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    1. Cao, H; Yuen, J; Hegele, RA
      Single nucleotide polymorphisms of the fukutin gene

      JOURNAL OF HUMAN GENETICS
    2. 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
    3. 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
    4. Gleeson, JG
      Neuronal migration disorders

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    5. 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
    6. 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
    7. 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
    8. 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
    9. 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
    10. Philpot, J; Counsell, S; Bydder, G; Sewry, CA; Dubowitz, V; Muntoni, F
      Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?

      NEUROMUSCULAR DISORDERS
    11. 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
    12. 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
    13. 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
    14. 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
    15. Bingol-Kologlu, M; Tanyel, FC; Akcoren, Z; Topaloglu, H; Gogus, S; Buyukpamukcu, N; Hicsonmez, A
      A comparative histopathologic and immunohistopathologic evaluation of cremaster muscles from boys with various inguinoscrotal pathologies

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    16. 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
    17. Kaye, EM
      Update on genetic disorders affecting white matter

      PEDIATRIC NEUROLOGY
    18. 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
    19. Kuzniecky, RI; Barkovich, AJ
      Malformations of cortical development and epilepsy

      BRAIN & DEVELOPMENT
    20. van der Flier, A; Sonnenberg, A
      Function and interactions of integrins

      CELL AND TISSUE RESEARCH
    21. Previtali, SC; Feltri, ML; Archelos, JJ; Quattrini, A; Wrabetz, L; Hartung, HP
      Role of integrins in the peripheral nervous system

      PROGRESS IN NEUROBIOLOGY
    22. Hoeltzenbein, M; Tome, FMS
      Oppenheim's myatonia congenita

      NEUROPEDIATRICS
    23. Subahi, SA
      Distinguishing cardiac features of a novel form of congenital muscular dystrophy (Salih CMD)

      PEDIATRIC CARDIOLOGY
    24. Guerrini, R; Carrozzo, R
      Epilepsy and genetic malformations of the cerebral cortex

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Ross, ME; Walsh, CA
      Human brain malformations and their lessons for neuronal migration

      ANNUAL REVIEW OF NEUROSCIENCE
    26. Sasaki, M; Oikawa, H; Ehara, S; Tamakawa, Y; Takahashi, S; Tohgi, H
      Disorganised unilateral cerebellar folia: a mild form of cerebellar cortical dysplasia?

      NEURORADIOLOGY
    27. 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
    28. 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
    29. Kakita, A; Wakabayashi, K; Piao, YS; Takahashi, H
      Experimentally induced leptomeningeal glioneuronal heterotopia and underlying cortical dysplasia of the lateral limbic area in rats treated transplacentally with methylmercury

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    30. 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
    31. Kobayashi, K; Sasaki, J; Kondo-Iida, E; Fukuda, Y; Kinoshita, M; Sunada, Y; Nakamura, Y; Toda, T
      Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin

      FEBS LETTERS
    32. 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
    33. Cserhalmi-Friedman, PB; Olson, PF; Koch, M; Champliaud, MF; Brunken, WJ; Burgeson, RE; Christiano, AM
      Structural analysis and mutation detection strategy for the human LamC3 gene

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    34. 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
    35. Komatsu, S; Sakata-Haga, H; Sawada, K; Hisano, S; Fukui, Y
      Prenatal exposure to ethanol induces leptomeningeal heterotopia in the cerebral cortex of the rat fetus

      ACTA NEUROPATHOLOGICA
    36. 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
    37. Tunggal, P; Smyth, N; Paulsson, M; Ott, MC
      Laminins: Structure and genetic regulation

      MICROSCOPY RESEARCH AND TECHNIQUE
    38. Patton, BL
      Laminins of the neuromuscular system

      MICROSCOPY RESEARCH AND TECHNIQUE
    39. McGowan, KA; Marinkovich, MP
      Laminins and human disease

      MICROSCOPY RESEARCH AND TECHNIQUE
    40. Belkin, AM; Stepp, MA
      Integrins as receptors for laminins

      MICROSCOPY RESEARCH AND TECHNIQUE
    41. Miyagoe-Suzuki, Y; Nakagawa, M; Takeda, S
      Merosin and congenital muscular dystrophy

      MICROSCOPY RESEARCH AND TECHNIQUE
    42. Colognato, H; Yurchenco, PD
      Form and function: The laminin family of heterotrimers

      DEVELOPMENTAL DYNAMICS
    43. Novak, U; Kaye, AH
      Extracellular matrix and the brain: components and function

      JOURNAL OF CLINICAL NEUROSCIENCE
    44. Sasaki, J; Ishikawa, K; Kobayashi, K; Kondo-Iida, E; Fukayama, M; Mizusawa, H; Takashima, S; Sakakihara, Y; Nakamura, Y; Toda, T
      Neuronal expression of the fukutin gene

