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    1. Rambukkana, A
      Molecular basis for the peripheral nerve predilection of Mycobacterium leprae

      CURRENT OPINION IN MICROBIOLOGY
    2. Tubridy, N; Fontaine, B; Eymard, B
      Congenital myopathies and congenital muscular dystrophies

      CURRENT OPINION IN NEUROLOGY
    3. 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
    4. Ruggieri, V; Lubieniecki, F; Meli, F; Diaz, D; Ferragut, E; Saito, K; Brockington, M; Muntoni, F; Fukuyama, Y; Taratuto, AL
      Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular-eye-brain loci: report of three siblings

      NEUROMUSCULAR DISORDERS
    5. Hayashi, YK; Tezak, Z; Momoi, T; Nonaka, I; Garcia, CA; Hoffman, EP; Arahata, K
      Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy

      NEUROMUSCULAR DISORDERS
    6. Kaariainen, M; Liljamo, T; Pelto-Huikko, M; Heino, J; Jarvinen, M; Kalimo, H
      Regulation of alpha 7 integrin by mechanical stress during skeletal muscleregeneration

      NEUROMUSCULAR DISORDERS
    7. Mercuri, E; Rutherford, M; De Vile, C; Counsell, S; Sewry, C; Brown, S; Bydder, G; Dubowitz, V; Muntoni, F
      Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophy

      NEUROMUSCULAR DISORDERS
    8. 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
    9. Nakagawa, M; Miyagoe-Suzuki, Y; Ikezoe, K; Miyata, Y; Nonaka, I; Harii, K; Takeda, S
      Schwann cell myelination occurred without basal lamina formation in laminin alpha 2 chain-null mutant (dy(3K)/dy(3K)) mice

      GLIA
    10. 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
    11. Trevisan, CP; Pastorello, E; Tonello, S; Armani, M; Rigoni, MT; Tormene, AP; Freda, MP; Zortea, M; Lombardi, S
      Ataxia and Congenital Muscular Dystrophy: the follow-up of a new specific phenotype

      BRAIN & DEVELOPMENT
    12. Draviam, R; Billington, L; Senchak, A; Hoffman, EP; Watkins, SC
      Confocal analysis of the dystrophin protein complex in muscular dystrophy

      MUSCLE & NERVE
    13. Cormand, B; Pihko, H; Bayes, M; Valanne, L; Santavuori, P; Talim, B; Gershoni-Baruch, R; Ahmad, A; van Bokhoven, H; Brunner, HG; Voit, T; Topaloglu, H; Dobyns, WB; Lehesjoki, AE
      Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease

      NEUROLOGY
    14. O'Brien, DP; Johnson, GC; Liu, LA; Guo, LT; Engvall, E; Powell, HC; Shelton, GD
      Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    15. Jones, KJ; Morgan, G; Johnston, H; Tobias, V; Ouvrier, RA; Wilkinson, I; North, KN
      The expanding phenotype of laminin alpha 2 chain (merosin) abnormalities: case series and review

      JOURNAL OF MEDICAL GENETICS
    16. Di Blasi, C; He, Y; Morandi, L; Cornelio, F; Guicheney, P; Mora, M
      Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping

      BRAIN
    17. North, PE; Waner, M; Mizeracki, A; Mrak, RE; Nicholas, R; Kincannon, J; Suen, JY; Mihm, MC
      A unique microvascular phenotype shared by juvenile hemangiomas and human placenta

      ARCHIVES OF DERMATOLOGY
    18. Brockington, M; Blake, DJ; Prandini, P; Brown, SC; Torelli, S; Benson, MA; Ponting, CP; Estournet, B; Romero, NB; Mercuri, E; Voit, T; Sewry, CA; Guicheney, P; Muntoni, F
      Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha 2 deficiency and abnormal glycosylation of alpha-dystroglycan

      AMERICAN JOURNAL OF HUMAN GENETICS
    19. Talim, B; Kale, G; Topaloglu, H; Akcoren, Z; Caglar, M; Gogus, S; Elkay, M
      Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophy

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    20. Sewry, CA
      Immunocytochemical analysis of human muscular dystrophy

      MICROSCOPY RESEARCH AND TECHNIQUE
    21. Talim, B; Ferreiro, A; Cormand, B; Vignier, N; Oto, A; Gogus, S; Cila, A; Lehesjoki, AE; Pihko, H; Guicheney, P; Topaloglu, H
      Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci

