Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words 'PERIODIC PARALYSIS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 399 riferimenti
Si mostrano 100 riferimenti a partire da 1
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Lin, SH; Lin, YF; Halperin, ML
      Hypokalaemia and paralysis

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    2. Salifu, MO; Otah, K; Carroll, HJ; Ifudu, O; Friedman, EA; Oh, MS; Aytug, S
      Thyrotoxic hypokalaemic paralysis in a Black man

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    3. Celesia, GG
      Disorders of membrane channels or channelopathies

      CLINICAL NEUROPHYSIOLOGY
    4. Lawson, K; Dunne, MJ
      Peripheral channelopathies as targets for potassium channel openers

      EXPERT OPINION ON INVESTIGATIONAL DRUGS
    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 - Second of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    6. Davies, NP; Hanna, MG
      The skeletal muscle channelopathies: basic science, clinical genetics and treatment

      CURRENT OPINION IN NEUROLOGY
    7. Foppen, RJG; van Mil, HGJ; van Heukelom, JS
      Osmolality influences bistability of membrane potential under hypokalemic conditions in mouse skeletal muscle: an experimental and theoretical study

      COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR AND INTEGRATIVE PHYSIOLOGY
    8. Froemming, GR; Ohlendieck, K
      The role of ion-regulatory membrane proteins of excitation-contraction coupling and relaxation in inherited muscle diseases

      FRONTIERS IN BIOSCIENCE
    9. Bockenhauer, D
      Ion channels in disease

      CURRENT OPINION IN PEDIATRICS
    10. Grunder, S; Geisler, HS; Rainier, S; Fink, JK
      Acid-sensing ion channel (ASCI) 4 gene: physical mapping, genomic organisation, and evaluation as a candidate for paroxysmal dystonia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    11. Falk, T; Kilani, RK; Yool, AJ; Sherman, SJ
      Viral vector-mediated expression of K+ channels regulates electrical excitability in skeletal muscle

      GENE THERAPY
    12. Alekov, AK; Rahman, M; Mitrovic, N; Lehmann-Horn, F; Lerche, H
      Enhanced inactivation and acceleration of activation of the sodium channelassociated with epilepsy in man

      EUROPEAN JOURNAL OF NEUROSCIENCE
    13. Ruszymah, BHI; Zaiton, Z; Aminuddin, S; Khalid, BAK
      11 beta-hydroxysteroid dehydrogenase bioactivity is increased in the colonbut not kidneys of rats given supplementary thyroxine.

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    14. Zinngrebe, EB; Steffgen, J; Muller, GA; Strutz, F
      Severe hypokalaemia and paralysis in a Chinese scientist

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    15. Chen, YC; Fang, JT; Chang, CT; Chou, HH
      Thyrotoxic periodic paralysis in a patient abusing thyroxine for weight reduction

      RENAL FAILURE
    16. Schofield, PR
      Genetics, an alternative way to discover, characterize and understand ion channels

      CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
    17. Alekov, AK; Peter, WG; Mitrovic, N; Lehmann-Horn, F; Lerche, H
      Two mutations in the IV/S4-S5 segment of the human skeletal muscle Na+ channel disrupt fast and enhance slow inactivation

      NEUROSCIENCE LETTERS
    18. Pertovaara, M; Korpela, M; Pasternack, A
      Factors predictive of renal involvement in patients with primary Sjogren'ssyndrome

      CLINICAL NEPHROLOGY
    19. Wappler, F
      Malignant hyperthermia

      EUROPEAN JOURNAL OF ANAESTHESIOLOGY
    20. Khodorova, A; Meissner, K; Leeson, S; Strichartz, GR
      Lidocaine selectively blocks abnormal impulses arising from noninactivating Na channels

      MUSCLE & NERVE
    21. Chemali, KR; Suarez, JI; Katirji, B
      Acute hypokalemic paralysis associated with long-term lithium therapy

      MUSCLE & NERVE
    22. Obuobie, K; Ogunko, A; Lazarus, JH
      Paralysis after a diarrhoeal illness

