These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

191 related items for PubMed ID: 10766892

  • 1. A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.
    Münchau A, Valente EM, Shahidi GA, Eunson LH, Hanna MG, Quinn NP, Schapira AH, Wood NW, Bhatia KP.
    J Neurol Neurosurg Psychiatry; 2000 May; 68(5):609-14. PubMed ID: 10766892
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. New family with paroxysmal exercise-induced dystonia and epilepsy.
    Kamm C, Mayer P, Sharma M, Niemann G, Gasser T.
    Mov Disord; 2007 Apr 30; 22(6):873-7. PubMed ID: 17290464
    [Abstract] [Full Text] [Related]

  • 4. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.
    Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, Verier A, Echenne B, Lopez de Munain A, Bousser MG, Tournier-Lasserve E.
    Ann Neurol; 1997 Dec 30; 42(6):885-90. PubMed ID: 9403481
    [Abstract] [Full Text] [Related]

  • 5. 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 21; 79(8):777-84. PubMed ID: 22875091
    [Abstract] [Full Text] [Related]

  • 6. Idiopathic epilepsy and paroxysmal dyskinesia.
    Guerrini R.
    Epilepsia; 2001 Aug 21; 42 Suppl 3():36-41. PubMed ID: 11520321
    [Abstract] [Full Text] [Related]

  • 7. The clinical and genetic heterogeneity of paroxysmal dyskinesias.
    Gardiner AR, Jaffer F, Dale RC, Labrum R, Erro R, Meyer E, Xiromerisiou G, Stamelou M, Walker M, Kullmann D, Warner T, Jarman P, Hanna M, Kurian MA, Bhatia KP, Houlden H.
    Brain; 2015 Dec 21; 138(Pt 12):3567-80. PubMed ID: 26598494
    [Abstract] [Full Text] [Related]

  • 8. Genetic heterogeneity in Italian families with familial hemiplegic migraine.
    Carrera P, Piatti M, Stenirri S, Grimaldi LM, Marchioni E, Curcio M, Righetti PG, Ferrari M, Gelfi C.
    Neurology; 1999 Jul 13; 53(1):26-33. PubMed ID: 10408532
    [Abstract] [Full Text] [Related]

  • 9. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
    Ophoff RA, Terwindt GM, Vergouwe MN, Frants RR, Ferrari MD.
    Neurologia; 1997 Dec 13; 12 Suppl 5():31-7. PubMed ID: 9436352
    [Abstract] [Full Text] [Related]

  • 10. Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family.
    Lee WL, Tay A, Ong HT, Goh LM, Monaco AP, Szepetowski P.
    Hum Genet; 1998 Nov 13; 103(5):608-12. PubMed ID: 9860304
    [Abstract] [Full Text] [Related]

  • 11. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy.
    Elliott MA, Peroutka SJ, Welch S, May EF.
    Ann Neurol; 1996 Jan 13; 39(1):100-6. PubMed ID: 8572654
    [Abstract] [Full Text] [Related]

  • 12. Familial (idiopathic) paroxysmal dyskinesias: an update.
    Bhatia KP.
    Semin Neurol; 2001 Jan 13; 21(1):69-74. PubMed ID: 11346027
    [Abstract] [Full Text] [Related]

  • 13. Genetic heterogeneity of familial hemiplegic migraine.
    Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR.
    Genomics; 1994 Jul 01; 22(1):21-6. PubMed ID: 7959770
    [Abstract] [Full Text] [Related]

  • 14. Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.
    Guerrini R, Bonanni P, Nardocci N, Parmeggiani L, Piccirilli M, De Fusco M, Aridon P, Ballabio A, Carrozzo R, Casari G.
    Ann Neurol; 1999 Mar 01; 45(3):344-52. PubMed ID: 10072049
    [Abstract] [Full Text] [Related]

  • 15. Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
    Striano P, Lispi ML, Gennaro E, Madia F, Traverso M, Bordo L, Aridon P, Martinelli Boneschi F, Barone B, dalla Bernardina B, Bianchi A, Capovilla G, De Marco P, Dulac O, Gaggero R, Gambardella A, Nabbout R, Prud'homme JF, Day R, Vanadia F, Vecchi M, Veggiotti P, Vigevano F, Viri M, Minetti C, Zara F.
    Epilepsia; 2006 Jun 01; 47(6):1029-34. PubMed ID: 16822249
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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 01; 33(6):288-93. PubMed ID: 12571782
    [Abstract] [Full Text] [Related]

  • 18. Infantile convulsions and paroxysmal choreoathetosis in a consanguineous family.
    Demir E, Prud'homme JF, Topçu M.
    Pediatr Neurol; 2004 May 01; 30(5):349-53. PubMed ID: 15165638
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.
    Marini C, Conti V, Mei D, Battaglia D, Lettori D, Losito E, Bruccini G, Tortorella G, Guerrini R.
    Neurology; 2012 Nov 20; 79(21):2109-14. PubMed ID: 23077026
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.