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La ricerca find articoli where soggetti phrase all words 'MITOCHONDRIAL MYOPATHY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 245 riferimenti
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    1. Steensberg, A; Vissing, J; Pedersen, BK
      Lack of IL-6 production during exercise in patients with mitochondrial myopathy

      EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY
    2. Muller, C; Schubert, M; Dengler, R; Wohlfarth, K
      Clinico-neurophysiological study on muscular fatigue in mitochondrial myopathy

      KLINISCHE NEUROPHYSIOLOGIE
    3. Stobiecki, M
      Applications of separation techniques hyphenated to mass spectrometer for metabolic profiling

      CURRENT ORGANIC CHEMISTRY
    4. Gupta, S; Blaivas, M; Ike, RW; Crofford, LJ
      Polymyositis evolving after rhabdomyolysis associated with HMG-CoA reductase inhibitors: A report of two cases

      JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
    5. Flaherty, KR; Wald, J; Weisman, IM; Zeballos, RJ; Schork, MA; Blaivas, M; Rubenfire, M; Martinez, FJ
      Unexplained exertional limitation - Characterization of patients with a mitochondrial myopathy

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    6. Gabrielli, A; Caruso, L
      Early recognition of acute cardiovascular beriberi by interpretation of hemodynamics

      JOURNAL OF CLINICAL ANESTHESIA
    7. Stollberger, C; Finsterer, J; Blazek, G
      Isolated left ventricular abnormal trabeculation: Follow-up and association with neuromuscular disorders

      CANADIAN JOURNAL OF CARDIOLOGY
    8. Ohta, H; Shintaku, M; Kurimoto, C; Kaneda, D
      Ga-67 scintigraphy in a case of mitochondrial myopathy

      CLINICAL NUCLEAR MEDICINE
    9. Finsterer, J; Stollberger, C; Wegmann, R; Jarius, C; Janssen, B
      Left ventricular hypertrabeculation in myotonic dystrophy Type 1

      HERZ
    10. Baker, SK; Tarnopolsky, MA; Bonen, A
      Expression of MCT1 and MCT4 in a patient with mitochondrial myopathy

      MUSCLE & NERVE
    11. Strachan, J; McLellan, A; Kirkpatrick, M; Hume, R; Mechan, D
      Ketoacidosis: an unusual presentation of MELAS

      JOURNAL OF INHERITED METABOLIC DISEASE
    12. Stollberger, C; Finsterer, J
      Echocardiography in storage and neuromuscular disorders

      WIENER KLINISCHE WOCHENSCHRIFT
    13. Lalla, A; Alleyne, T; Andrews, Y
      Understanding the mechanism of action of cytochrome (c)under-bar oxidase in normal and disease states: Shark heart enzyme, a potential model

      WEST INDIAN MEDICAL JOURNAL
    14. Melacini, P; Gambino, A; Caforio, A; Barchitta, A; Valente, ML; Angelini, A; Fanin, M; Thiene, G; Angelini, C; Casarotto, D; Danieli, GA; Dalla-Volta, S
      Heart transplantation in patients with inherited myopathies associated with end-stage cardiomyopathy: Molecular and biochemical defects on cardiac and skeletal muscle

      TRANSPLANTATION PROCEEDINGS
    15. Hameed, R; Raafat, F; Ramani, P; Gray, G; Roper, HP; Milford, DV
      Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological disease

      POSTGRADUATE MEDICAL JOURNAL
    16. Mudhar, HS; Wagner, BE; Suvarna, SK
      Electron microscopy of myocardial tissue. A nine year review

      JOURNAL OF CLINICAL PATHOLOGY
    17. Finsterer, J; Stollberger, C; Wanschitz, J; Jaksch, M; Budka, H
      Nail-patella syndrome associated with respiratory chain disorder

      EUROPEAN NEUROLOGY
    18. Clay, AS; Behnia, M; Brown, KK
      Mitochondrial disease - A pulmonary and critical-care medicine perspective

