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    1. Keedwell, R
      Evaluation of radio transmitters for measuring chick mortality in the Banded Dotterel

      WATERBIRDS
    2. Fedczyna, TO; Lutz, J; Pachman, LM
      Expression of TNF alpha by muscle fibers in biopsies from children with untreated juvenile dermatomyositis: Association with the TNF alpha-308A allele

      CLINICAL IMMUNOLOGY
    3. Sanoudou, D; Beggs, AH
      Clinical and genetic heterogeneity in nemaline myopathy - a disease of skeletal muscle thin filaments

      TRENDS IN MOLECULAR MEDICINE
    4. Artlett, CM; Miller, FW; Rider, LG
      Persistent maternally derived peripheral microchimerism is associated withthe juvenile idiopathic inflammatory myopathies

      RHEUMATOLOGY
    5. Steensberg, A; Vissing, J; Pedersen, BK
      Lack of IL-6 production during exercise in patients with mitochondrial myopathy

      EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY
    6. Asaka, T; Ikeuchi, K; Okino, S; Takizawa, Y; Satake, R; Nitta, E; Komai, K; Endo, K; Higuchi, S; Oyake, T; Yoshimura, T; Suenaga, A; Uyama, E; Saito, T; Konagaya, M; Sunohara, N; Namba, R; Takada, H; Honke, K; Nishina, M; Tanaka, H; Shinagawa, M; Tanaka, K; Matsushima, A; Tsuji, S; Takamori, M
      Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)

      JOURNAL OF HUMAN GENETICS
    7. Muller, C; Schubert, M; Dengler, R; Wohlfarth, K
      Clinico-neurophysiological study on muscular fatigue in mitochondrial myopathy

      KLINISCHE NEUROPHYSIOLOGIE
    8. Corvera, S
      Phosphatidylinositol 3-kinase and the control of endosome dynamics: New players defined by structural motifs

      TRAFFIC
    9. Trojaborg, W; Weimer, LH; Hays, AP
      Electrophysiologic studies in critical illness associated weakness: myopathy or neuropathy - a reappraisal

      CLINICAL NEUROPHYSIOLOGY
    10. Finsterer, J; Fuglsang-Frederiksen, A
      Concentric-needle versus macro EMG II. Detection of neuromuscular disorders

      CLINICAL NEUROPHYSIOLOGY
    11. Montagna, P; Liguori, R; Monari, L; Strong, PN; Riva, R; Di Stasi, V; Gandini, G; Cipone, M
      Equine muscular dystrophy with myotonia

      CLINICAL NEUROPHYSIOLOGY
    12. Priori, A; Cinnante, C; Pesenti, A; Gallanti, A; Cappellari, A; Scarlato, G; Barbieri, S
      Decreased EMG inhibition following electrical stimulation over muscle tendons in myopathies

      CLINICAL NEUROPHYSIOLOGY
    13. Stobiecki, M
      Applications of separation techniques hyphenated to mass spectrometer for metabolic profiling

      CURRENT ORGANIC CHEMISTRY
    14. Pao, D; Watson, C; Peters, B; Lucas, SB; Miller, RF
      Hyperlactataemia and hepatic steatosis: mitochondrial toxicity of nucleoside reverse transcriptase inhibitors

      SEXUALLY TRANSMITTED INFECTIONS
    15. Zhang, ZY
      Protein tyrosine phosphatases: prospects for therapeutics

      CURRENT OPINION IN CHEMICAL BIOLOGY
    16. Lang, CH; Kimball, SR; Frost, RA; Vary, TC
      Alcohol myopathy: impairment of protein synthesis and translation initiation

      INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
    17. Larner, AJ; Williamson, C; Ward, NS; Acheson, JF; Robinson, S; Farmer, SF
      Isolated familial hypomagnesaemia with novel neurological features: causallink or chance concurrence?

      EUROPEAN JOURNAL OF NEUROLOGY
    18. Heckmann, JG; Stefan, H; Heuss, D; Hopp, P; Neundorfer, B
      Isolated muscular sarcoidosis

      EUROPEAN JOURNAL OF NEUROLOGY
    19. Heesen, C; Gbadamosi, J; Schoser, BGH; Pohlau, D
      Autoimmune hyperthyroidism in multiple sclerosis under treatment with glatiramer acetate - a case report

      EUROPEAN JOURNAL OF NEUROLOGY
    20. Tubridy, N; Fontaine, B; Eymard, B
      Congenital myopathies and congenital muscular dystrophies

      CURRENT OPINION IN NEUROLOGY
    21. Hund, E
      Critical illness polyneuropathy

