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La ricerca find articoli where soggetti phrase all words 'PROTEOLIPID PROTEIN GENE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 94 riferimenti
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    1. Berger, J; Moser, HW; Forss-Petter, S
      Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment

      CURRENT OPINION IN NEUROLOGY
    2. Fuss, B; Afshari, FS; Colello, RJ; Macklin, WB
      Normal CNS myelination in transgenic mice overexpressing MHC class IH-2L(d) in oligodendrocytes

      MOLECULAR AND CELLULAR NEUROSCIENCE
    3. Casari, G; Rugarli, E
      Molecular basis of inherited spastic paraplegias

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    4. Kaye, EM
      Update on genetic disorders affecting white matter

      PEDIATRIC NEUROLOGY
    5. de los Monteros, AE; Baba, H; Zhao, PM; Pan, T; Chang, R; de Vellis, J; Ikenaka, K
      Remyelination of the adult demyelinated mouse brain by grafted oligodendrocyte progenitors and the effect of B-104 cografts

      NEUROCHEMICAL RESEARCH
    6. Beesley, JS; Lavy, L; Eraydin, NB; Siman, R; Grinspan, JB
      Caspase-3 activation in oligodendrocytes from the myelin-deficient rat

      JOURNAL OF NEUROSCIENCE RESEARCH
    7. Von Budingen, HC; Tanuma, N; Villoslada, P; Ouallet, JC; Hauser, SL; Genain, CP
      Immune responses against the myelin/oligodendrocyte glycoprotein in experimental autoimmune demyelination

      JOURNAL OF CLINICAL IMMUNOLOGY
    8. Kwiecien, JM; Blanco, M; Fox, JG; Delaney, KH; Fletch, AL
      Neuropathology of Bouncer Long Evans, a novel dysmyelinated rat

      COMPARATIVE MEDICINE
    9. Porter, BE; Tennekoon, G
      Myelin and disorders that affect the formation and maintenance of this sheath

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    10. Woodward, K; Kirtland, K; Dlouhy, S; Raskind, W; Bird, T; Malcolm, S; Abeliovich, D
      X inactivation phenotype in carriers of Pelizaeus-Merzbacher disease: skewed in carriers of a duplication and random in carriers of point mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    11. Cailloux, F; Gauthier-Barichard, F; Mimault, C; Isabelle, V; Courtois, V; Giraud, G; Dastugue, B; Boespflug-Tanguy, O
      Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    12. Baerwald, KD; Corbin, JG; Popko, B
      Major histocompatibility complex heavy chain accumulation in the endoplasmic reticulum of oligodendrocytes results in myelin abnormalities

      JOURNAL OF NEUROSCIENCE RESEARCH
    13. Ziereisen, F; Dan, B; Christiaens, F; Deltenre, P; Boutemy, R; Christophe, C
      Connatal Pelizaeus-Merzbacher disease in two girls

      PEDIATRIC RADIOLOGY
    14. Spalice, A; Popolizio, T; Parisi, P; Scarabino, T; Iannetti, P
      Proton MR spectroscopy in connatal Pelizaeus-Merzbacher disease

      PEDIATRIC RADIOLOGY
    15. 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
    16. Barkovich, AJ
      Concepts of myelin and myelination in neuroradiology

      AMERICAN JOURNAL OF NEURORADIOLOGY
    17. Tamagaki, A; Shima, M; Tomita, R; Okumura, M; Shibata, M; Morichika, S; Kurahashi, H; Giddings, JC; Yoshioka, A; Yokobayashi, Y
      Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Lewis, RA; Sumner, AJ; Shy, ME
      Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis

      MUSCLE & NERVE
    19. Percy, AK
      Pelizaeus-Merzbacher disease - Splice sites are nice sites for disease expression

      NEUROLOGY
    20. Dobretsova, A; Kokorina, NA; Wight, PA
      Functional characterization of a cis-acting DNA antisilencer region that modulates myelin proteolipid protein gene expression

