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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. Kramer, EM; Schardt, A; Nave, KA
      Membrane traffic in myelinating oligodendrocytes

      MICROSCOPY RESEARCH AND TECHNIQUE
    3. Southwood, C; Gow, A
      Molecular pathways of oligodendrocyte apoptosis revealed by mutations in the proteolipid protein gene

      MICROSCOPY RESEARCH AND TECHNIQUE
    4. Wegner, M
      Expression of transcription factors during oligodendroglial development

      MICROSCOPY RESEARCH AND TECHNIQUE
    5. Casari, G; Rugarli, E
      Molecular basis of inherited spastic paraplegias

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    6. Uschkureit, T; Sporkel, O; Bussow, H; Stoffel, W
      Rumpshaker-like proteolipid protein (PLP) ratio in a mouse model with unperturbed structural and functional integrity of the myelin sheath and axons in the central nervous system

      GLIA
    7. Kaye, EM
      Update on genetic disorders affecting white matter

      PEDIATRIC NEUROLOGY
    8. Wang, PJ; Hwu, WL; Shen, YZ
      Epileptic seizures and electroencephalographic evolution in genetic leukodystrophies

      JOURNAL OF CLINICAL NEUROPHYSIOLOGY
    9. Billings-Gagliardi, S; Nunnari, JJ; Wolf, MK
      Rumpshaker behaves like juvenile-lethal Plp mutations when combined with shiverer in double mutant mice

      DEVELOPMENTAL NEUROSCIENCE
    10. Inoue, K; Tanaka, H; Scaglia, F; Araki, A; Shaffer, LG; Lupski, JR
      Compensating for central nervous system dysmyelination: Females with a proteolipid protein gene duplication and sustained clinical improvement

      ANNALS OF NEUROLOGY
    11. Beesley, JS; Lavy, L; Eraydin, NB; Siman, R; Grinspan, JB
      Caspase-3 activation in oligodendrocytes from the myelin-deficient rat

      JOURNAL OF NEUROSCIENCE RESEARCH
    12. Pingault, V; Bondurand, N; Le Caignec, C; Tardieu, S; Lemort, N; Dubourg, O; Le Guern, E; Goossens, M; Boespflug-Tanguy, O
      The SOX10 transcription factor: evaluation as a candidate gene for centraland peripheral hereditary myelin disorders

      JOURNAL OF NEUROLOGY
    13. Fink, JK
      Progressive spastic paraparesis: Hereditary spastic paraplegia and its relation to primary and amyotrophic lateral sclerosis

      SEMINARS IN NEUROLOGY
    14. Regis, S; Filocamo, M; Mazzotti, R; Cusano, R; Corsolini, F; Bonuccelli, G; Stroppiano, M; Gatti, R
      Prenatal diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene duplication by quantitative fluorescent multiplex PCR

      PRENATAL DIAGNOSIS
    15. Baumann, N; Pham-Dinh, D
      Biology of oligodendrocyte and myelin in the mammalian central nervous system

      PHYSIOLOGICAL REVIEWS
    16. Bonavita, S; Schiffmann, R; Moore, DF; Frei, K; Choi, B; Patronas, N; Virta, A; Boespflug-Tanguy, O; Tedeschi, G
      Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations

      NEUROLOGY
    17. Herrera, J; Yang, H; Zhang, SC; Proschel, C; Tresco, P; Duncan, ID; Luskin, M; Mayer-Proschel, M
      Embryonic-derived glial-restricted precursor cells (GRP cells) can differentiate into astrocytes and oligodendrocytes in vivo

      EXPERIMENTAL NEUROLOGY
    18. van der Knaap, MS
      Magnetic resonance in childhood white-matter disorders - The 2001 Ronnie MacKeith lecture

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    19. Sanders, CR; Ismail-Beigi, F; McEnery, MW
      Mutations of peripheral myelin protein 22 result in defective trafficking through mechanisms which may be common to diseases involving tetraspan membrane proteins

      BIOCHEMISTRY
    20. Aridor, M; Hannan, LA
      Traffic jam: A compendium of human diseases that affect intracellular transport processes

      TRAFFIC
    21. Porter, BE; Tennekoon, G
      Myelin and disorders that affect the formation and maintenance of this sheath

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    22. Vanslyke, JK; Deschenes, SM; Musil, LS
      Intracellular transport, assembly, and degradation of wild-type and disease-linked mutant gap junction proteins

