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.
145 related articles for article (PubMed ID: 32305686)
1. Late-onset KMT2B-related dystonia in an Indian patient with normal cognition, dystonic opisthotonus and lack of oromandibular and laryngeal involvement. Pandey S; Bhattad S; Panda AK; Mahadevan L Parkinsonism Relat Disord; 2020 May; 74():33-35. PubMed ID: 32305686 [No Abstract] [Full Text] [Related]
2. An atypical case of early-onset dystonia with a novel missense variant in KMT2B. Zhou XY; Wu JJ; Sun YM Parkinsonism Relat Disord; 2019 Jun; 63():224-226. PubMed ID: 30253925 [No Abstract] [Full Text] [Related]
3. Generalized dystonia associated with mutation in the histone methyltransferase gene KMT2B (DYT28) and white matter abnormalities. Baizabal-Carvallo JF; Alonso-Juarez M Parkinsonism Relat Disord; 2018 Apr; 49():116-117. PubMed ID: 29396090 [No Abstract] [Full Text] [Related]
4. Early-onset oromandibular-laryngeal dystonia and Charlot gait: New phenotype of DYT-KMT2B. Brás A; Ribeiro JA; Sobral F; Moreira F; Morgadinho A; Januário C Neurology; 2019 May; 92(19):919. PubMed ID: 31061210 [No Abstract] [Full Text] [Related]
5. De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient. Klein C; Baumann H; Olschewski L; Hanssen H; Münchau A; Ferbert A; Brüggemann N; Lohmann K Parkinsonism Relat Disord; 2019 Jul; 64():337-339. PubMed ID: 30935829 [No Abstract] [Full Text] [Related]
6. An inherited KMT2B duplication variant in a Chinese family with dystonia and/or development delay. Dai L; Ding C; Fang F Parkinsonism Relat Disord; 2019 Jun; 63():227-228. PubMed ID: 30196991 [No Abstract] [Full Text] [Related]
7. KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation. Cif L; Demailly D; Lin JP; Barwick KE; Sa M; Abela L; Malhotra S; Chong WK; Steel D; Sanchis-Juan A; Ngoh A; Trump N; Meyer E; Vasques X; Rankin J; Allain MW; Applegate CD; Attaripour Isfahani S; Baleine J; Balint B; Bassetti JA; Baple EL; Bhatia KP; Blanchet C; Burglen L; Cambonie G; Seng EC; Bastaraud SC; Cyprien F; Coubes C; d'Hardemare V; ; Doja A; Dorison N; Doummar D; Dy-Hollins ME; Farrelly E; Fitzpatrick DR; Fearon C; Fieg EL; Fogel BL; Forman EB; Fox RG; ; Gahl WA; Galosi S; Gonzalez V; Graves TD; Gregory A; Hallett M; Hasegawa H; Hayflick SJ; Hamosh A; Hully M; Jansen S; Jeong SY; Krier JB; Krystal S; Kumar KR; Laurencin C; Lee H; Lesca G; François LL; Lynch T; Mahant N; Martinez-Agosto JA; Milesi C; Mills KA; Mondain M; Morales-Briceno H; ; Ostergaard JR; Pal S; Pallais JC; Pavillard F; Perrigault PF; Petersen AK; Polo G; Poulen G; Rinne T; Roujeau T; Rogers C; Roubertie A; Sahagian M; Schaefer E; Selim L; Selway R; Sharma N; Signer R; Soldatos AG; Stevenson DA; Stewart F; Tchan M; ; Verma IC; de Vries BBA; Wilson JL; Wong DA; Zaitoun R; Zhen D; Znaczko A; Dale RC; de Gusmão CM; Friedman J; Fung VSC; King MD; Mohammad SS; Rohena L; Waugh JL; Toro C; Raymond FL; Topf M; Coubes P; Gorman KM; Kurian MA Brain; 2020 Dec; 143(11):3242-3261. PubMed ID: 33150406 [TBL] [Abstract][Full Text] [Related]
8. Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia. Zech M; Boesch S; Maier EM; Borggraefe I; Vill K; Laccone F; Pilshofer V; Ceballos-Baumann A; Alhaddad B; Berutti R; Poewe W; Haack TB; Haslinger B; Strom TM; Winkelmann J Am J Hum Genet; 2016 Dec; 99(6):1377-1387. PubMed ID: 27839873 [TBL] [Abstract][Full Text] [Related]
11. Review of the phenotype of early-onset generalised progressive dystonia due to mutations in KMT2B. Gorman KM; Meyer E; Kurian MA Eur J Paediatr Neurol; 2018 Mar; 22(2):245-256. PubMed ID: 29289525 [TBL] [Abstract][Full Text] [Related]
12. Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile. Ciolfi A; Foroutan A; Capuano A; Pedace L; Travaglini L; Pizzi S; Andreani M; Miele E; Invernizzi F; Reale C; Panteghini C; Iascone M; Niceta M; Gavrilova RH; Schultz-Rogers L; Agolini E; Bedeschi MF; Prontera P; Garibaldi M; Galosi S; Leuzzi V; Soliveri P; Olson RJ; Zorzi GS; Garavaglia BM; Tartaglia M; Sadikovic B Clin Epigenetics; 2021 Aug; 13(1):157. PubMed ID: 34380541 [TBL] [Abstract][Full Text] [Related]
13. Low Voice, Spasmodic Dysphonia, and Hand Dystonia as Clinical Clues for KMT2B-Associated Early-Onset Dystonia. Hackenberg A; Wagner M; Pahnke J; Zeitler P; Boltshauser E Neuropediatrics; 2018 Oct; 49(5):356. PubMed ID: 29913530 [No Abstract] [Full Text] [Related]
14. [KMT2B variants responsible for children dystonia 28: report of two cases]. Dai LF; Ding CH; Fang T; Xie ZH; Liu TH; Zhang WH; Wang XH; Ren XT; Liu M; Tian XJ; Wu HS; Fang F Zhonghua Er Ke Za Zhi; 2019 Jul; 57(7):564-566. PubMed ID: 31269560 [TBL] [Abstract][Full Text] [Related]
15. A Novel Mutation in Padmanabha H; Awati AM; Thomas K; K Sarma GR Neurol India; 2021; 69(5):1400-1401. PubMed ID: 34747823 [TBL] [Abstract][Full Text] [Related]
16. Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study. Carecchio M; Invernizzi F; Gonzàlez-Latapi P; Panteghini C; Zorzi G; Romito L; Leuzzi V; Galosi S; Reale C; Zibordi F; Joseph AP; Topf M; Piano C; Bentivoglio AR; Girotti F; Morana P; Morana B; Kurian MA; Garavaglia B; Mencacci NE; Lubbe SJ; Nardocci N Mov Disord; 2019 Oct; 34(10):1516-1527. PubMed ID: 31216378 [TBL] [Abstract][Full Text] [Related]
17. A New Pathologic Owczarzak LR; Hogan KE; Dineen RT; Gill CE; Li MH Tremor Other Hyperkinet Mov (N Y); 2022; 12():7. PubMed ID: 35415007 [TBL] [Abstract][Full Text] [Related]
18. Failure to thrive - an overlooked manifestation of KMT2B-related dystonia: a case presentation. Ng A; Galosi S; Salz L; Wong T; Schwager C; Amudhavalli S; Gelineau-Morel R; Chowdhury S; ; Friedman J BMC Neurol; 2020 Jun; 20(1):246. PubMed ID: 32546208 [TBL] [Abstract][Full Text] [Related]