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    1. Mirnics, K; Lewis, DA
      Genes and subtypes of schizophrenia

      TRENDS IN MOLECULAR MEDICINE
    2. Akita, J; Abe, S; Shinkawa, H; Kimberling, WJ; Usami, S
      Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese

      JOURNAL OF HUMAN GENETICS
    3. 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
    4. Priori, SG; Bloise, R; Crotti, L
      The long QT syndrome

      EUROPACE
    5. Baulac, S; Huberfeld, G; Gourfinkel-An, I; Mitropoulou, G; Beranger, A; Prud'homme, JF; Baulac, M; Brice, A; Bruzzone, R; LeGuern, E
      First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma 2-subunit gene

      NATURE GENETICS
    6. Wallace, RH; Marini, C; Petrou, S; Harkin, LA; Bowser, DN; Panchal, RG; Williams, DA; Sutherland, GR; Mulley, JC; Scheffer, IE; Berkovic, SF
      Mutant GABA(A) receptor gamma 2-subunit in childhood absence epilepsy and febrile seizures

      NATURE GENETICS
    7. Moore, T; Hecquet, S; McLellann, A; Ville, D; Grid, D; Picard, F; Moulard, B; Asherson, P; Makoff, AJ; McCormick, D; Nasef, L; Froguel, P; Arzimanoglou, A; LeGuern, E; Bailleul, B
      Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME

      EPILEPSY RESEARCH
    8. Skradski, SL; Clark, AM; Jiang, HM; White, HS; Fu, YH; Ptacek, LJ
      A novel gene causing a mendelian audiogenic mouse epilepsy

      NEURON
    9. Yang, XF; Rothman, SM
      Focal cooling rapidly terminates experimental neocortical seizures

      ANNALS OF NEUROLOGY
    10. Fernandez, M; Raskind, W; Wolff, J; Matsushita, M; Yuen, E; Graf, W; Lipe, H; Bird, T
      Familial dyskinesia and facial myokymia (FDFM): A novel movement disorder

      ANNALS OF NEUROLOGY
    11. Durner, M; Keddache, MA; Tomasini, L; Shinnar, S; Resor, SR; Cohen, J; Harden, C; Moshe, SL; Rosenbaum, D; Kang, H; Ballaban-Gil, K; Hertz, S; Labar, DR; Luciano, D; Wallace, S; Yohai, D; Klotz, I; Dicker, E; Greenberg, DA
      Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type

      ANNALS OF NEUROLOGY
    12. Goossens, D; Del-Favero, J; Van Broeckhoven, C
      Trinucleotide repeat expansions: Do they contribute to bipolar disorder?

      BRAIN RESEARCH BULLETIN
    13. Van Brederode, JFM; Rho, JM; Cerne, R; Tempel, BL; Spain, WJ
      Evidence of altered inhibition in layer V pyramidal neurons from neocortexof kcna1-null mice

      NEUROSCIENCE
    14. Vaswani, M; Kapur, S
      Genetic basis of schizophrenia: Trinucleotide repeats - An update

      PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
    15. Ohara, K
      Anticipation, imprinting, trinucleotide repeat expansions and psychoses

      PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
    16. Bhatia, KP
      Familial (idiopathic) paroxysmal dyskinesias: An update

      SEMINARS IN NEUROLOGY
    17. Smith, JS; Iannotti, CA; Dargis, P; Christian, EP; Aiyar, J
      Differential expression of KCNQ2 splice variants: Implications to M current function during neuronal development

      JOURNAL OF NEUROSCIENCE
    18. Fry, M; Paterno, G; Moody-Corbett, F
      Cloning and expression of three K+ channel cDNAs from Xenopus muscle

      MOLECULAR BRAIN RESEARCH
    19. Ujike, H; Yamamoto, A; Tanaka, Y; Takehisa, Y; Takaki, M; Taked, T; Kodama, M; Kuroda, S
      Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder

      PSYCHIATRY RESEARCH
    20. Steinlein, OK
      Genes and mutations in idiopathic epilepsy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Sobetzko, D; Sander, T; Becker, CM
      Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    22. Liguori, R; Avoni, P; Baruzzi, A; Di Stasi, V; Montagna, P
      Familial continuous motor unit activity and epilepsy

      MUSCLE & NERVE
    23. Keating, MT; Sanguinetti, MC
      Molecular and cellular mechanisms of cardiac arrhythmias