      NEUROMUSCULAR DISORDERS
    22. Anderson, LVB; Harrison, RM; Pogue, R; Vafiadaki, E; Pollitt, C; Davison, K; Moss, JA; Keers, S; Pyle, A; Shaw, PJ; Mahjneh, I; Argov, Z; Greenberg, CR; Wrogemann, K; Bertorini, T; Goebel, HH; Beckmann, JS; Bashir, R; Bushby, KMD
      Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

      NEUROMUSCULAR DISORDERS
    23. Tardif-de Gery, S; Vilquin, JT; Carlier, P; Raynaud, JS; Wary, C; Schwartz, K; Leroy-Willig, A
      Muscular transverse relaxation time measurement by magnetic resonance imaging at 4 Tesla in normal and dystrophic dy/dy and dy(2j)/dy(2j) mice

      NEUROMUSCULAR DISORDERS
    24. Dubowitz, DJ; Tyszka, JM; Sewry, CA; Moats, RA; Scadeng, M; Dubowitz, V
      High resolution magnetic resonance imaging of the brain in the dy/dy mousewith merosin-deficient congenital muscular dystrophy

      NEUROMUSCULAR DISORDERS
    25. Kaariainen, M; Kaariainen, J; Jarvinen, TLN; Nissinen, L; Heino, J; Jarvinen, M; Kalimo, H
      Integrin and dystrophin associated adhesion protein complexes during regeneration of shearing-type muscle injury

      NEUROMUSCULAR DISORDERS
    26. Auranen, M; Rapola, J; Pihko, H; Haltia, M; Leivo, I; Soinila, S; Virtanen, I; Kalimo, H; Anderson, LVB; Santavuori, P; Somer, H
      Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease

      NEUROMUSCULAR DISORDERS
    27. Vilquin, JT; Vignier, N; Tremblay, JP; Engvall, E; Schwartz, K; Fiszman, M
      Identification of homozygous and heterozygous dy(2J) mice by PCR

      NEUROMUSCULAR DISORDERS
    28. Vajsar, J; Ackerley, C; Chitayat, D; Becker, LE
      Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome

      PEDIATRIC NEUROLOGY
    29. Di Blasi, C; Mora, M; Pareyson, D; Farina, L; Sghirlanzoni, A; Vignier, N; Blasevich, F; Cornelio, F; Guicheney, P; Morandi, L
      Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis

      ANNALS OF NEUROLOGY
    30. Dubowitz, T
      Congenital muscular dystrophy: An expanding clinical syndrome

      ANNALS OF NEUROLOGY
    31. Flanigan, KM; Kerr, M; Bromberg, MB; Leonard, C; Tsuruda, J; Zhang, P; Gonzalez-Gomez, I; Cohn, R; Campbell, KP; Leppert, M
      Congenital muscular dystrophy with rigid spine syndrome: A clinical, pathological, radiological, and genetic study

      ANNALS OF NEUROLOGY
    32. Mercuri, E; Sewry, CA; Brown, SC; Brockington, M; Jungbluth, H; DeVile, C; Counsell, S; Manzur, A; Muntoni, F
      Congenital muscular dystrophy with secondary merosin deficiency and normalbrain MRI: A novel entity?

      NEUROPEDIATRICS
    33. Pegoraro, E; Fanin, M; Trevisan, CP; Angelini, C; Hoffman, EP
      A novel laminin alpha 2 isoform in severe laminin alpha 2 deficient congenital muscular dystrophy

      NEUROLOGY
    34. Chadani, Y; Kondoh, T; Kamimura, N; Matsumoto, T; Matsuzaka, T; Kobayashi, O; Kondo-Iida, E; Kobayashi, K; Nonaka, I; Toda, T
      Walker-Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    35. Naom, I; D'Alessandro, M; Sewry, CA; Jardine, P; Ferlini, A; Moss, T; Dubowitz, J; Muntoni, F
      Mutations in the laminin alpha 2-chain gene in two children with early-onset muscular dystrophy

      BRAIN
    36. Lattanzi, G; Muntoni, F; Sabatelli, P; Squarzoni, S; Maraldi, NM; Cenni, V; Villanova, M; Columbaro, M; Merlini, L; Marmiroli, S
      Unusual laminin alpha 2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophy

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    37. Zhao, G; Mizuta, T; Ozaki, I; Kajihara, S; Yamamoto, K; Sakai, T
      Laminin 2 (merosin), but not laminin 1 (EHS-laminin), may be a major laminin isoform present in normal and fibrotic rat liver