      CHEST
    19. Finsterer, J; Gharehbaghi-Schnell, E; Stollberger, C; Fheodoroff, K; Seiser, A
      Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophy

      CLINICAL GENETICS
    20. Fiore, C; Arlot-Guilligay, D; Trezeguet, V; Lauquin, GJM; Brandolin, G
      Fluorometric detection of ADP/ATP carrier deficiency in human muscle

      CLINICA CHIMICA ACTA
    21. Smith, WQ; Abu-Harb, M
      Undiagnosed cardiomyopathy in a neonate: significance of low oxygen saturation during anaesthesia

      BRITISH JOURNAL OF ANAESTHESIA
    22. Ansved, T
      Muscle training in muscular dystrophies

      ACTA PHYSIOLOGICA SCANDINAVICA
    23. Vladutiu, GD; Bennett, MJ; Smail, D; Wong, LJ; Taggart, RT; Lindsley, HB
      A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene

      MOLECULAR GENETICS AND METABOLISM
    24. Shoubridge, EA
      A debut for mito-mouse

      NATURE GENETICS
    25. Calore, EE; Weg, R; Haraguchi, M; Calore, NMP; Cavaliere, MJ; Sesso, A
      Mitochondrial metabolism impairment in muscle fibres of rats chronically intoxicated with Senna occidentalis seeds

      EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY
    26. O'Rourke, KS
      Myopathies in the elderly

      RHEUMATIC DISEASE CLINICS OF NORTH AMERICA
    27. Finsterer, J; Obermann, I; Milvay, E
      Diagnostic yield of the lactate stress test in 160 patients with suspectedrespiratory chain disorder

      METABOLIC BRAIN DISEASE
    28. Pavlakis, SG; Kingsley, PB; Bialer, MG
      Stroke in children: Genetic and metabolic issues

      JOURNAL OF CHILD NEUROLOGY
    29. Moundras, JM; Wattrisse, G; Leroy, B; Decocq, J; Krivosic-Horber, R
      Labour analgesia in a patient with carnitine palmityl transferase deficiency.

      ANNALES FRANCAISES D ANESTHESIE ET DE REANIMATION
    30. Pourmand, R
      Metabolic myopathies - A diagnostic evaluation

      NEUROLOGIC CLINICS
    31. Kon, K; Inagaki, M; Kaga, M; Sasaki, M; Hanaoka, S
      Otoacoustic emission in patients with neurological disorders who have auditory brainstem response abnormality

      BRAIN & DEVELOPMENT
    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. Shaer, AJ; Rastegar, A
      Lactic acidosis in the setting of antiretroviral therapy for the acquired immunodeficiency syndrome - A case report and review of the literature

      AMERICAN JOURNAL OF NEPHROLOGY
    34. Tasaka, AC; Weg, R; Calore, EE; Sinhorini, IL; Dagli, MLZ; Haraguchi, M; Gorniak, SL
      Toxicity testing of senna occidentalis seed in rabbits

      VETERINARY RESEARCH COMMUNICATIONS
    35. Rubio, JC; Martin, MA; Del Hoyo, P; Bautista, J; Campos, Y; Segura, D; Navarro, C; Ricoy, JR; Cabello, A; Arenas, J
      Molecular analysis of Spanish patients with AMP deaminase deficiency

      MUSCLE & NERVE
    36. 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
    37. Robinson, BH
      Human cytochrome oxidase deficiency

      PEDIATRIC RESEARCH
    38. Ohshita, T; Oka, M; Imon, Y; Watanabe, C; Katayama, S; Yamaguchi, S; Kajima, T; Mimori, Y; Nakamura, S
      Serial diffusion-weighted imaging in MELAS

      NEURORADIOLOGY
    39. Fernandez, J; Montemayor, T; Bautista, J; Marquez, R; Jimenez, L; Arenas, J; Campos, Y; Castillo, J
      Role of cardiopulmonary exercise test in patients with mitochondrial myopathies

      MEDICINA CLINICA
    40. Bilzer, T; Neumann, J
      Necrotising myopathies in dogs - Differential diagnosis, therapy and own observations