      MOLECULAR BIOLOGY OF THE CELL
    23. 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
    24. 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
    25. Schwartz, CE; Gillessen-Kaesbach, G; May, M; Cappa, M; Gorski, J; Steindl, K; Neri, G
      Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    26. Yool, DA; Edgar, JM; Montague, P; Malcolm, S
      The proteolipid protein gene and myelin disorders in man and animal models

      HUMAN MOLECULAR GENETICS
    27. Pritchard, L; Sloane-Stanley, JA; Sharpe, JA; Aspinwall, R; Lu, WN; Buckle, V; Strmecki, L; Walker, D; Ward, CJ; Alpers, CE; Zhou, J; William, WG; Harris, PC
      A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype

      HUMAN MOLECULAR GENETICS
    28. Bronstein, JM
      Function of tetraspan proteins in the myelin sheath

      CURRENT OPINION IN NEUROBIOLOGY
    29. Wegner, M
      Transcriptional control in myelinating glia: The basic recipe

      GLIA
    30. Ramelli, GP; Remonda, L; Lovblad, KO; Hirsiger, H; Moser, H
      Abnormal myelination in a patient with deletion 14q11.2q13.1

      PEDIATRIC NEUROLOGY
    31. Kon, K; Inagaki, M; Kaga, M; Sasaki, M; Hanaoka, S
      Otoacoustic emission in patients with neurological disorders who have auditory brainstem response abnormality

      BRAIN & DEVELOPMENT
    32. 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
    33. Stecca, B; Southwood, CM; Gragerov, A; Kelley, KA; Friedrich, VL; Gow, A
      The evolution of lipophilin genes from invertebrates to tetrapods: DM-20 cannot replace proteolipid protein in CNS myelin

      JOURNAL OF NEUROSCIENCE
    34. Barkovich, AJ
      Concepts of myelin and myelination in neuroradiology

      AMERICAN JOURNAL OF NEURORADIOLOGY
    35. 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
    36. Lewis, RA; Sumner, AJ; Shy, ME
      Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis

      MUSCLE & NERVE
    37. McDermott, CJ; White, K; Bushby, K; Shaw, PJ
      Hereditary spastic paraparesis: a review of new developments

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    38. Frank, M; Atanasoski, S; Sancho, S; Magyar, JP; Rulicke, RT; Schwab, ME; Suter, U
      Progressive segregation of unmyelinated axons in peripheral nerves, myelinalterations in the CNS, and cyst formation in the kidneys of myelin and lymphocyte protein-overexpressing mice

      JOURNAL OF NEUROCHEMISTRY
    39. Jiang, HY; Duchala, CS; Awatramani, R; Shumas, S; Carlock, L; Kamholz, J; Garbern, J; Scherer, SS; Shy, ME; Macklin, WB
      Proteolipid protein mRNA stability is regulated by axonal contact in the rodent peripheral nervous system

      JOURNAL OF NEUROBIOLOGY
    40. Hudson, LD
      Breaking away from home

      AMERICAN JOURNAL OF HUMAN GENETICS
    41. Sasaki, A; Miyanaga, K; Ototsuji, M; Iwaki, A; Iwaki, T; Takahashi, S; Nakazato, Y
      Two autopsy cases with Pelizaeus-Merzbacher disease phenotype of adult onset, without mutation of proteolipid protein gene

      ACTA NEUROPATHOLOGICA
    42. Wong, K; Armstrong, RC; Gyure, KA; Morrison, AL; Rodriguez, D; Matalon, R; Johnson, AB; Wollmann, R; Gilbert, E; Le, TQ; Bradley, CA; Crutchfield, K; Schiffmann, R
      Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome

      ACTA NEUROPATHOLOGICA
    43. Aridor, M; Balch, WE
      Integration of endoplasmic reticulum signaling in health and disease

      NATURE MEDICINE
    44. Forsting, M
      MR imaging of the brain: metabolic and toxic white matter diseases

      EUROPEAN RADIOLOGY
    45. Sivakumar, K; Sambuughin, N; Selenge, B; Nagle, JW; Baasanjav, D; Hudson, LD; Goldfarb, LG
      Novel exon 3B proteolipid protein gene mutation causing late-onset spasticparaplegia type 2 with variable penetrance in female family members

