BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

315 related articles for article (PubMed ID: 10937138)

  • 1. Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
    Singh R; Macdonell RA; Scheffer IE; Crossland KM; Berkovic SF
    Epileptic Disord; 1999 Jun; 1(2):93-9. PubMed ID: 10937138
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins.
    Castiglioni C; López I; Riant F; Bertini E; Terracciano A
    Eur J Paediatr Neurol; 2013 May; 17(3):254-8. PubMed ID: 23182655
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree.
    Cuenca-Leon E; Cormand B; Thomson T; Macaya A
    Neuropediatrics; 2002 Dec; 33(6):288-93. PubMed ID: 12571782
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New family with paroxysmal exercise-induced dystonia and epilepsy.
    Kamm C; Mayer P; Sharma M; Niemann G; Gasser T
    Mov Disord; 2007 Apr; 22(6):873-7. PubMed ID: 17290464
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.
    Terwindt GM; Ophoff RA; Lindhout D; Haan J; Halley DJ; Sandkuijl LA; Brouwer OF; Frants RR; Ferrari MD
    Epilepsia; 1997 Aug; 38(8):915-21. PubMed ID: 9579893
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.
    Costa C; Prontera P; Sarchielli P; Tonelli A; Bassi MT; Cupini LM; Caproni S; Siliquini S; Donti E; Calabresi P
    Cephalalgia; 2014 Jan; 34(1):68-72. PubMed ID: 23918834
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Paroxysmal kinesigenic choreoathetosis: from first discovery in 1892 to genetic linkage with benign familial infantile convulsions.
    Kato N; Sadamatsu M; Kikuchi T; Niikawa N; Fukuyama Y
    Epilepsy Res; 2006 Aug; 70 Suppl 1():S174-84. PubMed ID: 16901678
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome.
    Rochette J; Roll P; Fu YH; Lemoing AG; Royer B; Roubertie A; Berquin P; Motte J; Wong SW; Hunter A; Robaglia-Schlupp A; Ptacek LJ; Szepetowski P
    Epileptic Disord; 2010 Sep; 12(3):199-204. PubMed ID: 20716510
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions.
    van Vliet R; Breedveld G; de Rijk-van Andel J; Brilstra E; Verbeek N; Verschuuren-Bemelmans C; Boon M; Samijn J; Diderich K; van de Laar I; Oostra B; Bonifati V; Maat-Kievit A
    Neurology; 2012 Aug; 79(8):777-84. PubMed ID: 22875091
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic forms of epilepsies and other paroxysmal disorders.
    Olson HE; Poduri A; Pearl PL
    Semin Neurol; 2014 Jul; 34(3):266-79. PubMed ID: 25192505
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial dyskinesia and facial myokymia (FDFM): a novel movement disorder.
    Fernandez M; Raskind W; Wolff J; Matsushita M; Yuen E; Graf W; Lipe H; Bird T
    Ann Neurol; 2001 Apr; 49(4):486-92. PubMed ID: 11310626
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Familial hemiplegic migraine].
    Thomsen LL; Olesen J; Russell MB
    Ugeskr Laeger; 1998 Sep; 160(37):5325-9. PubMed ID: 9748855
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Non-epileptic paroxysmal movement disorders].
    Klein C; Vieregge P
    Nervenarzt; 1998 Aug; 69(8):647-59. PubMed ID: 9757415
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Benign familial and non-familial infantile seizures: a study of 64 patients.
    Caraballo RH; Cersósimo RO; Espeche A; Fejerman N
    Epileptic Disord; 2003 Mar; 5(1):45-9. PubMed ID: 12773296
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy.
    Elliott MA; Peroutka SJ; Welch S; May EF
    Ann Neurol; 1996 Jan; 39(1):100-6. PubMed ID: 8572654
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
    Spacey SD; Valente EM; Wali GM; Warner TT; Jarman PR; Schapira AH; Dixon PH; Davis MB; Bhatia KP; Wood NW
    Mov Disord; 2002 Jul; 17(4):717-25. PubMed ID: 12210861
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetics of infantile seizures with paroxysmal dyskinesia: the infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes.
    Rochette J; Roll P; Szepetowski P
    J Med Genet; 2008 Dec; 45(12):773-9. PubMed ID: 19047496
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.
    Liu XR; Wu M; He N; Meng H; Wen L; Wang JL; Zhang MP; Li WB; Mao X; Qin JM; Li BM; Tang B; Deng YH; Shi YW; Su T; Yi YH; Tang BS; Liao WP
    Genes Brain Behav; 2013 Mar; 12(2):234-40. PubMed ID: 23190448
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
    de Vries B; Stam AH; Kirkpatrick M; Vanmolkot KR; Koenderink JB; van den Heuvel JJ; Stunnenberg B; Goudie D; Shetty J; Jain V; van Vark J; Terwindt GM; Frants RR; Haan J; van den Maagdenberg AM; Ferrari MD
    Epilepsia; 2009 Nov; 50(11):2503-4. PubMed ID: 19874388
    [No Abstract]   [Full Text] [Related]  

  • 20. A review of the genetic relation between migraine and epilepsy.
    Haan J; Terwindt GM; van den Maagdenberg AM; Stam AH; Ferrari MD
    Cephalalgia; 2008 Feb; 28(2):105-13. PubMed ID: 18197881
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.