      KLEINTIERPRAXIS
    41. 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
    42. Spicer, Z; Miller, ML; Andringa, A; Riddle, TM; Duffy, JJ; Doetschman, T; Shull, GE
      Stomachs of mice lacking the gastric H,K-ATPase alpha-subunit have achlorhydria, abnormal parietal cells, and ciliated metaplasia

      JOURNAL OF BIOLOGICAL CHEMISTRY
    43. Higgins, C; Gray, G; Ramani, P; Poulton, K; Whitehouse, W
      Transient cytochrome oxidase deficiency with Ohtahara syndrome

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    44. Rahman, S; Lake, BD; Taanman, JW; Hanna, MG; Cooper, JM; Schapira, AHV; Leonard, JV
      Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms

      BRAIN
    45. Stuerenburg, HJ
      The roles of carnosine in aging of skeletal muscle and in neuromuscular diseases

      BIOCHEMISTRY-MOSCOW
    46. Brenner, O; Wakshlag, JJ; Summers, BA; de Lahunta, A
      Alaskan Husky encephalopathy - a canine neurodegenerative disorder resembling subacute necrotizing encephalomyelopathy (Leigh syndrome)

      ACTA NEUROPATHOLOGICA
    47. Hirata, K; Nakagawa, M; Higuchi, I; Hashimoto, K; Hanada, K; Takahashi, K; Niiyama, T; Izumi, K; Sakoda, S; Yamada, H; Osame, M
      Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution

      JOURNAL OF HUMAN GENETICS
    48. Haviv, YS; Zimmerman, M; Berkman, N; Safadi, R
      Fumaric acid ester-induced diffuse renal tubular injury presenting as Fanconi syndrome and osteomalacia

      CLINICAL DRUG INVESTIGATION
    49. Calore, EE; Calore, NMP; Weg, R; Cavaliere, MJ; Da Rosa, AR; Dias, SD
      The lysosomal enzymes acid phosphatase and cathepsin D in rats intoxicatedwith Senna occidentalis seeds

      JOURNAL OF SUBMICROSCOPIC CYTOLOGY AND PATHOLOGY
    50. 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
    51. Fujimoto, S; Mizuno, K; Shibata, H; Kanayama, M; Kobayashi, M; Sugiyama, N; Ban, K; Ishikawa, T; Itoh, T; Togari, H; Wada, Y
      Serial electroencephalographic findings in patients with MELAS

      PEDIATRIC NEUROLOGY
    52. Yim, SY; Lee, IY; Kim, TS
      Enzyme histochemical study of germanium dioxide-induced mitochondrial myopathy in rats

      YONSEI MEDICAL JOURNAL
    53. Andreu, AL; Tanji, K; Bruno, C; Hadjigeorgiou, GM; Sue, CM; Jay, C; Ohnishi, T; Shanske, S; Bonilla, E; DiMauro, S
      Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene

      ANNALS OF NEUROLOGY
    54. Honorati, MC; Facchini, A
      Rheumatoid epitopes and CD4+immunodominant regions of recombinant hepatitis B surface antigen

      JOURNAL OF RHEUMATOLOGY
    55. Gonzalez-Crespo, MR; Arenas, J; Gomez-Reino, JJ; Campos, Y; Borstein, B; Martin, MA; Cabello, A; Garcia-Ryo, R; Ricoy, JR
      Muscle dysfunction in elderly individuals with hip fracture

      JOURNAL OF RHEUMATOLOGY
    56. Shoffner, JM
      Oxidative phosphorylation disease diagnosis

      SEMINARS IN NEUROLOGY
    57. Towbin, JA; Lipshultz, SE
      Genetics of neonatal cardiomyopathy

      CURRENT OPINION IN CARDIOLOGY
    58. Roy, PM; Gouello, JP; Pennison-Besnier, I; Chennebault, JM
      Severe lactic acidosis induced by nucleoside analogues in an HIV-infected man

