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La ricerca find articoli where soggetti phrase all words 'SPINOCEREBELLAR ATAXIA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 454 riferimenti
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    1. Di Donato, S; Gellera, C; Mariotti, C
      The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias

      NEUROLOGICAL SCIENCES
    2. Ichikawa, Y; Goto, J; Hattori, M; Toyoda, A; Ishii, K; Jeong, SY; Hashida, H; Masuda, N; Ogata, K; Kasai, F; Hirai, M; Maciel, P; Rouleau, GA; Sakaki, Y; Kanazawa, I
      The genomic structure and expression of MJD, the Machado-Joseph disease gene

      JOURNAL OF HUMAN GENETICS
    3. Takashima, M; Ishikawa, K; Nagaoka, U; Shoji, S; Mizusawa, H
      A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan

      JOURNAL OF HUMAN GENETICS
    4. Bonini, NM
      Drosophila as a genetic approach to human neurodegenerative disease

      PARKINSONISM & RELATED DISORDERS
    5. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; LeGuern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    6. Yuan, QP; Lindblad-Toh, K; Zander, C; Burgess, C; Durr, A; Schalling, M
      A cloning strategy for identification of genes containing trinucleotide repeat expansions

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    7. Bockenhauer, D
      Ion channels in disease

      CURRENT OPINION IN PEDIATRICS
    8. Grattan-Smith, PJ; Healey, S; Grigg, JR; Christodoulou, J
      Spinocerebellar ataxia type 7: A distinctive form of autosomal dominant cerebellar ataxia with retinopathy and marked genetic anticipation

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    9. Schilling, G; Jinnah, HA; Gonzales, V; Coonfield, ML; Kim, Y; Wood, JD; Price, DL; Li, XJ; Jenkins, N; Copeland, N; Moran, T; Ross, CA; Borchelt, DR
      Distinct behavioral and neuropathological abnormalities in transgenic mouse models of HD and DRPLA

      NEUROBIOLOGY OF DISEASE
    10. Fan, XP; Dion, P; Laganiere, J; Brais, B; Rouleau, GA
      Oligomerization of polyalanine expanded PABPN1 facilitates nuclear proteinaggregation that is associated with cell death

      HUMAN MOLECULAR GENETICS
    11. Choudhry, S; Mukerji, M; Srivastava, AK; Jain, S; Brahmachari, SK
      CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms

      HUMAN MOLECULAR GENETICS
    12. Richards, RI
      Dynamic mutations: a decade of unstable expanded repeats in human genetic disease

      HUMAN MOLECULAR GENETICS
    13. Orr, HT; Zoghbi, HY
      SCA1 molecular genetics: a history of a 13 year collaboration against glutamines

      HUMAN MOLECULAR GENETICS
    14. Cummings, CJ; Sun, YL; Opal, P; Antalffy, B; Mestril, R; Orr, HT; Dillmann, WH; Zoghbi, HY
      Over-expression of inducible HSP70 chaperone suppresses neuropathology andimproves motor function in SCA1 mice

      HUMAN MOLECULAR GENETICS
    15. Richetta, A; Ottini, L; Falchetti, M; Innocenzi, D; Bottoni, U; Faiola, R; Mariani-Costantini, R; Calvieri, S
      Instability at sequence repeats in melanocytic tumours

      MELANOMA RESEARCH
    16. Leroi, I; O'Hearn, E; Margolis, RL
      Psychiatric syndromes in cerebellar degeneration

      INTERNATIONAL REVIEW OF PSYCHIATRY
    17. Kiehl, TR; Shibata, H; Vo, T; Huynh, DP; Pulst, SM
      Identification and expression of a mouse ortholog of A2BP1

      MAMMALIAN GENOME
    18. Grierson, AJ; Shaw, CE; Miller, CCJ
      Androgen induced cell death in SHSY5Y neuroblastoma cells expressing wild-type and spinal bulbar muscular atrophy mutant androgen receptors

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    19. Orr, HT
      Beyond the Qs in the polyglutamine diseases

      GENES & DEVELOPMENT
    20. Paulson, H; Ammache, Z
      Ataxia and hereditary disorders

      NEUROLOGIC CLINICS
    21. Seranski, P; Hoff, C; Radelof, U; Hennig, S; Reinhardt, R; Schwartz, CE; Heiss, NS; Poustka, A
      RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients

      GENE
    22. Fischbeck, KH
      Polyglutamine expansion neurodegenerative disease

      BRAIN RESEARCH BULLETIN
    23. Piccioni, F; Simeoni, S; Andriola, I; Armatura, E; Bassanini, S; Pozzi, P; Poletti, A
      Polyglutamine tract expansion of the androgen receptor in a motoneuronal model of spinal and bulbar muscular atrophy

      BRAIN RESEARCH BULLETIN
    24. Goossens, D; Del-Favero, J; Van Broeckhoven, C
      Trinucleotide repeat expansions: Do they contribute to bipolar disorder?

