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 *

625 related articles for article (PubMed ID: 19504443)

  • 1. [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]  

  • 2. Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation.
    Fink JK; Hedera P
    Semin Neurol; 1999; 19(3):301-9. PubMed ID: 12194386
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.
    Dick KJ; Al-Mjeni R; Baskir W; Koul R; Simpson MA; Patton MA; Raeburn S; Crosby AH
    Neurology; 2008 Jul; 71(4):248-52. PubMed ID: 18463364
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.
    Meijer IA; Cossette P; Roussel J; Benard M; Toupin S; Rouleau GA
    Ann Neurol; 2004 Oct; 56(4):579-82. PubMed ID: 15455396
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.
    Sauter S; Miterski B; Klimpe S; Bönsch D; Schöls L; Visbeck A; Papke T; Hopf HC; Engel W; Deufel T; Epplen JT; Neesen J
    Hum Mutat; 2002 Aug; 20(2):127-32. PubMed ID: 12124993
    [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. 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]  

  • 9. 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]  

  • 10. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
    Schüle R; Bonin M; Dürr A; Forlani S; Sperfeld AD; Klimpe S; Mueller JC; Seibel A; van de Warrenburg BP; Bauer P; Schöls L
    Neurology; 2009 Jun; 72(22):1893-8. PubMed ID: 19357379
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.
    Klebe S; Azzedine H; Durr A; Bastien P; Bouslam N; Elleuch N; Forlani S; Charon C; Koenig M; Melki J; Brice A; Stevanin G
    Brain; 2006 Jun; 129(Pt 6):1456-62. PubMed ID: 16434418
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects.
    Warnecke T; Duning T; Schirmacher A; Mohammadi S; Schwindt W; Lohmann H; Dziewas R; Deppe M; Ringelstein EB; Young P
    Mov Disord; 2010 Mar; 25(4):413-20. PubMed ID: 20108356
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.
    Elleuch N; Depienne C; Benomar A; Hernandez AM; Ferrer X; Fontaine B; Grid D; Tallaksen CM; Zemmouri R; Stevanin G; Durr A; Brice A
    Neurology; 2006 Mar; 66(5):654-9. PubMed ID: 16534102
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetics of hereditary spastic paraplegias.
    Schüle R; Schöls L
    Semin Neurol; 2011 Nov; 31(5):484-93. PubMed ID: 22266886
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 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. [Advances of genetic research on the SPG4 gene].
    Yang HR; Qi Y; Song Z; Deng H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Jun; 27(3):282-5. PubMed ID: 20533266
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.
    Sauter SM; Engel W; Neumann LM; Kunze J; Neesen J
    Hum Mutat; 2004 Jan; 23(1):98. PubMed ID: 14695538
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary spastic paraplegia.
    Roşulescu E; Stănoiu C; Buteică E; Stănoiu B; Burada F; Zăvăleanu M
    Rom J Morphol Embryol; 2009; 50(2):299-303. PubMed ID: 19434327
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.