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 *

220 related articles for article (PubMed ID: 29368828)

  • 21. Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia.
    Zhao M; Chen YJ; Wang MW; Lin XH; Dong EL; Chen WJ; Wang N; Lin X
    Mol Diagn Ther; 2019 Dec; 23(6):781-789. PubMed ID: 31630374
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.
    Dürr A; Camuzat A; Colin E; Tallaksen C; Hannequin D; Coutinho P; Fontaine B; Rossi A; Gil R; Rousselle C; Ruberg M; Stevanin G; Brice A
    Arch Neurol; 2004 Dec; 61(12):1867-72. PubMed ID: 15596607
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia.
    Kadnikova VA; Rudenskaya GE; Stepanova AA; Sermyagina IG; Ryzhkova OP
    Sci Rep; 2019 Oct; 9(1):14412. PubMed ID: 31594988
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.
    Erichsen AK; Inderhaug E; Mattingsdal M; Eiklid K; Tallaksen CM
    Eur J Neurol; 2007 Jul; 14(7):809-14. PubMed ID: 17594340
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic, structural and clinical analysis of spastic paraplegia 4.
    Varghaei P; Estiar MA; Ashtiani S; Veyron S; Mufti K; Leveille E; Yu E; Spiegelman D; Rioux MF; Yoon G; Tarnopolsky M; Boycott KM; Dupre N; Suchowersky O; Trempe JF; Rouleau GA; Gan-Or Z
    Parkinsonism Relat Disord; 2022 May; 98():62-69. PubMed ID: 35487127
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene.
    Bönsch D; Schwindt A; Navratil P; Palm D; Neumann C; Klimpe S; Schickel J; Hazan J; Weiller C; Deufel T; Liepert J
    J Neurol Neurosurg Psychiatry; 2003 Aug; 74(8):1109-12. PubMed ID: 12876245
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mental deficiency in three families with SPG4 spastic paraplegia.
    Ribaï P; Depienne C; Fedirko E; Jothy AC; Viveweger C; Hahn-Barma V; Brice A; Durr A
    Eur J Hum Genet; 2008 Jan; 16(1):97-104. PubMed ID: 17957230
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.
    Crippa F; Panzeri C; Martinuzzi A; Arnoldi A; Redaelli F; Tonelli A; Baschirotto C; Vazza G; Mostacciuolo ML; Daga A; Orso G; Profice P; Trabacca A; D'Angelo MG; Comi GP; Galbiati S; Lamperti C; Bonato S; Pandolfo M; Meola G; Musumeci O; Toscano A; Trevisan CP; Bresolin N; Bassi MT
    Arch Neurol; 2006 May; 63(5):750-5. PubMed ID: 16682546
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis.
    Lindsey JC; Lusher ME; McDermott CJ; White KD; Reid E; Rubinsztein DC; Bashir R; Hazan J; Shaw PJ; Bushby KM
    J Med Genet; 2000 Oct; 37(10):759-65. PubMed ID: 11015453
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability.
    Kawarai T; Montecchiani C; Miyamoto R; Gaudiello F; Caltagirone C; Izumi Y; Kaji R; Orlacchio A
    J Neurol Sci; 2017 Sep; 380():92-97. PubMed ID: 28870597
    [TBL] [Abstract][Full Text] [Related]  

  • 32. New cellular imaging-based method to distinguish the SPG4 subtype of hereditary spastic paraplegia.
    Sardina F; Valente D; Fattorini G; Cioffi E; Zanna GD; Tessa A; Trisciuoglio D; Soddu S; Santorelli FM; Casali C; Rinaldo C
    Eur J Neurol; 2023 Jun; 30(6):1734-1744. PubMed ID: 36815539
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hereditary spastic paraplegias.
    Lau KK; Ching CK; Mak CM; Chan YW
    Hong Kong Med J; 2009 Jun; 15(3):217-20. PubMed ID: 19494379
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Large deletion involving the 5'-UTR in the spastin gene caused mild phenotype of autosomal dominant hereditary spastic paraplegia.
    Iwanaga H; Tsujino A; Shirabe S; Eguchi H; Fukushima N; Niikawa N; Yoshiura K; Eguchi K
    Am J Med Genet A; 2005 Feb; 133A(1):13-7. PubMed ID: 15637712
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Autonomic dysfunction in hereditary spastic paraplegia type 4.
    González-Salazar C; Takazaki KAG; Martinez ARM; Pimentel-Silva LR; Jacinto-Scudeiro LA; Nakagawa ÉY; Fujiwara Murakami CE; Saute JAM; Pedroso JL; Barsottini OGP; Teive HAG; França MC
    Eur J Neurol; 2019 Apr; 26(4):687-693. PubMed ID: 30489674
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia.
    Lan MY; Fu SC; Chang YY; Wu-Chou YH; Lai SC; Chen RS; Lu CS
    J Formos Med Assoc; 2012 Jul; 111(7):380-5. PubMed ID: 22817815
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Japanese SPG4 Patient with a Confirmed De Novo Mutation of the SPAST Gene.
    Nan H; Okamoto K; Gao L; Morishima Y; Ichinose Y; Koh K; Hashiyada M; Adachi N; Takiyama Y
    Intern Med; 2020 Sep; 59(18):2311-2315. PubMed ID: 32522921
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.
    Patrono C; Scarano V; Cricchi F; Melone MA; Chiriaco M; Napolitano A; Malandrini A; De Michele G; Petrozzi L; Giraldi C; Santoro L; Servidei S; Casali C; Filla A; Santorelli FM
    Hum Mutat; 2005 May; 25(5):506. PubMed ID: 15841487
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spastin related hereditary spastic paraplegia with dysplastic corpus callosum.
    Alber B; Pernauer M; Schwan A; Rothmund G; Hoffmann KT; Brummer D; Sperfeld AD; Uttner I; Binder H; Epplen JT; Dullinger J; Ludolph AC; Meyer T
    J Neurol Sci; 2005 Sep; 236(1-2):9-12. PubMed ID: 16009377
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families.
    Loureiro JL; Miller-Fleming L; Thieleke-Matos C; Magalhães P; Cruz VT; Coutinho P; Sequeiros J; Silveira I
    Acta Neurol Scand; 2009 Feb; 119(2):113-8. PubMed ID: 18664244
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.