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La ricerca find articoli where soggetti phrase all words 'channelopathy' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 20 riferimenti
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    1. Swinn, MJ; Fowler, CJ
      Isolated urinary retention in young women, or Fowler's syndrome

      CLINICAL AUTONOMIC RESEARCH
    2. Sharp, AH; Black, JL; Dubel, SJ; Sundarraj, S; Shen, JP; Yunker, AMR; Copeland, TD; McEnery, MW
      Biochemical and anatomical evidence for specialized voltage-dependent calcium channel gamma isoform expression in the epileptic and ataxic mouse, stargazer

      NEUROSCIENCE
    3. Kearney, JA; Plummer, NW; Smith, MR; Kapur, J; Cummins, TR; Waxman, SG; Goldin, AL; Meisler, MH
      A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities

      NEUROSCIENCE
    4. Schofield, PR
      Genetics, an alternative way to discover, characterize and understand ion channels

      CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
    5. Jeck, N; Derst, C; Wischmeyer, E; Ott, H; Weber, S; Rudin, C; Seyberth, HW; Daut, J; Karschin, A; Konrad, M
      Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome

      KIDNEY INTERNATIONAL
    6. Sugawara, T; Tsurubuchi, Y; Agarwala, KL; Ito, M; Fukuma, G; Mazaki-Miyazaki, E; Nagafuji, H; Noda, M; Imoto, K; Wada, K; Mitsudome, A; Kaneko, S; Montal, M; Nagata, K; Hirose, S; Yamakawa, K
      A missense mutation of the Na+ channel alpha(II) subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    7. Hirose, S; Okada, M; Kaneko, S; Mitsudome, A
      Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis

      EPILEPSY RESEARCH
    8. Allain, H; Schuck, S; Mauduit, N; Saiag, B; Pinel, JF; Bentue-Ferrer, D
      The pathophysiology of migraine.

      PATHOLOGIE BIOLOGIE
    9. Restituito, S; Thompson, RM; Eliet, J; Raike, RS; Riedl, M; Charnet, P; Gomez, CM
      The polyglutamine expansion in spinocerebellar ataxia type 6 causes a betasubunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes

      JOURNAL OF NEUROSCIENCE
    10. Lory, P; Monteil, A; Chemin, J; Leuranguer, V; Bourinet, E; Nargeot, J
      Molecular diversity of voltage-gated calcium channels

      THERAPIE
    11. Jurkat-Rott, K; Mitrovic, N; Hang, C; Kouzmekine, A; Iaizzo, P; Herzog, J; Lerche, H; Nicole, S; Vale-Santos, J; Chauveau, D; Fontaine, B; Lehmann-Horn, F
      Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    12. Davies, NP; Eunson, LH; Gregory, RP; Mills, KR; Morrison, PJ; Hanna, MG
      Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenita

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    13. Hart, IK
      Acquired neuromyotonia: A new autoantibody-mediated neuronal potassium channelopathy

      AMERICAN JOURNAL OF THE MEDICAL SCIENCES
    14. Finsterer, J; Stollberger, C
      Subclinical skeletal muscle involvement in long-QT syndrome

      JOURNAL OF ELECTROMYOGRAPHY AND KINESIOLOGY
    15. Davies, NP; Hanna, MG
      Neurological channelopathies: diagnosis and therapy in the new millennium

      ANNALS OF MEDICINE
    16. Hans, M; Luvisetto, S; Williams, ME; Spagnolo, M; Urrutia, A; Tottene, A; Brust, PF; Johnson, EC; Harpold, MM; Stauderman, KA; Pietrobon, D
      Functional consequences of mutations in the human alpha(1A) calcium channel subunit linked to familial hemiplegic migraine

      JOURNAL OF NEUROSCIENCE
    17. Matsuo, H; Kamakura, K; Matsushita, S; Ohmori, T; Okano, M; Tadano, Y; Tsuji, S; Higuchi, S
      Mutational analysis of the anion exchanger 3 gene in familial paroxysmal dystonic choreoathetosis linked to chromosome 2q

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Greenberg, DA
      Neuromuscular disease and calcium channels

      MUSCLE & NERVE
    19. Hirose, S; Iwata, H; Akiyoshi, H; Kobayashi, K; Ito, M; Wada, K; Kaneko, S; Mitsudome, A
      A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy

      NEUROLOGY
    20. PTACEK LJ
      CHANNELOPATHIES - ION-CHANNEL DISORDERS OF MUSCLE AS A PARADIGM FOR PAROXYSMAL DISORDERS OF THE NERVOUS-SYSTEM

      Neuromuscular disorders


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/10/20 alle ore 15:41:54