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    1. Hand, CK; Khoris, J; Salachas, F; Gros-Louis, F; Lopes, AAS; Mayeux-Portas, V; Brown, RH; Meininger, V; Camu, W; Rouleau, GA
      A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Wang, S; Ma, N; Gao, SJ; Yu, H; Leong, KW
      Transgene expression in the brain stem effected by intramuscular injectionof polyethylenimine/DNA complexes

      MOLECULAR THERAPY
    3. Cordes, SP
      Molecular genetics of cranial nerve development in mouse

      NATURE REVIEWS NEUROSCIENCE
    4. Urushitani, M; Shimohama, S
      The role of nitric oxide in amyotrophic lateral sclerosis

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    5. Beghi, E; Logroscino, G; Micheli, A; Millul, A; Perini, M; Riva, R; Salmoiraghi, F; Vitelli, E
      Validity of hospital discharge diagnoses for the assessment of the prevalence and incidence of amyotrophic lateral sclerosis

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    6. Santos-Bento, M; de Carvalho, M; Evangelista, T; Luis, MLS
      Sympathetic sudomotor function and amyotrophic lateral sclerosis

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    7. Miller, RG
      Examining the evidence about treatment in ALS/MND

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    8. Desnuelle, C; Dib, M; Garrel, C; Favier, A
      A double-blind, placebo-controlled randomized clinical trial of alpha-tocopherol (vitamin E) in the treatment of amyotrophic lateral sclerosis

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    9. Swash, M
      ALS 2000: the past points to the future

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    10. Mitsumoto, H
      Clinical trials: present and future

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    11. Nobile-Orazio, E; Carpo, M; Meucci, N
      Are there immunologically treatable motor neuron diseases?

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    12. Andersen, PM
      Genetics of sporadic ALS

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    13. Gellera, C
      Genetics of ALS in Italian families

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    14. Appel, SH; Beers, D; Siklos, L; Engelhardt, JI; Mosier, DR
      Calcium: the Darth Vader of ALS

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    15. Beck, M; Karch, C; Wiese, S; Sendtner, M
      Motoneuron cell death and neurotrophic factors: Basic models for development of new therapeutic strategies in ALS

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    16. Silani, V; Braga, M; Botturi, A; Cardin, V; Bez, A; Pizzuti, A; Scarlato, G
      Human developing motor neurons as a tool to study ALS

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    17. Gangwani, L; Mikrut, M; Theroux, S; Sharma, M; Davis, RJ
      Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein

      NATURE CELL BIOLOGY
    18. Serrao, M; Parisi, L; Pierelli, F; Rossi, P
      Cutaneous afferents mediating the cutaneous silent period in the upper limbs: evidences for a role of low-threshold sensory fibres

      CLINICAL NEUROPHYSIOLOGY
    19. Mall, V; Glocker, FX; Fietzek, U; Heinen, F; Berweck, S; Korinthenberg, R; Rosler, KM
      Inhibitory conditioning stimulus in transcranial magnetic stimulation reduces the number of excited spinal motor neurons

      CLINICAL NEUROPHYSIOLOGY
    20. Stetkarova, I; Kofler, M; Leis, AA
      Cutaneous and mixed nerve silent periods in syringomyelia

      CLINICAL NEUROPHYSIOLOGY
    21. Kunishige, M; Hill, KA; Riemer, AM; Farwell, KD; Halangoda, A; Heinmoller, E; Moore, SR; Turner, DM; Sommer, SS
      Mutation frequency is reduced in the cerebellum of Big Blue (R) mice overexpressing a human wild type SOD1 gene

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    22. Hodges, JR; Miller, B
      The classification, genetics and neuropathology of frontotemporal dementia. Introduction to the special topic papers: Part I

      NEUROCASE
    23. Skvortsova, VI; Limborska, SA; Slominsky, PA; Levitskaya, NI; Levitsky, GN; Shadrina, MI; Kondratyeva, EA
      Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia

      EUROPEAN JOURNAL OF NEUROLOGY
    24. Sendtner, M
      Molecular mechanisms in spinal muscular atrophy: models and perspectives

      CURRENT OPINION IN NEUROLOGY
    25. Duff, K; Rao, MV
      Progress in the modeling of neurodegenerative diseases in transgenic mice

