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La ricerca find articoli where soggetti phrase all words 'FAMILIAL HEMIPLEGIC MIGRAINE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 152 riferimenti
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    1. Celesia, GG
      Disorders of membrane channels or channelopathies

      CLINICAL NEUROPHYSIOLOGY
    2. Sandor, PS; Mascia, A; Seidel, L; de Pasqua, V; Schoenen, J
      Subclinical cerebellar impairment in the common types of migraine: A threedimensional analysis of reaching movements

      ANNALS OF NEUROLOGY
    3. Frontali, M
      Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder?

      BRAIN RESEARCH BULLETIN
    4. Knight, YE; Goadsby, PJ
      The periaqueductal grey matter modulates trigeminovascular input: A role in migraine?

      NEUROSCIENCE
    5. Ambrosini, A; De Noordhout, AM; Schoenen, J
      Neuromuscular transmission in migraine patients with prolonged aura

      ACTA NEUROLOGICA BELGICA
    6. Ikeda, K; Kobayashi, T; Ichikawa, T; Kumanishi, T; Niki, H; Yano, R
      The untranslated region of mu-opioid receptor mRNA contributes to reduced opioid sensitivity in CXBK mice

      JOURNAL OF NEUROSCIENCE
    7. Piedras-Renteria, ES; Watase, K; Harata, N; Zhuchenko, O; Zoghbi, HY; Lee, CC; Tsien, RW
      Increased expression of alpha(1A) Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6

      JOURNAL OF NEUROSCIENCE
    8. Lea, RA; Curtain, RP; Hutchins, C; Brimage, PJ; Griffiths, LR
      Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Jen, J; Wan, J; Graves, M; Yu, H; Mock, AF; Coulin, CJ; Kim, G; Yue, Q; Papazian, DM; Baloh, RW
      Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission

      NEUROLOGY
    10. Terwindt, GM; Ophoff, RA; van Eijk, R; Vergouwe, MN; Haan, J; Frants, RR; Sandkuijl, LA; Ferrari, MD
      Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura

      NEUROLOGY
    11. Ambrosini, A; de Noordhout, AM; Schoenen, J
      Neuromuscular transmission in migraine - A single-fiber EMG study in clinical subgroups

      NEUROLOGY
    12. Breslau, N; Rasmussen, BK
      The impact of migraine - Epidemiology, risk factors, and co-morbidities

      NEUROLOGY
    13. Nahab, FB; Worrell, GA; Weinshenker, BG
      25-year-old man with recurring headache and confusion

      MAYO CLINIC PROCEEDINGS
    14. Rogers, KL; Grice, ID; Griffiths, LR
      Modulation of in vitro platelet 5-HT release by species of Erythrina and Cymbopogon

      LIFE SCIENCES
    15. Bousser, MG; Tournier-Lasserve, E
      Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: from stroke to vessel wall physiology

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    16. Scoggan, KA; Chandra, T; Nelson, R; Hahn, AF; Bulman, DE
      Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2

      JOURNAL OF MEDICAL GENETICS
    17. Berjukow, S; Marksteiner, R; Sokolov, S; Weiss, RG; Margreiter, E; Hering, S
      Amino acids in segment IVS6 and beta-subunit interaction support distinct conformational changes during Ca(v)2.1 inactivation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    18. Mulleners, WM; Chronicle, EP; Palmer, JE; Koehler, PJ; Vredeveld, JW
      Visual cortex excitability in migraine with and without aura

      HEADACHE
    19. Ophoff, RA; van den Maagdenberg, AMJM; Roon, KI; Ferrari, MD; Frants, RR
      The impact of pharmacogenetics for migraine

      EUROPEAN JOURNAL OF PHARMACOLOGY
    20. Ptacek, LJ; Fu, YH
      Channelopathies: Episodic disorders of the nervous system

      EPILEPSIA
    21. Guerrini, R
      Idiopathic epilepsy and paroxysmal dyskinesia

      EPILEPSIA
    22. Jen, J; Geschwind, DH
      Ataxia and calcium channels - What a headache!