      CURRENT OPINION IN NEUROLOGY
    22. Sidibe, EH; Diop, AN; Thiam, A; Diagne, PM; Sarr, A; Toure, M; Diop, M
      Hoffmann's syndrome in hypothyroid myopathy. Report of a case in an African

      JOINT BONE SPINE
    23. Liu, YF; Steinacker, JM
      Changes in skeletal muscle heat shock proteins: Pathological significance

      FRONTIERS IN BIOSCIENCE
    24. Dalakas, MC
      Peripheral neuropathy and antiretroviral drugs

      JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
    25. Nakada, K; Inoue, K; Ono, T; Isobe, K; Ogura, A; Goto, Y; Nonaka, I; Hayashi, JI
      Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA

      NATURE MEDICINE
    26. 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
    27. Folzenlogen, D
      A case of atorvastatin combined toxic myopathy and inflammatory myositis

      JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
    28. 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
    29. Gehr, LC; Sessler, CN
      Neuromuscular blockade in the intensive care unit

      SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE
    30. Muller-Hocker, J; Schafer, S; Li, K
      Immunocytochemical localization of mitochondrial single-stranded DNA-binding protein in mitochondria-rich cells of normal and neoplastic human tissue

      APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY
    31. Eisenberg, I; Avidan, N; Potikha, T; Hochner, H; Chen, M; Olender, T; Barash, M; Shemesh, M; Sadeh, M; Grabov-Nardini, G; Shmilevich, I; Friedmann, A; Karpati, G; Bradley, WG; Baumbach, L; Lancet, D; Ben Asher, E; Beckmann, JS; Argov, Z; Mitrani-Rosenbaum, S
      The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene ismutated in recessive hereditary inclusion body myopathy

      NATURE GENETICS
    32. Chapman, KL; Mortier, GR; Chapman, K; Loughlin, J; Grant, ME; Briggs, MD
      Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasia

      NATURE GENETICS
    33. Brenner, M; Johnson, AB; Boespflug-Tanguy, O; Rodriguez, D; Goldman, JE; Messing, A
      Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

      NATURE GENETICS
    34. Omar, MA; Wilson, JP; Cox, TS
      Rhabdomyolysis and HMG-CoA reductase inhibitors

      ANNALS OF PHARMACOTHERAPY
    35. Goudeau, B; Dagvadorj, A; Rodrigues-Lima, F; Nedellec, P; Casteras-Simon, M; Perret, E; Langlois, S; Goldfarb, L; Vicart, P
      Structural and functional analysis of a new desmin variant causing desmin-related myopathy

      HUMAN MUTATION
    36. Nariai, R; Ohno, K; Ohta, Y; Hirakawa, K; Ishii, I; Senda, M
      Discordance between cerebral oxygen and glucose metabolism, and hemodynamics in a mitochondrial encephalomyopathy, lactic acidosis, and strokelike episode patient

      JOURNAL OF NEUROIMAGING
    37. Hartl, E; Finsterer, J; Grossegger, C; Kroiss, A; Stollberger, C
      Relationship between thyroid function and skeletal muscle involvement in subclinical and overt hypothyroidism

      ENDOCRINOLOGIST
    38. Gaist, D; Rodriguez, LAG; Huerta, C; Hallas, J; Sindrup, SH
      Lipid-lowering drugs and risk of myopathy: A population based follow-up study

      EPIDEMIOLOGY
    39. Oldfors, A; Fyhr, IM
      Inclusion body myositis: genetic factors, aberrant protein expression, andautoimmunity

      CURRENT OPINION IN RHEUMATOLOGY
    40. Ko, CH; Lam, CW; Tse, PWT; Kong, CK; Chan, AKH; Wong, LJC
      De novo mutation in the mitochondrial tRNA(Leu(UUR)) gene (A3243G) with rapid segregation resulting in MELAS in the offspring

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    41. Eisenberg, I; Hochner, H; Shemesh, M; Levi, T; Potikha, T; Sadeh, M; Argov, Z; Jackson, CL; Mitrani-Rosenbaum, S
      Physical and transcriptional map of the hereditary inclusion body myopathylocus on chromosome 9p12-p13

      EUROPEAN JOURNAL OF HUMAN GENETICS
    42. Rodriguez-Santiago, B; Casademont, J; Nunes, V
      Is mitochondrial DNA depletion involved in Alzheimer's disease?

