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La ricerca find articoli where soggetti phrase all words 'muscular dystrophy' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 3377 riferimenti
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    1. De Bruin, PF; Ueki, J; Bush, A; Manzur, AY; Watson, A; Pride, NB
      Inspiratory flow reserve in boys with Duchenne muscular dystrophy

      PEDIATRIC PULMONOLOGY
    2. Hawke, TJ; Garry, DJ
      Myogenic satellite cells: physiology to molecular biology

      JOURNAL OF APPLIED PHYSIOLOGY
    3. Natterlund, B; Ahlstrom, G
      Activities of daily living and quality of life in persons with muscular dystrophy

      JOURNAL OF REHABILITATION MEDICINE
    4. Nair, KPS; Vasanth, A; Gourie-Devi, M; Taly, AB; Rao, S; Gayathri, N; Murali, T
      Disabilities in children with Duchenne muscular dystrophy: A profile

      JOURNAL OF REHABILITATION MEDICINE
    5. Vestergaard, P; Glerup, H; Steffensen, BF; Rejnmark, L; Rahbek, J; Mosekilde, L
      Fracture risk in patients with muscular dystrophy and spinal muscular atrophy

      JOURNAL OF REHABILITATION MEDICINE
    6. Scriver, CR
      Human genetics: Lessons from Quebec populations

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    7. Leppig, KA; Disteche, CM
      Ring X and other structural X chromosome abnormalities: X inactivation andphenotype

      SEMINARS IN REPRODUCTIVE MEDICINE
    8. Hartigan-O'Connor, D; Kirk, CJ; Crawford, R; Mule, JJ; Chamberlain, JS
      Immune evasion by muscle-specific gene expression in dystrophic muscle

      MOLECULAR THERAPY
    9. Guibinga, GH; Ebihara, S; Nalbantoglu, J; Holland, P; Karpati, G; Petrof, BJ
      Forced myofiber regeneration promotes dystrophin gene transfer and improved muscle function despite advanced disease in old dystrophic mice

      MOLECULAR THERAPY
    10. Liu, F; Nishikawa, M; Clemens, PR; Huang, L
      Transfer of full-length Dmd to the diaphragm muscle of Dmd(mdx/mdx) mice through systemic administration of plasmid DNA

      MOLECULAR THERAPY
    11. Pizarro, M; Lissi, EA; Marshall, G; San Martin, A; Leighton, F
      Spontaneous urinary chemiluminescence and diet. An intervention study in humans

      LUMINESCENCE
    12. Spencer, MJ; Montecino-Rodriguez, E; Dorshkind, K; Tidball, JG
      Helper (CD4(+)) and cytotoxic (CD8(+))T cells promote the pathology of dystrophin-deficient muscle

      CLINICAL IMMUNOLOGY
    13. Faulkner, G; Lanfranchi, G; Valle, G
      Telethonin and other new proteins of the Z-disc of skeletal muscle

      IUBMB LIFE
    14. Chien, KR
      Genomic circuits and the integrative biology of cardiomyopathies

      EUROPEAN HEART JOURNAL SUPPLEMENTS
    15. Hegele, RA
      Molecular basis of partial lipodystrophy and prospects for therapy

      TRENDS IN MOLECULAR MEDICINE
    16. Lai, LW; Lien, YHH
      Therapeutic application of chimeric RNA/DNA oligonucleotide based gene therapy

      EXPERT OPINION ON BIOLOGICAL THERAPY
    17. Sanes, JR; Lichtman, JW
      Induction, assembly, maturation and maintenance of a postsynaptic apparatus

      NATURE REVIEWS NEUROSCIENCE
    18. Guillemin, K; Williams, T; Krasnow, MA
      A nuclear lamin is required for cytoplasmic organization and egg polarity in Drosophila

      NATURE CELL BIOLOGY
    19. Ma, LL; Yamada, S; Wirtz, D; Coulombe, PA
      A 'hot-spot' mutation alters the mechanical properties of keratin filamentnetworks

      NATURE CELL BIOLOGY
    20. Wilson, KL; Benavente, R; Burke, B; Craigie, R; Foisner, R; Furukawa, K; Gerace, L; Goldman, RD; Gruenbaum, Y; Harris, C; Hutchison, CJ; Krohne, G; Morris, GE; Otto, H; Simon, AJ; Worman, HJ
      Problems with LAP nomenclature