      CELL
    24. Towbin, JA; Wang, ZQ; Li, H
      Genotype and severity of long QT syndrome

      DRUG METABOLISM AND DISPOSITION
    25. Steckley, JL; Ebers, GC; Cader, MZ; McLachlan, RS
      An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus

      NEUROLOGY
    26. Miyoshi, Y; Yamada, T; Tanimura, M; Taniwaki, T; Arakawa, K; Ohyagi, Y; Furuya, H; Yamamoto, K; Sakai, K; Sasazuki, T; Kira, J
      A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1

      NEUROLOGY
    27. Casimiro, MC; Knollmann, BC; Ebert, SN; Vary, JC; Greene, AE; Franz, MR; Grinberg, A; Huang, SP; Pfeifer, K
      Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    28. Kuebler, D; Zhang, HG; Ren, XY; Tanouye, MA
      Genetic suppression of seizure susceptibility in Drosophila

      JOURNAL OF NEUROPHYSIOLOGY
    29. Johnson, MR; Johnson, MR; Sander, JWAS; Sander, JWAS
      The clinical impact of epilepsy genetics

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    30. Syrris, P; Murray, A; Carter, ND; McKenna, WM; Jeffery, S
      Mutation detection in long QT syndrome: a comprehensive set of primers andPCR conditions

      JOURNAL OF MEDICAL GENETICS
    31. Seebohm, G; Scherer, CR; Busch, AE; Lerche, C
      Identification of specific pore residues mediating KCNQ1 inactivation - A novel mechanism for long QT syndrome

      JOURNAL OF BIOLOGICAL CHEMISTRY
    32. Singh, R; Andermann, E; Whitehouse, WPA; Harvey, AS; Keene, DL; Seni, MH; Crossland, KM; Andermann, F; Berkovic, SF; Scheffer, IE
      Severe myoclonic epilepsy of infancy: Extended spectrum of GEFS(+)?

      EPILEPSIA
    33. Berkovic, SF; Scheffer, IE
      Genetics of the epilepsies

      EPILEPSIA
    34. Ptacek, LJ; Fu, YH
      Channelopathies: Episodic disorders of the nervous system

      EPILEPSIA
    35. Roden, DM
      Principles in pharmacogenetics

      EPILEPSIA
    36. Guerrini, R
      Idiopathic epilepsy and paroxysmal dyskinesia

      EPILEPSIA
    37. Hong, Y; Rautaharju, PM; Hopkins, PN; Arnett, DK; Djousse, L; Pankow, JS; Sholinsky, P; Rao, DC; Province, MA
      Familial aggregation of QT-interval variability in a general population: results from the NHLBI Family Heart Study

      CLINICAL GENETICS
    38. Huang, LQ; Bitner-Glindzicz, M; Tranebjaerg, L; Tinker, A
      A spectrum of functional effects for disease causing mutations in the Jervell and Lange-Nielsen syndrome

      CARDIOVASCULAR RESEARCH
    39. Towbin, JA; Wang, ZQ; Li, H
      Genotype and severity of long QT syndrome

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    40. Malacarne, M; Gennaro, E; Madia, F; Pozzi, S; Vacca, D; Barone, B; dalla Bernardina, B; Bianchi, A; Bonanni, P; De Marco, P; Gambardella, A; Giordano, L; Lispi, ML; Romeo, A; Santorum, E; Vanadia, F; Vecchi, M; Veggiotti, P; Vigevano, F; Viri, F; Bricarelli, FD; Zara, F
      Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity

      AMERICAN JOURNAL OF HUMAN GENETICS
    41. Caraballo, R; Pavek, S; Lemainque, A; Gastaldi, M; Echenne, B; Motte, J; Genton, P; Cersosimo, R; Humbertclaude, V; Fejerman, N; Monaco, AP; Lathrop, MG; Rochette, J; Szepetowski, P
      Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    42. Bowen, T; Ashworth, L; Kirov, G; Guy, CA; Jones, IR; McCandless, F; Craddock, N; O-Donovan, MC; Owen, MJ
      No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder

      BIPOLAR DISORDERS
    43. Roden, DM
      Impact of recent molecular studies on evaluation of ventricular arrhythmias

      JOURNAL OF INTERVENTIONAL CARDIAC ELECTROPHYSIOLOGY
    44. Chowdari, KV; Wood, J; Ganguli, R; Gottesman, II; Nimgaonkar, VL
      Lack of association between schizophrenia and a CAG repeat polymorphism ofthe hSKCa3 gene in a North Eastern US sample

      MOLECULAR PSYCHIATRY
    45. Guimaraes, J; Santos, JV
      Paroxysmal dystonia induced by exercise and acetazolamide

      EUROPEAN JOURNAL OF NEUROLOGY
    46. Berkovic, SF; Ottman, R
      Molecular genetics of the idiopathic epilepsies: the next steps...

