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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 16511635

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.
    Hedera P, DiMauro S, Bonilla E, Wald J, Eldevik OP, Fink JK.
    Neurology; 1999 Jul 13; 53(1):44-50. PubMed ID: 10408535
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 305(1-2):67-70. PubMed ID: 21440262
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
    Hanein S, Dürr A, Ribai P, Forlani S, Leutenegger AL, Nelson I, Babron MC, Elleuch N, Depienne C, Charon C, Brice A, Stevanin G.
    Hum Genet; 2007 Nov 15; 122(3-4):261-73. PubMed ID: 17605047
    [Abstract] [Full Text] [Related]

  • 9. Autosomal recessive spastic paraplegia (SPG45) with mental retardation maps to 10q24.3-q25.1.
    Dursun U, Koroglu C, Kocasoy Orhan E, Ugur SA, Tolun A.
    Neurogenetics; 2009 Oct 15; 10(4):325-31. PubMed ID: 19415352
    [Abstract] [Full Text] [Related]

  • 10. A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.
    Boukhris A, Feki I, Elleuch N, Miladi MI, Boland-Augé A, Truchetto J, Mundwiller E, Jezequel N, Zelenika D, Mhiri C, Brice A, Stevanin G.
    Neurogenetics; 2010 Oct 15; 11(4):441-8. PubMed ID: 20593214
    [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 15; 129(Pt 6):1456-62. PubMed ID: 16434418
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 37(2):59-66. PubMed ID: 16773502
    [Abstract] [Full Text] [Related]

  • 13. Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).
    Bouslam N, Benomar A, Azzedine H, Bouhouche A, Namekawa M, Klebe S, Charon C, Durr A, Ruberg M, Brice A, Yahyaoui M, Stevanin G.
    Ann Neurol; 2005 Apr 15; 57(4):567-71. PubMed ID: 15786464
    [Abstract] [Full Text] [Related]

  • 14. X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.
    Bonneau D, Rozet JM, Bulteau C, Berthier M, Mettey R, Gil R, Munnich A, Le Merrer M.
    J Med Genet; 1993 May 15; 30(5):381-4. PubMed ID: 8320699
    [Abstract] [Full Text] [Related]

  • 15. A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy.
    Al-Yahyaee S, Al-Gazali LI, De Jonghe P, Al-Barwany H, Al-Kindi M, De Vriendt E, Chand P, Koul R, Jacob PC, Gururaj A, Sztriha L, Parrado A, Van Broeckhoven C, Bayoumi RA.
    Neurology; 2006 Apr 25; 66(8):1230-4. PubMed ID: 16636240
    [Abstract] [Full Text] [Related]

  • 16. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.
    Zhao GH, Hu ZM, Shen L, Jiang H, Ren ZJ, Liu XM, Xia K, Guo P, Pan Q, Tang BS.
    Chin Med J (Engl); 2008 Mar 05; 121(5):430-4. PubMed ID: 18364116
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.
    Gucuyener K, Hirfanoglu T, Ok I, Cansu A, Serdaroglu A.
    J Child Neurol; 2007 Feb 05; 22(2):214-7. PubMed ID: 17621486
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.