      JOURNAL OF THE ROYAL SOCIETY OF MEDICINE
    23. Plaster, NM; Tawil, R; Tristani-Firouzi, M; Canun, S; Bendahhou, S; Tsunoda, A; Donaldson, MR; Iannaccone, ST; Brunt, E; Barohn, R; Clark, J; Deymeer, F; George, AL; Fish, FA; Hahn, A; Nitu, A; Ozdemir, C; Serdaroglu, P; Subramony, SH; Wolfe, G; Fu, YH; Ptacek, LJ
      Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

      CELL
    24. Vilin, YY; Fujimoto, E; Ruben, PC
      A novel mechanism associated with idiopathic ventricular fibrillation (IVF) mutations R1232W and T1620M in human cardiac sodium channels

      PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
    25. Desaphy, JF; De Luca, A; Tortorella, P; De Vito, D; George, AL; Camerino, DC
      Gating of myotonic Na channel mutants defines the response to mexiletine and a potent derivative

      NEUROLOGY
    26. Wu, FF; Takahashi, MP; Pegoraro, E; Angelini, C; Colleselli, P; Cannon, SC; Hoffman, EP
      A new mutation in a family with cold-aggravated myotonia disrupts Na+ channel inactivation

      NEUROLOGY
    27. Gajewska, M; Mikulska, M; Wirth-Dzieciolowska, E
      Molecular diagnosis in testing genetic diseases in horses

      MEDYCYNA WETERYNARYJNA
    28. Bennett, ES
      Channel cytoplasmic loops alter voltage-dependent sodium channel activation in an isoform-specific manner

      JOURNAL OF PHYSIOLOGY-LONDON
    29. Imbert, N; Vandebrouck, C; Duport, G; Raymond, G; Hassoni, AA; Constantin, B; Cullen, MJ; Cognard, C
      Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes

      JOURNAL OF PHYSIOLOGY-LONDON
    30. Ellerkmann, RK; Riazanski, V; Elger, CE; Urban, BW; Beck, H
      Slow recovery from inactivation regulates the availability of voltage-dependent Na+ channels in hippocampal granule cells, hilar neurons and basket cells

      JOURNAL OF PHYSIOLOGY-LONDON
    31. Kim, J; Hahn, Y; Sohm, EH; Lee, YJ; Yun, JH; Kim, JM; Chung, JH
      Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    32. Hilber, K; Sandtner, W; Kudlacek, O; Glaaser, IW; Weisz, E; Kyle, JW; French, RJ; Fozzard, HA; Dudley, SC; Todt, H
      The selectivity filter of the voltage-gated sodium channel is involved in channel activation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    33. Ptacek, LJ; Fu, YH
      Channelopathies: Episodic disorders of the nervous system

      EPILEPSIA
    34. Sternberg, D; Maisonobe, T; Jurkat-Rott, K; Nicole, S; Launay, E; Chauveau, D; Tabti, N; Lehmann-Horn, F; Hainque, B; Fontaine, B
      Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 inthe muscle sodium channel gene SCN4A

      BRAIN
    35. Desaphy, JF; Pierno, S; Leoty, C; George, AL; De Luca, A; Camerino, DC
      Skeletal muscle disuse induces fibre type-dependent enhancement of Na+ channel expression

      BRAIN
    36. O'Reilly, JP; Wang, SY; Wang, GK
      Residue-specific effects on slow inactivation at V787 in D2-S6 of Na(v)1.4sodium channels

      BIOPHYSICAL JOURNAL
    37. Hofer, C; Zalunardo, MP; Zollinger, A
      Total intravenous anaesthesia in a patient with familial hypokalaemic periodic paralysis

      ANAESTHESIA
    38. Soma, LR; Uboh, CE; Guan, FY; Birks, EK; Teleis, DC; Rudy, JA; Tsang, DS; Watson, AO
      Disposition, elimination, and bioavailability of phenytoin and its major metabolite in horses