      NATURE CELL BIOLOGY
    21. Mustfa, N; Moxham, J
      Respiratory muscle assessment in motor neurone disease

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    22. Cao, H; Yuen, J; Hegele, RA
      Single nucleotide polymorphisms of the fukutin gene

      JOURNAL OF HUMAN GENETICS
    23. Hegele, RA; Yuen, J; Cao, HN
      Single-nucleotide polymorphisms of the nuclear lamina proteome

      JOURNAL OF HUMAN GENETICS
    24. 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
    25. Corti, S; Salani, S; Del Bo, R; Torrente, Y; Strazzer, S; Belicchi, M; Paganoni, S; Li, Z; Comi, GP; Bresolin, N; Paulin, D; Scarlato, G
      T-antigen regulated expression reduces apoptosis of Tag-transformed human myoblasts

      CELLULAR AND MOLECULAR LIFE SCIENCES
    26. Burke, B; Mounkes, LC; Stewart, C
      The nuclear envelope in muscular dystrophy and cardiovascular diseases

      TRAFFIC
    27. Fahnehjelm, KT; Ygge, J; Engman, ML; Mosskin, M; Santavuori, P; Malm, G
      A child with Muscle-Eye-Brain disease - Ophthalmological and neurological characteristics

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    28. Mochizuki, H; Hanajima, R; Kowa, H; Motoyoshi, Y; Ashida, H; Kamakura, K; Motoyoshi, K; Ugawa, Y
      Somatosensory evoked potential recovery in myotonic dystrophy

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

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

      CLINICAL NEUROPHYSIOLOGY
    31. Chisari, C; Simonella, C; Rossi, B
      A surface EMG analysis of sarcolemma excitability alteration and myofibre degeneration in Steinert disease

      CLINICAL NEUROPHYSIOLOGY
    32. Ray, PF; Vekemans, M; Munnich, A
      Single cell multiplex PCR amplification of five dystrophin gene exons combined with gender determination

      MOLECULAR HUMAN REPRODUCTION
    33. Hinton, VJ; De Vivo, DC; Nereo, NE; Goldstein, E; Stern, Y
      Selective deficits in verbal working memory associated with a known genetic etiology: The neuropsychological profile of Duchenne muscular dystrophy

      JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY
    34. Walter, MC; Lochmuller, H
      Novel approaches to treat muscular dystrophies

      EXPERT OPINION ON INVESTIGATIONAL DRUGS
    35. Lynch, GS
      Novel therapies for muscular dystrophy and other muscle wasting conditions

      EXPERT OPINION ON THERAPEUTIC PATENTS
    36. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; LeGuern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    37. Udd, B; Griggs, R
      Distal myopathies

      CURRENT OPINION IN NEUROLOGY
    38. Serio, R; Bonvissuto, F; Mule, F
      Altered electrical activity in colonic smooth muscle cells from dystrophic(mdx) mice

      NEUROGASTROENTEROLOGY AND MOTILITY
    39. O'Brien, KF; Kunkel, LM
      Dystrophin and muscular dystrophy: Past, present, and future

      MOLECULAR GENETICS AND METABOLISM
    40. Mistry, DJ; Moorman, JR; Reddy, S; Mounsey, JP
      Skeletal muscle Na currents in mice heterozygous for Six5 deficiency

      PHYSIOLOGICAL GENOMICS
    41. Grange, RW; Isotani, E; Lau, KS; Kamm, KE; Huang, PL; Stull, JT
      Nitric oxide contributes to vascular smooth muscle relaxation in contracting fast-twitch muscles

      PHYSIOLOGICAL GENOMICS
    42. Adams, V; Gielen, S; Hambrecht, R; Schuler, G
      Apoptosis in skeletal muscle

      FRONTIERS IN BIOSCIENCE
    43. Enigk, RE; Maimone, MM
      Cellular and molecular properties of alpha-dystrobrevin in skeletal muscle

      FRONTIERS IN BIOSCIENCE
    44. Ponting, CP; Mott, R; Bork, P; Copley, RR
      Novel protein domains and repeats in Drosophila melanogaster: Insights into structure, function, and evolution

      GENOME RESEARCH
    45. Gleeson, JG
      Neuronal migration disorders

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    46. Louboutin, JP; Rouger, K; Tinsley, JM; Halldorson, J; Wilson, JM
      iNOS expression in dystrophinopathies can be reduced by somatic gene transfer of dystrophin or utrophin

