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La ricerca find articoli where soggetti phrase all words 'PERIPHERAL MYELIN' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 316 riferimenti
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    1. Bennett, CL; Chance, PF
      Molecular pathogenesis of hereditary motor, sensory and autonomic neuropathies

      CURRENT OPINION IN NEUROLOGY
    2. Kursula, P
      The current status of structural studies on proteins of the myelin sheath (review)

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    3. Lee, MJ; Calle, E; Brennan, A; Ahmed, S; Sviderskaya, E; Jessen, KR; Mirsky, R
      In early development of the rat mRNA for the major myelin protein P-0 is expressed in nonsensory areas of the embryonic inner ear, notochord, entericnervous system, and olfactory ensheathing cells

      DEVELOPMENTAL DYNAMICS
    4. Robert, F; Guennoun, R; Desarnaud, F; Do-Thi, A; Benmessahel, Y; Baulieu, EE; Schumacher, M
      Synthesis of progesterone in Schwann cells: regulation by sensory neurons

      EUROPEAN JOURNAL OF NEUROSCIENCE
    5. Hamacher, M; Pippirs, U; Kohler, A; Muller, HW; Bosse, F
      Plasmolipin: genomic structure, chromosomal localization, protein expression pattern, and putative association with Bardet-Biedl syndrome

      MAMMALIAN GENOME
    6. Gago, N; Akwa, Y; Sananes, N; Guennoun, R; Baulieu, EE; El-Etr, M; Schumacher, M
      Progesterone and the oligodendroglial lineage: Stage-dependent biosynthesis and metabolism

      GLIA
    7. Hughes, RAC
      Chronic inflammatory demyelinating polyradiculoneuropathy

      ANNALS OF NEUROLOGY
    8. Takeda, Y; Notsu, T; Kitamura, K; Uyemura, K
      Functional analysis for peripheral myelin protein PASII/PMP22: Is it a member of claudin superfamily?

      NEUROCHEMICAL RESEARCH
    9. Yoshida, M; Colman, DR
      Rapid functional analysis in Xenopus oocytes of Po protein adhesive interactions

      NEUROCHEMICAL RESEARCH
    10. Pfend, G; Matthieu, JM; Garin, N; Tosic, M
      Implication of the extracellular disulfide bond on myelin protein zero expression

      NEUROCHEMICAL RESEARCH
    11. Lane, JE; Foulkes, GD; Hope, TD; Mayorov, VI; Adkison, L
      Hereditary neuropathy with liability to pressure palsies mimicking multifocal compression neuropathy

      JOURNAL OF HAND SURGERY-AMERICAN VOLUME
    12. Ceuterick-de Groote, C; De Jonghe, P; Timmerman, V; Van Goethem, G; Lofgren, A; Ceulemans, B; Van Broeckhoven, C; Martin, JJ
      Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsy

      PATHOLOGY RESEARCH AND PRACTICE
    13. Faist, V; Erbersdobler, HF
      Metabolic transit and in vivo effects of melanoidins and precursor compounds deriving from the Maillard reaction

      ANNALS OF NUTRITION AND METABOLISM
    14. Guennoun, R; Benmessahel, Y; Delespierre, B; Gouezou, M; Rajkowski, KM; Baulieu, E; Schumacher, M
      Progesterone stimulates Krox-20 gene expression in Schwann cells

      MOLECULAR BRAIN RESEARCH
    15. Shiina, M; Kusunoki, S; Miyazaki, T; Kanazawa, I
      Variability in immunohistochemistries of IgM M-proteins binding to sulfated glucuronyl paragloboside

      JOURNAL OF NEUROIMMUNOLOGY
    16. Kwa, MSG; van Schaik, IN; Brand, A; Baas, F; Vermeulen, M
      Investigation of serum response to PMP22, connexin 32 and P-0 in inflammatory neuropathies

      JOURNAL OF NEUROIMMUNOLOGY
    17. Young, P; Suter, U
      Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Tooth disease