      JOURNAL OF NEUROCHEMISTRY
    21. Wrabetz, L; Feltri, ML; Quattrini, A; Imperiale, D; Previtali, S; D'Antonio, M; Martini, R; Yin, XH; Trapp, BD; Zhou, L; Chiu, SY; Messing, A
      P-0 glycoprotein overexpression causes congenital hypomyelination of peripheral nerves

      JOURNAL OF CELL BIOLOGY
    22. Hudson, LD
      Breaking away from home

      AMERICAN JOURNAL OF HUMAN GENETICS
    23. Komaki, H; Sasaki, M; Yamamoto, T; Iai, M; Takashima, S
      Connatal Pelizaeus-Merzbacher disease associated with the jimpy(msd) mice mutation

      PEDIATRIC NEUROLOGY
    24. Osaka, H; Kawanishi, C; Inoue, K; Onishi, H; Kobayashi, T; Sugiyama, N; Kosaka, K; Nezu, A; Fujii, K; Sugita, K; Kodama, K; Murayama, K; Murayama, S; Kanazawa, I; Kimura, S
      Pelizaeus-Merzbacher disease: Three novel mutations and implication for locus heterogeneity

      ANNALS OF NEUROLOGY
    25. Tohyama, Y; Kasama-Yoshida, H; Sakuma, M; Kobayashi, Y; Cao, Y; Hasegawa, M; Kojima, H; Tamai, Y; Tanokura, M; Kurihara, T
      Gene structure and amino acid sequence of Latimeria chalumnae (Coelacanth)myelin DM20: Phylogenetic relation of the fish

      NEUROCHEMICAL RESEARCH
    26. Popko, B; Baerwald, KD
      Oligodendroglial response to the immune cytokine interferon gamma

      NEUROCHEMICAL RESEARCH
    27. Illarioshkin, SN; Allen, KM; Gleeson, JG; Tsuji, S; Ikeuchi, T; Markova, ED; Walsh, CA; Ivanova-Smolenskaya, IA
      Studies of the candidate genes in X-linked congenital cerebellar hypoplasia

      JOURNAL OF NEUROLOGY
    28. Bradl, M
      Myelin dysfunction/degradation in the central nervous system: why are myelin sheaths susceptible to damage?

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    29. Bjartmar, C; Yin, XH; Trapp, BD
      Axonal pathology in myelin disorders

      JOURNAL OF NEUROCYTOLOGY
    30. Woodward, K; Palmer, R; Rao, K; Malcolm, S
      Prenatal diagnosis by FISH in a family with Pelizaeus-Merzbacher disease caused by duplication of the PLP gene

      PRENATAL DIAGNOSIS
    31. Hodes, ME; Zimmerman, AW; Aydanian, A; Naidu, S; Miller, NR; Oller, JLG; Barker, B; Aleck, KA; Hurley, TD; Dlouhy, SR
      Different mutations in the same codon of the proteolipid protein gene, PLP, way help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    32. Anderson, TJ; Griffiths, IR
      Pelizaeus-Merzbacher disease

      LABORATORY ANIMAL SCIENCE
    33. Garbern, J; Cambi, F; Shy, M; Kamholz, J
      The molecular pathogenesis of Pelizaeus-Merzbacher disease

      ARCHIVES OF NEUROLOGY
    34. Mimault, C; Giraud, G; Courtois, V; Cailloux, F; Boire, JY; Dastugue, B; Boespflug-Tanguy, O
      Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher disease: Duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not

      AMERICAN JOURNAL OF HUMAN GENETICS
    35. LASSMANN H
      NEUROPATHOLOGY IN MULTIPLE-SCLEROSIS - NEW CONCEPTS

      Multiple sclerosis
    36. GRIFFITHS I; KLUGMAN M; ANDERSON T; THOMSON C; VOUYIOUKLIS D; NAVE KA
      CURRENT CONCEPTS OF PLP AND ITS ROLE IN THE NERVOUS-SYSTEM

      Microscopy research and technique
    37. WERNER H; JUNG M; KLUGMANN M; SEREDA M; GRIFFITHS IR; NAVE KA
      MOUSE MODELS OF MYELIN DISEASES

      Brain pathology
    38. NEZU A; KIMURA S; TAKESHITA S; OSAKA H; KIMURA K; INOUE K
      AN MRI AND MRS STUDY OF PELIZAEUS-MERZBACHER-DISEASE