      HEPATOLOGY RESEARCH
    38. Sewry, CA; Muntoni, F
      Inherited disorders of the extracellular matrix

      CURRENT OPINION IN NEUROLOGY
    39. Vilquin, JT; Guerette, B; Puymirat, J; Yaffe, D; Tome, FMS; Fardeau, M; Fiszman, M; Schwartz, K; Tremblay, JP
      Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles

      GENE THERAPY
    40. Frost, EE; Buttery, PC; Milner, R; ffrench-Constant, C
      Integrins mediate a neuronal survival signal for oligodendrocytes

      CURRENT BIOLOGY
    41. Philpot, J; Cowan, F; Pennock, J; Sewry, C; Dubowitz, V; Bydder, G; Muntoni, F
      Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging

      NEUROMUSCULAR DISORDERS
    42. Taratuto, A; Lubieniecki, F; Diaz, D; Schultz, M; Ruggieri, V; Saccoliti, M; Dubrovsky, A
      Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study

      NEUROMUSCULAR DISORDERS
    43. Bernasconi, P; Di Blasi, C; Mora, M; Morandi, L; Galbiati, S; Confalonieri, P; Cornelio, F; Mantegazza, R
      Transforming growth factor-beta 1 and fibrosis in congenital muscular dystrophies

      NEUROMUSCULAR DISORDERS
    44. Reed, UC; Tsanaclis, AMC; Vainzof, M; Marie, SK; Carvalho, MS; Roizenblatt, J; Pedreira, CC; Diament, A; Levy, JA
      Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation

      BRAIN & DEVELOPMENT
    45. Nass, D; Goldberg, I; Sadeh, M
      Laminin alpha 2 deficient congenital muscular dystrophy: prenatal diagnosis

      EARLY HUMAN DEVELOPMENT
    46. Sallinen, R; Kuang, W; Engvall, E; Palotie, A; Wessman, M; Horelli-Kuitunen, N
      Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization

      CYTOGENETICS AND CELL GENETICS
    47. Han, J; Jenq, WM; Kefalides, NA
      Integrin alpha(2)beta(1) recognizes laminin-2 and induces C-erb B-2 tyrosine phosphorylation in metastatic human melanoma cells

      CONNECTIVE TISSUE RESEARCH
    48. Talts, JF; Andac, Z; Gohring, W; Brancaccio, A; Timpl, R
      Binding of the G domains of laminin alpha 1 and alpha 2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins

      EMBO JOURNAL
    49. Tome, FMS
      The saga of congenital muscular dystrophy

      NEUROPEDIATRICS
    50. Mahjneh, I; Bushby, K; Anderson, L; Muntoni, F; Tolvanen-Mahjneh, H; Bashir, R; Pizzi, A; Brockington, M; Marconi, G
      Merosin-positive congenital muscular dystrophy: A large inbred family

      NEUROPEDIATRICS
    51. Eeg-Olofsson, KE
      Congenital muscular dystrophy care of children and families

      SCANDINAVIAN JOURNAL OF REHABILITATION MEDICINE
    52. Chou, FL; Angelini, C; Daentl, D; Garcia, C; Greco, C; Hausmanowa-Petrusewicz, I; Fidzianska, A; Wessel, H; Hoffman, EP
      Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population

      NEUROLOGY
    53. Weilbach, FX; Kress, W; Strassburg, HM; Muller, CR; Gold, R
      Diagnostic approach to muscular dystrophies - recent developments and casereports

      NERVENARZT
    54. Shimoji, Y; Ng, V; Matsumura, K; Fischetti, VA; Rambukkana, A
      A 21-kDa surface protein of Mycobacterium leprae binds peripheral nerve laminin-2 and mediates Schwann cell invasion

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    55. McArdle, A; Maglara, A; Appleton, P; Watson, AJM; Grierson, I; Jackson, MJ
      Apoptosis in multinucleated skeletal muscle myotubes

      LABORATORY INVESTIGATION
    56. Kuang, W; Xu, H; Vilquin, JT; Engvall, E
      Activation of the lama2 gene in muscle regeneration: Abortive regenerationin laminin alpha 2-deficiency

      LABORATORY INVESTIGATION
    57. Hoffman, EP
      Counting muscular dystrophies in the post-molecular census