      CURRENT OPINION IN NEUROLOGY
    26. Pasqualetti, M; Rijli, FM
      Homeobox gene mutations and brain-stem developmental disorders: learning from knockout mice

      CURRENT OPINION IN NEUROLOGY
    27. Martin, LJ
      Neuronal cell death in nervous system development, disease, and injury (Review)

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    28. Lee, SK; Pfaff, SL
      Transcriptional networks regulating neuronal identity in the developing spinal cord

      NATURE NEUROSCIENCE
    29. Balaban, PM; Bravarenko, NI; Maksimova, OA; Nikitin, E; Ierusalimsky, VN; Zakharov, IS
      A single serotonergic modulatory cell can mediate reinforcement in the withdrawal network of the terrestrial snail

      NEUROBIOLOGY OF LEARNING AND MEMORY
    30. MacKenzie, AE; Gendron, NH
      Tudor reign

      NATURE STRUCTURAL BIOLOGY
    31. Shaw, PJ
      Genetic inroads in familial ALS

      NATURE GENETICS
    32. Grohmann, K; Schuelke, M; Diers, A; Hoffmann, K; Lucke, B; Adams, C; Bertini, E; Leonhardt-Horti, H; Muntoni, F; Ouvrier, R; Pfeufer, A; Rossi, R; Van Maldergem, L; Wilmshurst, JM; Wienker, TR; Sendtner, M; Rudnik-Schoneborn, S; Zerres, K; Hubner, C
      Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

      NATURE GENETICS
    33. Del Brio, MA; Riera, P; Peruzzo, B; Rodriguez, EM
      Hindbrain floor plate of the rat: Ultrastructural changes occurring duringdevelopment

      MICROSCOPY RESEARCH AND TECHNIQUE
    34. Gofflot, F; Gaoua, W; Bourguignon, L; Roux, C; Picard, JJ
      Expression of Sonic Hedgehog downstream genes is modified in rat embryos exposed in utero to a distal inhibitor of cholesterol biosynthesis

      DEVELOPMENTAL DYNAMICS
    35. Kenn, W; Ochs, G; Pabst, TA; Hahn, D
      H-1 spectroscopy in patients with amyotrophic lateral sclerosis

      JOURNAL OF NEUROIMAGING
    36. Alberta, JA; Park, SK; Mora, J; Yuk, DI; Pawlitzky, I; Iannarelli, P; Vartanian, T; Stiles, CD; Rowitch, DH
      Sonic hedgehog is required during an early phase of oligodendrocyte development in mammalian brain

      MOLECULAR AND CELLULAR NEUROSCIENCE
    37. Pradat, PF; Finiels, F; Kennel, P; Naimi, S; Orsini, C; Delaere, P; Revah, F; Mallet, J
      Partial prevention of cisplatin-induced neuropathy by electroporation-mediated nonviral gene transfer

      HUMAN GENE THERAPY
    38. Haider, MZ; Moosa, A; Dalal, H; Habib, Y; Reynold, L
      Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes

      JOURNAL OF BIOMEDICAL SCIENCE
    39. Scheffer, H; Cobben, JM; Matthijs, G; Wirth, B
      Best practice guidelines for molecular analysis in spinal muscular atrophy

      EUROPEAN JOURNAL OF HUMAN GENETICS
    40. Sossi, V; Giuli, A; Vitali, T; Tiziano, F; Mirabella, M; Antonelli, A; Neri, G; Brahe, C
      Premature termination mutations in exon 3 of the SMN1 gene are associated with exon skipping and a relatively mild SMA phenotype

      EUROPEAN JOURNAL OF HUMAN GENETICS
    41. Cho, K; Ryu, K; Lee, E; Won, S; Kim, J; Yoo, OJ; Hahn, S
      Correlation between genotype and phenotype in Korean patients with spinal muscular atrophy

      MOLECULES AND CELLS
    42. Schmalbruch, H; Haase, G
      Spinal muscular atrophy: Present state

      BRAIN PATHOLOGY
    43. de Carvalho, M; Johnsen, B; Fuglsang-Frederiksen, A
      Medical technology assessment - Electrodiagnosis in motor neuron diseases and amyotrophic lateral sclerosis

      NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY
    44. Pernas-Alonso, R; Perrone-Capano, C; Volpicelli, F; di Porzio, U
      Regionalized neurofilament accumulation and motoneuron degeneration are linked phenotypes in wobbler neuromuscular disease