      BRAIN RESEARCH REVIEWS
    18. Orstavik, K; Heier, MS; Young, P; Stogbauer, F
      Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies

      MUSCLE & NERVE
    19. Weiss, MD; Luciano, CA; Quarles, RH
      Nerve conduction abnormalities in aging mice deficient for myelin-associated glycoprotein

      MUSCLE & NERVE
    20. Fabrizi, GM; Ferrarini, M; Cavallaro, T; Jarre, L; Polo, A; Rizzuto, N
      A somatic and germline mosaic mutation in MPZ/P-0 mimics recessive inheritance of CMT1B

      NEUROLOGY
    21. Aarskog, NK; Aadland, S; Gjerde, IO; Vedeler, CA
      Molecular genetic analysis of Charcot-Marie-Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    22. Lagueny, A; Latour, P; Vital, G; Le Masson, G; Rouanet, M; Ferrer, X; Vital, C; Vandenberghe, A
      Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ gene

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    23. Fabrizi, GM; Simonati, A; Taioli, F; Cavallaro, T; Ferrarini, M; Rigatelli, F; Pini, A; Mostacciuolo, ML; Rizzuto, N
      PMP22 related congenital hypomyelination neuropathy

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    24. Rowland, JS; Barton, DE; Taylor, GR
      A comparison of methods for gene dosage analysis in HMSN type 1

      JOURNAL OF MEDICAL GENETICS
    25. Melcangi, RC; Magnaghi, V; Galbiati, M; Martini, L
      Steroid effects on the gene expression of peripheral myelin proteins

      HORMONES AND BEHAVIOR
    26. Kunz-Schughart, LA; Heyder, P; Schroeder, J; Knuechel, R
      A heterologous 3-D coculture model of breast tumor cells and fibroblasts to study tumor-associated fibroblast differentiation

      EXPERIMENTAL CELL RESEARCH
    27. Sancho, S; Young, P; Suter, U
      Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A

      BRAIN
    28. Wang, CX; Wadehra, M; Fisk, BC; Goodglick, L; Braun, J
      Epithelial membrane protein 2, a 4-transmembrane protein that suppresses B-cell lymphoma tumorigenicity

      BLOOD
    29. Storch, J; Thumser, AEA
      The fatty acid transport function of fatty acid-binding proteins

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    30. Brancolini, C; Edomi, P; Marzinotto, S; Schneider, C
      Exposure at the cell surface is required for Gas3/PMP22 to regulate both cell death and cell spreading: Implication for the Charcot-Marie-Tooth type 1A and Dejerine-Sottas diseases

      MOLECULAR BIOLOGY OF THE CELL
    31. Senderek, J; Hermanns, B; Lehmann, U; Bergmann, C; Marx, G; Kabus, C; Timmerman, V; Stoltenburg-Didinger, G; Schroder, JM
      Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: Two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124Met

      BRAIN PATHOLOGY
    32. Isaacs, AM; Davies, KE; Hunter, AJ; Nolan, PM; Vizor, L; Peters, J; Gale, DG; Kelsell, DP; Latham, ID; Chase, JM; Fisher, EMC; Bouzyk, MM; Potter, A; Masih, M; Walsh, FS; Sims, MA; Doncaster, KE; Parsons, CA; Martin, J; Brown, SDM; Rastan, S; Spurr, NK; Gray, IC
      Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

      HUMAN MOLECULAR GENETICS
    33. Dubourg, O; Mouton, P; Brice, A; LeGuern, E; Bouche, P
      Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies

      NEUROMUSCULAR DISORDERS
    34. Bronstein, JM
      Function of tetraspan proteins in the myelin sheath

      CURRENT OPINION IN NEUROBIOLOGY
    35. Casella, GTB; Wieser, R; Bunge, RP; Margitich, IS; Katz, J; Olson, L; Wood, PM
      Density dependent regulation of human Schwann cell proliferation

