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La ricerca find articoli where soggetti phrase all words 'PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 180 riferimenti
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    1. Spelbrink, JN; Li, FY; Tiranti, V; Nikali, K; Yuan, QP; Tariq, M; Wanrooij, S; Garrido, N; Comi, G; Morandi, L; Santoro, L; Toscano, A; Fabrizi, GM; Somer, H; Croxen, R; Beeson, D; Poulton, L; Suomalainen, A; Jacobs, HT; Zeviani, M; Larsson, C
      Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene LF-like protein localized in mitochondria

      NATURE GENETICS
    2. Shoubridge, EA
      Nuclear genetic defects of oxidative phosphorylation

      HUMAN MOLECULAR GENETICS
    3. Nagashima, T; Kato, H; Maguchi, S; Chuma, T; Mano, Y; Goto, Y; Nonaka, I; Nagashima, K
      A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA

      NEUROMUSCULAR DISORDERS
    4. Spagnolo, M; Tomelleri, G; Vattemi, G; Filosto, M; Rizzuto, N; Tonin, P
      A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia

      NEUROMUSCULAR DISORDERS
    5. 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
    6. Shoffner, JM
      An introduction: Oxidative phosphorylation diseases

      SEMINARS IN NEUROLOGY
    7. Biousse, V; Newman, NJ
      Neuro-ophthalmology of mitochondrial diseases

      SEMINARS IN NEUROLOGY
    8. Sladky, JT
      Histopathological features of peripheral nerve and muscle in mitochondrialdisease

      SEMINARS IN NEUROLOGY
    9. Hirano, M; Davidson, M; DiMauro, S
      Mitochondria and the heart

      CURRENT OPINION IN CARDIOLOGY
    10. Pulkes, T; Hanna, MG
      Human mitochondrial DNA diseases

      ADVANCED DRUG DELIVERY REVIEWS
    11. Finsterer, J; Milvay, E
      Diagnostic yield of the lactate stress test in respiratory chain disordersunder absolute and relative workload

      JOURNAL OF NEUROSCIENCE METHODS
    12. Suomalainen, A; Kaukonen, J
      Diseases caused by nuclear genes affecting mtDNA stability

      AMERICAN JOURNAL OF MEDICAL GENETICS
    13. Wallace, DC
      Mouse models for mitochondrial disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    14. Nardin, RA; Johns, DR
      Mitochondrial dysfunction and neuromuscular disease

      MUSCLE & NERVE
    15. Tanji, K; Bonilla, E
      Optical imaging techniques (Histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria

      METHODS IN CELL BIOLOGY, VOL 65
    16. Solano, A; Playan, A; Lopez-Perez, MJ; Montoya, J
      Genetic diseases of the mitochondrial DNA.

      SALUD PUBLICA DE MEXICO
    17. Jaksch, M; Kleinle, S; Scharfe, C; Klopstock, T; Pongratz, D; Muller-Hocker, J; Gerbitz, KD; Liechti-Gallati, S; Lochmuller, H; Horvath, R
      Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies

      JOURNAL OF MEDICAL GENETICS
    18. Kelley, SO; Steinberg, SV; Schimmel, P
      Fragile T-stem in disease-associated human mitochondrial tRNA sensitizes structure to local and distant mutations

      JOURNAL OF BIOLOGICAL CHEMISTRY
    19. Lewis, S; Hutchison, W; Di Nezza, L; Thyagarajan, D; Marotta, R; Dahl, H
      Refinement of the adPEO linked locus on Chr10 and analysis of MRS4 and three other candidate genes

      FEBS LETTERS
    20. Seneca, S; Verhelst, H; De Meirleir, L; Meire, F; Groote, CCD; Lissens, W; Van Coster, R
      A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome

      ARCHIVES OF NEUROLOGY
    21. Larsson, NG; Oldfors, A
      Mitochondrial myopathies

      ACTA PHYSIOLOGICA SCANDINAVICA
    22. Lopez, ME; Van Zeeland, NL; Dahl, DB; Weindruch, R; Aiken, JM
      Cellular phenotypes of age-associated skeletal muscle mitochondrial abnormalities in rhesus monkeys

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    23. Saiwaki, T; Shiga, K; Fukuyama, R; Tsutsumi, Y; Fushiki, S
      A unique junctional palindromic sequence in mitochondrial DNA from a patient with progressive external ophthalmoplegia

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    24. Fernandez-Moreno, MA; Bornstein, B; Petit, N; Garesse, R
      The pathophysiology of mitochondrial biogenesis: Towards four decades of mitochondrial DNA research