      Pediatric neurology
    39. CUDDON PA; LIPSITZ D; DUNCAN ID
      MYELIN MOSAICISM AND BRAIN PLASTICITY IN HETEROZYGOUS FEMALES OF A CANINE X-LINKED TRAIT

      Annals of neurology
    40. GRINSPAN JB; COULALAGLOU M; BEESLEY JS; CARPIO DF; SCHERER SS
      MATURATION-DEPENDENT APOPTOTIC CELL-DEATH OF OLIGODENDROCYTES IN MYELIN-DEFICIENT RATS

      Journal of neuroscience research
    41. BARRESE N; MAK B; FISHER L; MOSCARELLO MA
      MECHANISM OF DEMYELINATION IN DM20 TRANSGENIC MICE INVOLVES INCREASEDFATTY ACYLATION

      Journal of neuroscience research
    42. VOUYIOUKLIS DA; WERNER H; GRIFFITHS IR; STEWART GJ; ARMINNAVE K; THOMSON CE
      MOLECULAR-CLONING AND TRANSFECTION STUDIES OF M6B-2, A NOVEL SPLICE VARIANT OF A MEMBER OF THE PLP-DM20 M6 GENE FAMILY/

      Journal of neuroscience research
    43. LIPSITZ D; GOETZ BD; DUNCAN ID
      APOPTOTIC GLIAL-CELL DEATH AND KINETICS IN THE SPINAL-CORD OF THE MYELIN-DEFICIENT RAT

      Journal of neuroscience research
    44. HUXLEY C
      MYELIN DISORDERS

      Neuropathology and applied neurobiology
    45. VELA JM; GONZALEZ B; CASTELLANO B
      UNDERSTANDING GLIAL ABNORMALITIES ASSOCIATED WITH MYELIN DEFICIENCY IN THE JIMPY MUTANT MOUSE

      Brain research reviews
    46. HODES ME; HADJISAVVAS A; BUTLER IJ; AYDANIAN A; DLOUHY SR
      X-LINKED SPASTIC PARAPLEGIA DUE TO A MUTATION (C506T SER169PHE) IN EXON-4 OF THE PROTEOLIPID PROTEIN GENE (PLP)

      American journal of medical genetics
    47. WEINER JA; HECHT JH; CHUN J
      LYSOPHOSPHATIDIC ACID RECEPTOR GENE VZG-1 LP(A1)/EDG-2 IS EXPRESSED BY MATURE OLIGODENDROCYTES DURING MYELINATION IN THE POSTNATAL MURINE BRAIN/

      Journal of comparative neurology
    48. PEARSALL GB; NADON NL; WOLF MK; BILLINGSGAGLIARDI S
      JIMPY-4J MOUSE HAS A MISSENSE MUTATION IN EXON-2 OF THE PLP GENE

      Developmental neuroscience
    49. ORIAN JM; SLAVIN A; AYERS MM; BERNARD CAC
      DELAYED AND INCOMPLETE MYELINATION IN A TRANSGENIC MOUSE MUTANT WITH ABNORMAL OLIGODENDROCYTES

      Journal of neuroscience research
    50. TOSIC M; MATTHEY B; GOW A; LAZZARINI RA; MATTHIEU JM
      INTRACELLULAR-TRANSPORT OF THE DM-20 BEARING SHAKING PUP (SHP) MUTATION AND ITS POSSIBLE PHENOTYPIC CONSEQUENCES

      Journal of neuroscience research
    51. PEYRON F; TIMSIT S; THOMAS JL; KAGAWA T; IKENAKA K; ZALC B
      IN-SITU EXPRESSION OF PLP DM-20, MBP, AND CNP DURING EMBRYONIC AND POSTNATAL-DEVELOPMENT OF THE JIMPY MUTANT AND OF TRANSGENIC MICE OVEREXPRESSING PLP/

      Journal of neuroscience research
    52. YIN X; PETERSON J; GRAVEL M; BRAUN PE; TRAPP BD
      CNP OVEREXPRESSION INDUCES ABERRANT OLIGODENDROCYTE MEMBRANES AND INHIBITS MBP ACCUMULATION AND MYELIN COMPACTION

