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 *

235 related articles for article (PubMed ID: 22752065)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients.
    Huang XJ; Wang T; Wang JL; Liu XL; Che XQ; Li J; Mao X; Zhang M; Bi GH; Wu L; Zhang Y; Wang JY; Shen JY; Tang BS; Cao L; Chen SD
    Neurology; 2015 Nov; 85(18):1546-53. PubMed ID: 26446061
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Phenotypic overlap among paroxysmal dyskinesia subtypes: Lesson from a family with PRRT2 gene mutation.
    Wang K; Zhao X; Du Y; He F; Peng G; Luo B
    Brain Dev; 2013 Aug; 35(7):664-6. PubMed ID: 22902309
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. PRRT2 truncated mutations lead to nonsense-mediated mRNA decay in Paroxysmal Kinesigenic Dyskinesia.
    Wu L; Tang HD; Huang XJ; Zheng L; Liu XL; Wang T; Wang JY; Cao L; Chen SD
    Parkinsonism Relat Disord; 2014 Dec; 20(12):1399-404. PubMed ID: 25457817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia].
    Yang X; Zhang Y; Xu X; Yang Z; Wang S; Wu Y; Wu X
    Zhonghua Er Ke Za Zhi; 2015 Aug; 53(8):621-5. PubMed ID: 26717662
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation.
    Fabbri M; Marini C; Bisulli F; Di Vito L; Elia A; Guerrini R; Mei D; Tinuper P
    Epileptic Disord; 2013 Jun; 15(2):123-7. PubMed ID: 23771590
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions.
    Ono S; Yoshiura K; Kinoshita A; Kikuchi T; Nakane Y; Kato N; Sadamatsu M; Konishi T; Nagamitsu S; Matsuura M; Yasuda A; Komine M; Kanai K; Inoue T; Osamura T; Saito K; Hirose S; Koide H; Tomita H; Ozawa H; Niikawa N; Kurotaki N
    J Hum Genet; 2012 May; 57(5):338-41. PubMed ID: 22399141
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.