      NEUROBIOLOGY OF DISEASE
    45. Cisterni, C; Kallenbach, S; Jordier, F; Bagnis, C; Pettmann, B
      Death of motoneurons induced by trophic deprivation or by excitotoxicity is not prevented by overexpression of SMN

      NEUROBIOLOGY OF DISEASE
    46. Zhang, ML; Lorson, CL; Androphy, EJ; Zhou, J
      An in vivo reporter system for measuring increased inclusion of exon 7 in SMN2 mRNA: potential therapy of SMA

      GENE THERAPY
    47. Clarke, S; Hickey, A; O'Boyle, C; Hardiman, O
      Assessing individual quality of life in amyotrophic lateral sclerosis

      QUALITY OF LIFE RESEARCH
    48. Gellera, C; Castellotti, B; Riggio, MC; Silani, V; Morandi, L; Testa, D; Casali, C; Taroni, F; Di Donato, S; Zeviani, M; Mariotti, C
      Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations

      NEUROMUSCULAR DISORDERS
    49. Grohme, K; von Maravic, M; Gasser, T; Borasio, GD
      A case of amyotrophic lateral sclerosis with a very slow progression over 44 years

      NEUROMUSCULAR DISORDERS
    50. Bigini, P; Bastone, A; Mennini, T
      Glutamate transporters in the spinal cord of the wobbler mouse

      NEUROREPORT
    51. Doroudchi, MM; Minotti, S; Figlewicz, DA; Durham, HD
      Nitrotyrosination contributes minimally to toxicity of mutant SOD1 associated with ALS

      NEUROREPORT
    52. Tomkins, J; Banner, SJ; McDermott, CJ; Shaw, PJ
      Mutation screening of manganese superoxide dismutase in amyotrophic lateral sclerosis

      NEUROREPORT
    53. Obal, I; Jakab, JSK; Siklos, L; Engelhardt, JI
      Recruitment of activated microglia cells in the spinal cord of mice by ALSIgG

      NEUROREPORT
    54. Briscoe, J; Ericson, J
      Specification of neuronal fates in the ventral neural tube

      CURRENT OPINION IN NEUROBIOLOGY
    55. Sharma, K; Belmonte, JCI
      Development of the limb neuromuscular system

      CURRENT OPINION IN CELL BIOLOGY
    56. Traiffort, E; Moya, KL; Faure, H; Hassig, R; Ruat, M
      High expression and anterograde axonal transport of aminoterminal sonic hedgehog in the adult hamster brain

      EUROPEAN JOURNAL OF NEUROSCIENCE
    57. Mezler, M; Muller, T; Raming, K
      Cloning and functional expression of GABA(B) receptors from Drosophila

      EUROPEAN JOURNAL OF NEUROSCIENCE
    58. Lewis, KE; Eisen, JS
      Hedgehog signaling is required for primary motoneuron induction in zebrafish

      DEVELOPMENT
    59. Lu, HC; Swindell, EC; Sierralta, WD; Eichele, G; Thaller, C
      Evidence for a role of protein kinase C in FGF signal transduction in the developing chick limb bud

      DEVELOPMENT
    60. Chen, WB; Burgess, S; Hopkins, N
      Analysis of the zebrafish smoothened mutant reveals conserved and divergent functions of hedgehog activity

      DEVELOPMENT
    61. Altun-Gultekin, Z; Andachi, Y; Tsalik, EL; Pilgrim, D; Kohara, Y; Hobert, O
      A regulatory cascade of three homeobox genes, ceh-10 ttx-3 and ceh-23, controls cell fate specification of a defined interneuron class in C-elegans

      DEVELOPMENT
    62. Ferrier, DEK; Brooke, NM; Panopoulou, G; Holland, PWH
      The Mnx homeobox gene class defined by HB9, MNR2 and amphioxus AmphiMnx

      DEVELOPMENT GENES AND EVOLUTION
    63. Pathi, S; Pagan-Westphal, S; Baker, DP; Garber, EA; Rayhorn, P; Bumcrot, D; Tabin, CJ; Pepinsky, RB; Williams, KP
      Comparative biological responses to human Sonic, Indian, and Desert hedgehog