      ARCHIVES OF NEUROLOGY
    23. Denier, C; Ducros, A; Durr, A; Eymard, B; Chassande, B; Tournier-Lasserve, E
      Missense CACNA1A mutation causing episodic ataxia type 2

      ARCHIVES OF NEUROLOGY
    24. Soong, BW; Liu, RS; Wu, LC; Lu, YC; Lee, HY
      Metabolic characterization of spinocerebellar ataxia type 6

      ARCHIVES OF NEUROLOGY
    25. Guida, S; Trettel, F; Pagnutti, S; Mantuano, E; Tottene, A; Veneziano, L; Fellin, T; Spadaro, M; Stauderman, KA; Williams, ME; Volsen, S; Ophoff, RA; Frants, RR; Jodice, C; Frontali, M; Pietrobon, D
      Complete loss of P/Q calcium channel activity caused by a CACNA1A missensemutation carried by patients with episodic ataxia type 2

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. Afra, J; Cecchini, AP; Sandor, PS; Schoenen, J
      Comparison of visual and auditory evoked cortical potentials in migraine patients between attacks

      CLINICAL NEUROPHYSIOLOGY
    27. LaPoint, SF; Patel, U; Rubio, A
      Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

      ADVANCES IN ANATOMIC PATHOLOGY
    28. Weinreich, F; Jentsch, TJ
      Neurological diseases caused by ion-channel mutations

      CURRENT OPINION IN NEUROBIOLOGY
    29. Klockgether, T; Wullner, U; Spauschus, A; Evert, B
      The molecular biology of the autosomal-dominant cerebellar ataxias

      MOVEMENT DISORDERS
    30. Allain, H; Schuck, S; Mauduit, N; Saiag, B; Pinel, JF; Bentue-Ferrer, D
      The pathophysiology of migraine.

      PATHOLOGIE BIOLOGIE
    31. Manivet, P; Soliman, HR; Callebert, J; Laplanche, JL; Launay, JM
      Biochemical mechanisms in the physiopathology of migraines.

      PATHOLOGIE BIOLOGIE
    32. Couraud, F; Seagar, M
      Calcium channels and migraine.

      PATHOLOGIE BIOLOGIE
    33. Ducros, A
      Genetics of migraine

      PATHOLOGIE BIOLOGIE
    34. Geraud, G
      Rare and atypical forms of migraine

      PATHOLOGIE BIOLOGIE
    35. Sappey-Marinier, D; Broussolle, E; Vighetto, A
      Magnetic resonance spectroscopy of episodic ataxia type 2 and migraine - Reply

      ANNALS OF NEUROLOGY
    36. Haan, J; Kors, EE; Terwindt, GM; Vermeulen, FLMG; Vergouwe, MN; van den Maagdenberg, AMJM; Gill, DS; Pascual, J; Ophoff, RA; Frants, RR; Ferrari, MD
      Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene

      CEPHALALGIA
    37. Judit, A; Sandor, PS; Schoenen, J
      Habituation of visual and intensity dependence of auditory evoked corticalpotentials tends to normalize just before and during the migraine attack

      CEPHALALGIA
    38. Montagna, P
      Molecular genetics of migraine headaches: a review

      CEPHALALGIA
    39. Werhahn, KJ; Wiseman, K; Herzog, J; Forderreuther, S; Dichgans, M; Straube, A
      Motor cortex excitability in patients with migraine with aura and hemiplegic migraine

      CEPHALALGIA
    40. Chaudhuri, A; Watson, WS; Pearn, J; Behan, PO
      The symptoms of chronic fatigue syndrome are related to abnormal ion channel function

      MEDICAL HYPOTHESES
    41. Ayata, C; Shimizu-Sasamata, M; Lo, EH; Noebels, JL; Moskowitz, MA
      Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha 1A subunit of P/Q typecalcium channels

      NEUROSCIENCE
    42. 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
    43. Cowan, WM; Harter, DH; Kandel, ER
      The emergence of modern neuroscience: Some implications for neurology and psychiatry

      ANNUAL REVIEW OF NEUROSCIENCE
    44. Mogil, JS; Yu, L; Basbaum, AI
      Pain genes?: Natural variation and transgenic mutants

      ANNUAL REVIEW OF NEUROSCIENCE
    45. 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
    46. Lorenzon, NM; Beam, KG
      Calcium channelopathies

      KIDNEY INTERNATIONAL
    47. Geraud, G
      Rare and atypical forms of migraine.