      Journal of neuroscience research
    53. ANDERSON TJ; MONTAGUE P; NADON N; NAVE KA; GRIFFITHS IR
      MODIFICATION OF SCHWANN-CELL PHENOTYPE WITH PLP TRANSGENES - EVIDENCETHAT THE PLP AND DM20 ISOPROTEINS ARE TARGETED TO DIFFERENT CELLULAR DOMAINS

      Journal of neuroscience research
    54. PRINGLE NP; NADON NL; RHODE DM; RICHARDSON WD; DUNCAN ID
      NORMAL TEMPORAL AND SPATIAL-DISTRIBUTION OF OLIGODENDROCYTE PROGENITORS IN THE MYELIN-DEFICIENT (MD) RAT

      Journal of neuroscience research
    55. MANDAI K; MATSUMOTO M; KITAGAWA K; MATSUSHITA K; OHTSUKI T; MABUCHI T; COLMAN DR; KAMADA T; YANAGIHARA T
      ISCHEMIC DAMAGE AND SUBSEQUENT PROLIFERATION OF OLIGODENDROCYTES IN FOCAL CEREBRAL-ISCHEMIA

      Neuroscience
    56. DICKINSON PJ; GRIFFITHS IR; BARRIE JM; KYRIAKIDES E; POLLOCK GF; BARNETT SC
      EXPRESSION OF THE DM-20 ISOFORM OF THE PLP GENE IN OLFACTORY NERVE ENSHEATHING CELLS - EVIDENCE FROM DEVELOPMENTAL STUDIES

      Journal of neurocytology
    57. CARROZZO R; ARRIGO G; ROSSI E; BARDONI B; CAMMARATA M; GANDULLIA P; GATTI R; ZUFFARDI O
      MULTIPLE CONGENITAL-ANOMALIES, BRAIN HYPOMYELINATION, AND OCULAR ALBINISM IN A FEMALE WITH DUP(X)(PTER-]Q24--Q21.32-]QTER) AND RANDOM X-INACTIVATION

      American journal of medical genetics
    58. NAIDU S; DLOUHY SR; GERAGHTY MT; HODES ME
      A MALE CHILD WITH THE RUMPSHAKER MUTATION, X-LINKED SPASTIC PARAPLEGIA PELIZAEUS-MERZBACHER DISEASE AND LYSINURIA

      Journal of inherited metabolic disease
    59. GOW A; LAZZARINI RA
      A CELLULAR MECHANISM GOVERNING THE SEVERITY OF PELIZAEUS-MERZBACHER DISEASE

      Nature genetics
    60. GRAVEL M; PETERSON J; YONG VW; KOTTIS V; TRAPP B; BRAUN PE
      OVEREXPRESSION OF 2',3'-CYCLIC NUCLEOTIDE 3'-PHOSPHODIESTERASE IN TRANSGENIC MICE ALTERS OLIGODENDROCYTE DEVELOPMENT AND PRODUCES ABERRANT MYELINATION

      Molecular and cellular neurosciences
    61. BRADL M; LININGTON C
      ANIMAL-MODELS OF DEMYELINATION

      Brain pathology
    62. FANARRAGA ML; DICKINSON PJ; SOMMER I; MONTAGUE P; KYRIAKIDES E; GRIFFITHS IR
      EVIDENCE THAT SOME OLIGODENDROCYTE PROGENITORS IN THE DEVELOPING OPTIC PATHWAY EXPRESS THE PLP GENE

      Glia
    63. GILGENKRANTZ S
      DM20 SUPPORT OF PLP CELLULAR TRAFFICKING INFLUENCES THE SEVERITY OF DISEASES DUE TO PLP GENE ANOMALIES

      MS. Medecine sciences
    64. KAGAWA T; OBA A; OKUMURA S; IKENAKA K
      LOCALIZATION OF MESSENGER-RNA FOR UDP-GALACTOSE - CERAMIDE GALACTOSYLTRANSFERASE IN THE BRAIN DURING MOUSE DEVELOPMENT