      MECHANISMS OF DEVELOPMENT
    64. Coulouarn, Y; Fernex, C; Jegou, S; Henderson, CE; Vaudry, H; Lihrmann, I
      Specific expression of the urotensin II gene in sacral motoneurons of developing rat spinal cord

      MECHANISMS OF DEVELOPMENT
    65. Ott, T; Parrish, M; Bond, K; Schwaeger-Nickolenko, A; Monaghan, AP
      A new member of the spall like zinc finger protein family, Msal-3, is expressed in the CNS and sites of epithelial/mesenchymal interaction

      MECHANISMS OF DEVELOPMENT
    66. Seaman, C; Cooper, HM
      Netrin-3 protein is localized to the axons of motor, sensory, and sympathetic neurons

      MECHANISMS OF DEVELOPMENT
    67. Kraus, F; Haenig, B; Kispert, A
      Cloning and expression analysis of the mouse T-box gene Tbx20

      MECHANISMS OF DEVELOPMENT
    68. Moran, AP; Prendergast, MM
      Molecular mimicry in Campylobacter jejuni and Helicobacter pylori lipopolysaccharides: Contribution of gastrointestinal infections to autoimmunity

      JOURNAL OF AUTOIMMUNITY
    69. Kessaris, N; Pringle, N; Richardson, WD
      Ventral neurogenesis and the neuron-glial switch

      NEURON
    70. Mizuguchi, R; Sugimori, M; Takebayashi, H; Kosako, H; Nagao, M; Yoshida, S; Nabeshima, Y; Shimamura, K; Nakafuku, M
      Combinatorial roles of Olig2 and Neurogenin2 in the coordinated induction of pan-neuronal and subtype-specific properties of motoneurons

      NEURON
    71. Scardigli, R; Schuurmans, C; Gradwohl, G; Guillemot, F
      Crossregulation between Neurogenin2 and pathways specifying neuronal identity in the spinal cord

      NEURON
    72. Nguyen, MD; Lariviere, RC; Julien, JP
      Deregulation of Cdk5 in a mouse model of ALS: Toxicity alleviated by perikaryal neurofilament inclusions

      NEURON
    73. Pierani, A; Moran-Rivard, L; Sunshine, MJ; Littman, DR; Goulding, M; Jessell, TM
      Control of interneuron fate in the developing spinal cord by the progenitor homeodomain protein Dbx1

      NEURON
    74. Moran-Rivard, L; Kagawa, T; Saueressig, H; Gross, MK; Burill, J; Goulding, M
      Evx1 is a postmitotic determinant of V0 interneuron identity in the spinalcord

      NEURON
    75. Wong, PC; Cai, HB; Borchelt, DR; Price, DL
      Genetically engineered models relevant to neurodegenerative disorders - Their value for understanding disease mechanisms and designing/testing experimental therapeutics

      JOURNAL OF MOLECULAR NEUROSCIENCE
    76. Williams, K; Alvarez, X; Lackner, AA
      Central nervous system perivascular cells are immunoregulatory cells that connect the CNS with the peripheral immune system

      GLIA
    77. Boillee, S; Viala, L; Peschanski, M; Dreyfus, PA
      Differential microglial response to progressive neurodegeneration in the murine mutant wobbler

      GLIA
    78. Ingham, PW; McMahon, AP
      Hedgehog signaling in animal development: paradigms and principles

      GENES & DEVELOPMENT
    79. Hebert, MD; Szymczyk, PW; Shpargel, KB; Matera, AG
      Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein

      GENES & DEVELOPMENT
    80. Martin, N; Jaubert, J; Glaser, P; Szatanik, M; Guenet, JL
      Genetic and physical delineation of the region overlapping the progressivemotor neuropathy (pmn) locus on mouse chromosome 13

      GENOMICS
    81. Wong, V; Chan, V
      Molecular genetic study of a childhood form of spinal muscular atrophy

      JOURNAL OF CHILD NEUROLOGY
    82. Guettier-Sigrist, S; Coupin, G; Braun, S; Rogovitz, D; Courdier, I; Warter, JM; Poindron, P
      On the possible role of muscle in the pathogenesis of spinal muscular atrophy

      FUNDAMENTAL & CLINICAL PHARMACOLOGY
    83. Frugier, T; Cifuentes-Diaz, C; Tiziano, FD; Melki, J
      Animal models of spinal muscular atrophies: towards a better understandingof pathophysiology and development of therapeutics

