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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 22870186)

  • 1. PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort.
    Lee YC; Lee MJ; Yu HY; Chen C; Hsu CH; Lin KP; Liao KK; Chang MH; Liao YC; Soong BW
    PLoS One; 2012; 7(8):e38543. PubMed ID: 22870186
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
    Gardiner AR; Bhatia KP; Stamelou M; Dale RC; Kurian MA; Schneider SA; Wali GM; Counihan T; Schapira AH; Spacey SD; Valente EM; Silveira-Moriyama L; Teive HA; Raskin S; Sander JW; Lees A; Warner T; Kullmann DM; Wood NW; Hanna M; Houlden H
    Neurology; 2012 Nov; 79(21):2115-21. PubMed ID: 23077024
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.
    Cloarec R; Bruneau N; Rudolf G; Massacrier A; Salmi M; Bataillard M; Boulay C; Caraballo R; Fejerman N; Genton P; Hirsch E; Hunter A; Lesca G; Motte J; Roubertie A; Sanlaville D; Wong SW; Fu YH; Rochette J; Ptácek LJ; Szepetowski P
    Neurology; 2012 Nov; 79(21):2097-103. PubMed ID: 23077017
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Novel PRRT2 Variant in Chinese Patients Suffering from Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsion.
    Baldi S; Zhu JL; Hu QY; Wang JL; Zhang JB; Zhang SH
    Behav Neurol; 2020; 2020():2097059. PubMed ID: 32509037
    [TBL] [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; 79(8):777-84. PubMed ID: 22875091
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.
    Yang X; Zhang Y; Xu X; Wang S; Yang Z; Wu Y; Liu X; Wu X
    BMC Neurol; 2013 Dec; 13():209. PubMed ID: 24370076
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases.
    Wang JL; Mao X; Hu ZM; Li JD; Li N; Guo JF; Jiang H; Shen L; Li J; Shi YT; Xia K; Liu JY; Liao WP; Tang BS
    Neurosci Lett; 2013 Sep; 552():40-5. PubMed ID: 23896529
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population.
    Méneret A; Grabli D; Depienne C; Gaudebout C; Picard F; Dürr A; Lagroua I; Bouteiller D; Mignot C; Doummar D; Anheim M; Tranchant C; Burbaud P; Jedynak CP; Gras D; Steschenko D; Devos D; Billette de Villemeur T; Vidailhet M; Brice A; Roze E
    Neurology; 2012 Jul; 79(2):170-4. PubMed ID: 22744660
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PRRT2-related disorders: further PKD and ICCA cases and review of the literature.
    Becker F; Schubert J; Striano P; Anttonen AK; Liukkonen E; Gaily E; Gerloff C; Müller S; Heußinger N; Kellinghaus C; Robbiano A; Polvi A; Zittel S; von Oertzen TJ; Rostasy K; Schöls L; Warner T; Münchau A; Lehesjoki AE; Zara F; Lerche H; Weber YG
    J Neurol; 2013 May; 260(5):1234-44. PubMed ID: 23299620
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia cases.
    Mao CY; Shi CH; Song B; Wu J; Ji Y; Qin J; Li YS; Wang JJ; Shang DD; Sun SL; Xu YM
    J Neurol Sci; 2014 May; 340(1-2):91-3. PubMed ID: 24661410
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Re-evaluation of PRRT2 mutations in paroxysmal disorders.
    Guo XN; Lu Q; Zhou XQ; Liu Q; Zhang X; Cui LY
    J Neurol; 2014 May; 261(5):951-3. PubMed ID: 24609974
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression.
    Liu Q; Qi Z; Wan XH; Li JY; Shi L; Lu Q; Zhou XQ; Qiao L; Wu LW; Liu XQ; Yang W; Liu Y; Cui LY; Zhang X
    J Med Genet; 2012 Feb; 49(2):79-82. PubMed ID: 22209761
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia.
    Okumura A; Shimojima K; Kurahashi H; Numoto S; Shimada S; Ishii A; Ohmori I; Takahashi S; Awaya T; Kubota T; Sakakibara T; Ishihara N; Hattori A; Torisu H; Tohyama J; Inoue T; Haibara A; Nishida T; Yuhara Y; Miya K; Tanaka R; Hirose S; Yamamoto T
    Seizure; 2019 Oct; 71():1-5. PubMed ID: 31154286
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia.
    Groffen AJ; Klapwijk T; van Rootselaar AF; Groen JL; Tijssen MA
    J Neurol; 2013 Jan; 260(1):93-9. PubMed ID: 22752065
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients.
    Wang HX; Li HF; Liu GL; Wen XD; Wu ZY
    Chin Med J (Engl); 2016 May; 129(9):1017-21. PubMed ID: 27098784
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures.
    Zhao G; Liu X; Zhang Q; Wang K
    Int J Neurosci; 2018 Aug; 128(8):751-760. PubMed ID: 29285950
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 138(Pt 12):3567-80. PubMed ID: 26598494
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.