      MOLECULAR MEDICINE
    47. Marcus, CL
      Sleep-disordered breathing in children

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    48. Mehta, S; Hill, NS
      Noninvasive ventilation

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    49. Jakobs, PM; Hanson, EL; Crispell, KA; Toy, W; Keegan, H; Schilling, K; Icenogle, TB; Litt, M; Hershberger, RE
      Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

      JOURNAL OF CARDIAC FAILURE
    50. Burton, EA; Wechuck, JB; Wendell, SK; Goins, WF; Fink, DJ; Glorioso, JC
      Multiple applications for replication-defective herpes simplex virus vectors

      STEM CELLS
    51. Zimprich, A; Grabowski, M; Asmus, F; Naumann, M; Berg, D; Bertram, M; Scheidtmann, K; Kern, P; Winkelmann, F; Muller-Myhsok, B; Riedel, L; Bauer, M; Muller, T; Castro, M; Meitinger, T; Strom, TM; Gasser, T
      Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome

      NATURE GENETICS
    52. Betz, RC; Schoser, BGH; Kasper, D; Ricker, K; Ramirez, A; Stein, V; Torbergsen, T; Lee, YA; Nothen, MM; Wienker, TF; Malin, JP; Propping, P; Reis, A; Mortier, W; Jentsch, TJ; Vorgerd, M; Kubisch, C
      Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease

      NATURE GENETICS
    53. Grewal, PK; Holzfeind, PJ; Bittner, RE; Hewitt, JE
      Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycanin the myodystrophy mouse

      NATURE GENETICS
    54. Chan, KG; Galasko, CSB; Delaney, C
      Hip subluxation and dislocation in Duchenne Muscular Dystrophy

      JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B
    55. Heller, KD; Wirtz, DC; Siebert, CH; Forst, R
      Spinal stabilization in Duchenne muscular dystrophy: Principles of treatment and record of 31 operative treated cases

      JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B
    56. Grozdanovic, Z
      NO message from muscle

      MICROSCOPY RESEARCH AND TECHNIQUE
    57. Wakayama, Y; Inoue, M; Kojima, H; Murahashi, M; Shibuya, S; Oniki, H
      Localization of sarcoglycan, neuronal nitric oxide synthase, beta-dystroglycan, and dystrophin molecules in normal skeletal myofiber: Triple immunogold labeling electron microscopy

      MICROSCOPY RESEARCH AND TECHNIQUE
    58. Miyagoe-Suzuki, Y; Takeda, SI
      Association of neuronal nitric oxide synthase (nNOS) with alpha 1-syntrophin at the sarcolemma

      MICROSCOPY RESEARCH AND TECHNIQUE
    59. Blottner, D; Luck, G
      Just in time and place: NOS/NO system assembly in neuromuscular junction formation

      MICROSCOPY RESEARCH AND TECHNIQUE
    60. Gosztonyi, G; Naschold, U; Grozdanovic, Z; Stoltenburg-Didinger, G; Gossrau, R
      Expression of Leu-19 (CD56, N-CAM) and nitric oxide synthase (NOS) I in denervated and reinnervated human skeletal muscle

      MICROSCOPY RESEARCH AND TECHNIQUE
    61. Galbiati, F; Volonte, D; Liu, J; Capozza, F; Frank, PG; Zhu, L; Pestell, RG; Lisanti, MP
      Caveolin-1 expression negatively regulates cell cycle progression by inducing G(0)/G(1) arrest via a p53/p21(WAF1/Cip1)-dependent mechanism

      MOLECULAR BIOLOGY OF THE CELL
    62. Tolonen, N; Doglio, L; Schleich, S; Locker, JK
      Vaccinia virus DNA replication occurs in endoplasmic reticulum-enclosed cytoplasmic mini-nuclei

      MOLECULAR BIOLOGY OF THE CELL
    63. Mykkanen, OM; Gronholm, M; Ronty, M; Lalowski, M; Salmikangas, P; Suila, H; Carpen, O
      Characterization of human palladin, a microfilament-associated protein

      MOLECULAR BIOLOGY OF THE CELL
    64. Dominov, JA; Houlihan-Kamamoto, CA; Swap, CJ; Miller, JB
      Pro- and anti-apoptotic members of the Bcl-2 family in skeletal muscle: A distinct role for Bcl-2 in later stages of myogenesis