      MOLECULAR GENETICS AND METABOLISM
    25. Kelley, SO; Steinberg, SV; Schimmel, P
      Functional defects of pathogenic human mitochondrial tRNAs related to structural fragility

      NATURE STRUCTURAL BIOLOGY
    26. Paul, R; Desnuelle, C; Pouget, J; Pellissier, JF; Richelme, C; Monfort, MF; Butori, C; Saunieres, A; Paquis-Flucklinger, V
      Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions

      EUROPEAN JOURNAL OF HUMAN GENETICS
    27. Hirano, M; Vu, TH
      Defects of intergenomic communication: Where do we stand?

      BRAIN PATHOLOGY
    28. Kajander, OA; Rovio, AT; Majamaa, K; Poulton, J; Spelbrink, JN; Holt, IJ; Karhunen, PJ; Jacobs, HT
      Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states

      HUMAN MOLECULAR GENETICS
    29. Finsterer, J; Eichberger, H; Jarius, C
      Lactate-stress testing in 54 patients with mitochondriopathy

      EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
    30. Marin-Garcia, J; Goldenthal, MJ
      Mitochondrial biogenesis defects and neuromuscular disorders

      PEDIATRIC NEUROLOGY
    31. Shoffner, JM
      Mitochondrial myopathy diagnosis

      NEUROLOGIC CLINICS
    32. Vielhaber, S; Kudin, A; Schroder, R; Elger, CE; Kunz, WS
      Muscle fibres: applications for the study of the metabolic consequences ofenzyme deficiencies in skeletal muscle

      BIOCHEMICAL SOCIETY TRANSACTIONS
    33. Vu, TH; Tanji, K; Pallotti, F; Golzi, V; Hirano, M; DiMauro, S; Bonilla, E
      Analysis of mtDNA deletions in muscle by in situ hybridization

      MUSCLE & NERVE
    34. Malik, S; Sudoyo, H; Marzuki, S
      Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy

      JOURNAL OF INHERITED METABOLIC DISEASE
    35. Kaukonen, J; Juselius, JK; Tiranti, V; Kyttala, A; Zeviani, M; Comi, GP; Keranen, S; Peltonen, L; Suomalainen, A
      Role of adenine nucleotide translocator 1 in mtDNA maintenance

      SCIENCE
    36. Laforet, P; Ziegler, F; Sternberg, D; Rouche, A; Frachon, P; Fardeau, M; Eymard, B; Lombes, A
      MELAS (A3243G) mutation of mitochondrial DNA: a study of the relationshipsbetween the clinical phenotype in 19 patients and morphological and molecular data.

      REVUE NEUROLOGIQUE
    37. Solin, ML; Pitkanen, S; Taanman, JW; Holthofer, H
      Mitochondrial dysfunction in congenital nephrotic syndrome

      LABORATORY INVESTIGATION
    38. Schroder, R; Vielhaber, S; Wiedemann, FR; Kornblum, C; Papassotiropoulos, A; Broich, P; Zierz, S; Elger, CE; Reichmann, H; Seibel, P; Klockgether, T; Kunz, WS
      New insights into the metabolic consequences of large-scale mtDNA deletions: A quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    39. Van Goethem, G; Lofgren, A; Martin, JJ; Van Broeckhoven, C
      Further evidence for genetic heterogeneity of autosomal dominant disorderswith accumulation of multiple deletions of mitochondrial DNA

      JOURNAL OF MEDICAL GENETICS
    40. Moslemi, AR; Selimovic, N; Bergh, CH; Oldfors, A
      Fatal dilated cardiomyopathy associated with a mitochondrial DNA deletion

      CARDIOLOGY
    41. Rahman, S; Lake, BD; Taanman, JW; Hanna, MG; Cooper, JM; Schapira, AHV; Leonard, JV
      Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms

      BRAIN
    42. Chinnery, PF; Elliott, C; Green, GR; Rees, A; Coulthard, A; Turnbull, DM; Griffiths, TD
      The spectrum of hearing loss due to mitochondrial DNA defects

      BRAIN
    43. Houstek, J
      Genetic aspects of mitochondrial encephalomyoptahies

      BIOLOGIA
    44. Koga, Y; Akita, Y; Takane, N; Sato, Y; Kato, H
      Heterogeneous presentation in A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene

      ARCHIVES OF DISEASE IN CHILDHOOD
    45. Wiedemann, FR; Vielhaber, S; Schroder, R; Elger, CE; Kunz, WS
      Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples

      ANALYTICAL BIOCHEMISTRY
    46. Koga, Y; Koga, A; Iwanaga, R; Akita, Y; Tubone, J; Matsuishi, T; Takane, N; Sato, Y; Kato, H
      Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypes

      ACTA NEUROPATHOLOGICA
    47. Bauer, MF; Gempel, K; Hofmann, S; Jaksch, M; Philbrook, C; Gerbitz, KD
      Mitochondrial disorders. A diagnostic challenge in clinical chemistry

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    48. Rovio, A; Tiranti, V; Bednarz, AL; Suomalainen, A; Spelbrink, JN; Lecrenier, N; Melberg, A; Zeviani, M; Poulton, J; Foury, F; Jacobs, HT
      Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals

      EUROPEAN JOURNAL OF HUMAN GENETICS
    49. Andrews, RM; Griffiths, PG; Chinnery, PF; Turnbull, DM
      Evaluation of bupivacaine-induced muscle regeneration in the treatment of ptosis in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome

      EYE
    50. Pang, CY; Huang, CC; Yen, MY; Wang, EK; Kao, KP; Chen, SS; Wei, YH
      Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    51. Seyrantepe, V; Kale, G; Topaloglu, H; Alikasifoglu, A; Ozguc, M
      Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibers

      BRAIN & DEVELOPMENT
    52. Lertrit, P; Imsumran, A; Karnkirawattana, P; Devahasdin, V; Sangruchi, T; Atchaneeyasakul, L; Mungkornkarn, C; Neungton, N
      A unique 3.5-kb deletion of the mitochondrial genome in Thai patients withKearns-Sayre syndrome

      HUMAN GENETICS
    53. Grunewald, T; Porschke, H; Goebel, H; Reichmann, H; Seibel, P
      Chronic progressive external ophthalmoplegia with a novel mitochondrial DNA deletion and a mutation in the tRNA(Leu(UUR)) gene

      DRUG DEVELOPMENT RESEARCH
    54. Shoffner, JM
      Oxidative phosphorylation disease diagnosis

      SEMINARS IN NEUROLOGY
    55. Lacey, B; Chang, W; Rootman, J
      Nonthyroid causes of extraocular muscle disease

      SURVEY OF OPHTHALMOLOGY
    56. Barrera-Ramirez, CF; Barragan-Campos, HM; Sanchez-Guerrero, J; Garcia-Ramos, G; Vega-Boada, F; Estanol, B
      The other genome: Clinical spectrum of mitochondrial cytopathies or oxidative phosphorylation diseases

      REVISTA DE INVESTIGACION CLINICA
    57. Simon, DK; Pulst, SM; Sutton, JP; Browne, SE; Beal, MF; Johns, DR
      Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation

      NEUROLOGY
    58. Li, FY; Tariq, M; Croxen, R; Morten, K; Squier, W; Newsom-Davis, J; Beeson, D; Larsson, C
      Mapping of autosomal dominant progressive external ophthalmoplegia to a 7-cM critical region on 10q24

      NEUROLOGY
    59. Carrozzo, R; Davidson, MM; Walker, WF; Hirano, M; Miranda, AF
      Cellular and molecular studies in muscle and cultures from patients with multiple mitochondrial DNA deletions

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    60. Chinnery, PF; Howell, N; Andrews, RM; Turnbull, DM
      Mitochondrial DNA analysis: Polymorphisms and pathogenicity

      JOURNAL OF MEDICAL GENETICS
    61. Chinnery, PF; Howell, N; Andrews, RM; Turnbull, DM
      Clinical mitochondrial genetics

      JOURNAL OF MEDICAL GENETICS
    62. Schapira, AHV; Cock, HR
      Mitochondrial myopathies and encephalomyopathies

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    63. Cock, H; Schapira, AHV
      Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy

      EPILEPSIA
    64. Morgan-Hughes, JA; Hanna, MG
      Mitochondrial encephalomyopathies: the enigma of genotype versus phenotype

      BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
    65. Nishizaki, K; Fukushiama, K; Oda, Y; Masuda, A; Hayashi, S; Nagayasu, N; Yoshino, T; Kashihara, K; Takahashi, K; Masuda, Y
      Cochlear implantation for symptomatic hereditary deafness