      HUMAN MOLECULAR GENETICS
    45. Villanova, M; Mercuri, E; Bertini, E; Sabatelli, P; Morandi, L; Mora, M; Sewry, C; Brockington, M; Brown, SC; Ferreiro, A; Maraldi, NM; Toda, T; Guicheney, P; Merlini, L; Muntoni, F
      Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome

      NEUROMUSCULAR DISORDERS
    46. 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
    47. 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
    48. 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
    49. Toda, T; Kobayashi, K; Kondo-Iida, E; Sasaki, J; Nakamura, Y
      The Fukuyama congenital muscular dystrophy story

      NEUROMUSCULAR DISORDERS
    50. Jong, YJ; Kobayashi, K; Toda, T; Kondo-lida, E; Huang, SC; Shen, YZ; Nonaka, I; Fukuyama, Y
      Genetic heterogeneity in three Chinese children with Fukuyama congenital muscular dystrophy

      NEUROMUSCULAR DISORDERS
    51. 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
    52. Vilquin, JT; Vignier, N; Tremblay, JP; Engvall, E; Schwartz, K; Fiszman, M
      Identification of homozygous and heterozygous dy(2J) mice by PCR

      NEUROMUSCULAR DISORDERS
    53. Lammens, M
      Neuronal migration disorders in man

      EUROPEAN JOURNAL OF MORPHOLOGY
    54. Uziyel, Y; Hall, S; Cohen, J
      In fluence of laminin-2 on Schwann cell-axon interactions

      GLIA
    55. Kato, T; Funahashi, M; Matsui, A; Takashima, S; Suzuki, Y
      MRI of disseminated developmental dysmyelination in fukuyama type of CMD

      PEDIATRIC NEUROLOGY
    56. Vajsar, J; Ackerley, C; Chitayat, D; Becker, LE
      Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome

      PEDIATRIC NEUROLOGY
    57. Asano, Y; Minagawa, K; Okuda, A; Matsui, T; Ando, K; Kondo-Iida, E; Kobayashi, O; Toda, T; Nonaka, I; Tanizawa, T
      A case of Walker-Warburg syndrome

      BRAIN & DEVELOPMENT
    58. 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
    59. Gomez, JL; Garcia-Ayllon, MS; Campoy, FJ; Vidal, CJ
      Muscular dystrophy alters the processing of light acetylcholinesterase butnot butyrylcholinesterase forms in liver of Lama2(dy) mice

      JOURNAL OF NEUROSCIENCE RESEARCH
    60. Libby, RT; Champliaud, MF; Claudepierre, T; Xu, Y; Gibbons, EP; Koch, M; Burgeson, RE; Hunter, DD; Brunken, WJ
      Laminin expression in adult and developing retinae: Evidence of two novel CNS laminins

      JOURNAL OF NEUROSCIENCE
    61. Soto-Ares, G; Delmaire, C; Deries, B; Vallee, L; Pruvo, JP
      Cerebellar cortical dysplasia: MR findings in a complex entity

      AMERICAN JOURNAL OF NEURORADIOLOGY
    62. 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
    63. De Arcangelis, A; Georges-Labouesse, E
      Integrin and ECM functions - roles in vertebrate development

      TRENDS IN GENETICS
    64. Landrieu, P
      Progress in pediatric neurology.

      REVUE NEUROLOGIQUE
    65. 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
    66. Pedrosa-Domellof, F; Tiger, CF; Virtanen, I; Thornell, LE; Gullberg, D
      Laminin chains in developing and adult human myotendinous junctions

      JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
    67. Hammarberg, H; Wallquist, W; Piehl, F; Risling, M; Cullheim, S
      Regulation of laminin-associated integrin subunit mRNAs in rat spinal motoneurons during postnatal development and after axonal injury

      JOURNAL OF COMPARATIVE NEUROLOGY
    68. Kortesmaa, J; Yurchenco, P; Tryggvason, K
      Recombinant laminin-8 (alpha(4)beta(1)gamma(1)) - Production, purification, and interactions with integrins

      JOURNAL OF BIOLOGICAL CHEMISTRY
    69. Iwao, M; Fukada, S; Harada, T; Tsujikawa, K; Yagita, H; Hiramine, C; Miyagoe, Y; Takeda, S; Yamamoto, H
      Interaction of merosin (laminin 2) with very late activation antigen-6 is necessary for the survival of CD4(+) CD8(+) immature thymocytes

      IMMUNOLOGY
    70. Holt, KH; Crosbie, RH; Venzke, DP; Campbell, KP
      Biosynthesis of dystroglycan: processing of a precursor propeptide

      FEBS LETTERS
    71. Gustafsson, E; Fassler, R
      Insights into extracellular matrix functions from mutant mouse models