      ANNALS OF NEUROLOGY
    46. 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
    47. Faerber, EN; Melvin, JJ; Smergel, EM
      MRI appearances of metachromatic leukodystrophy

      PEDIATRIC RADIOLOGY
    48. Bjartmar, C; Yin, XH; Trapp, BD
      Axonal pathology in myelin disorders

      JOURNAL OF NEUROCYTOLOGY
    49. Thomson, CE; Anderson, TJ; McCulloch, MC; Dickinson, P; Vouyiouklis, DA; Griffiths, IR
      The early phenotype associated with the jimpy mutation of the proteolipid protein gene

      JOURNAL OF NEUROCYTOLOGY
    50. Fink, JK; Hedera, P
      Hereditary spastic paraplegia, genetic heterogeneity and genotype-phenotype correlation

      SEMINARS IN NEUROLOGY
    51. Tobler, AR; Notterpek, L; Naef, R; Taylor, V; Suter, U; Shooter, EM
      Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction

      JOURNAL OF NEUROSCIENCE
    52. 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
    53. 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
    54. Sindou, P; Anani, T; Garbay, B; Couratier, P; Lagrange, E; Vallat, JM
      Involvement of myelin proteins in hereditary neuropathies.

      REVUE NEUROLOGIQUE
    55. van der Knaap, MS; Breiter, SN; Naidu, S; Hart, AAM; Valk, J
      Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach

      RADIOLOGY
    56. Dobretsova, A; Wight, PA
      Antisilencing: Myelin proteolipid protein gene expression in oligodendrocytes is regulated via derepression

      JOURNAL OF NEUROCHEMISTRY
    57. Correa-Cerro, L; Garcia-Cruz, D; Ruiz, MX; Sanchez-Corona, J
      De novo duplication Xq22-q23 in a girl with short stature and gonadal dysgenesis

      ANNALES DE GENETIQUE
    58. Bradl, M; Bauer, J; Inomata, T; Zielasek, J; Nave, KA; Toyka, K; Lassmann, H; Wekerle, H
      Transgenic Lewis rats overexpressing the proteolipid protein gene: myelin degeneration and its effect on T cell-mediated experimental autoimmune encephalomyelitis

      ACTA NEUROPATHOLOGICA
    59. NAGAO M; KADOWAKI J
      CONNATAL PELIZAEUS-MERZBACHER-DISEASE - A MISSENSE MUTATION IN EXON-4OF THE PROTEOLIPID PROTEIN (PLP) GENE

      JOURNAL OF HUMAN GENETICS
    60. 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
    61. WERNER H; JUNG M; KLUGMANN M; SEREDA M; GRIFFITHS IR; NAVE KA
      MOUSE MODELS OF MYELIN DISEASES

      Brain pathology
    62. HAYES MW; OUVRIER RA; EVANS W; SOMERVILLE E; MORRIS JGL
      X-LINKED DYSTONIA-DEAFNESS SYNDROME

      Movement disorders
    63. CUDDON PA; LIPSITZ D; DUNCAN ID
      MYELIN MOSAICISM AND BRAIN PLASTICITY IN HETEROZYGOUS FEMALES OF A CANINE X-LINKED TRAIT

      Annals of neurology
    64. HUXLEY C
      MYELIN DISORDERS

      Neuropathology and applied neurobiology
    65. NEZU A; KIMURA S; TAKESHITA S; OSAKA H; TANAKA M
      MAGNETIC STIMULATION OF THE CORTICOSPINAL TRACTS IN PELIZAEUS-MERZBACHER DISEASE

      Electroencephalography and clinical neurophysiology. Evoked potentials
    66. VELA JM; GONZALEZ B; CASTELLANO B
      UNDERSTANDING GLIAL ABNORMALITIES ASSOCIATED WITH MYELIN DEFICIENCY IN THE JIMPY MUTANT MOUSE

      Brain research reviews
    67. 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
    68. GRIFFITHS I; KLUGMANN M; ANDERSON T; YOOL D; THOMSON C; SCHWAB MH; SCHNEIDER A; ZIMMERMANN F; MCCULLOCH M; NADON N; NAVE KA
      AXONAL SWELLINGS AND DEGENERATION IN MICE LACKING THE MAJOR PROTEOLIPID OF MYELIN