      EPILEPTIC DISORDERS
    47. Scheffer, IE
      Autosomal dominant rolandic epilepsy with speech dyspraxia

      EPILEPTIC DISORDERS
    48. Stafstrom, CE; Tempel, BL
      Epilepsy genes: The link between molecular dysfunction and pathophysiology

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    49. 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
    50. Berul, CI
      Neonatal long QT syndrome and sudden cardiac death

      PROGRESS IN PEDIATRIC CARDIOLOGY
    51. Steenman, M; Westerveld, A; Mannens, M
      Genetics of Beckwith-Wiedemann syndrome-associated tumors: Common genetic pathways

      GENES CHROMOSOMES & CANCER
    52. Chiurazzi, P; Oostra, BA
      Genetics of mental retardation

      CURRENT OPINION IN PEDIATRICS
    53. Scheffer, IE; Berkovic, SF
      Genetics of the epilepsies

      CURRENT OPINION IN PEDIATRICS
    54. Ranta, S; Zhang, YH; Ross, B; Takkunen, E; Hirvasniemi, A; de la Chapelle, A; Gilliam, TC; Lehesjoki, AE
      Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    55. del Giudice, EM; Coppola, G; Scuccimarra, G; Cirillo, G; Bellini, G; Pascotto, A
      Benign familial neonatal convulsions (BFNC) resulting from mutation of theKCNQ2 voltage sensor

      EUROPEAN JOURNAL OF HUMAN GENETICS
    56. Sander, T; Schulz, H; Saar, K; Gennaro, E; Riggio, MC; Bianchi, A; Zara, F; Luna, D; Bulteau, C; Kaminska, A; Ville, D; Cieuta, C; Picard, F; Prud'homme, JF; Bate, L; Sundquist, A; Gardiner, RM; Janssen, GAMAJ; de Haan, GJ; Kasteleijn-Nolst-Trenite, DGA; Bader, A; Lindhout, D; Riess, O; Wienker, TF; Janz, D; Reis, A
      Genome search for susceptibility loci of common idiopathic generalised epilepsies

      HUMAN MOLECULAR GENETICS
    57. Stober, G; Meyer, J; Nanda, I; Wienker, TF; Saar, K; Jatzke, S; Schmid, M; Lesch, KP; Beckmann, H
      hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodiccatatonia, a familial subtype of schizophrenia

      EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
    58. Landrieu, P
      Advances in pediatric neurology?

      ARCHIVES DE PEDIATRIE
    59. Mizuno, K; Okada, M; Murakami, T; Kamata, A; Zhu, G; Kawata, Y; Wada, K; Kaneko, S
      Effects of carbamazepine on acetylcholine release and metabolism

      EPILEPSY RESEARCH
    60. Goodwin, H; Curran, N; Chioza, B; Blower, J; Nashef, L; Asherson, P; Makoff, AJ
      No association found between polymorphisms in genes encoding mGluR7 and mGluR8 and idiopathic generalised epilepsy in a case control study

      EPILEPSY RESEARCH
    61. Sugimoto, Y; Morita, R; Amano, K; Fong, CYG; Shah, PU; Castroviejo, IP; Khan, S; Delgado-Escueta, AV; Yamakawa, K
      Childhood absence epilepsy in 8q24: Refinement of candidate region and construction of physical map

      GENOMICS
    62. Klockgether, T; Wullner, U; Spauschus, A; Evert, B
      The molecular biology of the autosomal-dominant cerebellar ataxias

      MOVEMENT DISORDERS
    63. Bhatia, KP; Griggs, RC; Ptacek, LJ
      Episodic movement disorders as channelopathies

      MOVEMENT DISORDERS
    64. Chiang, CE; Roden, DM
      The Long QT Syndromes: Genetic basis and clinical implications