      ANNALS OF EMERGENCY MEDICINE
    59. Korres, SG; Manta, PB; Balatsouras, DG; Papageorgiou, CT
      Audiological assessment in patients with mitochondrial myopathy

      SCANDINAVIAN AUDIOLOGY
    60. Hadjigeorgiou, GM; Kim, SH; Fischbeck, KH; Andreu, AL; Berry, GT; Bingham, P; Shanske, S; Bonilla, E; DiMauro, S
      A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    61. Abe, K; Matsuo, Y; Kadekawa, J; Inoue, S; Yanagihara, T
      Effect of coenzyme Q10 in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): Evaluation by noninvasive tissue oximetry

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    62. Platt, SR; Chrisman, CL; Shelton, GD
      Lipid storage myopathy in a cocker spaniel

      JOURNAL OF SMALL ANIMAL PRACTICE
    63. Freyssenet, D; DiCarlo, M; Escobar, P; Grey, J; Schneider, J; Hood, DA
      Zidovudine (AZT) induced alterations in mitochondrial biogenesis in rat striated muscles

      CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
    64. Sharfstein, SR; Gordon, MF; Libman, RB; Malkin, ES
      Adult-onset MELAS presenting as herpes encephalitis

      ARCHIVES OF NEUROLOGY
    65. Famularo, G; De Simone, C; Cifone, G
      Carnitine stands on its own in HIV infection treatment

      ARCHIVES OF INTERNAL MEDICINE
    66. Tsuchiya, K; Miyazaki, H; Akabane, H; Yamamoto, M; Kondo, H; Mizusawa, H; Ikeda, K
      MELAS with prominent white matter gliosis and atrophy of the cerebellar granular layer: a clinical, genetic, and pathological study

      ACTA NEUROPATHOLOGICA
    67. WALLACE JJ; PERNDT H; SKINNER M
      ANESTHESIA AND MITOCHONDRIAL DISEASE

      Paediatric anaesthesia
    68. PRZEDBORSKI S; SCHON EA
      LOSS OF ROS - A RADICAL RESPONSE

      Nature genetics
    69. SILVESTRI G; RANA M; DIMUZIO A; UNCINI A; TONALI P; SERVIDEI S
      A LATE-ONSET MITOCHONDRIAL MYOPATHY IS ASSOCIATED WITH A NOVEL MITOCHONDRIAL-DNA (MTDNA) POINT MUTATION IN THE TRNA(TRP) GENE

      Neuromuscular disorders
    70. Campos, Y; Martin, MA; Garcia-Silva, T; del Hoyo, P; Rubio, JC; Castro-Gago, M; Garcia-Penas, J; Casas, J; Cabello, A; Ricoy, JR; Arenas, J
      Clinical heterogeneity associated with mitochondrial DNA depletion in muscle

      NEUROMUSCULAR DISORDERS
    71. CHEAM EWS; CRITCHLEY LAH
      ANESTHESIA FOR A CHILD WITH COMPLEX-I RESPIRATORY-CHAIN ENZYME DEFICIENCY

      Journal of clinical anesthesia
    72. YANG CC; HWANG CC; PANG CY; WEI YH
      MITOCHONDRIAL MYOPATHY WITH PREDOMINANT RESPIRATORY DYSFUNCTION IN A PATIENT WITH A3243G MUTATION IN THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE

      Journal of the Formosan Medical Association
    73. OBRIEN A; BLAIVAS M; ALBERS J; WALD J; WATTS C
      A CASE OF RESPIRATORY MUSCLE WEAKNESS DUE TO CYTOCHROME-C-OXIDASE ENZYME DEFICIENCY

      The European respiratory journal
    74. JARADAT SA; KO MSH; GROSSMAN LI
      TISSUE-SPECIFIC EXPRESSION AND MAPPING OF THE COX7AH GENE IN MOUSE

      Genomics
    75. TOPALOGLU H; SEYRANTEPE V; KANDEMIR N; AKCOREN Z; OZGUC M
      MTDNA NT3243 MUTATION, EXTERNAL OPHTHALMOPLEGIA, AND HYPOGONADISM IN AN ADOLESCENT GIRL