      Science
    69. ANDERSON TJ; SCHNEIDER A; BARRIE JA; KLUGMANN M; MCCULLOCH MC; KIRKHAM D; KYRIAKIDES E; NAVE KA; GRIFFITHS IR
      LATE-ONSET NEURODEGENERATION IN MICE WITH INCREASED DOSAGE OF THE PROTEOLIPID PROTEIN GENE

      Journal of comparative neurology
    70. DEMICHELE G; DEFUSCO M; CAVALCANTI F; FILLA A; MARCONI R; VOLPE G; MONTICELLI A; BALLABIO A; CASARI G; COCOZZA S
      A NEW LOCUS FOR AUTOSOMAL RECESSIVE HEREDITARY SPASTIC PARAPLEGIA MAPS TO CHROMOSOME 16Q24.3

      American journal of human genetics
    71. NAEF R; ADLKOFER K; LESCHER B; SUTER U
      ABERRANT PROTEIN TRAFFICKING IN TREMBLER SUGGESTS A DISEASE MECHANISMFOR HEREDITARY HUMAN PERIPHERAL NEUROPATHIES

      Molecular and cellular neurosciences
    72. MORI M; NISHIMURA M
      A SERINE-TO-PROLINE MUTATION IN THE COPPER-TRANSPORTING P-TYPE ATPASEGENE OF THE MACULAR MOUSE

      Mammalian genome
    73. GARBERN JY; CAMBI F; TANG XM; SIMA AAF; VALLAT JM; BOSCH EP; LEWIS R; SHY M; SOHI J; KRAFT G; CHEN KL; JOSHI I; LEONARD DGB; JOHNSON W; RASKIND W; DLOUHY SR; PRATT V; HODES ME; BIRD T; KAMHOLZ J
      PROTEOLIPID PROTEIN IS NECESSARY IN PERIPHERAL AS WELL AS CENTRAL MYELIN

      Neuron
    74. KLUGMANN M; SCHWAB MH; PUHLHOFER A; SCHNEIDER A; ZIMMERMANN F; GRIFFITHS IR; NAVE KA
      ASSEMBLY OF CNS MYELIN IN THE ABSENCE OF PROTEOLIPID PROTEIN

      Neuron
    75. ONO J; HARADA K; MANO T; SAKURAI K; OKADA S
      DIFFERENTIATION OF DYSMYELINATION AND DEMYELINATION USING DIFFUSIONALANISOTROPY

      Pediatric neurology
    76. ONO J; HARADA K; MANO T; SAKURAI K; OKADA S
      DIFFERENTIATION OF DYSMYELINATION AND DEMYELINATION USING DIFFUSIONALANISOTROPY

      Pediatric neurology
    77. GOW A
      REDEFINING THE LIPOPHILIN FAMILY OF PROTEOLIPID PROTEINS

      Journal of neuroscience research
    78. 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
    79. 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
    80. YANG XY; SKOFF RP
      PROTEOLIPID PROTEIN REGULATES THE SURVIVAL AND DIFFERENTIATION OF OLIGODENDROCYTES

      The Journal of neuroscience
    81. AWATRAMANI R; SCHERER S; GRINSPAN J; COLLARINI E; SKOFF R; OHAGAN D; GARBERN J; KAMHOLZ J
      EVIDENCE THAT THE HOMEODOMAIN PROTEIN GTX IS INVOLVED IN THE REGULATION OF OLIGODENDROCYTE MYELINATION

      The Journal of neuroscience
    82. KIM TS; KIM IO; KIM WS; CHOI YS; LEE JY; KIM OW; YEON KM; KIM KJ; HWANG YS
      MR OF CHILDHOOD METACHROMATIC LEUKODYSTROPHY

      American journal of neuroradiology
    83. TAKANASHI J; SUGITA K; OSAKA H; ISHII M; NIIMI H
      PROTON MR SPECTROSCOPY IN PELIZAEUS-MERZBACHER DISEASE

      American journal of neuroradiology
    84. 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
    85. HEIM P; CLAUSSEN M; HOFFMANN B; CONZELMANN E; GARTNER J; HARZER K; HUNNEMAN DH; KOHLER W; KURLEMANN G; KOHLSCHUTTER A
      LEUKODYSTROPHY INCIDENCE IN GERMANY

      American journal of medical genetics
    86. BOND C; SI XL; CRISP M; WONG P; PAULSON GW; BOESEL CP; DLOUHY SR; HODES ME
      PELIZAEUS-MERZBACHER DISEASE X-LINKED SPASTIC PARAPLEGIA PROTEOLIPID PROTEIN NONSENSE MUTATION

