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1. Sciacco, M; Prelle, A; Comi, GP; Napoli, L; Battistel, A; Bresolin, N; Tancredi, L; Lamperti, C; Bordoni, A; Fagiolari, G; Ciscato, P; Chiveri, L; Perini, MP; Fortunato, F; Adobbati, L; Messina, S; Toscano, A; Martinelli-Boneschi, F; Papadimitriou, A; Scarlato, G; Moggio, M
   Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation
   JOURNAL OF NEUROLOGY
   
   M. Sciacco et al., "Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation", J NEUROL, 248(9), 2001, pp. 778-788
2. Sciacco, M; Fagiolari, G; Lamperti, C; Messina, S; Bazzi, P; Napoli, L; Chiveri, L; Prelle, A; Comi, GP; Bresolin, N; Scarlato, G; Moggio, M
   Lack of apoptosis in mitochondrial encephalomyopathies
   NEUROLOGY
   
   M. Sciacco et al., "Lack of apoptosis in mitochondrial encephalomyopathies", NEUROLOGY, 56(8), 2001, pp. 1070-1074
3. Bazzi, P; Tancredi, L; Scarpini, E; Messina, S; Sciacco, M; Livraghi, S; Vanoli, M; Prelle, A; Scarlato, G; Moggio, M
   Severe polyneuropathy in a patient with Churg-Strauss syndrome
   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
   
   P. Bazzi et al., "Severe polyneuropathy in a patient with Churg-Strauss syndrome", J PERIPH N, 5(2), 2000, pp. 106-110
4. Prelle, A; Sciacco, M; Comi, GP; Messina, S; Carpo, M; Ciscato, P; Orazio, EN; Fortunato, F; Mora, G; Bignotti, V; Fagiolari, G; Moggio, M; Scarlato, G
   A sporadic, atypical case of desminopathy: morphological and immunologicalcharacterization
   CLINICAL NEUROPATHOLOGY
   
   A. Prelle et al., "A sporadic, atypical case of desminopathy: morphological and immunologicalcharacterization", CLIN NEUR, 19(4), 2000, pp. 208-212
5. Bazzi, P; Moggio, M; Prelle, A; Sciacco, M; Messina, S; Barbieri, S; Tonin, P; Tomelleri, G; Battistel, A; Adobbati, L; Checcarelli, N; Veschi, G; Scarlato, G
   Critically ill patients: immunological evidence of inflammation in muscle biopsy
   CLINICAL NEUROPATHOLOGY
   
   P. Bazzi et al., "Critically ill patients: immunological evidence of inflammation in muscle biopsy", CLIN NEUR, 18(1), 1999, pp. 23-30
6. COMI GP; BORDONI A; SALANI S; FRANCESCHINA L; SCIACCO M; PRELLE A; FORTUNATO F; ZEVIANI M; NAPOLI L; BRESOLIN N; MOGGIO M; AUSENDA CD; TAANMAN JW; SCARLATO G
   CYTOCHROME-C-OXIDASE SUBUNIT-I MICRODELETION IN A PATIENT WITH MOTOR-NEURON DISEASE
   Annals of neurology
   
   G.P. Comi et al., "CYTOCHROME-C-OXIDASE SUBUNIT-I MICRODELETION IN A PATIENT WITH MOTOR-NEURON DISEASE", Annals of neurology, 43(1), 1998, pp. 110-116
7. FRANCESCHINA L; SALANI S; BORDONI A; SCIACCO M; NAPOLI L; COMI GP; PRELLE A; FORTUNATO F; HADJIGEORGIOU GM; FARINA E; BRESOLIN N; DANGELO MG; SCARLATO G
   A NOVEL MITOCHONDRIAL TRNA(ILE) POINT MUTATION IN CHRONIC PROGRESSIVEEXTERNAL OPHTHALMOPLEGIA
   Journal of neurology
   
   L. Franceschina et al., "A NOVEL MITOCHONDRIAL TRNA(ILE) POINT MUTATION IN CHRONIC PROGRESSIVEEXTERNAL OPHTHALMOPLEGIA", Journal of neurology, 245(11), 1998, pp. 755-758
8. SCIACCO M; GASPARORIPPA P; VU TH; TANJI K; SHANSKE S; MENDELL JR; SCHON EA; DIMAURO S; BONILLA E
   STUDY OF MITOCHONDRIAL-DNA DEPLETION IN MUSCLE BY SINGLE-FIBER POLYMERASE-CHAIN-REACTION
   Muscle & nerve
   
   M. Sciacco et al., "STUDY OF MITOCHONDRIAL-DNA DEPLETION IN MUSCLE BY SINGLE-FIBER POLYMERASE-CHAIN-REACTION", Muscle & nerve, 21(11), 1998, pp. 1374-1381
9. PAPADIMITRIOU A; COMI GP; HADJIGEORGIOU GM; BORDONI A; SCIACCO M; NAPOLI L; PRELLE A; MOGGIO M; FAGIOLARI G; BRESOLIN N; SALANI S; ANASTASOPOULOS I; GIASSAKIS G; DIVARI R; SCARLATO G
   PARTIAL DEPLETION AND MULTIPLE DELETIONS OF MUSCLE MTDNA IN FAMILIAL MNGIE SYNDROME
   Neurology
   
