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 *

290 related articles for article (PubMed ID: 18663179)

  • 1. SPG11 compound mutations in spastic paraparesis with thin corpus callosum.
    Samaranch L; Riverol M; Masdeu JC; Lorenzo E; Vidal-Taboada JM; Irigoyen J; Pastor MA; de Castro P; Pastor P
    Neurology; 2008 Jul; 71(5):332-6. PubMed ID: 18663179
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel mutations c.[5121_5122insAG]+[6859C>T] of the SPG11 gene associated with cerebellum hypometabolism in a Chinese case of hereditary spastic paraplegia with thin corpus callosum.
    Ma J; Xiong L; Chang Y; Jing X; Huang W; Hu B; Shi X; Xu W; Wang Y; Li X
    Parkinsonism Relat Disord; 2014 Feb; 20(2):256-9. PubMed ID: 24315199
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum.
    Liao SS; Shen L; Du J; Zhao GH; Wang XY; Yang Y; Xiao ZQ; Yuan Y; Jiang H; Li N; Sun HD; Wang JL; Wang CY; Zhou YF; Mo XY; Xia K; Tang BS
    J Neurol Sci; 2008 Dec; 275(1-2):92-9. PubMed ID: 18835492
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum.
    Abdel Aleem A; Abu-Shahba N; Swistun D; Silhavy J; Bielas SL; Sattar S; Gleeson JG; Zaki MS
    Eur J Med Genet; 2011; 54(1):82-5. PubMed ID: 20971220
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia, cross section hospital base study.
    Alfaidi N; Sobahy T; Ali Q; Al Said Y; Karim G; Khan H; Kurdi K; Cupler E
    J Neurol Sci; 2022 Mar; 434():120144. PubMed ID: 35074613
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.
    Hehr U; Bauer P; Winner B; Schule R; Olmez A; Koehler W; Uyanik G; Engel A; Lenz D; Seibel A; Hehr A; Ploetz S; Gamez J; Rolfs A; Weis J; Ringer TM; Bonin M; Schuierer G; Marienhagen J; Bogdahn U; Weber BH; Topaloglu H; Schols L; Riess O; Winkler J
    Ann Neurol; 2007 Dec; 62(6):656-65. PubMed ID: 18067136
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cognitive profile in spastic paraplegia with thin corpus callosum and mutations in SPG11.
    Siri L; Battaglia FM; Tessa A; Rossi A; Rocco MD; Facchinetti S; Mascaretti M; Santorelli FM; Veneselli E; Biancheri R
    Neuropediatrics; 2010 Feb; 41(1):35-8. PubMed ID: 20571989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case report of SPG11 mutations in a Chinese ARHSP-TCC family.
    Zhang L; McFarland KN; Jiao J; Jiao Y
    BMC Neurol; 2016 Jun; 16():87. PubMed ID: 27256065
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Forceps minor region signal abnormality "ears of the lynx": an early MRI finding in spastic paraparesis with thin corpus callosum and mutations in the spatacsin gene (SPG11) on chromosome 15.
    Riverol M; Samaranch L; Pascual B; Pastor P; Irigoyen J; Pastor MA; de Castro P; Masdeu JC
    J Neuroimaging; 2009 Jan; 19(1):52-60. PubMed ID: 19040626
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity.
    Pippucci T; Panza E; Pompilii E; Donadio V; Borreca A; Babalini C; Patrono C; Zuntini R; Kawarai T; Bernardi G; Liguori R; Romeo G; Montagna P; Orlacchio A; Seri M
    Eur J Neurol; 2009 Jan; 16(1):121-6. PubMed ID: 19087158
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.
    Lossos A; Stevanin G; Meiner V; Argov Z; Bouslam N; Newman JP; Gomori JM; Klebe S; Lerer I; Elleuch N; Silverstein S; Durr A; Abramsky O; Ben-Nariah Z; Brice A
    Arch Neurol; 2006 May; 63(5):756-60. PubMed ID: 16682547
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
    Orlén H; Melberg A; Raininko R; Kumlien E; Entesarian M; Söderberg P; Påhlman M; Darin N; Kyllerman M; Holmberg E; Engler H; Eriksson U; Dahl N
    Am J Med Genet B Neuropsychiatr Genet; 2009 Oct; 150B(7):984-92. PubMed ID: 19194956
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia.
    Paisan-Ruiz C; Dogu O; Yilmaz A; Houlden H; Singleton A
    Neurology; 2008 Apr; 70(16 Pt 2):1384-9. PubMed ID: 18337587
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
    Boukhris A; Stevanin G; Feki I; Denis E; Elleuch N; Miladi MI; Truchetto J; Denora P; Belal S; Mhiri C; Brice A
    Arch Neurol; 2008 Mar; 65(3):393-402. PubMed ID: 18332254
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
    Stevanin G; Azzedine H; Denora P; Boukhris A; Tazir M; Lossos A; Rosa AL; Lerer I; Hamri A; Alegria P; Loureiro J; Tada M; Hannequin D; Anheim M; Goizet C; Gonzalez-Martinez V; Le Ber I; Forlani S; Iwabuchi K; Meiner V; Uyanik G; Erichsen AK; Feki I; Pasquier F; Belarbi S; Cruz VT; Depienne C; Truchetto J; Garrigues G; Tallaksen C; Tranchant C; Nishizawa M; Vale J; Coutinho P; Santorelli FM; Mhiri C; Brice A; Durr A;
    Brain; 2008 Mar; 131(Pt 3):772-84. PubMed ID: 18079167
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary spastic paraplegia with a thin corpus callosum.
    Somasundaram S; Raghavendra S; Singh A; Kesavadas C; Nair M
    Pediatr Radiol; 2007 May; 37(5):503-5. PubMed ID: 17387465
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
    Denora PS; Schlesinger D; Casali C; Kok F; Tessa A; Boukhris A; Azzedine H; Dotti MT; Bruno C; Truchetto J; Biancheri R; Fedirko E; Di Rocco M; Bueno C; Malandrini A; Battini R; Sickl E; de Leva MF; Boespflug-Tanguy O; Silvestri G; Simonati A; Said E; Ferbert A; Criscuolo C; Heinimann K; Modoni A; Weber P; Palmeri S; Plasilova M; Pauri F; Cassandrini D; Battisti C; Pini A; Tosetti M; Hauser E; Masciullo M; Di Fabio R; Piccolo F; Denis E; Cioni G; Massa R; Della Giustina E; Calabrese O; Melone MA; De Michele G; Federico A; Bertini E; Durr A; Brockmann K; van der Knaap MS; Zatz M; Filla A; Brice A; Stevanin G; Santorelli FM
    Hum Mutat; 2009 Mar; 30(3):E500-19. PubMed ID: 19105190
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.