BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 33681653)

  • 61. White matter alterations in familial cortical myoclonic tremor with epilepsy type 1.
    Wang B; Wang H; Cen Z; Yuan J; Yang D; Chen X; Xie F; Wang L; Wu S; Ouyang Z; Zang YF; Luo W
    Epilepsia; 2022 May; 63(5):1093-1103. PubMed ID: 35247271
    [TBL] [Abstract][Full Text] [Related]  

  • 62. FAME 3: a novel form of progressive myoclonus and epilepsy.
    Carr JA; van der Walt PE; Nakayama J; Fu YH; Corfield V; Brink P; Ptacek L
    Neurology; 2007 Apr; 68(17):1382-9. PubMed ID: 17452583
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Coherence analysis differentiates between cortical myoclonic tremor and essential tremor.
    van Rootselaar AF; Maurits NM; Koelman JH; van der Hoeven JH; Bour LJ; Leenders KL; Brown P; Tijssen MA
    Mov Disord; 2006 Feb; 21(2):215-22. PubMed ID: 16200541
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype.
    Striano P; Zara F; Striano S
    Acta Neurol Scand; 2005 Apr; 111(4):211-7. PubMed ID: 15740570
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2.
    Guerrini R; Bonanni P; Patrignani A; Brown P; Parmeggiani L; Grosse P; Brovedani P; Moro F; Aridon P; Carrozzo R; Casari G
    Brain; 2001 Dec; 124(Pt 12):2459-75. PubMed ID: 11701600
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disability.
    Poulat AL; Ville D; de Bellescize J; André-Obadia N; Cacciagli P; Milh M; Villard L; Lesca G
    Epilepsy Res; 2015 Mar; 111():72-7. PubMed ID: 25769375
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Familial cortical myoclonic tremor as a unique form of cortical reflex myoclonus.
    Terada K; Ikeda A; Mima T; Kimura M; Nagahama Y; Kamioka Y; Murone I; Kimura J; Shibasaki H
    Mov Disord; 1997 May; 12(3):370-7. PubMed ID: 9159732
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitability.
    Depienne C; van den Maagdenberg AMJM; Kühnel T; Ishiura H; Corbett MA; Tsuji S
    Epilepsia; 2023 Jun; 64 Suppl 1():S31-S38. PubMed ID: 36622139
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Epilepsy and electroencephalogram evolution in YWHAG gene mutation: A new phenotype and review of the literature.
    Stern T; Orenstein N; Fellner A; Lev-El Halabi N; Shuldiner AR; Gonzaga-Jauregui C; Lidzbarsky G; Basel-Salmon L; Goldberg-Stern H
    Am J Med Genet A; 2021 Mar; 185(3):901-908. PubMed ID: 33393734
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Clinical anticipation in Japanese families of benign adult familial myoclonus epilepsy.
    Hitomi T; Kondo T; Kobayashi K; Matsumoto R; Takahashi R; Ikeda A
    Epilepsia; 2012 Feb; 53(2):e33-6. PubMed ID: 22150818
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy.
    Coppola A; Santulli L; Del Gaudio L; Minetti C; Striano S; Zara F; Striano P
    Epilepsia; 2011 Jul; 52(7):1245-50. PubMed ID: 21426326
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Nationwide survey in Japan endorsed diagnostic criteria of benign adult familial myoclonus epilepsy.
    Kobayashi K; Hitomi T; Matsumoto R; Watanabe M; Takahashi R; Ikeda A
    Seizure; 2018 Oct; 61():14-22. PubMed ID: 30053653
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Cerebellar Atrophy in Cortical Myoclonic Tremor and Not in Hereditary Essential Tremor-a Voxel-Based Morphometry Study.
    Buijink AW; Broersma M; van der Stouwe AM; Sharifi S; Tijssen MA; Speelman JD; Maurits NM; van Rootselaar AF
    Cerebellum; 2016 Dec; 15(6):696-704. PubMed ID: 26519379
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Familial cortical tremor with epilepsy: an under-recognized familial tremor.
    Okuma Y; Shimo Y; Shimura H; Hatori K; Hattori T; Tanaka S; Kondo T; Mizuno Y
    Clin Neurol Neurosurg; 1998 Mar; 100(1):75-8. PubMed ID: 9637212
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Current treatment options for familial adult myoclonus epilepsy.
    Coppola A; Dubbioso R; Cuccurullo C; Licchetta L; Carreno M; Hirsch E; Bilo L
    Epilepsia; 2023 Jun; 64 Suppl 1():S58-S63. PubMed ID: 36947106
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Electroencephalogram and clinical focalities in juvenile myoclonic epilepsy.
    So GM; Thiele EA; Sanger T; Schmid R; Riviello JJ
    J Child Neurol; 1998 Nov; 13(11):541-5. PubMed ID: 9853646
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Familial infantile myoclonic epilepsy: clinical features in a large kindred with autosomal recessive inheritance.
    de Falco FA; Majello L; Santangelo R; Stabile M; Bricarelli FD; Zara F
    Epilepsia; 2001 Dec; 42(12):1541-8. PubMed ID: 11879364
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Familial benign myoclonus epilepsy of adult onset: a previously unrecognized myoclonic disorder.
    Okino S
    J Neurol Sci; 1997 Jan; 145(1):113-8. PubMed ID: 9073039
    [TBL] [Abstract][Full Text] [Related]  

  • 79. SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features.
    Selmer KK; Lund C; Brandal K; Undlien DE; Brodtkorb E
    Epilepsy Behav; 2009 Nov; 16(3):555-7. PubMed ID: 19782004
    [TBL] [Abstract][Full Text] [Related]  

  • 80. [Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy].
    Zhang YH; Sun HH; Liu XY; Ma XW; Yang ZX; Xiong H; Qin J; Lin Q; Wu XR
    Zhonghua Er Ke Za Zhi; 2008 Oct; 46(10):769-73. PubMed ID: 19099883
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.