      GLIA
    36. Saberan-Djoneidi, D; Sanguedolce, V; Assouline, Z; Levy, N; Passage, E; Fontes, M
      Molecular dissection of the Schwann cell specific promoter of the PMP22 gene

      GENE
    37. Gao, Y; Li, WH; Filbin, MT
      Acylation of myelin Po protein is required for adhesion

      JOURNAL OF NEUROSCIENCE RESEARCH
    38. Bronstein, JM; Tiwari-Woodruff, S; Buznikov, AG; Stevens, DB
      Involvement of OSP/Claudin-11 in oligodendrocyte membrane interactions: Role in biology and disease

      JOURNAL OF NEUROSCIENCE RESEARCH
    39. Young, P; Stogbauer, F; Eller, B; de Jonghe, P; Lofgren, A; Timmerman, V; Rautenstrauss, B; Oexle, K; Grehl, H; Kuhlenbaumer, G; Van Broeckhoven, C; Ringelstein, EB; Funke, H
      PMP22 Thr118Met is not a clinically relevant CMT1 marker

      JOURNAL OF NEUROLOGY
    40. Schneider, C; Reiners, K; Friedl, W; Ebner, R; Toyka, KV
      Involvement of the visual pathway in hereditary neuropathy with liability to pressure palsies

      JOURNAL OF NEUROLOGY
    41. Peirano, RI; Goerich, DE; Riethmacher, D; Wegner, M
      Protein zero gene expression is regulated by the glial transcription factor Sox10

      MOLECULAR AND CELLULAR BIOLOGY
    42. Uschkureit, T; Sporkel, O; Stracke, J; Bussow, H; Stoffel, W
      Early onset of axonal degeneration in double (plp-/-mag-/-) and hypomyelinosis in triple (plp-/-mbp-/-mag-/-) mutant mice

      JOURNAL OF NEUROSCIENCE
    43. Calida, DM; Kremlev, SG; Fujioka, T; Hilliard, B; Ventura, E; Constantinescu, CS; Lavi, E; Rostami, A
      Experimental allergic neuritis in the SJL/J mouse: induction of severe andreproducible disease with bovine peripheral nerve myelin and pertussis toxin with or without interleukin-12

      JOURNAL OF NEUROIMMUNOLOGY
    44. Gabriel, CM; Gregson, NA; Hughes, RAC
      Anti-PMP22 antibodies in patients with inflammatory neuropathy

      JOURNAL OF NEUROIMMUNOLOGY
    45. Ritz, MF; Lechner-Scott, J; Scott, RJ; Fuhr, P; Malik, N; Erne, B; Taylor, V; Suter, U; Schaeren-Wiemers, N; Steck, AJ
      Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and acquired neuropathies

      JOURNAL OF NEUROIMMUNOLOGY
    46. Zielasek, J; Martini, R; Suter, U; Toyka, KV
      Neuromyotonia in mice with hereditary myelinopathies

      MUSCLE & NERVE
    47. Stogbauer, F; Young, P; Kuhlenbaumer, G; De Jonghe, P; Timmerman, V
      Hereditary recurrent focal neuropathies - Clinical and molecular features

      NEUROLOGY
    48. Iyer, S; Bianchi, R; Eichberg, J
      Tyrosine phosphorylation of PNS myelin P-0 occurs in the cytoplasmic domain and is maximal during early development

      JOURNAL OF NEUROCHEMISTRY
    49. Yin, X; Kidd, GJ; Wrabetz, L; Feltri, ML; Messing, A; Trapp, BD
      Schwann cell myelination requires timely and precise targeting of P-0 protein

      JOURNAL OF CELL BIOLOGY
    50. Bissar-Tadmouri, N; Parman, Y; Boutrand, L; Deymeer, F; Serdaroglu, P; Vandenberghe, A; Battaloglu, E
      Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type I and HNPP patients