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    65. Hattori, H; Fujii, T; Nigami, H; Higuchi, Y; Tsuji, M; Hamada, Y
      Co-segregation of benign infantile convulsions and paroxysmal kinesigenic choreoathetosis

      BRAIN & DEVELOPMENT
    66. Hirose, S; Zenri, F; Akiyoshi, H; Fukuma, G; Iwata, H; Inoue, T; Yonetani, M; Tsutsumi, M; Muranaka, H; Kurokawa, T; Hanai, T; Wada, K; Kaneko, S; Mitsudome, A
      A novel mutation of KCNQ3 (c.925T -> C) in a Japanese family with benign familial neonatal convulsions

      ANNALS OF NEUROLOGY
    67. Bianchi, L; Priori, SG; Napolitano, C; Surewicz, KA; Dennis, AT; Memmi, M; Schwartz, PJ; Brown, AM
      Mechanisms of I-Ks suppression in LQT1 mutants

      AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
    68. Gardiner, RM
      Impact of our understanding of the genetic aetiology of epilepsy

      JOURNAL OF NEUROLOGY
    69. Schulze-Bahr, E; Haverkamp, W; Borggrefe, M; Wedekind, H; Monnig, G; Mergenthaler, J; Assmann, G; Funke, H; Breithardt, G
      Molecular genetics of arrhythmias - a new paradigm

      ZEITSCHRIFT FUR KARDIOLOGIE
    70. Vatta, M; Li, H; Towbin, JA
      Molecular biology of arrhythmic syndromes

      CURRENT OPINION IN CARDIOLOGY
    71. LaPlante, JM; O'Rourke, F; Lu, XH; Fein, A; Olsen, A; Feinstein, MB
      Cloning of human Ca2+ homoeostasis endoplasmic reticulum protein (CHERP): regulated expression of antisense cDNA depletes CHERP, inhibits intracellular Ca2+ mobilization and decreases cell proliferation

      BIOCHEMICAL JOURNAL
    72. Lee, WL; Biervert, C; Hallmann, K; Tay, A; Dean, JCS; Steinlein, OK
      A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family

      NEUROPEDIATRICS
    73. Li, H; Fuentes-Garcia, J; Towbin, JA
      Current concepts in long QT syndrome

      PEDIATRIC CARDIOLOGY
    74. Roberts, R; Brugada, R
      Genetic aspects of arrhythmias

      AMERICAN JOURNAL OF MEDICAL GENETICS
    75. Riley, BP; McGuffin, P
      Linkage and associated studies of schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    76. Vincent, JB; Paterson, AD; Strong, E; Petronis, A; Kennedy, JL
      The unstable trinucleotide repeat story of major psychosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    77. Towbin, JA; Vatta, M
      The genetics of cardiac arrhythmias

      PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY
    78. Moulard, B; Crespel, A; Malafosse, A; Baldy-Moulinier, M
      Recent insights about genetics of human idiopathic epilepsies and febrilesseizures

      REVUE NEUROLOGIQUE
    79. Berkovic, SF
      Familial epilepsies: Quality of life issues in genetic research

      NEUROLOGY
    80. Swoboda, KJ; Soong, BW; McKenna, C; Brunt, ERP; Litt, M; Bale, JF; Ashizawa, T; Bennett, LB; Bowcock, AM; Roach, ES; Gerson, D; Matsuura, T; Heydemann, PT; Nespeca, MP; Jankovic, J; Leppert, M; Ptacek, LJ
      Paroxysmal kinesigenic dyskinesia and infantile convulsions - Clinical andlinkage studies

      NEUROLOGY
    81. Gambardella, A; Annesi, G; De Fusco, M; Patrignani, A; Aguglia, U; Annesi, F; Pasqua, AA; Spadafora, P; Oliveri, RL; Valentino, P; Zappia, M; Ballabio, A; Casari, G; Quattrone, A
      A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps tochromosome 1

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

      NEUROLOGY
    83. Steinlein, OK
      Benign familial neonatal convulsions molecular pathology

      NERVENARZT
    84. Lees-Miller, JP; Duan, YJ; Teng, GQ; Duff, HJ
      Molecular determinant of high-affinity dofetilide binding to HERG1 expressed in Xenopus oocytes: Involvement of S6 sites