      Developmental neuroscience
    65. NADON NL; DUNCAN ID
      MOLECULAR ANALYSIS OF GLIAL-CELL DEVELOPMENT IN THE CANINE SHAKING PUP MUTANT

      Developmental neuroscience
    66. DICKINSON PJ; FANARRAGA ML; GRIFFITHS IR; BARRIE JM; KYRIAKIDES E; MONTAGUE P
      OLIGODENDROCYTE PROGENITORS IN THE EMBRYONIC SPINAL-CORD EXPRESS DM-20

      Neuropathology and applied neurobiology
    67. GRIFFITHS IR
      MYELIN MUTANTS - MODEL SYSTEMS FOR THE STUDY OF NORMAL AND ABNORMAL MYELINATION

      BioEssays
    68. TERREGINO C; CARDONA F; BARBETTI F; ANTONOZZI I; CARDUCCI C
      CLINICAL AND MOLECULAR EVALUATION OF ITALIAN PATIENTS AFFECTED BY PELIZAEUS-MERZBACHER DISEASE

      Journal of inherited metabolic disease
    69. WARNER LE; REITER LT; MURAKAMI T; LUPSKI JR
      MOLECULAR MECHANISMS FOR CHARCOT-MARIE-TOOTH-DISEASE AND RELATED DEMYELINATING PERIPHERAL NEUROPATHIES

      Cold Spring Harbor Symposia on Quantitative Biology
    70. YAMADA M; KAGAWA T; IKENAKA K
      DEVELOPMENT AND DIFFERENTIATION OF OLIGODENDROCYTES

      Japanese Journal of Physiology
    71. INOUE K; OSAKA H; SUGIYAMA N; KAWANISHI C; ONISHI H; NEZU A; KIMURA K; KIMURA S; YAMADA Y; KOSAKA K
      A DUPLICATED PLP GENE CAUSING PELIZAEUS-MERZBACHER DISEASE DETECTED BY COMPARATIVE MULTIPLEX PCR

      American journal of human genetics
    72. LUNN KF; FANARRAGA ML; DUNCAN ID
      MYELIN MUTANTS - NEW MODELS AND NEW OBSERVATIONS

      Microscopy research and technique
    73. WANG PJ; YOUNG CL; LIU HM; CHANG XC; SHEN YZ
      NEUROPHYSIOLOGIC STUDIES AND MRI IN PELIZAEUS-MERZBACHER DISEASE - COMPARISON OF CLASSIC AND CONNATAL FORMS

      Pediatric neurology
    74. SYPECKA J; GAJKOWSKA B; DOMANSKAJANIK K
      OLIGODENDROCYTE DEVELOPMENT IN PLP PT MUTANT RABBITS - GLYCOLIPID ANTIGENS AND PLP GENE-EXPRESSION

      Metabolic brain disease
    75. NEZU A
      NEUROPHYSIOLOGICAL STUDY IN PELIZAEUS-MERZBACHER DISEASE

      Brain & development
    76. BILLINGSGAGLIARDI S; KIRSCHNER DA; NADON NL; DIBENEDETTO LM; KARTHIGASAN J; LANE P; PEARSALL GB; WOLF MK
      JIMPY 4J - A NEW X-LINKED MOUSE MUTATION PRODUCING SEVERE CNS HYPOMYELINATION

      Developmental neuroscience
    77. NADON NL; DUNCAN ID
      GENE-EXPRESSION AND OLIGODENDROCYTE DEVELOPMENT IN THE MYELIN-DEFICIENT RAT

      Journal of neuroscience research
    78. FELTS PA; BLACK JA; WAXMAN SG
      EXPRESSION OF SODIUM-CHANNEL ALPHA-SUBUNITS AND BETA-SUBUNITS IN THE NERVOUS-SYSTEM OF THE MYELIN-DEFICIENT RAT

      Journal of neurocytology
    79. DUNCAN ID; NADON NL; HOFFMAN RL; LUNN KF; CSIZA C; WELLS MR
      OLIGODENDROCYTE SURVIVAL AND FUNCTION IN THE LONG-LIVED STRAIN OF THEMYELIN-DEFICIENT RAT