      American journal of medical genetics
    87. HODES ME; BLANK CA; PRATT VM; MORALES J; NAPIER J; DLOUHY SR
      NONSENSE MUTATION IN EXON-3 OF THE PROTEOLIPID PROTEIN GENE (PLP) IN A FAMILY WITH AN UNUSUAL FORM OF PELIZAEUS-MERZBACHER-DISEASE

      American journal of medical genetics
    88. ILLARIOSHKIN SN; IVANOVASMOLENSKAYA IA; MARKOVA ED; NIKOLSKAYA NN; TSUDZI S
      NEW FORM OF HEREDITARY ATAXIA - INBORN X- LINKED CEREBELLAR HYPOPLASIA (CLINICAL AND MOLECULAR-GENETIC ANALYSIS)

      Zurnal nevropatologii i psihiatrii im. S.S. Korsakova
    89. LEGUERN E
      NEUROGENETICS

      Revue neurologique
    90. VERHAGEN WIM; HUYGEN PLM; SMEETS HJM; RENIER WO; DEWIJS I
      A NEW PROTEOLIPID LIPOPROTEIN MUTATION IN PELIZAEUS-MERZBACHER-DISEASE

      Journal of the neurological sciences
    91. KAWANISHI C; OSAKA H; INOUE K; ONISHI H; YAMADA Y; KOSAKA K
      A NEW RESTRICTION-SITE POLYMORPHISM IN THE HUMAN PROTEOLIPID PROTEIN GENE

      Clinical genetics
    92. RAMAEKERS VT; HEIMANN G; REUL J; THRON A; JAEKEN J
      GENETIC-DISORDERS AND CEREBELLAR STRUCTURAL ABNORMALITIES IN CHILDHOOD

      Brain
    93. DONNELLY A; COLLEY A; CRIMMINS D; MULLEY J
      A NOVEL MUTATION IN EXON-6 (F236S) OF THE PROTEOLIPID PROTEIN GENE ISASSOCIATED WITH SPASTIC PARAPLEGIA

      Human mutation
    94. BRADL M; LININGTON C
      ANIMAL-MODELS OF DEMYELINATION

      Brain pathology
    95. GILGENKRANTZ S
      DM20 SUPPORT OF PLP CELLULAR TRAFFICKING INFLUENCES THE SEVERITY OF DISEASES DUE TO PLP GENE ANOMALIES

      MS. Medecine sciences
    96. NEZU A; KIMURA S; UEHARA S; OSAKA H; KOBAYASHI T; HARAGUCHI M; INOUE K; KAWANISHI C
      PELIZAEUS-MERZBACHER-LIKE DISEASE - FEMALE CASE-REPORT

      Brain & development
    97. KNAPP PE
      PROTEOLIPID PROTEIN - IS IT MORE THAN JUST A STRUCTURAL COMPONENT OF MYELIN

      Developmental neuroscience
    98. ILLARIOSHKIN SN; TANAKA H; MARKOVA ED; NIKOLSKAYA NN; IVANOVASMOLENSKAYA IA; TSUJI S
      X-LINKED NONPROGRESSIVE CONGENITAL CEREBELLAR HYPOPLASIA - CLINICAL DESCRIPTION AND MAPPING TO CHROMOSOME XQ

      Annals of neurology
    99. STEPHENS TS; PAKASKI M; LEES MB; POTTER NT
      IDENTIFICATION AND CHARACTERIZATION OF A B-CELL DETERMINANT WITHIN THE AMPHIPATHIC DOMAIN (RESIDUES-178-238) OF THE MYELIN PROTEOLIPID PROTEIN

      Journal of neuroscience research
    100. KREMER H; HAMEL BCJ; VANDENHELM B; ARTS WFM; DEWIJS IJ; SISTERMANS EA; ROPERS HH; MARIMAN ECM
      LOCALIZATION OF THE GENE (OR GENES) FOR A SYNDROME WITH X-LINKED MENTAL-RETARDATION, ATAXIA, WEAKNESS, HEARING IMPAIRMENT, LOSS OF VISION AND A FATAL COURSE IN EARLY-CHILDHOOD

      Human genetics


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Documento generato il 27/10/20 alle ore 17:14:17