      Pediatric neurology
    76. Arenas, J; Rubio, JC; Martin, MA; Campos, Y
      Biological roles of L-carnitine in perinatal metabolism

      EARLY HUMAN DEVELOPMENT
    77. SUE CM; LIPSETT LJ; CRIMMINS DS; TSANG CS; BOYAGES SC; PRESGRAVE CM; GIBSON WPR; BYRNE E; MORRIS JGL
      COCHLEAR ORIGIN OF HEARING-LOSS IN MELAS SYNDROME

      Annals of neurology
    78. Hughes, IP
      Diagnosis and control of genetic disease in small animals: Part I - Basic genetic principles and the diagnosis of genetic disease

      AUSTRALIAN VETERINARY PRACTITIONER
    79. VOGT AM; KUBLER W
      HEART-FAILURE - IS THERE AN ENERGY DEFICIT CONTRIBUTING TO CONTRACTILE DYSFUNCTION

      Basic research in cardiology
    80. DREIER JP; KORNER K; EBERT N; GORNER A; RUBIN I; BACK T; LINDAUER U; WOLF T; VILLRINGER A; EINHAUPL KM; LAURITZEN M; DIRNAGL U
      NITRIC-OXIDE SCAVENGING BY HEMOGLOBIN OR NITRIC-OXIDE SYNTHASE INHIBITION BY N-NITRO-L-ARGININE INDUCES CORTICAL SPREADING ISCHEMIA WHEN K+IS INCREASED IN THE SUBARACHNOID SPACE

      Journal of cerebral blood flow and metabolism
    81. 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
    82. TARNOPOLSKY MA; MAGUIRE J; MYINT T; APPLEGARTH D; ROBINSON BH
      CLINICAL, PHYSIOLOGICAL, AND HISTOLOGICAL FEATURES IN A KINDRED WITH THE T3271C MELAS MUTATION

      Muscle & nerve
    83. 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
    84. TAKAHASHI S; TOHGI H; YONEZAWA H; OBARA S; NAGANE Y
      CEREBRAL BLOOD-FLOW AND OXYGEN-METABOLISM BEFORE AND AFTER A STROKE-LIKE EPISODE IN PATIENTS WITH MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS AND STROKE-LIKE EPISODES (MELAS)

      Journal of the neurological sciences
    85. KATO T; MURASHITA J; SHIOIRI T; TERADA M; INUBUSHI T; KATO N
      PHOTIC STIMULATION-INDUCED ALTERATION OF BRAIN ENERGY-METABOLISM MEASURED BY P-31-MR SPECTROSCOPY IN PATIENTS WITH MELAS

      Journal of the neurological sciences
    86. SUE CM; CRIMMINS DS; SOO YS; PAMPHLETT R; PRESGRAVE CM; KOTSIMBOS N; JEANFRANCOIS MJB; BYRNE E; MORRIS JGL
      NEURORADIOLOGICAL FEATURES OF 6 KINDREDS WITH MELAS TRNA(LEU) A3243G POINT MUTATION - IMPLICATIONS FOR PATHOGENESIS

      Journal of Neurology, Neurosurgery and Psychiatry
    87. KOLLER H; STOLL G; NEUENJACOB E
      POSTPARTUM MANIFESTATION OF A NECROTIZING LIPID STORAGE MYOPATHY ASSOCIATED WITH MUSCLE CARNITINE DEFICIENCY

      Journal of Neurology, Neurosurgery and Psychiatry
    88. VISSING J; VISSING SF; MACLEAN DA; SALTIN B; QUISTORFF B; HALLER RG
      SYMPATHETIC ACTIVATION IN EXERCISE IS NOT DEPENDENT ON MUSCLE ACIDOSIS - DIRECT EVIDENCE FROM STUDIES IN METABOLIC MYOPATHIES