      EUROPEAN JOURNAL OF HUMAN GENETICS
    43. Bonsch, D; Scheer, P; Neumann, C; Lang-Roth, R; Seifert, E; Storch, P; Weiller, C; Lamprecht-Dinnesen, A; Deufel, T
      A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus

      EUROPEAN JOURNAL OF HUMAN GENETICS
    44. Bornemann, A; Goebel, HH
      Introduction: Recent advances in hereditary neuromuscular diseases of childhood

      BRAIN PATHOLOGY
    45. Bornemann, A; Goebel, HH
      Congenital myopathies

      BRAIN PATHOLOGY
    46. Ozawa, E; Nishino, I; Nonaka, I
      Sarcolemmopathy: Muscular dystrophies with cell membrane defects

      BRAIN PATHOLOGY
    47. Lee, MJ; Lee, JS; Lee, MC
      Apoptosis of skeletal muscle on steroid-induced myopathy in rats

      JOURNAL OF KOREAN MEDICAL SCIENCE
    48. Wirth, J; Back, E; Huttenhofer, A; Nothwang, HG; Lich, C; Gross, S; Menzel, C; Schinzel, A; Kioschis, P; Tommerup, N; Ropers, HH; Horsthemke, B; Buiting, K
      A translocation breakpoint cluster disrupts the newly defined 3 ' end of the SNURF-SNRPN transcription unit on chromosome 15

      HUMAN MOLECULAR GENETICS
    49. Monnier, N; Romero, NB; Lerale, J; Landrieu, P; Nivoche, Y; Fardeau, M; Lunardi, J
      Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor

      HUMAN MOLECULAR GENETICS
    50. Mankodi, A; Urbinati, CR; Yuan, QP; Moxley, RT; Sansone, V; Krym, M; Henderson, D; Schalling, M; Swanson, MS; Thornton, CA
      Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2

      HUMAN MOLECULAR GENETICS
    51. Matsuda, C; Hayashi, YK; Ogawa, M; Aoki, M; Murayama, K; Nishino, I; Nonaka, I; Arahata, K; Brown, RH
      The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

      HUMAN MOLECULAR GENETICS
    52. Bodyak, ND; Nekhaeva, E; Wei, JY; Khrapko, K
      Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues

      HUMAN MOLECULAR GENETICS
    53. Natterlund, B; Sjoden, PO; Ahlstrom, G
      The illness experience of adult persons with muscular dystrophy

      DISABILITY AND REHABILITATION
    54. Minami, N; Ikezoe, K; Kuroda, H; Nakabayashi, H; Satoyoshi, E; Nonaka, I
      Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy

      NEUROMUSCULAR DISORDERS
    55. Dorchies, OM; Laporte, J; Wagner, S; Hindelang, C; Warter, JM; Mandel, JL; Poindron, P
      Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system

      NEUROMUSCULAR DISORDERS
    56. Stojkovic, T; Maurage, CA; Moerman, A; Hurtevent, JF; Krivosic-Horber, R; Pellissier, JF; Vermersch, P
      Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibility

      NEUROMUSCULAR DISORDERS
    57. Chae, J; Minami, N; Jin, Y; Nakagawa, M; Murayama, K; Igarashi, F; Nonaka, I
      Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy

      NEUROMUSCULAR DISORDERS
    58. Cherin, P; Menard, D; Mouton, P; Viallard, JF; Le Hello, C; Authier, FJ; Gherardi, RK; Coquet, M; Herson, S; Leroi, JP
      Macrophagic myofasciitis associated with inclusion body myositis: a reportof three cases

      NEUROMUSCULAR DISORDERS
    59. 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
    60. Campos, Y; Gamez, J; Garcia, A; Andreu, AL; Rubio, JC; Martin, MA; del Hoyo, P; Navarro, C; Cervera, C; Garesse, R; Arenas, J
      A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy

      NEUROMUSCULAR DISORDERS
    61. Schneider, C; Wessig, C; Muller, CR; Brechtelsbauer, D; Grimm, T
      Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes

      NEUROMUSCULAR DISORDERS
    62. Romero, NB; De Lonlay, P; Llense, S; Leturcq, F; Touati, G; Urtizberea, JA; Saudubray, JM; Munnich, A; Kaplan, JC; Recan, D
      Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomaticcarrier with 'de novo' duplication of dystrophin gene

      NEUROMUSCULAR DISORDERS
    63. Chabrol, B; Figarella-Branger, D; Coquet, M; Mancini, J; Fontan, D; Pedespan, JM; Francannet, C; Pouget, J; Beaufrere, AM; Pellilssier, JF
      X-linked myopathy with excessive autophagy: a clinicopathological study offive new families