      REVUE NEUROLOGIQUE
    48. Evidente, VGH; Gwinn-Hardy, KA; Caviness, JN; Gilman, S
      Hereditary ataxias

      MAYO CLINIC PROCEEDINGS
    49. Hering, S; Berjukow, S; Sokolov, S; Marksteiner, R; Weiss, RG; Kraus, R; Timin, EN
      Molecular determinants of inactivation in voltage-gated Ca2+ channels

      JOURNAL OF PHYSIOLOGY-LONDON
    50. Sokolov, S; Weiss, RG; Timin, EN; Hering, S
      Modulation of slow inactivation in class A Ca2+ channels by beta-subunits

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

      JOURNAL OF MEDICAL GENETICS
    52. Toru, S; Murakoshi, T; Ishikawa, K; Saegusa, H; Fujigasaki, H; Uchihara, T; Nagayama, S; Osanai, M; Mizusawa, H; Tanabe, T
      Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function

      JOURNAL OF BIOLOGICAL CHEMISTRY
    53. Jeziorski, MC; Greenberg, RM; Anderson, PAV
      Calcium channel beta subunits differentially modulate recovery of the channel from inactivation

      FEBS LETTERS
    54. Hassan, A; Markus, HS
      Genetics and ischaemic stroke

      BRAIN
    55. Plomp, JJ; Vergouwe, MN; Van den Maagdenberg, AM; Ferrari, MD; Frants, RR; Molenaar, PC
      Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca2+ channel mutation

      BRAIN
    56. Dworakowska, B; Dolowy, K
      Ion channels-related diseases

      ACTA BIOCHIMICA POLONICA
    57. Benatar, MG
      Calcium channelopathies

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    58. Austin, CP; Holder, DJ; Ma, L; Mixson, LA; Caskey, CT
      Mapping of hKCa3 to chromosome 1q21 and investigation of linkage of CAG repeat polymorphism to schizophrenia

      MOLECULAR PSYCHIATRY
    59. Kors, EE; Haan, J; Ferrari, MD
      Genetics of primary headaches

      CURRENT OPINION IN NEUROLOGY
    60. Randall, A; Benham, CD
      Recent advances in the molecular understanding of voltage-gated Ca2+ channels

      MOLECULAR AND CELLULAR NEUROSCIENCE
    61. Frontali, M; Novelletto, A; Annesi, G; Jodice, C
      CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    62. Jen, J
      Calcium channelopathies in the central nervous system

      CURRENT OPINION IN NEUROBIOLOGY
    63. Davies, NP; Hanna, MG
      Neurological channelopathies: diagnosis and therapy in the new millennium

      ANNALS OF MEDICINE
    64. Bahra, A; Evers, S; Goadsby, PJ
      Comorbidity of depression and migraine - a review

      NERVENHEILKUNDE
    65. Gervil, M; Ulrich, V; Kyvik, KO; Olesen, J; Russell, MB
      Migraine without aura: A population-based twin study

      ANNALS OF NEUROLOGY
    66. Ulrich, V; Gervil, M; Kyvik, KO; Olesen, J; Russell, MB
      Evidence of a genetic factor in migraine with aura: A population-based Danish twin study

      ANNALS OF NEUROLOGY
    67. Friend, KL; Crimmins, D; Phan, TG; Sue, CM; Colley, A; Fung, VSC; Morris, JGL; Sutherland, GR; Richards, RI
      Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

      HUMAN GENETICS
    68. Mayer, M; Straube, A; Bruening, R; Uttner, I; Pongratz, D; Gasser, T; Dichgans, M; Muller-Hocker, J
      Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL

      JOURNAL OF NEUROLOGY
    69. Wang, W; Wang, GP; Ding, XL; Wang, YH
      Personality and response to repeated visual stimulation in migraine and tension-type headaches

      CEPHALALGIA
    70. Frants, RR
      The use of isolates in migraine genetic research

      CEPHALALGIA
    71. Becker, WJ
      The scientific basis of migraine management

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    72. Gardner, K
      The genetic basis of migraine: How much do we know?

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    73. Wang, W; Wang, YH; Fu, XM; Sun, ZM; Schoenen, J
      Auditory evoked potentials and multiple personality measures in migraine and post-traumatic headaches

      PAIN
    74. Ambrosini, A; de Noordhout, AM; Alagona, G; Dalpozzo, F; Schoenen, J
      Impairment of neuromuscular transmission in a subgroup of migraine patients

      NEUROSCIENCE LETTERS
    75. Hofmann, F; Lacinova, L; Klugbauer, N
      Voltage-dependent calcium channels: From structure to function

      REVIEWS OF PHYSIOLOGY BIOCHEMISTRY AND PHARMACOLOGY, VOL 139
    76. Dichgans, M; Gasser, T
      Clinical findings and diagnostic approach in CADASIL

      AKTUELLE NEUROLOGIE
    77. Leniger, T; Diener, HC
      Migraine and epilepsy - A relationship?