      BRAIN RESEARCH BULLETIN
    25. Ferro, P; dell'Eva, R; Pfeffer, U
      Are there CAG repeat expansion-related disorders outside the central nervous system?

      BRAIN RESEARCH BULLETIN
    26. Beauchemin, AMJ; Gottlieb, B; Beitel, LK; Elhaji, YA; Leonard, P; Trifiro, MA
      Cytochrome c oxidase subunit Vb interacts with human androgen receptor: A potential mechanism for neurotoxicity in spinobulbar muscular atrophy

      BRAIN RESEARCH BULLETIN
    27. Calabresi, V; Guida, S; Servadio, A; Jodice, C
      Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro

      BRAIN RESEARCH BULLETIN
    28. Fusco, FR; Viscomi, MT; Bernardi, G; Molinari, M
      Localization of ataxin-2 within the cerebellar cortex of the rat

      BRAIN RESEARCH BULLETIN
    29. Cellini, E; Forleo, P; Nacmias, B; Tedde, A; Latorraca, S; Piacentini, S; Parnetti, L; Gallai, V; Sorbi, S
      Clinical and genetic analysis of hereditary and sporadic ataxia in centralItaly

      BRAIN RESEARCH BULLETIN
    30. Schelhaas, HJ; Ippe, PF; Hageman, G; Sinke, RJ; van der Laan, EN; Beemer, FA
      Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia

      JOURNAL OF NEUROLOGY
    31. Ross, BM; Mamalias, N; Moszczynska, A; Rajput, AH; Kish, SJ
      Elevated activity of phospholipid biosynthetic enzymes in substantia nigraof patients with Parkinson's disease

      NEUROSCIENCE
    32. Nishimura, M; Kawakami, H; Maruyama, H; Izumi, Y; Kuno, S; Kaji, R; Nakamura, S
      Influence of interleukin-1 beta gene polymorphism on age-at-onset of spinocerebellar ataxia 6 (SCA6) in Japanese patients

      NEUROSCIENCE LETTERS
    33. Ohara, K
      Anticipation, imprinting, trinucleotide repeat expansions and psychoses

      PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
    34. Evert, BO; Vogt, IR; Kindermann, C; Ozimek, L; de Vos, RAI; Brunt, ERP; Schmitt, I; Klockgether, T; Wullner, U
      Inflammatory genes are upregulated in expanded ataxin-3-expressing cell lines and spinocerebellar ataxia type 3 brains

      JOURNAL OF NEUROSCIENCE
    35. Mori, M; Adachi, Y; Kusumi, M; Nakashima, K
      A genetic epidemiological study of spinocerebellar ataxias in Tottori Prefecture, Japan

      NEUROEPIDEMIOLOGY
    36. Manabe, Y; Honda, E; Shiro, Y; Sakai, K; Kohira, I; Kashihara, K; Shohmori, T; Abe, K
      Fractal dimension analysis of static stabilometry in Parkinson's disease and spinocerebellar ataxia

      NEUROLOGICAL RESEARCH
    37. Mariotti, C; Gellera, C; Grisoli, M; Mineri, R; Castucci, A; Di Donato, S
      Pathogenic effect of an intermediate-size SCA-6 allele (CAG)(19) in a homozygous patient

      NEUROLOGY
    38. Sobrido, MJ; Cholfin, JA; Perlman, S; Pulst, SM; Geschwind, DH
      SCA8 repeat expansions in ataxia: A controversial association

      NEUROLOGY
    39. Rantamaki, M; Krahe, R; Paetau, A; Cormand, B; Mononen, I; Udd, B
      Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family

      NEUROLOGY
    40. Storey, E; Gardner, RJM; Knight, MA; Kennerson, ML; Tuck, RR; Forrest, SM; Nicholson, GA
      A new autosomal dominant pure cerebellar ataxia

      NEUROLOGY
    41. O'Hearn, E; Holmes, SE; Calvert, PC; Ross, CA; Margolis, RL
      SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion

      NEUROLOGY
    42. Gomez, CM
      Polyglutamine aggregates in SCA6 Purkinje cells - A tail of two toxicities

      NEUROLOGY
    43. Ishikawa, K; Owada, K; Ishida, K; Fujigasaki, H; Li, MS; Tsunemi, T; Ohkoshi, N; Toru, S; Mizutani, T; Hayashi, M; Arai, N; Hasegawa, K; Kawanami, T; Kato, T; Makifuchi, T; Shoji, S; Tanabe, T; Mizusawa, H
      Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells

      NEUROLOGY
    44. Siyanova, EY; Mirkin, SM
      Expansion of trinucleotide repeats

      MOLECULAR BIOLOGY
    45. Hashida, H; Goto, J; Suzuki, T; Jeong, SY; Masuda, N; Ooie, T; Tachiiri, Y; Tsuchiya, H; Kanazawa, I
      Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA)

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    46. Namekawa, M; Takiyama, Y; Ando, Y; Sakoe, K; Muramatsu, S; Fujimoto, K; Nishizawa, M; Nakano, I
      Choreiform movements in spinocerebellar ataxia type 1

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    47. Shimazaki, H; Takiyama, Y; Sakoe, K; Amaike, M; Nagaki, H; Namekawa, M; Sasaki, H; Nakano, I; Nishizawa, M
      Meiotic instability of the CAG repeats in the SCA6/CACNA1A gene in two Japanese SCA6 families

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    48. Inoue, T; Lin, X; Kohlmeier, KA; Orr, HT; Zoghbi, HY; Ross, WN
      Calcium dynamics and electrophysiological properties of cerebellar Purkinje cells in SCA1 transgenic mice

      JOURNAL OF NEUROPHYSIOLOGY
    49. Takahashi, J; Tanaka, J; Arai, K; Funata, N; Hattori, T; Fukuda, T; Fujigasaki, H; Uchihara, T
      Recruitment of nonexpanded polyglutamine proteins to intranuclear aggregates in neuronal intranuclear hyaline inclusion disease

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    50. Mazzola, JL; Sirover, MA
      Reduction of glyceraldehyde-3-phosphate dehydrogenase activity in Alzheimer's disease and in Huntington's disease fibroblasts

      JOURNAL OF NEUROCHEMISTRY
    51. Alba, MM; Santibanez-Koref, MF; Hancock, JM
      The comparative genomics of polyglutamine repeats: Extreme difference in the codon organization of repeat-encoding regions between mammals and Drosophila

      JOURNAL OF MOLECULAR EVOLUTION
    52. Burk, S; Bosch, S; Globas, C; Zuhlke, C; Daum, I; Klockgether, T; Dichgans, J
      Executive dysfunction in spinocerebellar ataxia type 1

      EUROPEAN NEUROLOGY
    53. Marzouki, N; Belal, S; Benhamida, C; Benlemlih, M; Hentati, F
      Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families

      CLINICAL GENETICS
    54. Burk, K; Bosch, S; Muller, CA; Melms, A; Zuhlke, C; Stern, M; Besenthal, I; Skalej, M; Ruck, P; Ferber, S; Klockgether, T; Dichgans, J
      Sporadic cerebellar ataxia associated with gluten sensitivity

      BRAIN
    55. Etchebehere, ECSC; Cendes, F; Lopes-Cendes, I; Pereira, JA; Lima, MCL; Sansana, CR; Silva, CAM; Camargo, MFAG; Santos, AO; Ramos, CD; Camargo, EE
      Brain single-photon emission computed tomography and magnetic resonance imaging in Machado-Joseph disease

      ARCHIVES OF NEUROLOGY
    56. Maciel, P; Costa, MDC; Ferro, A; Rousseau, M; Santos, CS; Gaspar, C; Barros, J; Rouleau, GA; Coutinho, P; Sequeiros, J
      Improvement in the molecular diagnosis of Machado-Joseph disease

      ARCHIVES OF NEUROLOGY
    57. Gokhan, S; Mehler, MF
      Basis and clinical neuroscience applications of embryonic stem cells

      ANATOMICAL RECORD
    58. Berthelier, V; Hamilton, JB; Chen, SM; Wetzel, R
      A microtiter plate assay for polyglutamine aggregate extension