      ACTA OTO-LARYNGOLOGICA
    66. SHOUBRIDGE EA
      MITOCHONDRIAL ENCEPHALOMYOPATHIES

      Current opinion in neurology
    67. FEDERICO A; DOTTI MT; CARDAIOLI E; GRIECO G; MALANDRINI A; MANNESCHI L; PLEWNIA K; RUFA A; RENIERI A; BRUTTINI M; PERTICONI GF
      ASSOCIATION IN THE SAME PATIENT OF AUTOSOMAL-DOMINANT PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MULTIPLE MTDNA DELETIONS AND X-LINKED ICHTHYOSIS - CLINICAL, BIOCHEMICAL, HISTOLOGICAL, SUBMICROSCOPIC AND MOLECULAR-GENETIC STUDY

      Journal of submicroscopic cytology and pathology
    68. STERNBERG D; DANAN C; LOMBES A; LAFORET P; GIRODON E; GOOSSENS M; AMSELEM S
      EXHAUSTIVE SCANNING APPROACH TO SCREEN ALL THE MITOCHONDRIAL TRANSFER-RNA GENES FOR MUTATIONS AND ITS APPLICATION TO THE INVESTIGATION OF 35 INDEPENDENT PATIENTS WITH MITOCHONDRIAL DISORDERS

      Human molecular genetics
    69. SERVIDEI S
      MITOCHONDRIAL ENCEPHALOMYOPATHIES - GENE MUTATION

      Neuromuscular disorders
    70. TENGAN CH; MORAES CT
      DUPLICATION AND TRIPLICATION WITH STAGGERED BREAKPOINTS IN HUMAN MITOCHONDRIAL-DNA

      Biochimica et biophysica acta. Molecular basis of disease
    71. MULLERHOCKER J; JACOB U; SEIBEL P
      THE COMMON 4977-BASE-PAIR DELETION OF MITOCHONDRIAL-DNA PREFERENTIALLY ACCUMULATES IN THE CARDIAC CONDUCTION SYSTEM OF PATIENTS WITH KEARNS-SAYRE-SYNDROME

      Modern pathology
    72. ZANSSEN S; MOLNAR M; BUSE G; SCHRODER JM
      MITOCHONDRIAL CYTOCHROME-B GENE DELETION IN KEARNS-SAYRE-SYNDROME ASSOCIATED WITH A SUBCLINICAL TYPE OF PERIPHERAL NEUROPATHY

      Clinical neuropathology
    73. Scaioli, V; Antozzi, C; Villani, F; Rimoldi, M; Zeviani, M; Panzica, F; Avanzini, G
      Utility of multimodal evoked potential study and electroencephalography inmitochondrial encephalomyopathy

      ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES
    74. FISCHELGHODSIAN N
      MITOCHONDRIAL GENETICS AND HEARING-LOSS - THE MISSING LINK BETWEEN GENOTYPE AND PHENOTYPE

      Proceedings of the Society for Experimental Biology and Medicine
    75. OHKOSHI N; ISHII A; SHIRAIWA N; SHOJI S; YOSHIZAWA K
      DYSFUNCTION OF THE HYPOTHALAMIC-PITUITARY SYSTEM IN MITOCHONDRIAL ENCEPHALOMYOPATHIES

      Journal of medicine
    76. ILLA I; CASADEMONT J
      37-YEAR-OLD WOMAN WITH DEAFNESS, DECREASE IN VISUAL ACUTENESS, DYSARTHRIA, MYOCLONUS AND ALTERATIONS IN OCULAR MOVEMENTS OF 20 YEARS OF EVOLUTION

      Medicina Clinica
    77. VONBLOTZHEIM SG; BORRUAT FX; HIRT L
      OCULAR MITOCHONDRIAL MYOPATHY - A SPECTRU M OF CLINICAL PRESENTATIONS

      Klinische Monatsblatter fur Augenheilkunde
    78. HORVATH R; FU K; JOHNS T; GENGE A; KARPATI G; SHOUBRIDGE EA
      CHARACTERIZATION OF THE MITOCHONDRIAL-DNA ABNORMALITIES IN THE SKELETAL-MUSCLE OF PATIENTS WITH INCLUSION-BODY MYOSITIS

      Journal of neuropathology and experimental neurology
    79. SALVAN AM; VIONDURY J; CONFORTGOUNY S; SANGLA I; POUGET J; COZZONE PJ
      BRAIN METABOLIC PROFILES OBTAINED BY PROTON MRS IN 2 FORMS OF MITOCHONDRIOPATHIES - LEBERS HEREDITARY OPTIC NEUROPATHY AND CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA

      European neurology
    80. VILARINHO L; SANTORELLI FM; CARDOSO ML; COELHO T; GUIMARAES A; COUTINHO P
      MITOCHONDRIAL-DNA ANALYSIS IN OCULAR MYOPATHY - OBSERVATIONS IN 29 PORTUGUESE PATIENTS

      European neurology
    81. PORTEOUS WK; JAMES AM; SHEARD PW; PORTEOUS CM; PACKER MA; HYSLOP SJ; MELTON JV; PANG CY; WEI YH; MURPHY MP
      BIOENERGETIC CONSEQUENCES OF ACCUMULATING THE COMMON 4977-BP MITOCHONDRIAL-DNA DELETION

      European journal of biochemistry
    82. NISHIZUKA S; TAMURA G; GOTO Y; MURAYAMA K; KONNO T; HAKOZAKI M; NONAKA I; TOHGI H; SATODATE R
      TISSUE-SPECIFIC INVOLVEMENT OF MULTIPLE MITOCHONDRIAL-DNA DELETIONS IN FAMILIAR MITOCHONDRIAL MYOPATHY

      Biochemical and biophysical research communications
    83. HANNA MG; NELSON IP; RAHMAN S; LANE RJM; LAND J; HEALES S; COOPER MJ; SCHAPIRA AHV; MORGANHUGHES JA; WOOD NW
      CYTOCHROME-C-OXIDASE DEFICIENCY ASSOCIATED WITH THE FIRST STOP-CODON POINT MUTATION IN HUMAN MTDNA

      American journal of human genetics
    84. CHINNERY PF; TURNBULL DM
      MITOCHONDRIAL MEDICINE

      Quarterly Journal of Medicine
    85. ZEVIANI M; ANTOZZI C
      MITOCHONDRIAL DISORDERS

      Molecular human reproduction
    86. WARNER TT; SCHAPIRA AHV
      GENETIC-COUNSELING IN MITOCHONDRIAL DISEASES

      Current opinion in neurology
    87. KERR DS
      PROTEAN MANIFESTATIONS OF MITOCHONDRIAL DISEASES - A MINIREVIEW

      Journal of pediatric hematology/oncology
    88. MOSLEMI AR; LINDBERG C; OLDFORS A
      ANALYSIS OF MULTIPLE MITOCHONDRIAL-DNA DELETIONS IN INCLUSION-BODY MYOSITIS

      Human mutation

    89. MITOCHONDRIAL ENCEPHALOMYOPATHIES - GENE MUTATION

      Neuromuscular disorders

    90. MITOCHONDRIAL ENCEPHALOMYOPATHIES - GENE MUTATION

      Neuromuscular disorders

    91. MITOCHONDRIAL ENCEPHALOMYOPATHIES - GENE MUTATION

      Neuromuscular disorders

    92. MITOCHONDRIAL ENCEPHALOMYOPATHIES - GENE MUTATION

      Neuromuscular disorders
    93. SERVIDEI S
      MITOCHONDRIAL ENCEPHALOMYOPATHIES - GENE MUTATION

      Neuromuscular disorders

    94. MITOCHONDRIAL ENCEPHALOMYOPATHIES - GENE MUTATION

      Neuromuscular disorders
    95. ROWLAND LP; HIRANO M; DIMAURO S; SCHON EA
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY, OTHER OCULAR MYOPATHIES, AND PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA

      Neuromuscular disorders
    96. DILAZZARO V; RESTUCCIA D; SERVIDEI S; VALERIANI M; NARDONE R; MANFREDI G; SILVESTRI G; RICCI E; TONALI P
      FUNCTIONAL INVOLVEMENT OF CENTRAL-NERVOUS-SYSTEM IN MITOCHONDRIAL DISORDERS

      ELECTROMYOGRAPHY AND MOTOR CONTROL-ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY
    97. DIMAURO S; TANJI K
      MITOCHONDRIAL DISORDERS

      Japanese journal of human genetics
    98. SUOMALAINEN A
      MITOCHONDRIAL-DNA AND DISEASE

      Annals of medicine
    99. ROTIG A; LEHNERT A; CHRETIEN D; RUSTIN P; GUBLER MC; MUNNICH A; NIAUDET P
      KIDNEY INVOLVEMENT IN MITOCHONDRIAL DISOR DERS

      MS. Medecine sciences
    100. EWART RM; BURROWS RF
      PREGNANCY IN CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA - A CASE-REPORT

      American journal of perinatology


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Documento generato il 03/06/20 alle ore 02:01:15