      Journal of neurocytology
    80. TIMSIT S; MARTINEZ S; ALLINQUANT B; PEYRON F; PUELLES L; ZALC B
      OLIGODENDROCYTES ORIGINATE IN A RESTRICTED ZONE OF THE EMBRYONIC VENTRAL NEURAL-TUBE DEFINED BY DM-20 MESSENGER-RNA EXPRESSION

      The Journal of neuroscience
    81. KOBAYASHI H; HOFFMAN EP; MARKS HG
      THE RUMPSHAKER MUTATION IN SPASTIC PARAPLEGIA

      Nature genetics
    82. SUTER U; PATEL PI
      GENETIC-BASIS OF INHERITED PERIPHERAL NEUROPATHIES

      Human mutation
    83. KAYE EM; DOLL RF; NATOWICZ MR; SMITH FI
      PELIZAEUS-MERZBACHER DISEASE PRESENTING AS SPINAL MUSCULAR-ATROPHY - CLINICAL AND MOLECULAR STUDIES

      Annals of neurology
    84. INOUYE H; KIRSCHNER DA
      MEMBRANE TOPOLOGY OF PLP IN CNS MYELIN - EVALUATION OF MODELS

      Neurochemical research
    85. MULLER U; GRAEBER MB; HABERHAUSEN G; KOHLER A
      MOLECULAR-BASIS AND DIAGNOSIS OF NEUROGENETIC DISORDERS

      Journal of the neurological sciences
    86. NADON NL; ARNHEITER H; HUDSON LD
      A COMBINATION OF PLP AND DM20 TRANSGENES PROMOTES PARTIAL MYELINATIONIN THE JIMPY MOUSE

      Journal of neurochemistry
    87. KAGAWA T; NAKAO J; YAMADA M; SHIMIZU K; HAYAKAWA T; MIKOSHIBA K; IKENAKA K
      FATE OF JIMPY-TYPE OLIGODENDROCYTES IN JIMPY HETEROZYGOTE

      Journal of neurochemistry
    88. BOESPFLUGTANGUY O; MIMAULT C; MELKI J; CAVAGNA A; GIRAUD G; DINH DP; DASTUGUE B; DAUTIGNY A; AICARDI J; GOUTTIERES F; BAUMANN N; BERTINI E; DAVID A; HENOCQ A; LANDRIEU P; TARDIEU M; LEBERRE C; LEMAREC B; LYON G; MAYER M; PINARD JM; PONSOT G; MATHIEU M; SAINTIVE JP; SAURA R; VALLEE L
      GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES

      American journal of human genetics
    89. WILLIAMS KA; DEBER CM
      THE STRUCTURE AND FUNCTION OF CENTRAL-NERVOUS-SYSTEM MYELIN

      Critical reviews in clinical laboratory sciences
    90. STRAUTNIEKS S; MALCOLM S
      A G TO T MUTATION AT A SPLICE-SITE IN A CASE OF PELIZAEUS-MERZBACHER DISEASE

      Human molecular genetics
    91. MIKOL DD; RONGNOPARUT P; ALLWARDT BA; MARTON LS; STEFANSSON K
      THE OLIGODENDROCYTE MYELIN GLYCOPROTEIN OF MOUSE - PRIMARY STRUCTURE AND GENE STRUCTURE

      Genomics
    92. HODES ME; PRATT VM; DLOUHY SR
      GENETICS OF PELIZAEUS-MERZBACHER DISEASE

      Developmental neuroscience
    93. CHANCE PF; PLEASURE D
      CHARCOT-MARIE-TOOTH SYNDROME

      Archives of neurology
    94. FANARRAGA ML; GRIFFITHS IR; MCCULLOCH MC; BARRIE JA; KENNEDY PGE; BROPHY PJ
      RUMPSHAKER - AN X-LINKED MUTATION CAUSING HYPOMYELINATION - DEVELOPMENTAL DIFFERENCES IN MYELINATION AND GLIAL-CELLS BETWEEN THE OPTIC-NERVE AND SPINAL-CORD

      Glia


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Documento generato il 31/10/20 alle ore 08:44:06