      NEUROMUSCULAR DISORDERS
    64. Nakamura, A; Harrod, GV; Davies, KE
      Activation of calcineurin and stress activated protein kinase/p38-mitogen activated protein kinase in hearts of utrophin-dystrophin knockout mice

      NEUROMUSCULAR DISORDERS
    65. Piercy, RJ; Hinchcliff, KW; Morley, PS; DiSilvestro, RA; Reinhart, GA; Nelson, SL; Schmidt, KE; Craig, AM
      Vitamin E and exertional rhabdomyolysis during endurance sled dog racing

      NEUROMUSCULAR DISORDERS
    66. Pollitt, C; Anderson, LVB; Pogue, R; Davison, K; Pyle, A; Bushby, KMD
      The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach

      NEUROMUSCULAR DISORDERS
    67. Ueyama, H; Kumamoto, T; Nagao, S; Masuda, T; Horinouchi, H; Fujimoto, S; Tsuda, T
      A new dysferlin gene mutation in two Japanese families with limb-girdle muscular dystrophy 2B and Miyoshi myopathy

      NEUROMUSCULAR DISORDERS
    68. Sewry, CA; Brown, SC; Pelin, K; Jungbluth, H; Wallgren-Pettersson, C; Labeit, S; Manzur, A; Muntoni, F
      Abnormalities in the expression of nebulin in chromosome-2 linked nemalinemyopathy

      NEUROMUSCULAR DISORDERS
    69. Gurgel-Giannetti, J; Reed, U; Bang, ML; Pelin, K; Donner, K; Marie, SK; Carvalho, M; Fireman, MAT; Zanoteli, E; Oliveira, ASB; Zatz, M; Wallgren-Pettersson, C; Labeit, S; Vainzof, M
      Nebulin expression in patients with nemaline myopathy

      NEUROMUSCULAR DISORDERS
    70. Reijneveld, JC; Notermans, NC; Linssen, WHJP; Bar, PR; Wokke, JHJ
      Hyper-CK-aemia revisited

      NEUROMUSCULAR DISORDERS
    71. Goebel, HH; Warlo, IAP
      Surplus protein myopathies

      NEUROMUSCULAR DISORDERS
    72. Voit, T; Kutz, P; Leube, B; Neuen-Jacob, E; Schroder, JM; Cavallotti, D; Vaccario, ML; Schaper, J; Broich, P; Cohn, R; Baethmann, M; Gohlich-Ratmann, G; Scoppetta, C; Herrmann, R
      Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus

      NEUROMUSCULAR DISORDERS
    73. Mahjneh, I; Marconi, G; Bushby, K; Anderson, LVB; Tolvanen-Mahjneh, H; Somer, H
      Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations

      NEUROMUSCULAR DISORDERS
    74. Jungbluth, H; Sewry, CA; Brown, SC; Nowak, KJ; Laing, NG; Wallgren-Pettersson, C; Pelin, K; Manzur, AY; Mercuri, E; Dubowitz, V; Muntoni, F
      Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene

      NEUROMUSCULAR DISORDERS
    75. Olby, NJ; Sharp, NJH; Anderson, LVB; Kunkel, LM; Bonnemann, CG
      Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers

      NEUROMUSCULAR DISORDERS
    76. Pogue, R; Anderson, LVB; Pyle, A; Sewry, C; Pollitt, C; Johnson, MA; Davison, K; Moss, JA; Mercuri, E; Muntoni, F; Bushby, KMD
      Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies

      NEUROMUSCULAR DISORDERS
    77. Chan, TYK; Kwok, TCY
      Chronicity of neurological features in ciguatera fish poisoning

      HUMAN & EXPERIMENTAL TOXICOLOGY
    78. Khan, S; Hemalatha, R; Jeyaseelan, L; Oommen, A; Zachariah, A
      Neuroparalysis and oxime efficacy in organophosphate poisoning: a study ofbutyrylcholinesterase

      HUMAN & EXPERIMENTAL TOXICOLOGY
    79. Vafiadaki, E; Reis, A; Keers, S; Harrison, R; Anderson, LVB; Raffelsberger, T; Ivanova, S; Hoger, H; Bittner, RE; Bushby, K; Bashir, R
      Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation

      NEUROREPORT
    80. Simonsen, A; Wurmser, AE; Emr, SD; Stenmark, H
      The role of phosphoinositides in membrane transport

      CURRENT OPINION IN CELL BIOLOGY
    81. Tonks, NK; Neel, BG
      Combinatorial control of the specificity of protein tyrosine phosphatases