      M S-MEDECINE SCIENCES
    84. Knopman, DS
      An overview of common non-Alzheimer dementias

      CLINICS IN GERIATRIC MEDICINE
    85. Werth, JL
      Using the Youk-Kevorkian case to teach about euthanasia and other end-of-life issues

      DEATH STUDIES
    86. Cassada, DC; Tribble, CG; Laubach, VE; Nguyen, BN; Rieger, JM; Linden, J; Kaza, AK; Long, SM; Kron, IL; Kern, JA
      An adenosine A(2A) agonist, ATL-146e, reduces paralysis and apoptosis during rabbit spinal cord reperfusion

      JOURNAL OF VASCULAR SURGERY
    87. Borasio, GD; Voltz, R; Miller, RG
      Palliative care in amyotrophic lateral sclerosis

      NEUROLOGIC CLINICS
    88. Colcher, A; Simuni, T
      Other Parkinson syndromes

      NEUROLOGIC CLINICS
    89. Wakabayashi, K; Piao, YS; Hayashi, S; Kakita, A; Yamada, M; Takahashi, H
      Ubiquitinated neuronal inclusions in the neostriatum in patients with amyotrophic lateral sclerosis with and without dementia - A study of 60 patients 31 to 87 years of age

      CLINICAL NEUROPATHOLOGY
    90. Tran, TD; Kroepfl, T; Saito, M; Nagura, M; Ichiseki, H; Kubota, M; Toda, T; Sakakihara, Y
      The gene copy ratios of SMN1/SMN2 in Japanese carriers with type I spinal muscular atrophy

      BRAIN & DEVELOPMENT
    91. Nguyen, MD; Julien, JP; Rivest, S
      Induction of pro inflammatory molecules in mice with amyotrophic lateral sclerosis: No requirement for proapoptotic interleukin-1 beta in neurodegeneration

      ANNALS OF NEUROLOGY
    92. Mesulam, MM
      Primary progressive aphasia

      ANNALS OF NEUROLOGY
    93. Almer, G; Guegan, C; Teismann, P; Naini, A; Rosoklija, G; Hays, AP; Chen, CP; Przedborski, S
      Increased expression of the pro-inflammatory enzyme cyclooxygenase-2 in amyotrophic lateral sclerosis

      ANNALS OF NEUROLOGY
    94. Walker, MP; Schlaberg, R; Hays, AP; Bowser, R; Lipkin, WI
      Absence of echovirus sequences in brain and spinal cord of amyotrophic lateral sclerosis patients

      ANNALS OF NEUROLOGY
    95. Usuki, S; Ren, J; Utsunomiya, I; Cashman, NR; Inokuchi, J; Miyatake, T
      GM2 ganglioside regulates the function of ciliary neurotrophic factor receptor in murine immortalized motor neuron-like cells (NSC-34)

      NEUROCHEMICAL RESEARCH
    96. Urushitani, M; Nakamizo, T; Inoue, R; Sawada, H; Kihara, T; Honda, K; Akaike, A; Shimohama, S
      N-methyl-D-aspartate receptor-mediated mitochondrial Ca2+ overload in acute excitotoxic motor neuron death: A mechanism distinct from chronic neurotoxicity after Ca2+ influx

      JOURNAL OF NEUROSCIENCE RESEARCH
    97. Cusco, I; Barcelo, MJ; del Rio, E; Martin, Y; Hernandez-Chico, C; Bussaglia, E; Baiget, M; Tizzano, EF
      Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases

      HUMAN GENETICS
    98. Rochette, CF; Gilbert, N; Simard, LR
      SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens

      HUMAN GENETICS
    99. Mailman, MD; Hemingway, T; Darsey, RL; Glasure, CE; Huang, Y; Chadwick, RB; Heinz, JW; Papp, AC; Snyder, PJ; Sedra, MS; Schafer, RW; Abuelo, DN; Reich, EW; Theil, KS; Burghes, AHM; de la Chapelle, A; Prior, TW
      Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome

      HUMAN GENETICS
    100. Lafitte, C; Amoura, Z; Cacoub, P; Pradat-Diehl, P; Picq, C; Salachas, F; Leger, JM; Piette, JC; Delattre, JY
      Neurological complications of primary Sjogren's syndrome

      JOURNAL OF NEUROLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/02/20 alle ore 11:33:32