      EXPERIMENTAL CELL RESEARCH
    72. Sorokin, LM; Maley, MAL; Moch, H; von der Mark, H; von der Mark, K; Cadalbert, L; Karosi, S; Davies, MJ; McGeachie, JK; Grounds, MD
      Laminin alpha 4 and integrin alpha 6 are upregulated in regenerating dy/dyskeletal muscle: Comparative expression of laminin and integrin isoforms in muscles regenerating after crush injury

      EXPERIMENTAL CELL RESEARCH
    73. Rosen, GD; Galaburda, AM
      Single cause, polymorphic neuronal migration disorders: an animal model

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    74. Oliviero, P; Chassagne, C; Salichon, N; Corbier, A; Hamon, G; Marotte, F; Charlemagne, D; Rappaport, L; Samuel, JL
      Expression of laminin alpha 2 chain during normal and pathological growth of myocardium in rat and human

      CARDIOVASCULAR RESEARCH
    75. 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
    76. Sakuma, K; Watanabe, K; Sano, M; Uramoto, I; Totsuka, T
      Postnatal profiles of myogenic regulatory factors and the receptors of TGF-beta(2), LIF and IGF-I in the gastrocnemius and rectus femoris muscles of dy mouse

      ACTA NEUROPATHOLOGICA
    77. Kumada, S; Tsuchiya, K; Takahashi, M; Takesue, M; Shiotsu, H; Nomura, Y; Segawa, M; Ikeda, K; Hayashi, M
      The cerebellar and thalamic degeneration in Fukuyama-type congenital muscular dystrophy

      ACTA NEUROPATHOLOGICA
    78. Sewry, CA; Muntoni, F
      Inherited disorders of the extracellular matrix

      CURRENT OPINION IN NEUROLOGY
    79. Buttery, PC; ffrench-Constant, C
      Laminin-2/integrin interactions enhance myelin membrane formation by oligodendrocytes

      MOLECULAR AND CELLULAR NEUROSCIENCE
    80. 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
    81. Aravind, L; Koonin, EV
      The fukutin protein family - predicted enzymes modifying cell-surface molecules

      CURRENT BIOLOGY
    82. Frost, EE; Buttery, PC; Milner, R; ffrench-Constant, C
      Integrins mediate a neuronal survival signal for oligodendrocytes

      CURRENT BIOLOGY
    83. Belpaire-Dethiou, MC; Saito, K; Fukuyama, Y; Kondo-Iida, E; Toda, T; Duprez, T; Verellen-Dumoulin, C; Van den Bergh, PYK
      Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patient

      NEUROMUSCULAR DISORDERS
    84. 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
    85. 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
    86. 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
    87. Toda, T; Kobayashi, K
      Fukuyama-type congenital muscular dystrophy: the first human disease to becaused by an ancient retrotransposal integration

      JOURNAL OF MOLECULAR MEDICINE-JMM
    88. Salo, S; Haakana, H; Kontusaari, S; Hujanen, E; Kallunki, T; Tryggvason, K
      Laminin-5 promotes adhesion and migration of epithelial cells: identification of a migration-related element in the gamma 2 chain gene (LAMC2) with activity in transgenic mice

      MATRIX BIOLOGY
    89. Walsh, CA
      Genetic malformations of the human cerebral cortex

      NEURON
    90. Rice, DS; Curran, T
      Mutant mice with scrambled brains: understanding the signaling pathways that control cell positioning in the CNS

      GENES & DEVELOPMENT
    91. Lacy, SE; Bonnemann, CG; Buzney, EA; Kunkel, LM
      Identification of FLRT1, FLRT2, and FLRT3: A novel family of transmembraneleucine-rich repeat proteins

      GENOMICS
    92. 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
    93. Nass, D; Goldberg, I; Sadeh, M
      Laminin alpha 2 deficient congenital muscular dystrophy: prenatal diagnosis

      EARLY HUMAN DEVELOPMENT
    94. Smith, CD; Trevathan, ER; Zhang, M; Andersen, AH; Avison, MJ
      Functional magnetic resonance imaging evidence for task-specific activation of developmentally abnormal visual association cortex

      ANNALS OF NEUROLOGY
    95. 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
    96. Sztriha, L; Al-Gazali, LI; Varady, E; Goebel, HH; Nork, M
      Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis

      NEUROPEDIATRICS
    97. Tome, FMS
      The saga of congenital muscular dystrophy

      NEUROPEDIATRICS
    98. 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
    99. Oka, A; Itoh, M; Takashima, S
      The early induction of cyclooxygenase 2 associated with neurofibrillary degeneration in brains of patients with Fukuyama-type congenital muscular dystrophy

      NEUROPEDIATRICS
    100. Miner, JH
      Renal basement membrane components

      KIDNEY INTERNATIONAL


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 07/08/20 alle ore 18:10:50