162 related articles for article (PubMed ID: 28609135)
1. Primary familial brain calcifications linked with a novel SLC20A2 gene mutation in a Chinese family.
Mi TM; Mao W; Cai YN; Yang CX; Wang CD; Xu EH; Zhang H; Chan P
J Neurogenet; 2017 Sep; 31(3):149-152. PubMed ID: 28609135
[TBL] [Abstract][Full Text] [Related]
2. Primary familial brain calcification in a Norwegian family, caused by a novel SLC20A2 gene mutation.
Røsby O; Legati A; Coppola G
J Neurol; 2016 Mar; 263(3):594-6. PubMed ID: 26860091
[No Abstract] [Full Text] [Related]
3. A splice site mutation causing exon 6 skipping in SLC20A2 gene in a primary familial brain calcification family.
Huang YT; Zhang LH; Li MF; Cheng L; Zou GY; Zhou HH
Brain Res Bull; 2019 Aug; 150():261-265. PubMed ID: 30634018
[TBL] [Abstract][Full Text] [Related]
4. SLC20A2-related primary familial brain calcification with purely acute psychiatric symptoms: a case report.
Bu W; Hou L; Zhu M; Zhang R; Zhang X; Zhang X; Tang J; Liu X
BMC Neurol; 2022 Jul; 22(1):265. PubMed ID: 35850697
[TBL] [Abstract][Full Text] [Related]
5. A SLC20A2 mutation identified in an asymptomatic patient with brain calcification.
Gagliardi M; Morelli M; Iannello G; Colica C; Annesi G; Quattrone A
J Neurol Sci; 2017 Jan; 372():70-72. PubMed ID: 28017251
[No Abstract] [Full Text] [Related]
6. Clinical and radiological diversity in genetically confirmed primary familial brain calcification.
Koyama S; Sato H; Kobayashi R; Kawakatsu S; Kurimura M; Wada M; Kawanami T; Kato T
Sci Rep; 2017 Sep; 7(1):12046. PubMed ID: 28935882
[TBL] [Abstract][Full Text] [Related]
7. [Clinical features of familial idiopathic basal ganglia calcification caused by a novel mutation in the SLC20A2 gene].
Zhu M; Fang C; Li X; Zhou M; Wan H; Hong D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb; 32(1):64-8. PubMed ID: 25636102
[TBL] [Abstract][Full Text] [Related]
8. Novel SLC20A2 mutation in a Japanese pedigree with primary familial brain calcification.
Kuroi Y; Akagawa H; Yoneyama T; Kikuchi A; Maegawa T; Onda H; Kasuya H
J Neurol Sci; 2019 Apr; 399():183-185. PubMed ID: 30826713
[No Abstract] [Full Text] [Related]
9. Primary familial brain calcification with a novel SLC20A2 mutation: Analysis of PiT-2 expression and localization.
Taglia I; Formichi P; Battisti C; Peppoloni G; Barghigiani M; Tessa A; Federico A
J Cell Physiol; 2018 Mar; 233(3):2324-2331. PubMed ID: 28722801
[TBL] [Abstract][Full Text] [Related]
10. Update and Mutational Analysis of SLC20A2: A Major Cause of Primary Familial Brain Calcification.
Lemos RR; Ramos EM; Legati A; Nicolas G; Jenkinson EM; Livingston JH; Crow YJ; Campion D; Coppola G; Oliveira JR
Hum Mutat; 2015 May; 36(5):489-95. PubMed ID: 25726928
[TBL] [Abstract][Full Text] [Related]
11. Association between a novel mutation in SLC20A2 and familial idiopathic basal ganglia calcification.
Zhang Y; Guo X; Wu A
PLoS One; 2013; 8(2):e57060. PubMed ID: 23437308
[TBL] [Abstract][Full Text] [Related]
12. Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.
Chen WJ; Yao XP; Zhang QJ; Ni W; He J; Li HF; Liu XY; Zhao GX; Murong SX; Wang N; Wu ZY
Gene; 2013 Oct; 529(1):159-62. PubMed ID: 23939468
[TBL] [Abstract][Full Text] [Related]
13. SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia.
Baker M; Strongosky AJ; Sanchez-Contreras MY; Yang S; Ferguson W; Calne DB; Calne S; Stoessl AJ; Allanson JE; Broderick DF; Hutton ML; Dickson DW; Ross OA; Wszolek ZK; Rademakers R
Neurogenetics; 2014 Mar; 15(1):23-30. PubMed ID: 24135862
[TBL] [Abstract][Full Text] [Related]
14. Primary familial brain calcification: Genetic analysis and clinical spectrum.
Taglia I; Mignarri A; Olgiati S; Menci E; Petrocelli PL; Breedveld GJ; Scaglione C; Martinelli P; Federico A; Bonifati V; Dotti MT
Mov Disord; 2014 Nov; 29(13):1691-5. PubMed ID: 25284758
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of MYORG mutations as a novel cause of primary familial brain calcification.
Chen Y; Fu F; Chen S; Cen Z; Tang H; Huang J; Xie F; Zheng X; Yang D; Wang H; Huang X; Zhang Y; Zhou Y; Liu JY; Luo W
Mov Disord; 2019 Feb; 34(2):291-297. PubMed ID: 30589467
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification.
Guo XX; Zou XH; Wang C; Yao XP; Su HZ; Lai LL; Chen HT; Lai JH; Liu YB; Chen DP; Deng YC; Lin P; Lin HS; Hong BC; Yao QY; Chen XJ; Huang DQ; Fu HX; Peng JD; Niu YF; Zhao YY; Zhu XQ; Lu XP; Lin HL; Li YK; Liu CY; Huang GB; Wang N; Chen WJ
Hum Mutat; 2019 Apr; 40(4):392-403. PubMed ID: 30609140
[TBL] [Abstract][Full Text] [Related]
17. Novel SLC20A2 mutation in primary familial brain calcification with disturbance of sustained phonation and orofacial apraxia.
Nan H; Takaki R; Ichinose Y; Tsuchiya M; Koh K; Hanyu S; Shindo K; Takiyama Y
J Neurol Sci; 2018 Jul; 390():1-3. PubMed ID: 29801865
[No Abstract] [Full Text] [Related]
18. Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2.
Chiriaco C; Novellino F; Salsone M; Gagliardi M; Morelli M; Quattrone A
Neurol Sci; 2018 Feb; 39(2):379-380. PubMed ID: 28936702
[No Abstract] [Full Text] [Related]
19. First report of a de novo mutation at SLC20A2 in a patient with brain calcification.
Ferreira JB; Pimentel L; Keasey MP; Lemos RR; Santos LM; Oliveira MF; Santos S; Jensen N; Teixeira K; Pedersen L; Rocha CR; Dias da Silva MR; Oliveira JR
J Mol Neurosci; 2014 Dec; 54(4):748-51. PubMed ID: 24969325
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan.
Yamada M; Tanaka M; Takagi M; Kobayashi S; Taguchi Y; Takashima S; Tanaka K; Touge T; Hatsuta H; Murayama S; Hayashi Y; Kaneko M; Ishiura H; Mitsui J; Atsuta N; Sobue G; Shimozawa N; Inuzuka T; Tsuji S; Hozumi I
Neurology; 2014 Feb; 82(8):705-12. PubMed ID: 24463626
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
