CARNITINE PALMITOYLTRANSFERASE TO 1P13-P11 BY NONRADIOACTIVE IN-SITU HYBRIDIZATION (VOL 13, PG 1372, 1992)

      Genomics
    44. CORTI O; FINOCCHIARO G; ROSSI E; ZUFFARDI O; DIDONATO S
      MOLECULAR-CLONING OF CDNAS ENCODING HUMAN CARNITINE ACETYLTRANSFERASEAND MAPPING OF THE CORRESPONDING GENE TO CHROMOSOME 9Q34.1

      Genomics
    45. ANTONACCI R; COLOMBO I; ARCHIDIACONO N; VOLTA M; DIDONATO S; FINOCCHIARO G; ROCCHI M
      ASSIGNMENT OF THE GENE ENCODING THE BETA-SUBUNIT OF THE ELECTRON-TRANSFER FLAVOPROTEIN (ETFB) TO HUMAN-CHROMOSOME 19Q13.3

      Genomics
    46. PANDOLFO M; PIZZUTI A; REDOLFI E; MUNARO M; DIDONATO S; CAVALCANTI F; FILLA A; MONTICELLI A; PIANESE L; COCOZZA S
      ISOLATION OF A NEW GENE IN THE FRIEDREICH ATAXIA CANDIDATE REGION ON HUMAN-CHROMOSOME-9 BY CDNA DIRECT SELECTION

      Biochemical medicine and metabolic biology
    47. CORTI O; DIDONATO S; FINOCCHIARO G
      DIVERGENT SEQUENCES IN THE 5' REGION OF CDNA SUGGEST ALTERNATIVE SPLICING AS A MECHANISM FOR THE GENERATION OF CARNITINE ACETYLTRANSFERASESWITH DIFFERENT SUBCELLULAR LOCALIZATIONS

      Biochemical journal
    48. MONTERMINI L; WANG HW; VERDERIO E; TARONI F; DIDONATO S; FINOCCHIARO G
      IDENTIFICATION OF 5' REGULATORY REGIONS OF THE HUMAN CARNITINE PALMITOYLTRANSFERASE-II GENE

      Biochimica et biophysica acta, N. Gene structure and expression
    49. MAGNANI I; GUERNERI S; POLLO B; CIRENEI N; COLOMBO BM; BROGGI G; GALLI C; BUGIANI O; DIDONATO S; FINOCCHIARO G; CONTI AMF
      INCREASING COMPLEXITY OF THE KARYOTYPE IN 50 HUMAN GLIOMAS - PROGRESSIVE EVOLUTION AND DE-NOVO OCCURRENCE OF CYTOGENETIC ALTERATIONS

      Cancer genetics and cytogenetics
    50. RIMOLDI M; BERGOMI P; ROMEO A; DIDONATO S
      A NEW STABLE-ISOTOPE DILUTION METHOD FOR MEASUREMENT OF EROTIC ACID UTILIZING SOLVENT-EXTRACTED URINE

      Journal of inherited metabolic disease
    51. GELLERA C; DIDONATO S; TARONI F
      MOLECULAR STUDY OF FUMARASE DEFICIENCY

      Neurology
    52. GELLERA C; DIDONATO S; TARONI F
      MOLECULAR STUDY OF FUMARASE DEFICIENCY

      Neurology
    53. PAREYSON D; SGHIRLANZONI A; SCAIOLI V; CASTELLOTTI B; DIDONATO S; PANDOLFO M; LORENZETTI D; LUPSKI JR
      SUBMICROSCOPIC DELETION IN 17P11.2-P12 IN ITALIAN HNPP FAMILIES

      Neurology
    54. ANTOZZI C; GARAVAGLIA B; MORA M; RIMOLDI M; MORANDI L; URSINO E; DIDONATO S
      LATE-ONSET RIBOFLAVIN-RESPONSIVE MYOPATHY WITH COMBINED MULTIPLE ACYL-COENZYME-A DEHYDROGENASE AND RESPIRATORY-CHAIN DEFICIENCY

      Neurology
    55. MARIOTTI C; TIRANTI V; CARRARA F; DALLAPICCOLA B; DIDONATO S; ZEVIANI M
      DEFECTIVE RESPIRATORY CAPACITY AND MITOCHONDRIAL PROTEIN-SYNTHESIS INTRANSFORMANT CYBRIDS HARBORING THE TRNA(LEU(UUR)) MUTATION ASSOCIATEDWITH MATERNALLY INHERITED MYOPATHY AND CARDIOMYOPATHY

      The Journal of clinical investigation
    56. TARONI F; VERDERIO E; DWORZAK F; WILLEMS PJ; CAVADINI P; DIDONATO S
      IDENTIFICATION OF A COMMON MUTATION IN THE CARNITINE PALMITOYLTRANSFERASE II GENE IN FAMILIAL RECURRENT MYOGLOBINURIA PATIENTS

      Nature genetics
    57. JODICE C; FRONTALI M; PERSICHETTI F; NOVELLETTO A; PANDOLFO M; SPADARO M; GIUNTI P; SCHINAIA G; LULLI P; MALASPINA P; PLASMATI R; TOLA R; ANTONELLI A; DIDONATO S; MOROCUTTI C; WEISSENBACH J; CANN HM; TERRENATO L
      THE GENE FOR SPINAL CEREBELLAR ATAXIA-1 (SCA1) IS FLANKED BY 2 CLOSELY LINKED HIGHLY POLYMORPHIC MICROSATELLITE LOCI