      ANALYTICAL BIOCHEMISTRY
    59. Skinner, PJ; Vierra-Green, CA; Clark, HB; Zoghbi, HY; Orr, HT
      Altered trafficking of membrane proteins in Purkinje cells of SCA1 transgenic mice

      AMERICAN JOURNAL OF PATHOLOGY
    60. Le Roy-Duflos, I
      Possible causal relationships between cerebellar patterns of foliation andhindlimb coordination in laboratory mice: A quantitative trait locus analysis

      BEHAVIOR GENETICS
    61. Yabe, I; Sasaki, H; Yamashita, I; Takei, A; Tashiro, K
      Clinical trial of acetazolamide in SCA6, with assessment using the Ataxia Rating Scale and body stabilometry

      ACTA NEUROLOGICA SCANDINAVICA
    62. Cummings, CJ; Zoghbi, HY
      Trinucleotide repeats: Mechanisms and pathophysiology

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    63. Gusella, JF; MacDonald, ME
      Molecular genetics: Unmasking polyglutamine triggers in neurodegenerative disease

      NATURE REVIEWS NEUROSCIENCE
    64. Restivo, DA; Giuffrida, S; Rapisarda, G; Antonuzzo, A; Saponara, R; Reggio, A; Salinaro, AT; Raffaele, R; Domina, E; Trovato, A; Condorelli, DF; Pennisi, G
      Central motor conduction to lower limb after transcranial magnetic stimulation in spinocerebellar ataxia type 2 (SCA2)

      CLINICAL NEUROPHYSIOLOGY
    65. Bennett, P
      Microsatellites

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    66. Huynh, DP; Figueroa, K; Hoang, N; Pulst, SM
      Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

      NATURE GENETICS
    67. Kaushik, N; Malaspina, A; de Belleroche, J
      Characterization of trinucleotide- and tandem repeat-containing transcripts obtained from human spinal cord cDNA library by high-density filter hybridization

      DNA AND CELL BIOLOGY
    68. Jonasson, J; Juvonen, V; Sistonen, P; Ignatius, J; Johansson, D; Bjorck, EJ; Wahlstrom, J; Melberg, A; Holmgren, G; Forsgren, L; Holmberg, M
      Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    69. Broadstock, M; Michie, S; Marteau, T
      Psychological consequences of predictive genetic testing: a systematic review

      EUROPEAN JOURNAL OF HUMAN GENETICS
    70. Stevanin, G; Durr, A; Brice, A
      Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology

      EUROPEAN JOURNAL OF HUMAN GENETICS
    71. Lindenberg, KS; Yvert, G; Muller, K; Landwehrmeyer, GB
      Expression analysis of ataxin-7 mRNA and protein in human brain: Evidence for a widespread distribution and focal protein accumulation

      BRAIN PATHOLOGY
    72. Shibata, H; Huynh, DP; Pulst, SM
      A novel protein with RNA-binding motifs interacts with ataxin-2

      HUMAN MOLECULAR GENETICS
    73. Yanagisawa, H; Bundo, M; Miyashita, T; Okamura-Oho, Y; Tadokoro, K; Tokunaga, K; Yamada, M
      Protein binding of a DRPLA family through arginine-glutamic acid dipeptiderepeats is enhanced by extended polyglutamine

      HUMAN MOLECULAR GENETICS
    74. Lorenzetti, D; Watase, K; Xu, BS; Matzuk, MM; Orr, HT; Zoghbi, HY
      Repeat instability and motor incoordination in mice with a targeted expanded CAG repeat in the Sca1 locus

      HUMAN MOLECULAR GENETICS
    75. Moseley, ML; Schut, MJ; Bird, TD; Koob, MD; Day, JW; Ranum, LPW
      SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance

      HUMAN MOLECULAR GENETICS
    76. Simeoni, S; Mancini, MA; Stenoien, DL; Marcelli, M; Weigel, NL; Zanisi, M; Martini, L; Poletti, A
      Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tract

      HUMAN MOLECULAR GENETICS
    77. Kumagai, R; Kaseda, Y; Kawakami, H; Nakamura, S
      Electrophysiological studies in spinocerebellar ataxia type 6: a statistical approach

      NEUROREPORT
    78. Nagao, Y; Ishiguro, H; Nukina, N
      DMSO and glycerol reduce bacterial death induced by expression of truncated N-terminal huntingtin with expanded polyglutamine tracts

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    79. Klockgether, T; Wullner, U; Spauschus, A; Evert, B
      The molecular biology of the autosomal-dominant cerebellar ataxias

