311 related articles for article (PubMed ID: 32242913)
1. Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey.
Akçakaya NH; Özeş Ak B; Gonzalez MA; Züchner S; Battaloğlu E; Parman Y
Neurol Neurochir Pol; 2020; 54(2):176-184. PubMed ID: 32242913
[TBL] [Abstract][Full Text] [Related]
2. Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
Elert-Dobkowska E; Stepniak I; Krysa W; Rajkiewicz M; Rakowicz M; Sobanska A; Rudzinska M; Wasielewska A; Pilch J; Kubalska J; Lipczynska-Lojkowska W; Kulczycki J; Kurdziel K; Sikorska A; Beetz C; Zaremba J; Sulek A
J Neurol Sci; 2015 Dec; 359(1-2):35-9. PubMed ID: 26671083
[TBL] [Abstract][Full Text] [Related]
3. The investigation of genetic and clinical features in patients with hereditary spastic paraplegia in central-Southern China.
Wang C; Zhang YJ; Xu CH; Li D; Liu ZJ; Wu Y
Mol Genet Genomic Med; 2021 May; 9(5):e1627. PubMed ID: 33638609
[TBL] [Abstract][Full Text] [Related]
4. Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.
Balicza P; Grosz Z; Gonzalez MA; Bencsik R; Pentelenyi K; Gal A; Varga E; Klivenyi P; Koller J; Züchner S; Molnar JM
J Neurol Sci; 2016 May; 364():116-21. PubMed ID: 27084228
[TBL] [Abstract][Full Text] [Related]
5. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.
Olmez A; Uyanik G; Ozgül RK; Gross C; Cirak S; Elibol B; Anlar B; Winner B; Hehr U; Topaloglu H; Winkler J
Neuropediatrics; 2006 Apr; 37(2):59-66. PubMed ID: 16773502
[TBL] [Abstract][Full Text] [Related]
6. Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia.
Park H; Kang SH; Park S; Kim SY; Seo SH; Lee SJ; Lee JA; Cho SI; Sung JJ; Lee KW; Kim JY; Park SS; Seong MW
J Neurol Sci; 2015 Oct; 357(1-2):167-72. PubMed ID: 26208798
[TBL] [Abstract][Full Text] [Related]
7. Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia.
Lu X; Cen Z; Xie F; Ouyang Z; Zhang B; Zhao G; Luo W
J Neurol Sci; 2014 Dec; 347(1-2):368-71. PubMed ID: 25454648
[TBL] [Abstract][Full Text] [Related]
8. Anticipation Can Be More Common in Hereditary Spastic Paraplegia with
Hashemi SS; Hajati R; Davarzani A; Rohani M; DanaeeFard F; Rahimi Bidgoli MM; Fatehi F; Kariminejad A; Najmabadi H; Nafissi S; Alavi A
Can J Neurol Sci; 2022 Sep; 49(5):651-661. PubMed ID: 34353391
[TBL] [Abstract][Full Text] [Related]
9. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.
Alvarez V; Sánchez-Ferrero E; Beetz C; Díaz M; Alonso B; Corao AI; Gámez J; Esteban J; Gonzalo JF; Pascual-Pascual SI; López de Munain A; Moris G; Ribacoba R; Márquez C; Rosell J; Marín R; García-Barcina MJ; Del Castillo E; Benito C; Coto E;
BMC Neurol; 2010 Oct; 10():89. PubMed ID: 20932283
[TBL] [Abstract][Full Text] [Related]
10. A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings.
Polymeris AA; Tessa A; Anagnostopoulou K; Rubegni A; Galatolo D; Dinopoulos A; Gika AD; Youroukos S; Skouteli E; Santorelli FM; Pons R
J Neurol; 2016 Aug; 263(8):1604-11. PubMed ID: 27260292
[TBL] [Abstract][Full Text] [Related]
11. Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia.
Kim TH; Lee JH; Park YE; Shin JH; Nam TS; Kim HS; Jang HJ; Semenov A; Kim SJ; Kim DS
J Clin Neurol; 2014 Jul; 10(3):257-61. PubMed ID: 25045380
[TBL] [Abstract][Full Text] [Related]
12. Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients.
Erfanian Omidvar M; Torkamandi S; Rezaei S; Alipoor B; Omrani MD; Darvish H; Ghaedi H
J Neurol; 2021 Jun; 268(6):2065-2082. PubMed ID: 31745725
[TBL] [Abstract][Full Text] [Related]
13. Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes.
Elert-Dobkowska E; Stepniak I; Krysa W; Ziora-Jakutowicz K; Rakowicz M; Sobanska A; Pilch J; Antczak-Marach D; Zaremba J; Sulek A
Neurogenetics; 2019 Mar; 20(1):27-38. PubMed ID: 30778698
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
Perić S; Marković V; Candayan A; De Vriendt E; Momčilović N; Savić A; Dragašević-Mišković N; Svetel M; Stević Z; Božović I; Mesaroš Š; Drulović J; Basta I; Petrović I; Tamaš O; Mijajlović M; Novaković I; Sokić D; Jordanova A
Cells; 2022 Sep; 11(18):. PubMed ID: 36139378
[TBL] [Abstract][Full Text] [Related]
15. Exome sequencing identifies novel compound heterozygous mutations in SPG11 that cause autosomal recessive hereditary spastic paraplegia.
Zhao W; Zhu QY; Zhang JT; Liu H; Wang LJ; Chen ZQ; Guan LP; Huang XS; Yang L; Yu SY
J Neurol Sci; 2013 Dec; 335(1-2):112-7. PubMed ID: 24090761
[TBL] [Abstract][Full Text] [Related]
16. A complex form of hereditary spastic paraplegia in three siblings due to somatic mosaicism for a novel SPAST mutation in the mother.
Aulitzky A; Friedrich K; Gläser D; Gastl R; Kubisch C; Ludolph AC; Volk AE
J Neurol Sci; 2014 Dec; 347(1-2):352-5. PubMed ID: 25315759
[TBL] [Abstract][Full Text] [Related]
17. A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum.
Blumkin L; Lerman-Sagie T; Lev D; Yosovich K; Leshinsky-Silver E
J Neurol Sci; 2011 Jun; 305(1-2):67-70. PubMed ID: 21440262
[TBL] [Abstract][Full Text] [Related]
18. Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia.
Kadnikova VA; Rudenskaya GE; Stepanova AA; Sermyagina IG; Ryzhkova OP
Sci Rep; 2019 Oct; 9(1):14412. PubMed ID: 31594988
[TBL] [Abstract][Full Text] [Related]
19. Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia.
McCorquodale DS; Ozomaro U; Huang J; Montenegro G; Kushman A; Citrigno L; Price J; Speziani F; Pericak-Vance MA; Züchner S
Clin Genet; 2011 Jun; 79(6):523-30. PubMed ID: 20718791
[TBL] [Abstract][Full Text] [Related]
20. Mutation analysis of four Chinese families with pure hereditary spastic paraplegia: pseudo- X-linked dominant inheritance and male lethality due to a novel ATL1 mutation.
Zhao N; Sui Y; Li XF; Liu W; Lu YP; Feng WH; Ma C; Wang YW; Bao HX; Huang F; Wang H; Yi DX; Han WT; Jiang M
Genet Mol Res; 2015 Nov; 14(4):14690-7. PubMed ID: 26600529
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]