      DEVELOPMENTAL DYNAMICS
    65. Costa, C; Harding, B; Copp, AJ
      Neuronal migration defects in the Dreher (Lmx1a) mutant mouse: Role of disorders of the glial limiting membrane

      CEREBRAL CORTEX
    66. Dalloz, C; Claudepierre, T; Rodius, F; Mornet, D; Sahel, J; Rendon, A
      Differential distribution of the members of the dystrophin glycoprotein complex in mouse retina: Effect of the mdx(3Cv) mutation

      MOLECULAR AND CELLULAR NEUROSCIENCE
    67. Abdulrazzak, H; Noro, N; Simons, JP; Goldspink, G; Barnard, EA; Gorecki, DC
      Structural diversity despite strong evolutionary conservation in the 5 '-untranslated region of the P-type dystrophin transcript

      MOLECULAR AND CELLULAR NEUROSCIENCE
    68. Newey, SE; Gramolini, AO; Wu, J; Holzfeind, P; Jasmin, BJ; Davies, KE; Blake, DJ
      A novel mechanism for modulating synaptic gene expression: Differential localization of alpha-dystrobrevin transcripts in skeletal muscle

      MOLECULAR AND CELLULAR NEUROSCIENCE
    69. Jankowski, RJ; Haluszczak, C; Trucco, M; Huard, J
      Flow cytometric characterization of myogenic cell populations obtained viathe preplate technique: Potential for rapid isolation of muscle-derived stem cells

      HUMAN GENE THERAPY
    70. Kapsa, R; Quigley, A; Lynch, GS; Steeper, K; Kornberg, AJ; Gregorevic, P; Austin, L; Byrne, E
      In vivo and in vitro correction of the mdx dystrophin gene nonsense mutation by short-fragment homologous replacement

      HUMAN GENE THERAPY
    71. Holt, I; Clements, L; Manilal, S; Brown, SC; Morris, GE
      The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin

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

      BRAIN PATHOLOGY
    73. Ludwig, M; Geipel, A; Berg, C; Gembruch, U; Schwinger, E; Diedrich, K
      Is intracytoplasmic sperm injection itself an indication to perform preimplantation genetic diagnosis (PGD)? About PGD, invasive prenatal diagnosis and genetic sonography

      FETAL DIAGNOSIS AND THERAPY
    74. Chaturvedi, LS; Srivastava, S; Mukherjee, M; Mittal, RD; Phadke, SR; Pradhan, S; Mittal, B
      Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene

      INDIAN JOURNAL OF MEDICAL RESEARCH
    75. Zaccaria, ML; Perrone-Capano, C; Melucci-Vigo, G; Gaeta, L; Petrucci, TC; Paggi, P
      Differential regulation of transcripts for dystrophin isoforms, dystroglycan, and alpha 3AChR subunit in mouse sympathetic ganglia following postganglionic nerve crush

      NEUROBIOLOGY OF DISEASE
    76. Cao, B; Pruchnic, R; Ikezawa, M; Xiao, X; Li, J; Wickham, TJ; Kovesdi, I; Rudert, WA; Huard, J
      The role of receptors in the maturation-dependent adenoviral transduction of myofibers

      GENE THERAPY
    77. Roberts, ML; Athanasopoulos, T; Pohlschmidt, M; Duisit, G; Cosset, FL; Dickson, G
      Post-mitotic, differentiated myotubes efficiently produce retroviral vector from hybrid adeno-retrovirus templates

      GENE THERAPY
    78. Campeau, P; Chapdelaine, P; Seigneurin-Venin, S; Massie, B; Tremblay, JP
      Transfection of large plasmids in primary human myoblasts

      GENE THERAPY
    79. McMahon, JM; Signori, E; Wells, KE; Fazio, VM; Wells, DJ
      Optimisation of electrotransfer of plasmid into skeletal muscle by pretreatment with hyaluronidase - increased expression with reduced muscle damage

      GENE THERAPY
    80. Winder, SJ
      The complexities of dystroglycan

      TRENDS IN BIOCHEMICAL SCIENCES
    81. Cohen, M; Lee, KK; Wilson, KL; Gruenbaum, Y
      Transcriptional repression, apoptosis, human disease and the functional evolution of the nuclear lamina