      AMERICAN JOURNAL OF VETERINARY RESEARCH
    39. Meola, G; Sansone, V
      Therapy in myotonic disorders and in muscle channelopathies

      NEUROLOGICAL SCIENCES
    40. Benatar, M
      Neurological potassium channelopathies

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    41. Guimaraes, J; Santos, JV
      Paroxysmal dystonia induced by exercise and acetazolamide

      EUROPEAN JOURNAL OF NEUROLOGY
    42. Wada, T; Yachie, A; Fujita, S; Takei, K; Sumita, R; Ichihara, T; Koizumi, S
      Hypokalemic periodic paralysis and mutations in the CACNL1A3 gene: Case study in a Japanese family

      PEDIATRICS INTERNATIONAL
    43. Vainzof, M; Muniz, VP; Tsanaclis, AMC; Silva, HCA; Rusticci, MS
      Does the A3333G mutation in the CACNL1A3 gene, detected in malignant hyperthermia, also occur in central core disease?

      GENETIC TESTING
    44. McLaughlin, SA; Buchsbaum, MS
      Clinicopathological Conference: Weakness in the knees

      ACADEMIC EMERGENCY MEDICINE
    45. Dominguez-Moran, JA; Baron, M; De Blas, G; Orensanz, LM; Jimenez-Escrig, A
      Clinical-molecular study of a family with essential tremor, late onset seizures and periodic paralysis

      SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    46. Zwarts, MJ; Drost, G; Stegeman, DF
      Recent progress in the diagnostic use of surface EMG for neurological diseases

      JOURNAL OF ELECTROMYOGRAPHY AND KINESIOLOGY
    47. Terada, K; Tanaka, HA; Yoshizawa, S
      Two-parameter bifurcations in the Hodgkin-Huxley equations for muscle fibers

      ELECTRONICS AND COMMUNICATIONS IN JAPAN PART III-FUNDAMENTAL ELECTRONIC SCIENCE
    48. Xia, JH; Zhang, HL; Tang, DS; Tang, XX; Dai, HP; Pan, Q; Long, ZG; Liao, XD
      Identification and characterization of human neuronal voltage-gated calcium channel gamma 3 subunit gene

      CHINESE SCIENCE BULLETIN
    49. Georgesco, M; Salerno, A
      Spontaneous activity in electromyography: mechanisms and practical interest.

      NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY
    50. Sansone, V; Griggs, RC; Moxley, RT
      Hypothyroidism unmasking proximal myotonic myopathy

      NEUROMUSCULAR DISORDERS
    51. Weinreich, F; Jentsch, TJ
      Neurological diseases caused by ion-channel mutations

      CURRENT OPINION IN NEUROBIOLOGY
    52. Brand, S; Seeger, T; Alzheimer, C
      Enhancement of persistent Na+ current by sea anemone toxin (ATX II) exertsdual action on hippocampal excitability

      EUROPEAN JOURNAL OF NEUROSCIENCE
    53. Hirose, S; Okada, M; Kaneko, S; Mitsudome, A
      Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis

      EPILEPSY RESEARCH
    54. Catterall, WA
      From ionic currents to molecular mechanisms: The structure and function ofvoltage-gated sodium channels

      NEURON
    55. Moran, O
      Modulation of the rSkM1 sodium channel alpha-subunit by the beta(1)-subunit does not modify the inactivation kinetics

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    56. Bhatia, KP; Griggs, RC; Ptacek, LJ
      Episodic movement disorders as channelopathies

      MOVEMENT DISORDERS
    57. Birkhahn, RH; Gaeta, TJ; Melniker, L
      Thyrotoxic periodic paralysis and intravenous propranolol in the emergencysetting

      JOURNAL OF EMERGENCY MEDICINE
    58. Pourmand, R
      Metabolic myopathies - A diagnostic evaluation

      NEUROLOGIC CLINICS
    59. Horak, HA; Pourmand, R
      Endocrine myopathies

      NEUROLOGIC CLINICS
    60. Gong, B; Miki, T; Seino, S; Renaud, JM
      A K-ATP channel deficiency affects resting tension, not contractile force,during fatigue in skeletal muscle

      AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
    61. Surtees, R
      Inherited ion channel disorders

      EUROPEAN JOURNAL OF PEDIATRICS
    62. Wu, G; Dias, P; Wu, C; Li, GJ; Kumar, S; Singh, S
      Hyperglycemia, hyperlipemia, and periodic paralysis: A case report of new side effects of clozapine

      PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
    63. Struyk, AF; Scoggan, KA; Bulman, DE; Cannon, SC
      The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation

      JOURNAL OF NEUROSCIENCE
    64. Mori, Y; Wakamori, M; Oda, S; Fletcher, CF; Sekiguchi, N; Mori, E; Copeland, NG; Jenkins, NA; Matsushita, K; Matsuyama, Z; Imoto, K
      Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol))

      JOURNAL OF NEUROSCIENCE
    65. Kawasaki, F; Felling, R; Ordway, RW
      A temperature-sensitive paralytic mutant defines a primary synaptic calcium channel in Drosophila

      JOURNAL OF NEUROSCIENCE
    66. Chatot-Henry, C; Smadja, D; Longhi, R; Brebion, A; Sobesky, G
      Thyrotoxic periodic paralysis. Two news cases in black race patients.

      REVUE DE MEDECINE INTERNE
    67. van Oldruitenborgh-Oosterbaan, MMS; Goehring, LS
      Muscle and muscle disorders in the horse

      PFERDEHEILKUNDE
    68. Kuntzer, T; Flocard, F; Vial, C; Kohler, A; Magistris, MR; Labarre-Vila, A; Gonnaud, PM; Ochsner, F; Soichot, P; Chan, V; Monnier, G
      Exercise test in muscle channelopathies and other muscle disorders

      MUSCLE & NERVE
    69. Dumitru, D
      Physiologic basis of potentials recorded in electromyography

      MUSCLE & NERVE
    70. Boulos, PT; Heiman-Patterson, TD; Alexander, GM; Tahmoush, AJ
      Patch clamp studies of the thr1313met mutant sodium channel causing paramyotonia congenita

      MUSCLE & NERVE
    71. Jurkat-Rott, K; McCarthy, T; Lehmann-Horn, F
      Genetics and pathogenesis of malignant hyperthermia

      MUSCLE & NERVE
    72. Missiaen, L; Robberecht, W; Van Den Bosch, L; Callewaert, G; Parys, JB; Wuytack, F; Raeymaekers, L; Nilius, B; Eggermont, J; De Smedt, H
      Abnormal intracellular Ca2+ homeostasis and disease

      CELL CALCIUM
    73. George, AL; Hebert, S
      Forefronts in nephrology: Ion channelopathies: Hereditary dysfunction of ion channels - Skytop, Pennsylvania, USA - October 28-31, 1998 - Introduction

      KIDNEY INTERNATIONAL
    74. Lorenzon, NM; Beam, KG
      Calcium channelopathies

      KIDNEY INTERNATIONAL
    75. Parilo, MA; Gonzalez, CL
      Acute quadriplegia in a 34-year-old man

      SOUTHERN MEDICAL JOURNAL
    76. Sabau, I; Canonica, A
      Hypokalaemic periodic paralysis associated with controlled thyrotoxicosis

      SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT
    77. Didonna, D; D'Alessandro, G; De Michele, A; Conte, M; Storelli, A; Totaro, M; Altomare, E
      Thyrotoxic periodic paralysis in a Caucasian man in treatment for Graves' disease

      PANMINERVA MEDICA
    78. Ptacek, LJ
      Ligand-gated ion channelopathies - Mutations in different genes causing one disease

      NEUROLOGY
    79. Bennett, LB; Roach, ES; Bowcock, AM
      A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16

      NEUROLOGY
    80. Clausen, T; Overgaard, K
      The role of K+ channels in the force recovery elicited by Na+-K+ pump stimulation in Ba2+-paralysed rat skeletal muscle

