BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 21764335)

  • 21. Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes.
    Torisu H; Watanabe K; Shimojima K; Sugawara M; Sanefuji M; Ishizaki Y; Sakai Y; Yamashita H; Yamamoto T; Hara T
    Brain Dev; 2014 Apr; 36(4):342-5. PubMed ID: 23768507
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel SCN2A mutation in family with benign familial infantile seizures.
    Striano P; Bordo L; Lispi ML; Specchio N; Minetti C; Vigevano F; Zara F
    Epilepsia; 2006 Jan; 47(1):218-20. PubMed ID: 16417554
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 79(21):2109-14. PubMed ID: 23077026
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.
    Steinlein OK; Villain M; Korenke C
    Seizure; 2012 Nov; 21(9):740-2. PubMed ID: 22877996
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Benign familial infantile convulsions: phenotypic variability in a family.
    Demir E; Turanii G; Yalntzoglu D; Topcu M
    J Child Neurol; 2005 Jun; 20(6):535-8. PubMed ID: 15996407
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Spectrum of epilepsy in terminal 1p36 deletion syndrome.
    Bahi-Buisson N; Guttierrez-Delicado E; Soufflet C; Rio M; Daire VC; Lacombe D; Héron D; Verloes A; Zuberi S; Burglen L; Afenjar A; Moutard ML; Edery P; Novelli A; Bernardini L; Dulac O; Nabbout R; Plouin P; Battaglia A
    Epilepsia; 2008 Mar; 49(3):509-15. PubMed ID: 18031548
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. [Benign infantile familial convulsions].
    Caraballo R; Cersósimo R; Galicchio S; Fejerman N
    Rev Neurol; 1997 May; 25(141):682-4. PubMed ID: 9206591
    [TBL] [Abstract][Full Text] [Related]  

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

  • 31. Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine.
    Dale RC; Gardiner A; Antony J; Houlden H
    Dev Med Child Neurol; 2012 Oct; 54(10):958-60. PubMed ID: 22845787
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
    Gardella E; Becker F; Møller RS; Schubert J; Lemke JR; Larsen LH; Eiberg H; Nothnagel M; Thiele H; Altmüller J; Syrbe S; Merkenschlager A; Bast T; Steinhoff B; Nürnberg P; Mang Y; Bakke Møller L; Gellert P; Heron SE; Dibbens LM; Weckhuysen S; Dahl HA; Biskup S; Tommerup N; Hjalgrim H; Lerche H; Beniczky S; Weber YG
    Ann Neurol; 2016 Mar; 79(3):428-36. PubMed ID: 26677014
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
    Piver MS
    Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Unusual variability of PRRT2 linked phenotypes within a family.
    Brueckner F; Kohl B; Puest B; Gassner S; Osseforth J; Lindenau M; Stodieck S; Biskup S; Lohmann E
    Eur J Paediatr Neurol; 2014 Jul; 18(4):540-2. PubMed ID: 24755245
    [TBL] [Abstract][Full Text] [Related]  

  • 36. PRRT2 mutation causes benign familial infantile convulsions.
    de Vries B; Callenbach PM; Kamphorst JT; Weller CM; Koelewijn SC; ten Houten R; de Coo IF; Brouwer OF; van den Maagdenberg AM
    Neurology; 2012 Nov; 79(21):2154-5. PubMed ID: 23077019
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies.
    Swoboda KJ; Soong B; McKenna C; Brunt ER; Litt M; Bale JF; Ashizawa T; Bennett LB; Bowcock AM; Roach ES; Gerson D; Matsuura T; Heydemann PT; Nespeca MP; Jankovic J; Leppert M; Ptácek LJ
    Neurology; 2000 Jul; 55(2):224-30. PubMed ID: 10908896
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Electroclinical features of benign infantile seizures with mild gastroenteritis.
    Saadeldin IY
    Epileptic Disord; 2011 Mar; 13(1):8-17. PubMed ID: 21393100
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin.
    van Strien TW; van Rootselaar AF; Hilgevoord AA; Linssen WH; Groffen AJ; Tijssen MA
    Parkinsonism Relat Disord; 2012 Jun; 18(5):645-8. PubMed ID: 22464846
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.
    Labate A; Tarantino P; Palamara G; Gagliardi M; Cavalcanti F; Ferlazzo E; Sturniolo M; Incorpora G; Annesi G; Aguglia U; Gambardella A
    Epilepsy Res; 2013 May; 104(3):280-4. PubMed ID: 23352743
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.