      TRENDS IN BIOCHEMICAL SCIENCES
    82. Corbett, MA; Robinson, CS; Dunglison, GF; Yang, N; Joya, JE; Stewart, AW; Schnell, C; Gunning, PW; North, KN; Hardeman, EC
      A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy

      HUMAN MOLECULAR GENETICS
    83. Sunada, Y; Ohi, H; Hase, A; Ohi, H; Hosono, T; Arata, S; Higuchi, S; Matsumura, K; Shimizu, T
      Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity

      HUMAN MOLECULAR GENETICS
    84. Boyle, S; Gilchrist, S; Bridger, JM; Mahy, NL; Ellis, JA; Bickmore, WA
      The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells

      HUMAN MOLECULAR GENETICS
    85. Bastianutto, C; Bestard, JA; Lahnakoski, K; Broere, D; De Visser, M; Zaccolo, M; Pozzan, T; Ferlini, A; Muntoni, F; Patarnello, T
      Dystrophin muscle enhancer 1 is implicated in the activation of non-muscleisoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy

      HUMAN MOLECULAR GENETICS
    86. Fan, XP; Dion, P; Laganiere, J; Brais, B; Rouleau, GA
      Oligomerization of polyalanine expanded PABPN1 facilitates nuclear proteinaggregation that is associated with cell death

      HUMAN MOLECULAR GENETICS
    87. Gache, Y; Allegra, M; Bodemer, C; Pisani-Spadafora, A; de Prost, Y; Ortonne, JP; Meneguzzi, G
      Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with aging

      HUMAN MOLECULAR GENETICS
    88. 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
    89. De Repentigny, Y; Cote, PD; Pool, M; Bernier, G; Girard, S; Vidal, SM; Kothary, R
      Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a

      HUMAN MOLECULAR GENETICS
    90. van Deutekom, JCT; Bremmer-Bout, M; Janson, AAM; Ginjaar, IB; Baas, F; den Dunnen, JT; van Ommen, GJB
      Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells

      HUMAN MOLECULAR GENETICS
    91. Yamada, H; Saito, F; Fukuta-Ohi, H; Zhong, D; Hase, A; Arai, K; Okuyama, A; Maekawa, R; Shimizu, T; Matsumura, K
      Processing of beta-dystroglycan by matrix metalloproteinase disrupts the link between the extracellular matrix and cell membrane via the dystroglycancomplex

      HUMAN MOLECULAR GENETICS
    92. Mills, MA; Yang, N; Weinberger, RP; Vander Woude, DL; Beggs, AH; Easteal, S; North, KN
      Differential expression of the actin-binding proteins, alpha-actinin-2 and-3, in different species: implications for the evolution of functional redundancy

      HUMAN MOLECULAR GENETICS
    93. Del Bo, R; Torrente, Y; Corti, S; D'Angelo, MG; Comi, GP; Fagiolari, G; Salani, S; Cova, A; Pisati, F; Moggio, M; Ausenda, C; Scarlato, G; Bresolin, N
      In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: Evidence of programmed cell death after muscle cell transplantation

      CELL TRANSPLANTATION
    94. 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
    95. Connolly, AM; Keeling, RM; Mehta, S; Pestronk, A; Sanes, JR
      Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin alpha 2-deficient mice

      NEUROMUSCULAR DISORDERS
    96. Fisher, R; Tinsley, JM; Phelps, SR; Squire, SE; Townsend, ER; Martin, JE; Davies, KE
      Non-toxic ubiquitous over-expression of utrophin in the mdx mouse

      NEUROMUSCULAR DISORDERS
    97. Kaminski, H; Andrade, FH
      Nitric oxide: biologic effects on muscle and role in muscle diseases

      NEUROMUSCULAR DISORDERS
    98. Flanigan, KM; Coffeen, CM; Sexton, L; Stauffer, D; Brunner, S; Leppert, MF
      Genetic characterization of a large, historically significant Utah kindredwith facioscapulohumeral dystrophy

      NEUROMUSCULAR DISORDERS
    99. Kitaguchi, T; Matsubara, S; Sato, M; Miyamoto, K; Hirai, S; Schwartz, K; Bonne, G
      A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block

      NEUROMUSCULAR DISORDERS
    100. 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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/06/20 alle ore 23:26:05