      CURRENT OPINION IN CELL BIOLOGY
    82. Potter, MA; Bartolo, DCC
      Proctalgia fugax

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    83. Vestergaard, H; Lund, S; Pedersen, O
      Rosiglitazone treatment of patients with extreme insulin resistance and diabetes mellitus due to insulin receptor mutations has no effects on glucoseand lipid metabolism

      JOURNAL OF INTERNAL MEDICINE
    84. Gabrielli, A; Caruso, L
      Early recognition of acute cardiovascular beriberi by interpretation of hemodynamics

      JOURNAL OF CLINICAL ANESTHESIA
    85. Sabatelli, P; Bonaldo, P; Lattanzi, G; Braghetta, P; Bergamin, N; Capanni, C; Mattioli, E; Columbaro, M; Ognibene, A; Pepe, G; Bertini, E; Merlini, L; Maraldi, NM; Squarzoni, S
      Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts

      MATRIX BIOLOGY
    86. Hendriks, F; Kooman, JP; van der Sande, FM
      Massive rhabdomyolysis and life threatening hyperkalaemia in a patient with the combination of cerivastatin and gemfibrozil

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    87. Tung, YC; Tsau, YK; Chu, LW; Young, C; Shen, YZ
      Lipid myopathy associated with renal tubular acidosis and spastic diplegiain two brothers

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    88. Lien, LM; Yang, CC; Chen, WH; Chiu, HC
      Bethlem myopathy in a Taiwanese family

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    89. Mori, S; Hamada, H; Yokoyama, A; Kohno, N; Kondo, K; Hara, Y; Kawata, H; Hiwada, K
      Severe inclusion body myositis with interstitial pneumonia

      INTERNAL MEDICINE
    90. Higashikata, T; Koyama, J; Shimada, H; Yazaki, M; Owa, M; Ikeda, S
      An 80-year-old mitochondrial disease patient with A3243G tRNA(Leu) ((UUR))gene presenting cardiac dysfunction as the main symptom

      INTERNAL MEDICINE
    91. Lewis, MP; Machell, JRA; Hunt, NP; Sinanan, ACM; Tippett, HL
      The extracellular matrix of muscle - implications for manipulation of the craniofacial musculature

      EUROPEAN JOURNAL OF ORAL SCIENCES
    92. Vainzof, M; Anderson, LVB; McNally, EM; Davis, DB; Faulkner, G; Valle, G; Moreira, ES; Pavanello, RCM; Passos-Bueno, MR; Zatz, M
      Dysferlin protein analysis in limb-girdle muscular dystrophies

      JOURNAL OF MOLECULAR NEUROSCIENCE
    93. Aisen, PS; Marin, DB; Brickman, AM; Santoro, J; Fusco, M
      Pilot tolerability studies of hydroxychloroquine and colchicine in Alzheimer disease

      ALZHEIMER DISEASE & ASSOCIATED DISORDERS
    94. Shelton, GD; Liu, LA; Guo, LT; Smith, GK; Christiansen, JS; Thomas, WB; Smith, MO; Kline, KL; March, PA; Flegel, T; Engvall, E
      Muscular dystrophy in female dogs

      JOURNAL OF VETERINARY INTERNAL MEDICINE
    95. Razzaq, A; Robinson, IM; McMahon, HT; Skepper, JN; Su, Y; Zelhof, AC; Jackson, AP; Gay, NJ; O'Kane, CJ
      Amphiphysin is necessary for organization of the excitation-contraction coupling machinery of muscles, but not for synaptic vesicle endocytosis in Drosophila

      GENES & DEVELOPMENT
    96. Appel, S; Reichwald, K; Zimmermann, WG; Reis, A; Rosenthal, A; Hennies, HC
      Identification and localization of a new human myotubularin-related protein gene, MTMR8, on 8p22-p23

      GENOMICS
    97. Trauner, DA; Fahmy, RF; Mishler, DA
      Oral motor dysfunction and feeding difficulties in nephropathic cystinosis

      PEDIATRIC NEUROLOGY
    98. Banwell, BL
      Intermediate filament-related myopathies

      PEDIATRIC NEUROLOGY
    99. Rich, A; Leach, A; Ellershaw, J
      A case of difficult pain in a patient with chronic renal failure and calciphylaxis

      JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
    100. Whyte, MP; Podgornik, MN; Wollberg, VA; Eddy, MC; McAlister, WH
      Pseudo-(tumor-induced) rickets

      JOURNAL OF BONE AND MINERAL RESEARCH


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/05/20 alle ore 13:50:18