      The Journal of clinical investigation
    89. OKADA H; ARAGA S; TAKESHIMA T; NAKASHIMA K
      PLASMA LACTIC-ACID AND PYRUVIC-ACID LEVELS IN MIGRAINE AND TENSION-TYPE HEADACHE

      Headache
    90. Stollberger, C; Finsterer, J; Keller, H; Mamoli, B; Slany, J
      Progression of cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy during a 2-year follow-up

      CARDIOLOGY
    91. KIMATA KG; GORDAN L; AJAX ET; DAVIS PH; GRABOWSKI T
      A CASE OF LATE-ONSET MELAS

      Archives of neurology
    92. VANGOETHEM G; MARTIN JJ; LOFGREN A; DEHAENE I; TACK P; VANZANDYCKE M; VERVERKEN D; CEUTERICK C; VANBROECKHOVEN C
      UNUSUAL PRESENTATION AND CLINICAL VARIABILITY IN BELGIAN PEDIGREES WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND MULTIPLE DELETIONS OF MITOCHONDRIAL-DNA

      European journal of neurology
    93. PLEWNIA K; DOTTI MT; MALANDRINI A; MANNESCHI L; BATTISTI C; DESTEFANO N; RUFA A; MOTOLESE E; FEDERICO A
      A RARE ASSOCIATION OF MYASTHENIA-GRAVIS AND MITOCHONDRIAL MYOPATHY - A CLINICAL, BIOCHEMICAL AND MORPHOLOGIC STUDY OF ONE CASE

      Journal of submicroscopic cytology and pathology
    94. KIM SH; CHI JG; REITH A; KADENBACH B
      QUANTITATIVE-ANALYSIS OF MITOCHONDRIAL-DNA DELETION IN PARAFFIN-EMBEDDED MUSCLE TISSUES FROM PATIENTS WITH KSS AND CPEO

      Biochimica et biophysica acta. Molecular basis of disease
    95. KLEINER DE; GAFFEY MJ; SALLIE R; TSOKOS M; NICHOLS L; MCKENZIE R; STRAUS SE; HOOFNAGLE JH
      HISTOPATHOLOGIC CHANGES ASSOCIATED WITH FIALURIDINE HEPATOTOXICITY

      Modern pathology
    96. FERRERA PC; CURRAN CB; SWANSON H
      ETIOLOGY OF PEDIATRIC ISCHEMIC STROKE

      The American journal of emergency medicine
    97. KOROSHETZ WJ; JENKINS BG; ROSEN BR; BEAL MF
      ENERGY-METABOLISM DEFECTS IN HUNTINGTONS-DISEASE AND EFFECTS OF COENZYME Q(10)

      Annals of neurology
    98. RUBIOGOZALBO ME; RUITENBEEK W; BENTLAGE HACM; SCHAGGER H; SENGERS RCA; TRIJBELS JMF; TERLAAK HJ; MARIMAN ECM; BAKKER MM; DEJAGER J; SMEITINK JAM
      FAVORABLE CLINICAL COURSE IN AN INFANT WITH SEVERE DEFICIENCY OF COMPLEX-III OF THE RESPIRATORY-CHAIN COMBINED WITH LESS SEVERE DEFICIENCIES OF COMPLEX-I, COMPLEX-II AND COMPLEX-IV

      European journal of pediatrics
    99. KIMURA M; HASEGAWA Y; YASUDA K; SEJIMA H; INOUE M; YAMAGUCHI S; ANDO Y; OHNO S
      MAGNETIC-RESONANCE-IMAGING WITH FLUID-ATTENUATED INVERSION-RECOVERY PULSE SEQUENCES IN MELAS SYNDROME

      Pediatric radiology
    100. SPERL W; SKLADAL D; GNAIGER E; WYSS M; MAYR U; HAGER J; GELLERICH FN
      HIGH-RESOLUTION RESPIROMETRY OF PERMEABILIZED SKELETAL-MUSCLE FIBERS IN THE DIAGNOSIS OF NEUROMUSCULAR DISORDERS

      Molecular and cellular biochemistry


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 07/08/20 alle ore 06:12:59