      MOLECULAR PHARMACOLOGY
    85. Wigmore, MA; Lacey, MG
      Kv3-like persistent, outwardly rectifying, Cs+-permeable, K+ current in raf subthalamic nucleus neurones

      JOURNAL OF PHYSIOLOGY-LONDON
    86. Watanabe, H; Nagata, E; Kosakai, A; Nakamura, M; Yokoyama, M; Tanaka, K; Sasai, H
      Disruption of the epilepsy KCNQ2 gene results in neural hyperexcitability

      JOURNAL OF NEUROCHEMISTRY
    87. Kitada, K; Akimitsu, T; Shigematsu, Y; Kondo, A; Maihara, T; Yokoi, N; Kuramoto, T; Sasa, M; Serikawa, T
      Accumulation of N-acetyl-L-aspartate in the brain of the tremor rat, a mutant exhibiting absence-like seizure and spongiform degeneration in the central nervous system

      JOURNAL OF NEUROCHEMISTRY
    88. Towbin, JA; Vatta, M; Li, H
      Genetics of Brugada, long QT, and arrhythmogenic right ventricular dysplasia syndromes

      JOURNAL OF ELECTROCARDIOLOGY
    89. Lee, MP; Ravenel, JD; Hu, RJ; Lustig, LR; Tomaselli, G; Berger, RD; Brandenburg, SA; Litzi, TJ; Bunton, TE; Limb, C; Francis, H; Gorelikow, M; Gu, H; Washington, K; Argani, P; Goldenring, JR; Coffey, RJ; Feinberg, AP
      Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice

      JOURNAL OF CLINICAL INVESTIGATION
    90. Steinlein, OK
      Neuronal nicotinic receptors in human epilepsy

      EUROPEAN JOURNAL OF PHARMACOLOGY
    91. Maihara, T; Noda, A; Yamazoe, H; Voigt, B; Kitada, K; Serikawa, T
      Chromosomal mapping of genes for epilepsy in NER: A rat strain with tonic-clonic seizures

      EPILEPSIA
    92. Larsen, LA; Svendsen, IH; Jensen, AM; Kanters, JK; Andersen, PS; Moller, M; Sorensen, SA; Sandoe, E; Jacobsen, JR; Vuust, J; Christiansen, M
      Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2

      CLINICAL GENETICS
    93. Chouabe, C; Neyroud, N; Richard, P; Denjoy, I; Hainque, B; Romey, G; Drici, MD; Guicheney, P; Barhanin, J
      Novel mutations in KvLQT1 that affect I-ks activation through interactionswith Isk

      CARDIOVASCULAR RESEARCH
    94. Wakana, S; Sugaya, E; Naramoto, F; Yokote, N; Maruyama, C; Jin, W; Ohguchi, H; Tsuda, T; Sugaya, A; Kajiwara, K
      Gene mapping of SEZ group genes and determination of pentylenetetrazol susceptible quantitative trait loci in the mouse chromosome

      BRAIN RESEARCH
    95. Robinson, R; Gardiner, M
      Genetics of childhood epilepsy

      ARCHIVES OF DISEASE IN CHILDHOOD
    96. Zara, F; Gennaro, E; Stabile, M; Carbone, I; Malacarne, M; Majello, L; Santangelo, R; de Falco, FA; Bricarelli, FD
      Mapping of a locus for a familial autosomal recessive idiopathic myoclonicepilepsy of infancy to chromosome 16p13

      AMERICAN JOURNAL OF HUMAN GENETICS
    97. Ali, RHH; Zareba, W; Moss, AJ; Schwartz, PJ; Benhorin, J; Vincent, GM; Locati, EH; Priori, S; Napolitano, C; Towbin, JA; Hall, WJ; Robinson, JL; Andrews, ML; Zhang, L; Timothy, K; Medina, A
      Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with the long QT syndrome

      AMERICAN JOURNAL OF CARDIOLOGY
    98. Steinlein, OK
      Strategies to identify genes contributing to epilepsy in man

      ACTA NEUROLOGICA SCANDINAVICA
    99. Kors, EE; Haan, J; Ferrari, MD
      Genetics of primary headaches

      CURRENT OPINION IN NEUROLOGY
    100. Singh, R; Macdonell, RAL; Scheffer, IE; Crossland, KM; Berkovic, SF
      Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms

      EPILEPTIC DISORDERS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/10/20 alle ore 07:13:41