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 *

115 related articles for article (PubMed ID: 28437518)

  • 1. A Middle-aged Man With Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis.
    Kung NH; Van Stavern GP; Bucelli RC
    JAMA Neurol; 2017 Jun; 74(6):733-736. PubMed ID: 28437518
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene.
    Bhattacharjee S; Beauchamp N; Murray BE; Lynch T
    Neurosciences (Riyadh); 2017 Oct; 22(4):303-307. PubMed ID: 29057857
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early Onset Degenerative Parkinsonism - Consider SPG7 Mutation.
    Bhattacharjee S; Noushad M; Sadler M
    Neurol India; 2021; 69(4):1051-1052. PubMed ID: 34507444
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neurogenetics: The expanding horizons of diagnosis and disease pathogenesis.
    Gomez CM; Kawakami H
    Neurology; 2015 Mar; 84(11):1070-1. PubMed ID: 25681450
    [No Abstract]   [Full Text] [Related]  

  • 5. SPG7 mutations are a common cause of undiagnosed ataxia.
    Pfeffer G; Pyle A; Griffin H; Miller J; Wilson V; Turnbull L; Fawcett K; Sims D; Eglon G; Hadjivassiliou M; Horvath R; Németh A; Chinnery PF
    Neurology; 2015 Mar; 84(11):1174-6. PubMed ID: 25681447
    [No Abstract]   [Full Text] [Related]  

  • 6. Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS?
    Jacquemont S; Orrico A; Galli L; Sahota PK; Brunberg JA; Anichini C; Leehey M; Schaeffer S; Hagerman RJ; Hagerman PJ; Tassone F
    J Med Genet; 2005 Feb; 42(2):e14. PubMed ID: 15689437
    [No Abstract]   [Full Text] [Related]  

  • 7. Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: a diagnostic approach.
    Sedel F; Fontaine B; Saudubray JM; Lyon-Caen O
    J Inherit Metab Dis; 2007 Nov; 30(6):855-64. PubMed ID: 17957490
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spastin and paraplegin gene analysis in selected cases of motor neurone disease (MND).
    McDermott CJ; Roberts D; Tomkins J; Bushby KM; Shaw PJ
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2003 Jun; 4(2):96-9. PubMed ID: 14506940
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new paraplegin mutation in a patient with primary progressive multiple sclerosis.
    Bellinvia A; Pastò L; Niccolai C; Tessa A; Carrai R; Martinelli C; Moretti M; Amato MP; Santorelli FM; Sorbi S; Matà S
    Mult Scler Relat Disord; 2020 Sep; 44():102302. PubMed ID: 32570181
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Paraplegin gene analysis in hereditary spastic paraparesis (HSP) pedigrees in northeast England.
    McDermott CJ; Dayaratne RK; Tomkins J; Lusher ME; Lindsey JC; Johnson MA; Casari G; Turnbull DM; Bushby K; Shaw PJ
    Neurology; 2001 Feb; 56(4):467-71. PubMed ID: 11222789
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acquired progressive spastic paraparesis due to neurobrucellosis: a case report.
    Karaca S; Demiroglu YZ; Karataş M; Tan M
    Acta Neurol Belg; 2007 Dec; 107(4):118-21. PubMed ID: 18416286
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adrenomyeloneuropathy.
    Misra S; Ramesh R; Ramu ChS; Srirangalaxmi G; Radhakrishn H; Vajresware
    J Assoc Physicians India; 2012 Jul; 60():58-61. PubMed ID: 23405547
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel c.775_781dup,p(Thr261fs) mutation in
    Bhattacharjee S; Stinton V; Cairns D; Murray B
    Neurol India; 2017; 65(5):1141-1142. PubMed ID: 28879915
    [No Abstract]   [Full Text] [Related]  

  • 14. Elimination of INPP4A and SLC5A7 as candidate genes for congenital progressive ataxia and spastic paresis in pigs.
    Genini S; Nguyen TT; Bürgi E; Stranzinger G; Vögeli P; Giuffra E
    Anim Genet; 2009 Oct; 40(5):789-90. PubMed ID: 19397514
    [No Abstract]   [Full Text] [Related]  

  • 15. Friedreich's ataxia presenting as an isolated spastic paraparesis.
    Wilkinson PA; Bradley JL; Warner TT
    J Neurol Neurosurg Psychiatry; 2001 Nov; 71(5):709. PubMed ID: 11688498
    [No Abstract]   [Full Text] [Related]  

  • 16. Early-onset ataxia with progressive external ophthalmoplegia associated with POLG mutation: autosomal recessive mitochondrial ataxic syndrome or SANDO?
    Habek M; Barun B; Adamec I; Mitrović Z; Ozretić D; Brinar VV
    Neurologist; 2012 Sep; 18(5):287-9. PubMed ID: 22931735
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel presenilin 1 mutation (Y154N) in a patient with early onset Alzheimer's disease with spastic paraparesis.
    Hattori S; Sakuma K; Wakutani Y; Wada K; Shimoda M; Urakami K; Kowa H; Nakashima K
    Neurosci Lett; 2004 Sep; 368(3):319-22. PubMed ID: 15364419
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal dominant childhood onset slowly progressive leukodystrophy--a Japanese family with spastic paraparesis, ataxia, mental deterioration, and skeletal abnormality.
    Nomoto N; Iwasaki Y; Arasaki K; Fujioka T; Kurihara T; Wakata N
    J Neurol Sci; 2004 Jun; 221(1-2):35-9. PubMed ID: 15178211
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Adult-onset spastic paraparesis: an approach to diagnostic work-up.
    Zhovtis Ryerson L; Herbert J; Howard J; Kister I
    J Neurol Sci; 2014 Nov; 346(1-2):43-50. PubMed ID: 25263600
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Emotional detachment, gait ataxia, and cerebellar dysconnectivity associated with compound heterozygous mutations in the
    Ringman JM; Qiao Y; Garbin A; Fisher BE; Fogel B; Watari Knoell K; Chui HC; Shi Y; Rexach JE
    Neurocase; 2020 Oct; 26(5):299-304. PubMed ID: 32893728
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.