      CLINICAL GENETICS
    51. Nobile-Orazio, E; Meucci, N; Baldini, L; Di Troia, A; Scarlato, G
      Long-term prognosis of neuropathy associated with anti-MAG IgM M-proteins and its relationship to immune therapies

      BRAIN
    52. Xu, MJ; Zhao, RX; Sui, XW; Xu, FP; Zhao, ZZJ
      Tyrosine phosphorylation of myelin P-0 and its implication in signal transduction

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    53. Kusunoki, S
      Antiglycolipid antibodies in Guillain-Barre syndrome and autoimmune neuropathies

      AMERICAN JOURNAL OF THE MEDICAL SCIENCES
    54. Mersiyanova, IV; Perepelov, AV; Polyakov, AV; Sitnikov, VF; Dadali, EL; Oparin, RB; Petrin, AN; Evgrafov, OV
      A new variant of Charcot-Marie-Tooth disease type 2 is probably the resultof a mutation in the neurofilament-light gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    55. Kalaydjieva, L; Gresham, D; Gooding, R; Heather, L; Baas, F; de Jonge, R; Blechschmidt, K; Angelicheva, D; Chandler, D; Worsley, P; Rosenthal, A; King, RHM; Thomas, PK
      N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom

      AMERICAN JOURNAL OF HUMAN GENETICS
    56. Ohnishi, A; Yamamoto, T; Izawa, K; Yamamori, S; Takahashi, K; Mega, H; Jinnai, K
      Dejerine-Sottas disease with a novel de novo dominant mutation, Ser 149 Arg, of the peripheral myelin protein 22

      ACTA NEUROPATHOLOGICA
    57. Schenone, A; Mancardi, GL
      Molecular basis of inherited neuropathies

      CURRENT OPINION IN NEUROLOGY
    58. Brancolini, C; Marzinotto, S; Edomi, P; Agostoni, E; Fiorentini, C; Muller, HW; Schneider, C
      Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22

      MOLECULAR BIOLOGY OF THE CELL
    59. Keller, MP; Chance, PF
      Inherited neuropathies: From gene to disease

      BRAIN PATHOLOGY
    60. Steck, AJ; Erne, B; Gabriel, JM; Schaeren-Wiemers, N
      Paraproteinaemic neuropathies

      BRAIN PATHOLOGY
    61. Notterpek, L; Ryan, MC; Tobler, AR; Shooter, EM
      PMP22 accumulation in aggresomes: Implications for CMT1A pathology

      NEUROBIOLOGY OF DISEASE
    62. Hagedorn, L; Suter, U; Sommer, L
      P0 and PMP22 mark a multipotent neural crest-derived cell type that displays community effects in response to TGF-beta family factors

      DEVELOPMENT
    63. van de Wetering, RAC; Gabreels-Festen, AAWM; Kremer, H; Kalscheuer, VM; Gabreels, FJM; Mariman, EC
      Regulation and expression of the murine Pmp22 gene

      MAMMALIAN GENOME
    64. Carenini, S; Montag, D; Schachner, M; Martini, R
      Subtle roles of neural cell adhesion molecule and myelin-associated glycoprotein during Schwann cell spiralling in P0-deficient mice

      GLIA
    65. Lazakovitch, EM; She, BR; Lien, CL; Woo, WM; Ju, YT; Sue, LC
      The Gas7 gene encodes two protein isoforms differentially expressed withinthe brain

      GENOMICS
    66. Chance, PF
      Molecular genetics of hereditary neuropathies

      JOURNAL OF CHILD NEUROLOGY
    67. Agostoni, E; Gobessi, S; Brancolini, C; Schneider, C
      Identification and characterization of a new member of the gas3/PMP22 genefamily in C-elegans

      GENE
    68. Swisshelm, K; Machl, A; Planitzer, S; Robertson, R; Kubbies, M; Hosier, S
      SEMP1, a senescence-associated cDNA isolated from human mammary epithelialcells, is a member of an epithelial membrane protein superfamily