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    58. Brown, SC; Fassati, A; Popplewell, L; Page, AM; Henry, MD; Campbell, KP; Dickson, G
      Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan-laminin interaction

      JOURNAL OF CELL SCIENCE
    59. Relan, NK; Yang, Y; Beqaj, S; Miner, JH; Schuger, L
      Cell elongation induces laminin alpha 2 chain expression in mouse embryonic mesenchymal cells: Role in visceral myogenesis

      JOURNAL OF CELL BIOLOGY
    60. Saito, F; Masaki, T; Kamakura, K; Anderson, LVB; Fujita, S; Fukuta-Ohi, H; Sunada, Y; Shimizu, T; Matsumura, K
      Characterization of the transmembrane molecular architecture of the dystroglycan complex in Schwann cells

      JOURNAL OF BIOLOGICAL CHEMISTRY
    61. Talts, JF; Timpl, R
      Mutation of a basic sequence in the laminin alpha 2LG3 module leads to a lack of proteolytic processing and has different effects on beta 1 integrin-mediated cell adhesion and alpha-dystroglycan binding

      FEBS LETTERS
    62. Mukasa, T; Momoi, T; Momoi, MY
      Activation of caspase-3 apoptotic pathways in skeletal muscle fibers in laminin alpha 2-deficient mice

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    63. Hoffman, EP
      Muscular dystrophy - Identification and use of genes for diagnostics and therapeutics

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    64. Morandi, L; Di Blasi, C; Farina, L; Sorokin, L; Uziel, G; Azan, G; Pini, A; Toscano, A; Lanfossi, M; Galbiati, S; Cornelio, F; Mora, M
      Clinical correlations in 16 patients with total or partial laminin alpha 2deficiency characterized using antibodies against 2 fragments of the protein

      ARCHIVES OF NEUROLOGY
    65. Anderson, LVB; Davison, K
      Multiplex Western blotting system for the analysis of muscular dystrophy proteins

      AMERICAN JOURNAL OF PATHOLOGY
    66. TOTI P; VILLANOVA M; DEFELICE C; MEGHA T; BARTOLOMMEI S; TOSI P
      EXPRESSION OF LAMININ-1 AND LAMININ-2 IN BRAIN-TUMOR VESSELS - AN IMMUNOHISTOCHEMICAL STUDY

      Journal of submicroscopic cytology and pathology
    67. HAYASHI YK; CHOU FL; ENGVALL E; OGAWA M; MATSUDA C; HIRABAYASHI S; YOKOCHI K; ZIOBER BL; KRAMER RH; KAUFMAN SJ; OZAWA E; GOTO Y; NONAKA I; TSUKAHARA T; WANG JZ; HOFFMAN EP; ARAHATA K
      MUTATIONS IN THE INTEGRIN ALPHA-7 GENE CAUSE CONGENITAL MYOPATHY

      Nature genetics
    68. FLORESDELGADO G; BRINGAS P; WARBURTON D
      LAMININ-2 ATTACHMENT SELECTS MYOFIBROBLASTS FROM FETAL MOUSE LUNG

      American journal of physiology. Lung cellular and molecular physiology
    69. NAOM I; DALESSANDRO M; SEWRY CA; PHILPOT J; MANZUR AY; DUBOWITZ V; MUNTONI F
      LAMININ ALPHA-2-CHAIN GENE-MUTATIONS IN 2 SIBLINGS PRESENTING WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    70. TOPALOGLU H; TALIM B; VIGNIER N; HELBLINGLECLERC A; YETUK M; AFSIN IE; CAGLAR M; KALE G; GUICHENEY P
      MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY WITH SEVERE MENTAL-RETARDATION AND NORMAL CRANIAL MRI - A REPORT OF 2 SIBLINGS

      Neuromuscular disorders
    71. PORTER JD
      COMMENTARY - EXTRAOCULAR-MUSCLE SPARING IN MUSCULAR-DYSTROPHY - A CRITICAL-EVALUATION OF POTENTIAL PROTECTIVE MECHANISMS

      Neuromuscular disorders
    72. KANOFF RJ; CURLESS RG; PETITO C; FALCONE S; SIATKOWSKI RM; PEGORARO E
      WALKER-WARBURG-SYNDROME - NEUROLOGIC FEATURES AND MUSCLE MEMBRANE-STRUCTURE

