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 *

161 related articles for article (PubMed ID: 35572931)

  • 1. Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia.
    Shi Y; Wang A; Chen B; Wang X; Niu S; Li W; Li S; Zhang Z
    Front Neurol; 2022; 13():872927. PubMed ID: 35572931
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Clinical and Genetic Spectrum in a Large Cohort of Hereditary Spastic Paraplegia.
    Cao Y; Zheng H; Zhu Z; Yao L; Tian W; Cao L
    Mov Disord; 2024 Apr; 39(4):651-662. PubMed ID: 38291924
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients.
    Lu C; Li LX; Dong HL; Wei Q; Liu ZJ; Ni W; Gitler AD; Wu ZY
    J Mol Med (Berl); 2018 Jul; 96(7):701-712. PubMed ID: 29934652
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Hereditary spastic paraplegia: new insights into clinical variability and spasticity-ataxia phenotype, and novel mutations.
    Sahin I; Saat H
    Acta Neurol Belg; 2022 Dec; 122(6):1529-1535. PubMed ID: 34420199
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Expansion of the mutation and phenotypic spectrum of hereditary spastic paraplegia.
    Xing F; Du J
    Neurol Sci; 2022 Aug; 43(8):4989-4996. PubMed ID: 35348942
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic origin of patients having spastic paraplegia with or without other neurologic manifestations.
    Chen J; Zhao Z; Shen H; Bing Q; Li N; Guo X; Hu J
    BMC Neurol; 2022 May; 22(1):180. PubMed ID: 35578252
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic and clinical features of pediatric-onset hereditary spastic paraplegia: a single-center study in Japan.
    Ikeda A; Kumaki T; Tsuyusaki Y; Tsuji M; Enomoto Y; Fujita A; Saitsu H; Matsumoto N; Kurosawa K; Goto T
    Front Neurol; 2023; 14():1085228. PubMed ID: 37251230
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Genetic, structural and clinical analysis of spastic paraplegia 4.
    Varghaei P; Estiar MA; Ashtiani S; Veyron S; Mufti K; Leveille E; Yu E; Spiegelman D; Rioux MF; Yoon G; Tarnopolsky M; Boycott KM; Dupre N; Suchowersky O; Trempe JF; Rouleau GA; Gan-Or Z
    Parkinsonism Relat Disord; 2022 May; 98():62-69. PubMed ID: 35487127
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias.
    Wan N; Chen Z; Wan L; Yuan H; Tang Z; Liu M; Peng Y; Peng L; Lei L; Xie Y; Deng Q; Wang S; Wang C; Peng H; Hou X; Shi Y; Long Z; Qiu R; Xia K; Tang B; Jiang H
    Parkinsonism Relat Disord; 2021 Aug; 89():120-127. PubMed ID: 34284285
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese.
    Dong Y; Li XY; Wang XL; Xu F; Wang ZJ; Song Y; Li Q; Lin R; Wang C
    Neurosci Lett; 2021 Sep; 761():136108. PubMed ID: 34256108
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary spastic paraparesis: The real-world experience from a Neurogenetics outpatient clinic.
    Cunha IA; Ribeiro JA; Santos MC
    Eur J Med Genet; 2022 Mar; 65(3):104430. PubMed ID: 35065294
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.
    Finsterer J; Löscher W; Quasthoff S; Wanschitz J; Auer-Grumbach M; Stevanin G
    J Neurol Sci; 2012 Jul; 318(1-2):1-18. PubMed ID: 22554690
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.
    Pensato V; Castellotti B; Gellera C; Pareyson D; Ciano C; Nanetti L; Salsano E; Piscosquito G; Sarto E; Eoli M; Moroni I; Soliveri P; Lamperti E; Chiapparini L; Di Bella D; Taroni F; Mariotti C
    Brain; 2014 Jul; 137(Pt 7):1907-20. PubMed ID: 24833714
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.