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 *

169 related articles for article (PubMed ID: 21725714)

  • 1. Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia.
    Sánchez-Ferrero E; Coto E; Corao AI; Díaz M; Gámez J; Esteban J; Gonzalo JF; Pascual-Pascual SI; López De Munaín A; Morís G; Infante J; Del Castillo E; Márquez C; Alvarez V
    J Neurol; 2012 Feb; 259(2):246-50. PubMed ID: 21725714
    [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. 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]  

  • 4. High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia.
    Lan MY; Chang YY; Yeh TH; Lai SC; Liou CW; Kuo HC; Wu YR; Lyu RK; Hung JW; Chang YC; Lu CS
    BMC Neurol; 2014 Nov; 14():216. PubMed ID: 25421405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings.
    Polymeris AA; Tessa A; Anagnostopoulou K; Rubegni A; Galatolo D; Dinopoulos A; Gika AD; Youroukos S; Skouteli E; Santorelli FM; Pons R
    J Neurol; 2016 Aug; 263(8):1604-11. PubMed ID: 27260292
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary spastic paraplegia].
    Kanda T; Kobayashi H
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():429-32. PubMed ID: 12013904
    [No Abstract]   [Full Text] [Related]  

  • 8. Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.
    Tang B; Zhao G; Xia K; Pan Q; Luo W; Shen L; Long Z; Dai H; Zi X; Jiang H
    Arch Neurol; 2004 Jan; 61(1):49-55. PubMed ID: 14732620
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Isoform-specific increase of spastin stability by N-terminal missense variants including intragenic modifiers of SPG4 hereditary spastic paraplegia.
    Schickel J; Pamminger T; Ehrsam A; Münch S; Huang X; Klopstock T; Kurlemann G; Hemmerich P; Dubiel W; Deufel T; Beetz C
    Eur J Neurol; 2007 Dec; 14(12):1322-8. PubMed ID: 17916079
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary spastic paraplegia: the pace quickens.
    Fink JK
    Ann Neurol; 2002 Jun; 51(6):669-72. PubMed ID: 12112070
    [No Abstract]   [Full Text] [Related]  

  • 11. A founder mutation p.H701P identified as a major cause of SPG7 in Norway.
    Rydning SL; Wedding IM; Koht J; Chawla M; Øye AM; Sheng Y; Vigeland MD; Selmer KK; Tallaksen CM
    Eur J Neurol; 2016 Apr; 23(4):763-71. PubMed ID: 26756429
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.
    Brugman F; Veldink JH; Franssen H; de Visser M; de Jong JM; Faber CG; Kremer BH; Schelhaas HJ; van Doorn PA; Verschuuren JJ; Bruyn RP; Kuks JB; Robberecht W; Wokke JH; van den Berg LH
    Arch Neurol; 2009 Apr; 66(4):509-14. PubMed ID: 19364936
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion.
    Beetz C; Nygren AO; Deufel T; Reid E
    Neurogenetics; 2007 Nov; 8(4):317-8. PubMed ID: 17657515
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutation analysis of SPG4 and SPG3A genes and its implication in molecular diagnosis of Korean patients with hereditary spastic paraplegia.
    Park SY; Ki CS; Kim HJ; Kim JW; Sung DH; Kim BJ; Lee WY
    Arch Neurol; 2005 Jul; 62(7):1118-21. PubMed ID: 16009769
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy.
    Klebe S; Depienne C; Gerber S; Challe G; Anheim M; Charles P; Fedirko E; Lejeune E; Cottineau J; Brusco A; Dollfus H; Chinnery PF; Mancini C; Ferrer X; Sole G; Destée A; Mayer JM; Fontaine B; de Seze J; Clanet M; Ollagnon E; Busson P; Cazeneuve C; Stevanin G; Kaplan J; Rozet JM; Brice A; Durr A
    Brain; 2012 Oct; 135(Pt 10):2980-93. PubMed ID: 23065789
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical features of hereditary spastic paraplegia due to spastin mutation.
    McDermott CJ; Burness CE; Kirby J; Cox LE; Rao DG; Hewamadduma C; Sharrack B; Hadjivassiliou M; Chinnery PF; Dalton A; Shaw PJ;
    Neurology; 2006 Jul; 67(1):45-51. PubMed ID: 16832076
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia.
    Svenstrup K; Bross P; Koefoed P; Hjermind LE; Eiberg H; Born AP; Vissing J; Gyllenborg J; Nørremølle A; Hasholt L; Nielsen JE
    J Neurol Sci; 2009 Sep; 284(1-2):90-5. PubMed ID: 19423133
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
    Nielsen JE; Johnsen B; Koefoed P; Scheuer KH; Grønbech-Jensen M; Law I; Krabbe K; Nørremølle A; Eiberg H; Søndergård H; Dam M; Rehfeld JF; Krarup C; Paulson OB; Hasholt L; Sørensen SA
    Eur J Neurol; 2004 Dec; 11(12):817-24. PubMed ID: 15667412
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals.
    Sulek A; Elert E; Rajkiewicz M; Zdzienicka E; Stepniak I; Krysa W; Zaremba J
    Neurol Sci; 2013 Feb; 34(2):239-42. PubMed ID: 22203332
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.