      JOURNAL OF PHYSIOLOGY-LONDON
    81. 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
    82. Felix, R
      Channelopathies: ion channel defects linked to heritable clinical disorders

      JOURNAL OF MEDICAL GENETICS
    83. Mitrovic, N; George, AL; Horn, R
      Role of domain 4 in sodium channel slow inactivation

      JOURNAL OF GENERAL PHYSIOLOGY
    84. Scherf, H
      Hypokalemic thyrotoxic paroxysmal paralysis

      INTERNIST
    85. Haeseler, G; Mamarvar, M; Bufler, J; Dengler, R; Hecker, H; Aronson, JK; Piepenbrock, S; Leuwer, M
      Voltage-dependent blockade of normal and mutant muscle sodium channels by benzylalcohol

      BRITISH JOURNAL OF PHARMACOLOGY
    86. Vedantham, V; Cannon, SC
      Rapid and slow voltage-dependent conformational changes in segment IVS6 ofvoltage-gated Na+ channels

      BIOPHYSICAL JOURNAL
    87. O'Reilly, JP; Wang, SY; Wang, GK
      A point mutation in domain 4-segment 6 of the skeletal muscle sodium channel produces an atypical inactivation state

      BIOPHYSICAL JOURNAL
    88. Jourdain, P; Pousset, F; Girard, S; Komajda, M; Thomas, D
      Paralysing hypokalemic thyrotoxicosis.

      ARCHIVES DES MALADIES DU COEUR ET DES VAISSEAUX
    89. Alberts, MK; Clarke, CR; MacAllister, CG; Homer, LM
      Pharmacokinetics of acetazolamide after intravenous and oral administration in horses

      AMERICAN JOURNAL OF VETERINARY RESEARCH
    90. Dworakowska, B; Dolowy, K
      Ion channels-related diseases

      ACTA BIOCHIMICA POLONICA
    91. Scherf, H
      Hypokalemic thyrotoxic paroxysmal paralysis

      DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT
    92. Pertovaara, M; Korpela, M; Kouri, T; Pasternack, A
      The occurrence of renal involvement in primary Sjogren's syndrome: a studyof 78 patients

      RHEUMATOLOGY
    93. Famularo, G; Corsi, FM; Giacanelli, M
      Iatrogenic worsening of hypokalemia and neuromuscular paralysis associatedwith the use of glucose solutions for potassium replacement in a young woman with licorice intoxication and furosemide abuse

      ACADEMIC EMERGENCY MEDICINE
    94. Randall, A; Benham, CD
      Recent advances in the molecular understanding of voltage-gated Ca2+ channels

      MOLECULAR AND CELLULAR NEUROSCIENCE
    95. Inshasi, JS; Jose, VP; van der Merwe, CA; Gledhill, RF
      Dysfunction of sensory nerves during attacks of hypokalemic periodic paralysis

      NEUROMUSCULAR DISORDERS
    96. Desaphy, JF; Camerino, DC; Tortorella, V; De Luca, A
      Effect of mexiletine on sea anemone toxin-induced non-inactivating sodium channels of rat skeletal muscle: a model of sodium channel myotonia

      NEUROMUSCULAR DISORDERS
    97. Day, JW; Roelofs, R; Leroy, B; Pech, I; Benzow, K; Ranum, LPW
      Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)

      NEUROMUSCULAR DISORDERS
    98. Ohtani, H; Imai, H; Kodama, T; Hamai, K; Komatsuda, A; Wakui, H; Miura, AB
      Severe hypokalaemia and respiratory arrest due to renal tubular acidosis in a patient with Sjogren syndrome

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    99. Yeh, JH; Sun, MH; Chiu, HC
      Dominant-inherited hypokalemic periodic paralysis in a large Chinese family

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    100. Schleithoff, L; Mehrke, G; Reutlinger, B; Lehmann-Horn, F
      Genomic structure and functional expression of a human alpha(2)/delta calcium channel subunit gene (CACNA2)

      GENOMICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/10/20 alle ore 06:55:49