      Human molecular genetics
    58. PANDOLFO M; MUNARO M; COCOZZA S; REDOLFI EM; PIANESE L; CAVALCANTI F; MONTICELLI A; DIDONATO S
      A DINUCLEOTIDE REPEAT POLYMORPHISM (D9S202) IN THE FRIEDREICHS ATAXIAREGION ON CHROMOSOME-9Q13-Q21.1

      Human molecular genetics
    59. MONTERMINI L; DIDONATO S; FINOCCHIARO G
      IDENTIFICATION OF THE 5' REGULATORY REGION OF THE HUMAN CARNITINE PALMITOYLTRANSFERASE (CPT) GENE

      The FASEB journal
    60. TIRANTI V; ROCCHI M; DIDONATO S; ZEVIANI M
      CLONING OF HUMAN AND RAT CDNAS ENCODING THE MITOCHONDRIAL SINGLE-STRANDED DNA-BINDING PROTEIN (SSB)

      Gene
    61. COCOZZA S; ANTONELLI A; CAMPANELLA G; CAVALCANTI F; DEMICHELE G; DIDONATO S; FILLA A; MONTICELLI A; PIANESE L; PICCINELLI A; PORCELLINI A; REDOLFI E; VARRONE S; PANDOLFO M
      EVIDENCE OF A GENETIC-MARKER ASSOCIATED WITH EARLY-ONSET IN FRIEDREICHS ATAXIA

      Journal of neurology
    62. TARONI F; VERDERIO E; CAVADINI P; GELLERA C; DWORZAK F; DIDONATO S
      IDENTIFICATION OF THE MOST COMMON MUTATION UNDERLYING CARNITINE PALMITOYL TRANSFERASE-II (CPT-II) DEFICIENCY

      Neurology
    63. TIRANTI V; FABRIZI GM; MARIOTTI C; SAVARESE N; UZIEL G; DIDONATO S; ZEVIANI M
      MITOCHONDRIAL TRANSFER RNA(THR) MUTATION IN FATAL INFANTILE MYOPATHY WITH DEFICIENCY OF THE RESPIRATORY COMPLEX-I AND COMPLEX-IV

      Neurology
    64. FABRIZI GM; GUAZZI G; DIDONATO S; TIRANTI V; MALANDRINI A; FEDERICO A; MARIOTTI C; CARRARA F; ZEVIANI M
      A 9-BP MICRODUPLICATION IN THE MITOCHONDRIAL-DNA ASSOCIATED WITH A NEW MATERNALLY INHERITED ENCEPHALOMYOPATHY

      Neurology
    65. DIDONATO S; ZEVIANI M; GIOVANNINI P; SAVARESE N; RIMOLDI M; MARIOTTI C; GIROTTI F; CARACENI T
      RESPIRATORY-CHAIN AND MITOCHONDRIAL-DNA IN MUSCLE AND BRAIN IN PARKINSONS-DISEASE PATIENTS

      Neurology
    66. FINOCCHIARO G; COLOMBO I; GARAVAGLIA B; GELLERA C; VALDAMERI G; GARBUGLIO N; DIDONATO S
      CDNA CLONING AND MITOCHONDRIAL IMPORT OF THE BETA-SUBUNIT OF THE HUMAN ELECTRON-TRANSFER FLAVOPROTEIN

      European journal of biochemistry
    67. BIANCHI A; AVANZINI G; BERNARDINA BD; CANGER R; TASSINARI CA; VIGEVANO F; TIEZZI A; BUZZI G; FANI C; DEVERMANDOIS CR; ZOLO P; ANTONELLI A; BINELLI S; BUTI D; CANEVINI MP; CARULLO A; CIARMATORI C; COPPOLA G; DALESSANDRO P; DEFEO MR; DIDONATO S; DURISOTTI C; ROSO CF; FRANCIA A; GALIMBERTI CA; GALLI R; GAROFALO P; ROSSI PG; IANI C; MAI R; MANFREDI M; MARGIOTTA N; MASSETANI R; MAZZA S; MECARELLI O; PARMEGGIANI A; PASCOTTO A; RICCI S; ROCCHI R; ROMANO G; SALTARELI A; SANTUCCI M; SIDERI G; SPECCHIO L; TARTARA A; TIACCI C; VATTI G; VIGLIANO P; VOLPI L
      CONCORDANCE OF CLINICAL FORMS OF EPILEPSY IN FAMILIES WITH SEVERAL AFFECTED MEMBERS

      Epilepsia
    68. FINOCCHIARO G; TARONI F; DIDONATO S
      MITOCHONDRIAL DISEASES - MOLECULAR ASPECTS OF HUMAN DEFECTS OF BETA-OXIDATION

      Annales de biologie clinique
    69. CORTI O; FINOCCHIARO G; DIDONATO S
      DIVERGENT SEQUENCES IN THE 5' REGION OF CDNA SUGGEST A MECHANISM FOR MITOCHONDRIAL OR PEROXISOMAL LOCALIZATION OF HUMAN CARNITINE ACETYLTRANSFERASE

      American journal of human genetics
    70. TARONI F; VERDERIO E; CAVADINI P; LAMANTEA E; GELLERA C; DIDONATO S
      THE MOLECULAR-BASES OF CARNITINE PALMITOYLTRANSFERASE (CPT)-II DEFICIENCY

      American journal of human genetics
    71. VERDERIO E; CAVADINI P; MONTEMINI L; DIDONATO S; GELLERA C; TARONI F
      STRUCTURE OF THE HUMAN CARNITINE PALMITOYLTRANSFERASE (CPT)-II GENE -DETERMINATION OF THE EXON INTRON COMPOSITION USING INVERSE PCR/

      American journal of human genetics


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Documento generato il 21/10/20 alle ore 07:58:19