   A. Papadimitriou et al., "PARTIAL DEPLETION AND MULTIPLE DELETIONS OF MUSCLE MTDNA IN FAMILIAL MNGIE SYNDROME", Neurology, 51(4), 1998, pp. 1086-1092
10. VU TH; SCIACCO M; TANJI K; NICHTER C; BONILLA E; CHATKUPT S; MAERTENS P; SHANSKE S; MENDELL J; KOENIGSBERGER MR; SHARER L; SCHON EA; DIMAURO S; DEVIVO DC
    CLINICAL MANIFESTATIONS OF MITOCHONDRIAL-DNA DEPLETION
    Neurology
    
    T.H. Vu et al., "CLINICAL MANIFESTATIONS OF MITOCHONDRIAL-DNA DEPLETION", Neurology, 50(6), 1998, pp. 1783-1790
11. PRELLE A; COMI GP; TANCREDI L; RIGOLETTO C; CISCATO P; FORTUNATO F; NESTI S; SCIACCO M; ROBOTTI M; BAZZI P; FELISARI G; MOGGIO M; SCARLATO G
    SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS
    Acta Neuropathologica
    
    A. Prelle et al., "SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS", Acta Neuropathologica, 96(5), 1998, pp. 509-514
12. SCIACCO M; PRELLE A; NAPOLI L; COMI GP; BRESOLIN N; TOSCANO A; PAPADIMITRIOU A; MOGGIO M; SCARLATO G
    MITOCHONDRIAL ENCEPHALOMYOPATHIES - RETROSPECTIVE STUDY OF A POPULATION OF 220 PATIENTS SELECTED ACCORDING TO CLINICAL, MORPHOLOGICAL AND MOLECULAR-GENETIC CRITERIA
    Neurology
    
    M. Sciacco et al., "MITOCHONDRIAL ENCEPHALOMYOPATHIES - RETROSPECTIVE STUDY OF A POPULATION OF 220 PATIENTS SELECTED ACCORDING TO CLINICAL, MORPHOLOGICAL AND MOLECULAR-GENETIC CRITERIA", Neurology, 48(3), 1997, pp. 51001-51001
13. SANTORELLI FM; SCIACCO M; TANJI K; SHANSKE S; VU TH; GOLZI V; GRIGGS RC; MENDELL JR; HAYS AP; BERTORINI TE; PESTRONK A; BONILLA E; DIMAURO S
    MULTIPLE MITOCHONDRIAL-DNA DELETIONS IN SPORADIC INCLUSION-BODY MYOSITIS - A STUDY OF 56 PATIENTS
    Annals of neurology
    
    F.M. Santorelli et al., "MULTIPLE MITOCHONDRIAL-DNA DELETIONS IN SPORADIC INCLUSION-BODY MYOSITIS - A STUDY OF 56 PATIENTS", Annals of neurology, 39(6), 1996, pp. 789-795
14. PRELLE A; RIGOLETTO C; MOGGIO M; SCIACCO M; COMI GP; CISCATO P; FAGIOLARI G; RAPUZZI S; BIGNOTTI V; SCARLATO G
    ASYMPTOMATIC FAMILIAL HYPERCKEMIA ASSOCIATED WITH DESMIN ACCUMULATIONIN SKELETAL-MUSCLE
    Journal of the neurological sciences
    
    A. Prelle et al., "ASYMPTOMATIC FAMILIAL HYPERCKEMIA ASSOCIATED WITH DESMIN ACCUMULATIONIN SKELETAL-MUSCLE", Journal of the neurological sciences, 140(1-2), 1996, pp. 132-136
15. CHEN X; BONILLA E; SCIACCO M; SCHON EA
    PAUCITY OF DELETED MITOCHONDRIAL DNAS IN BRAIN-REGIONS OF HUNTINGTONS-DISEASE PATIENTS
    Biochimica et biophysica acta. Molecular basis of disease
    
    X. Chen et al., "PAUCITY OF DELETED MITOCHONDRIAL DNAS IN BRAIN-REGIONS OF HUNTINGTONS-DISEASE PATIENTS", Biochimica et biophysica acta. Molecular basis of disease, 1271(1), 1995, pp. 229-233
16. VU TH; SCIACCO M; TANJI K; BONILLA E; CHATKUPT S; SHANSKE S; DEVIVO D; NICHTER C; MENDELL J; KOENIGSBERGER MR; SHARER L; DIMAURO S
    MITOCHONDRIAL-DNA DEPLETION AND CLINICAL MANIFESTATIONS
    Annals of neurology
    