      AKTUELLE NEUROLOGIE
    78. 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
    79. Martelletti, P; Lulli, P; Morellini, M; Mariani, B; Pennesi, G; Cappellacci, S; Brioli, G; Giacovazzo, M; Trabace, S
      Chromosome 6p-encoded HLA-DR2 determinant discriminates migraine without aura from migraine with aura

      HUMAN IMMUNOLOGY
    80. Yousry, TA; Seelos, K; Mayer, M; Bruning, R; Uttner, I; Dichgans, M; Mammi, S; Straube, A; Mai, N; Filippi, M
      Characteristic MR lesion pattern and correlation of T1 and T2 lesion volume with neurologic and neuropsychological findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

      AMERICAN JOURNAL OF NEURORADIOLOGY
    81. Echenne, B; Ducros, A; Rivier, F; Joutel, A; Humbertclaude, V; Roubertie, A; Azais, M; Bousser, MG; Tournier-Lasserve, E
      Recurrent episodes of coma: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1

      NEUROPEDIATRICS
    82. Schuck, P; Bohmer, K; Resch, KL
      Migraine and migraine prophylaxis: is there a role for magnesium?

      SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT
    83. Lehmann-Horn, F; Jurkat-Rott, K
      Voltage-gated ion channels and hereditary disease

      PHYSIOLOGICAL REVIEWS
    84. Gervil, M; Ulrich, V; Kaprio, J; Olesen, J; Russell, MB
      The relative role of genetic and environmental factors in migraine withoutaura

      NEUROLOGY
    85. Burk, K; Klockgether, T; Dichgans, J
      Molecular genetics and pathogenic mechanisms of hereditary ataxia

      NERVENARZT
    86. Jun, K; Piedras-Renteria, ES; Smith, SM; Wheeler, DB; Lee, SB; Lee, TG; Chin, HM; Adams, ME; Scheller, RH; Tsien, RW; Shin, HS
      Ablation of P/Q-type Ca2+ channel currents, altered synaptic transmission,and progressive ataxia in mice lacking the alpha(1A)-subunit

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    87. Mogil, JS
      The genetic mediation of individual differences in sensitivity to pain andits inhibition

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    88. Campbell, DB; Hess, EJ
      L-type calcium channels contribute to the tottering mouse dystonic episodes

      MOLECULAR PHARMACOLOGY
    89. Ulrich, V; Gervil, M; Kyvik, KO; Olesen, J; Russell, MB
      The inheritance of migraine with aura estimated by means of structural equation modelling

      JOURNAL OF MEDICAL GENETICS
    90. Barclay, J; Rees, M
      Mouse models of spike-wave epilepsy

      EPILEPSIA
    91. DAVOUS P
      CADASIL - A REVIEW WITH PROPOSED DIAGNOSTIC-CRITERIA

      European journal of neurology
    92. BARCHI RL
      ION-CHANNEL MUTATIONS AFFECTING MUSCLE AND BRAIN

      Current opinion in neurology
    93. WELCH KMA
      CURRENT OPINIONS IN HEADACHE PATHOGENESIS - INTRODUCTION AND SYNTHESIS

      Current opinion in neurology
    94. PTACEK LJ
      THE PLACE OF MIGRAINE AS A CHANNELOPATHY

      Current opinion in neurology
    95. BALOH RW
      ADVANCES IN NEUROTOLOGY

      Current opinion in neurology
    96. PEROUTKA SJ
      GENETIC-BASIS OF MIGRAINE

      Clinical neuroscience
    97. TERWINDT GM; OPHOFF RA; HAAN J; SANDKUIJL LA; FRANTS RR; FERRARI MD
      MIGRAINE, ATAXIA AND EPILEPSY - A CHALLENGING SPECTRUM OF GENETICALLY-DETERMINED CALCIUM CHANNELOPATHIES

      European journal of human genetics
    98. AUBURGER G
      NEW GENETIC CONCEPTS AND STROKE PREVENTION

      Cerebrovascular diseases
    99. BRIN MF; KOLLER W
      EPIDEMIOLOGY AND GENETICS OF ESSENTIAL TREMOR

      Movement disorders
    100. GORDON N
      EPISODIC ATAXIA AND CHANNELOPATHIES

      Brain & development


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/02/20 alle ore 11:15:37