      Pediatric neurology
    73. TSAO CY; MENDELL JR; RUSIN J; LUQUETTE M
      CONGENITAL MUSCULAR-DYSTROPHY WITH COMPLETE LAMININ-ALPHA-2-DEFICIENCY, CORTICAL DYSPLASIA, AND CEREBRAL WHITE-MATTER CHANGES IN CHILDREN

      Journal of child neurology
    74. MACKAY MT; KORNBERG AJ; SHIELD L; PHELAN E; KEAN MJ; COLEMAN LT; DENNETT X
      CONGENITAL MUSCULAR-DYSTROPHY, WHITE-MATTER ABNORMALITIES, AND NEURONAL MIGRATION DISORDERS - THE EXPANDING CONCEPT

      Journal of child neurology
    75. VOIT T
      CONGENITAL MUSCULAR-DYSTROPHIES - 1997 UPDATE

      Brain & development
    76. SEWRY CA; UZIYEL Y; TORELLI S; BUCHANAN S; SOROKIN L; COHEN J; WATT DJ
      DIFFERENTIAL LABELING OF LAMININ ALPHA-2 IN MUSCLE AND NEURAL TISSUE OF DY DY MICE - ARE THERE ISOFORMS OF THE LAMININ ALPHA-2 CHAIN/

      Neuropathology and applied neurobiology
    77. TERLAAK HJ; LEYTEN QH; GABREELS FJM; KUPPEN H; RENIER WO; SENGERS RCA
      LAMININ-ALPHA(2) (MEROSIN), BETA-DYSTROGLYCAN, ALPHA-SARCOGLYCAN (ADHALIN), AND DYSTROPHIN EXPRESSION IN CONGENITAL MUSCULAR-DYSTROPHIES - AN IMMUNOHISTOCHEMICAL STUDY

      Clinical neurology and neurosurgery
    78. PORTER JD; KARATHANASIS P
      EXTRAOCULAR-MUSCLE IN MEROSIN-DEFICIENT MUSCULAR-DYSTROPHY - CATION HOMEOSTASIS IS MAINTAINED BUT IS NOT MECHANISTIC IN MUSCLE SPARING

      Cell and tissue research
    79. AGIUS E; COCHARD P
      COMPARISON OF NEURITE OUTGROWTH INDUCED BY INTACT AND INJURED SCIATIC-NERVES - A CONFOCAL AND FUNCTIONAL-ANALYSIS

      The Journal of neuroscience
    80. BARKOVICH AJ
      NEUROIMAGING MANIFESTATIONS AND CLASSIFICATION OF CONGENITAL MUSCULAR-DYSTROPHIES

      American journal of neuroradiology
    81. Salih, MAM; Al Rayess, M; Cutshall, S; Urtizberea, JA; Al-Turaiki, MHS; Ozo, CO; Straub, V; Akbar, M; Abid, M; Andeejani, A; Campbell, KP
      A novel form of familial congenital muscular dystrophy in two adolescents

      NEUROPEDIATRICS
    82. CONNOLLY AM; PESTRONK A; MEHTA S; ALLOZI M
      PRIMARY ALPHA-SARCOGLYCAN DEFICIENCY RESPONSIVE TO IMMUNOSUPPRESSION OVER 3 YEARS

      Muscle & nerve
    83. Rambukkana, A; Yamada, H; Zanazzi, G; Mathus, T; Salzer, JL; Yurchenco, PD; Campbell, KP; Fischetti, VA
      Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae

      SCIENCE
    84. Farina, L; Morandi, L; Milanesi, I; Ciceri, E; Mora, M; Moroni, I; Pantaleoni, C; Savoiardo, M
      Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients

      NEURORADIOLOGY
    85. MUNTONI F; SEWRY CA
      CONGENITAL MUSCULAR-DYSTROPHY - FROM RAGS TO RICHES

      Neurology
    86. COHN RD; HERRMANN R; SOROKIN L; WEWER UM; VOIT T
      LAMININ ALPHA-2 CHAIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY - VARIABLE EPITOPE EXPRESSION IN SEVERE AND MILD CASES

      Neurology
    87. PEGORARO E; MARKS H; GARCIA CA; CRAWFORD T; MANCIAS P; CONNOLLY AM; FANIN M; MARTINELLO F; TREVISAN CP; ANGELINI C; STELLA A; SCAVINA M; MUNK RL; SERVIDEI S; BONNEMANN CC; BERTORINI T; ACSADI G; THOMPSON CE; GAGNON D; HOGANSON G; CARVER V; ZIMMERMAN RA; HOFFMAN EP
      LAMININ ALPHA-2 MUSCULAR-DYSTROPHY - GENOTYPE PHENOTYPE STUDIES OF 22PATIENTS/