      MOVEMENT DISORDERS
    80. Tozaki, T; Inoue, S; Mashima, S; Ohta, M; Miura, N; Tomita, M
      Sequence analysis of trinucleotide repeat microsatellites from an enrichment library of the equine genome

      GENOME
    81. Yamashita, I; Sasaki, H; Yabe, I; Fukazawa, T; Nogoshi, S; Komeichi, K; Takada, A; Shiraishi, K; Takiyama, Y; Nishizawa, M; Kaneko, J; Tanaka, H; Tsuji, S; Tashiro, K
      A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter

      ANNALS OF NEUROLOGY
    82. Gilman, S
      The spinocerebellar ataxias

      CLINICAL NEUROPHARMACOLOGY
    83. Watanabe, H; Tanaka, F; Doyu, M; Riku, S; Yoshida, M; Hashizume, Y; Sobue, G
      Differential somatic CAG repeat instability in variable brain cell lineagein dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis

      HUMAN GENETICS
    84. Saleem, Q; Choudhry, S; Mukerji, M; Bashyam, L; Padma, MV; Chakravarthy, A; Maheshwari, MC; Jain, S; Brahmachari, SK
      Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation

      HUMAN GENETICS
    85. Hsieh, M; Lin, SJ; Chen, JF; Lin, HM; Hsiao, KM; Li, SY; Li, C; Tsai, CJ
      Identification of the spinocerebellar ataxia type 7 mutation in Taiwan: application of PCR-based Southern blot

      JOURNAL OF NEUROLOGY
    86. Montagna, P
      Molecular genetics of migraine headaches: a review

      CEPHALALGIA
    87. Tolbert, DL; Clark, BR
      Olivocerebellar projections modify hereditary Purkinje cell degeneration

      NEUROSCIENCE
    88. Nozawa, K; Suzuki, M; Takemura, M; Yoshida, S
      In vitro expansion of mammalian telomere repeats by DNA polymerase alpha-primase

      NUCLEIC ACIDS RESEARCH
    89. Erdemoglu, AK; Akbostanci, MC; Selcuki, D
      Familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy

      CLINICAL NEUROLOGY AND NEUROSURGERY
    90. Tsuji, S
      Dentatorubral-pallidoluysian atrophy (DRPLA)

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    91. Evert, BO; Wullner, U; Klockgether, T
      Cell death in polyglutamine diseases

      CELL AND TISSUE RESEARCH
    92. Lesort, M; Tucholski, J; Miller, ML; Johnson, GVW
      Tissue transglutaminase: a possible role in neurodegenerative diseases

      PROGRESS IN NEUROBIOLOGY
    93. Rolfsmeier, ML; Lahue, RS
      Stabilizing effects of interruptions on trinucleotide repeat expansions inSaccharomyces cerevisiae

      MOLECULAR AND CELLULAR BIOLOGY
    94. Yazawa, I
      Aberrant phosphorylation of dentatorubral-pallidoluysian atrophy (DRPLA) protein complex in brain tissue

      BIOCHEMICAL JOURNAL
    95. Zuhlke, C; Atici, J; Martorell, L; Gembruch, U; Kohl, M; Gopel, W; Schwinger, E
      Rapid detection of expansions by PCR and non-radioactive hybridization: application for prenatal diagnosis of myotonic dystrophy

      PRENATAL DIAGNOSIS
    96. Gibson, GE; Park, LCH; Sheu, KFR; Blass, JP; Calingasan, NY
      The alpha-ketoglutarate dehydrogenase complex in neurodegeneration

      NEUROCHEMISTRY INTERNATIONAL
    97. Manabe, Y; Shiro, Y; Takahashi, K; Kashihara, K; Abe, K
      A case of spinocerebellar ataxia accompanied by severe involvement of the motor neuron system

      NEUROLOGICAL RESEARCH
    98. Culjkovic, B; Stojkovic, O; Savic, D; Zamurovic, N; Nesic, M; Major, T; Keckarevic, D; Romac, S; Zamurovic, B; Vukosavic, S
      Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    99. Inukai, A; Doyu, M; Kato, T; Liang, YD; Kuru, S; Yamamoto, M; Kobayashi, Y; Sobue, G
      Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle

      MUSCLE & NERVE
    100. Lieberman, AP; Fischbeck, KH
      Triplet repeat expansion in neuromuscular disease

      MUSCLE & NERVE


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/12/19 alle ore 04:02:17