    T.H. Vu et al., "MITOCHONDRIAL-DNA DEPLETION AND CLINICAL MANIFESTATIONS", Annals of neurology, 38(3), 1995, pp. 541-541
17. MORAES CT; SCIACCO M; RICCI E; TENGAN CH; HAO H; BONILLA E; SCHON EA; DIMAURO S
    PHENOTYPE GENOTYPE CORRELATIONS IN SKELETAL-MUSCLE OF PATIENTS WITH MTDNA DELETIONS
    Muscle & nerve
    
    C.T. Moraes et al., "PHENOTYPE GENOTYPE CORRELATIONS IN SKELETAL-MUSCLE OF PATIENTS WITH MTDNA DELETIONS", Muscle & nerve, 1995, pp. 150-153
18. SCIACCO M; GASPARORIPPA P; SHANSKE S; MENDELL JR; SCHON EA; DIMAURO S; BONILLA E
    LATE-ONSET MUSCLE MITOCHONDRIAL-DNA (MTDNA) DEPLETION - DIAGNOSIS BY SINGLE-FIBER PCR
    Neurology
    
    M. Sciacco et al., "LATE-ONSET MUSCLE MITOCHONDRIAL-DNA (MTDNA) DEPLETION - DIAGNOSIS BY SINGLE-FIBER PCR", Neurology, 45(4), 1995, pp. 434-434
19. SCIACCO M; BONILLA E; SCHON EA; DIMAURO S; MORAES CT
    DISTRIBUTION OF WILD-TYPE AND COMMON DELETION FORMS OF MTDNA IN NORMAL AND RESPIRATION-DEFICIENT MUSCLE-FIBERS FROM PATIENTS WITH MITOCHONDRIAL MYOPATHY (VOL 3, PG 13, 1994)
    Human molecular genetics
    
    M. Sciacco et al., "DISTRIBUTION OF WILD-TYPE AND COMMON DELETION FORMS OF MTDNA IN NORMAL AND RESPIRATION-DEFICIENT MUSCLE-FIBERS FROM PATIENTS WITH MITOCHONDRIAL MYOPATHY (VOL 3, PG 13, 1994)", Human molecular genetics, 3(4), 1994, pp. 687-687
20. SCIACCO M; BONILLA E; SCHON EA; DIMAURO S; MORAES CT
    DISTRIBUTION OF WILD-TYPE AND COMMON DELETION FORMS OF MTDNA IN NORMAL AND RESPIRATION-DEFICIENT MUSCLE-FIBERS FROM PATIENTS WITH MITOCHONDRIAL MYOPATHY
    Human molecular genetics
    
    M. Sciacco et al., "DISTRIBUTION OF WILD-TYPE AND COMMON DELETION FORMS OF MTDNA IN NORMAL AND RESPIRATION-DEFICIENT MUSCLE-FIBERS FROM PATIENTS WITH MITOCHONDRIAL MYOPATHY", Human molecular genetics, 3(1), 1994, pp. 13-19
21. MOGGIO M; PRELLE A; FAGIOLARI G; CHECCARELLI N; SCIACCO M; CISCATO P; SCARLATO G
    ANIONIC PHOSPHOLIPIDS CALCIUM-BINDING SITES IN DUCHENNE AND MURINE X-LINKED MUSCULAR-DYSTROPHY
    Muscle & nerve
    
    M. Moggio et al., "ANIONIC PHOSPHOLIPIDS CALCIUM-BINDING SITES IN DUCHENNE AND MURINE X-LINKED MUSCULAR-DYSTROPHY", Muscle & nerve, 17(5), 1994, pp. 485-488
22. SANTORELLI FM; SCIACCO M; SHANSKE S; GRIGGS RC; MENDELL JR; BONILLA E; DIMAURO S
    MITOCHONDRIAL-DNA DELETIONS IN PATIENTS WITH INCLUSION-BODY MYOSITIS
    Neurology
    
    F.M. Santorelli et al., "MITOCHONDRIAL-DNA DELETIONS IN PATIENTS WITH INCLUSION-BODY MYOSITIS", Neurology, 44(4), 1994, pp. 10000131-10000131
23. SCIACCO M; MORAES CT; SCHON EA; DIMAURO S; BONILLA E
    ARE DELETED MITOCHONDRIAL DNAS FUNCTIONALLY DOMINANT OVER WILD-TYPE GENOMES
    Neurology
    
    M. Sciacco et al., "ARE DELETED MITOCHONDRIAL DNAS FUNCTIONALLY DOMINANT OVER WILD-TYPE GENOMES", Neurology, 43(4), 1993, pp. 403-403
24. SCARPINI E; BIANCHI R; MOGGIO M; SCIACCO M; FIORI MG; SCARLATO G
    DECREASE OF NERVE NA-ATPASE ACTIVITY IN THE PATHOGENESIS OF HUMAN DIABETIC NEUROPATHY(,K+)
    Journal of the neurological sciences
    
    E. Scarpini et al., "DECREASE OF NERVE NA-ATPASE ACTIVITY IN THE PATHOGENESIS OF HUMAN DIABETIC NEUROPATHY(,K+)", Journal of the neurological sciences, 120(2), 1993, pp. 159-167