      Neurology
    88. NONAKA I
      ANIMAL-MODELS OF MUSCULAR-DYSTROPHIES

      Laboratory animal science
    89. JONES KJ; KIM SS; NORTH KN
      ABNORMALITIES OF DYSTROPHIN, THE SARCOGLYCANS, AND LAMININ ALPHA-2 INTHE MUSCULAR-DYSTROPHIES

      Journal of Medical Genetics
    90. GUICHENEY P; VIGNIER N; ZHANG X; HE Y; CRUAUD C; FREY V; HELBLINGLECLERC A; RICHARD P; ESTOURNET B; MERLINI L; TOPALOGLU H; MORA M; HARPEY JP; HAENGGELI CA; BAROIS A; HAINQUE B; SCHWARTZ K; TOME FMS; FARDEAU M; TRYGGVASON K
      PCR BASED MUTATION SCREENING OF THE LAMININ ALPHA-2 CHAIN GENE (LAMA2) - APPLICATION TO PRENATAL-DIAGNOSIS AND SEARCH FOR FOUNDER EFFECTS IN CONGENITAL MUSCULAR-DYSTROPHY

      Journal of Medical Genetics
    91. KUANG W; XU H; VACHON PH; LIU L; LOECHEL F; WEWER UM; ENGVALL E
      MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY - PARTIAL GENETIC CORRECTION IN 2 MOUSE MODELS

      The Journal of clinical investigation
    92. MCDEARMON EL; BURWELL AL; COMBS AC; RENLEY BA; SDANO MT; ERVASTI JM
      DIFFERENTIAL HEPARIN SENSITIVITY OF ALPHA-DYSTROGLYCAN BINDING TO LAMININS EXPRESSED IN NORMAL AND DY DY MOUSE SKELETAL-MUSCLE/

      The Journal of biological chemistry
    93. TALTS JF; MANN K; YAMADA Y; TIMPL R
      STRUCTURAL-ANALYSIS AND PROTEOLYTIC PROCESSING OF RECOMBINANT G-DOMAIN OF MOUSE LAMININ ALPHA-2 CHAIN

      FEBS letters
    94. KUANG W; XU H; VACHON PH; ENGVALL E
      DISRUPTION OF THE LAMA2 GENE IN EMBRYONIC STEM-CELLS - LAMININ ALPHA-2 IS NECESSARY FOR SUSTENANCE OF MATURE MUSCLE-CELLS

      Experimental cell research
    95. MARTINELLO F; ANGELINI C; TREVISAN CP
      CONGENITAL MUSCULAR-DYSTROPHY WITH PARTIAL MEROSIN DEFICIENCY AND LATE-ONSET EPILEPSY

      European neurology
    96. VAJSAR J; CHITAYAT D; BECKER LE; HO M; BENZEEV B; JAY V
      SEVERE CLASSICAL CONGENITAL MUSCULAR-DYSTROPHY AND MEROSIN EXPRESSION

      Clinical genetics
    97. TOTI P; PELLEGRINO M; VILLANOVA M; FLORI ML; MIRACCO C; BARTOLOMMEI S; ANDREASSI L
      ALTERED EXPRESSION OF THE ALPHA-2 LAMININ CHAIN IN PSORIATIC SKIN - THE EFFECT OF TREATMENT WITH CYCLOSPORINE

      British journal of dermatology
    98. BUSHBY K; ANDERSON LVB; POLLITT C; NAOM I; MUNTONI F; BINDOFF L
      ABNORMAL MEROSIN IN ADULTS - A NEW FORM OF LATE-ONSET MUSCULAR-DYSTROPHY NOT LINKED TO CHROMOSOME 6Q2

      Brain
    99. MOGHADASZADEH B; DESGUERRE I; TOPALOGLU H; MUNTONI FN; PAVEK S; SEWRY C; MAYER M; FARDEAU M; TOME FMS; GUICHENEY P
      IDENTIFICATION OF A NEW LOCUS FOR A PECULIAR FORM OF CONGENITAL MUSCULAR-DYSTROPHY WITH EARLY RIGIDITY OF THE SPINE, ON CHROMOSOME 1P35-36

      American journal of human genetics
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 12/08/20 alle ore 17:01:43