BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 35331153)

  • 1. An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15.
    Vander Stichele G; Durr A; Yoon G; Schüle R; Blackstone C; Esposito G; Buffel C; Oliveira I; Freitag C; van Rooijen S; Hoffmann S; Thielemans L; Cowling BS
    BMC Neurol; 2022 Mar; 22(1):115. PubMed ID: 35331153
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7.
    Estiar MA; Yu E; Haj Salem I; Ross JP; Mufti K; Akçimen F; Leveille E; Spiegelman D; Ruskey JA; Asayesh F; Dagher A; Yoon G; Tarnopolsky M; Boycott KM; Dupre N; Dion PA; Suchowersky O; Trempe JF; Rouleau GA; Gan-Or Z
    Mov Disord; 2021 Jul; 36(7):1664-1675. PubMed ID: 33598982
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia.
    Battini R; Fogli A; Borghetti D; Michelucci A; Perazza S; Baldinotti F; Conidi ME; Ferreri MI; Simi P; Cioni G
    Eur J Neurol; 2011 Jan; 18(1):150-7. PubMed ID: 20550563
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
    Ruano L; Melo C; Silva MC; Coutinho P
    Neuroepidemiology; 2014; 42(3):174-83. PubMed ID: 24603320
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China.
    Dong EL; Wang C; Wu S; Lu YQ; Lin XH; Su HZ; Zhao M; He J; Ma LX; Wang N; Chen WJ; Lin X
    Mol Neurodegener; 2018 Jul; 13(1):36. PubMed ID: 29980238
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity.
    Boukhris A; Stevanin G; Feki I; Denora P; Elleuch N; Miladi MI; Goizet C; Truchetto J; Belal S; Brice A; Mhiri C
    Clin Genet; 2009 Jun; 75(6):527-36. PubMed ID: 19438933
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Retrospective Review of 18 Patients With Childhood-Onset Hereditary Spastic Paraplegia, Nine With Novel Variants.
    Kilic MA; Yildiz EP; Deniz A; Coskun O; Kurekci F; Avci R; Genc HM; Yesil G; Akbas S; Yesilyurt A; Kara B
    Pediatr Neurol; 2024 Mar; 152():189-195. PubMed ID: 38301322
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.
    Schüle R; Schlipf N; Synofzik M; Klebe S; Klimpe S; Hehr U; Winner B; Lindig T; Dotzer A; Riess O; Winkler J; Schöls L; Bauer P
    J Neurol Neurosurg Psychiatry; 2009 Dec; 80(12):1402-4. PubMed ID: 19917823
    [TBL] [Abstract][Full Text] [Related]  

  • 11. ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis.
    Vantaggiato C; Panzeri E; Castelli M; Citterio A; Arnoldi A; Santorelli FM; Liguori R; Scarlato M; Musumeci O; Toscano A; Clementi E; Bassi MT
    Autophagy; 2019 Jan; 15(1):34-57. PubMed ID: 30081747
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Autosomal dominant spastic paraplegias: a review of 89 families resulting from a portuguese survey.
    Loureiro JL; Brandão E; Ruano L; Brandão AF; Lopes AM; Thieleke-Matos C; Miller-Fleming L; Cruz VT; Barbosa M; Silveira I; Stevanin G; Pinto-Basto J; Sequeiros J; Alonso I; Coutinho P
    JAMA Neurol; 2013 Apr; 70(4):481-7. PubMed ID: 23400676
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [AAA ATPases and hereditary spastic paraplegia].
    Wang YG; Shen L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):298-301. PubMed ID: 19504443
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec.
    Haj Salem I; Beaudin M; Stumpf M; Estiar MA; Côté PO; Brunet F; Gamache PL; Rouleau GA; Mourabit-Amari K; Gan-Or Z; Dupré N
    Can J Neurol Sci; 2021 Sep; 48(5):655-665. PubMed ID: 33397523
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Investigation of mitochondrial function in hereditary spastic paraparesis.
    McDermott CJ; Taylor RW; Hayes C; Johnson M; Bushby KM; Turnbull DM; Shaw PJ
    Neuroreport; 2003 Mar; 14(3):485-8. PubMed ID: 12634509
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The high prevalence of hereditary spastic paraplegia in Sardinia, insular Italy.
    Racis L; Tessa A; Di Fabio R; Storti E; Agnetti V; Casali C; Santorelli FM; Pugliatti M
    J Neurol; 2014 Jan; 261(1):52-9. PubMed ID: 24141732
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.