      GENE
    69. Plante-Bordeneuve, V; Guiochon-Mantel, A; Lacroix, C; Lapresle, J; Said, G
      The Roussy-Levy family: From the original description to the gene

      ANNALS OF NEUROLOGY
    70. Mandich, P; Mancardi, GL; Varese, A; Soriani, S; Di Maria, E; Bellone, E; Bado, M; Gross, L; Windebank, AJ; Ajmar, F; Schenone, A
      Congenital hypomyelination due to myelin protein zero Q215X mutation

      ANNALS OF NEUROLOGY
    71. Sedzik, J; Kotake, Y; Uyemura, K
      Purification of P0 myelin glycoprotein by a Cu2+-immobilized metal affinity chromatography

      NEUROCHEMICAL RESEARCH
    72. Huhne, K; Park, O; Liehr, T; Rautenstrauss, B
      Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines

      JOURNAL OF NEUROSCIENCE RESEARCH
    73. Melcangi, RC; Magnaghi, V; Cavarretta, I; Zucchi, I; Bovolin, P; D'Urso, D; Martini, L
      Progesterone derivatives are able to influence peripheral myelin protein 22 and P-0 gene expression: Possible mechanisms of action

      JOURNAL OF NEUROSCIENCE RESEARCH
    74. Ben-Porath, I; Yanuka, O; Benvenisty, N
      The Tmp gene, encoding a membrane protein, is a c-Myc target with a tumorigenic activity

      MOLECULAR AND CELLULAR BIOLOGY
    75. D'Urso, D; Ehrhardt, P; Muller, HW
      Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin

      JOURNAL OF NEUROSCIENCE
    76. Brady, ST; Witt, AS; Kirkpatrick, LL; de Waegh, SM; Readhead, C; Tu, PH; Lee, VMY
      Formation of compact myelin is required for maturation of the axonal cytoskeleton

      JOURNAL OF NEUROSCIENCE
    77. Frei, R; Motzing, S; Kinkelin, I; Schachner, M; Koltzenburg, M; Martini, R
      Loss of distal axons and sensory Merkel cells and features indicative of muscle denervation in hindlimbs of P0-deficient mice

      JOURNAL OF NEUROSCIENCE
    78. Kashork, CD; Lupski, JR; Shaffer, LG
      Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridization

      PRENATAL DIAGNOSIS
    79. Magnaghi, V; Cavarretta, I; Zucchi, I; Susani, L; Rupprecht, R; Hermann, B; Martini, L; Melcangi, RC
      Po gene expression is modulated by androgens in the sciatic nerve of adultmale rats

      MOLECULAR BRAIN RESEARCH
    80. Weiss, MD; Dalakas, MC; Lauter, CJ; Willison, HJ; Quarles, RH
      Variability in the binding of anti-MAG and anti-SGPG antibodies to target antigens in demyelinating neuropathy and IgM paraproteinemia

      JOURNAL OF NEUROIMMUNOLOGY
    81. Zou, LP; Ma, DH; Levi, M; Wahren, B; Wei, L; Mix, E; van der Meide, PH; Link, H; Zhu, J
      Antigen-specific immunosuppression: nasal tolerance to P0 protein peptidesfor the prevention and treatment of experimental autoimmune neuritis in Lewis rats

      JOURNAL OF NEUROIMMUNOLOGY
    82. Hughes, RAC; Hadden, RDM; Gregson, NA; Smith, KJ
      Pathogenesis of Guillain-Barre syndrome

      JOURNAL OF NEUROIMMUNOLOGY
    83. Wulf, P; Suter, U
      Embryonic expression of epithelial membrane protein 1 in early neurons

      DEVELOPMENTAL BRAIN RESEARCH
    84. Sindou, P; Vallat, JM; Chapon, F; Archelos, JJ; Tabaraud, F; Anani, T; Braund, KG; Maisonobe, T; Hauw, JJ; Vandenberghe, A
      Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease

      MUSCLE & NERVE
    85. Toyka, KV
      Eighty three years of the Guillain-Barre Syndrome: clinical and immunopathologic aspects, current and future treatments

      REVUE NEUROLOGIQUE
    86. Lupski, JR
      Charcot-Marie-tooth polyneuropathy: Duplication, gene dosage, and genetic heterogeneity

      PEDIATRIC RESEARCH
    87. Fabrizi, GM; Cavallaro, T; Taioli, F; Orrico, D; Morbin, M; Simonati, A; Rizzuto, N
      Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a pointmutation of peripheral myelin protein-22

      NEUROLOGY
    88. Zucchi, I; Montagna, C; Susani, L; Montesano, R; Affer, M; Zanotti, S; Redolfi, E; Vezzoni, P; Dulbecco, R
      Genetic dissection of dome formation in a mammary cell line: Identification of two genes with opposing action

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    89. Frank, M; Schaeren-Wiemers, N; Schneider, R; Schwab, ME
      Developmental expression pattern of the myelin proteolipid MAL indicates different functions of MAL for immature Schwann cells and in a late step of CNS myelinogenesis

      JOURNAL OF NEUROCHEMISTRY
    90. Haney, CA; Sahenk, Z; Li, C; Lemmon, VP; Roder, J; Trapp, BD
      Heterophilic binding of L1 on unmyelinated sensory axons mediates schwann cell adhesion and is required for axonal survival

      JOURNAL OF CELL BIOLOGY
    91. Du Pasquier, L; Courtet, M; Chretien, I
      Duplication and MHC linkage of the CTX family of genes in Xenopus and in mammals

      EUROPEAN JOURNAL OF IMMUNOLOGY
    92. Yamauchi, Y; Abe, K; Mantani, A; Hitoshi, Y; Suzuki, M; Osuzu, F; Kuratani, S; Yamamura, K
      A novel transgenic technique that allows specific marking of the neural crest cell lineage in mice

      DEVELOPMENTAL BIOLOGY
    93. Sancho, S; Magyar, JP; Aguzzi, A; Suter, U
      Distal axonopathy in peripheral nerves of PMP22-mutant mice

      BRAIN
    94. Inouye, H; Tsuruta, H; Sedzik, J; Uyemura, K; Kirschner, DA
      Tetrameric assembly of full-sequence protein zero myelin glycoprotein by synchrotron X-ray scattering

      BIOPHYSICAL JOURNAL
    95. Matsuoka, H; Cheng, KC; Krug, MS; Yazawa, Y; Yoo, TJ
      Murine model of autoimmune hearing loss induced by myelin protein PO

      ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY
    96. Kovach, MJ; Lin, JP; Boyadjiev, S; Campbell, K; Mazzeo, L; Herman, K; Rimer, LA; Frank, W; Llewellyn, B; Jabs, EW; Gelber, D; Kimonis, VE
      A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness

      AMERICAN JOURNAL OF HUMAN GENETICS
    97. Vallat, JM; Sindou, P; Garbay, B; Preux, PM; Anani, T; Richard, L; Diot, M
      Expression of myelin proteins in the adult heterozygous Trembler mouse

      ACTA NEUROPATHOLOGICA
    98. MARTINI R; ZIELASEK J; TOYKA KV
      INHERITED DEMYELINATING NEUROPATHIES - FROM GENE TO DISEASE

      Current opinion in neurology
    99. LUPSKI JR
      CHARCOT-MARIE-TOOTH-DISEASE - LESSONS IN GENETIC MECHANISMS

      Molecular medicine
    100. SILANDER K; MERETOJA P; JUVONEN V; IGNATIUS J; PIHKO H; SAARINEN A; WALLDEN T; HERRGARD E; AULA P; SAVONTAUS ML
      SPECTRUM OF MUTATIONS IN FINNISH PATIENTS WITH CHARCOT-MARIE-TOOTH-DISEASE AND RELATED NEUROPATHIES

      Human mutation


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/08/20 alle ore 15:49:49