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 *

205 related articles for article (PubMed ID: 31646384)

  • 1. Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4).
    Rattay TW; Boldt A; Völker M; Wiethoff S; Hengel H; Schüle R; Schöls L
    J Neurol; 2020 Feb; 267(2):369-379. PubMed ID: 31646384
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutations.
    Servelhere KR; Faber I; Saute JA; Moscovich M; D'Abreu A; Jardim LB; Teive HA; Lopes-Cendes I; Franca MC
    Eur J Neurol; 2016 Feb; 23(2):408-11. PubMed ID: 26806216
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Urinary symptoms, quality of life, and patient satisfaction in genetic and sporadic hereditary spastic paraplegia.
    Schneider SA; Beckinger VE; Möller B; Knüpfer S; Hamann M; Deuschl G
    J Neurol; 2019 Jan; 266(1):207-211. PubMed ID: 30467602
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Resting state fMRI studies in SPG4-linked hereditary spastic paraplegia.
    Liao X; Huang M; Xing W; Wu X; Liao W; Wang X; Tang B; Shen L
    J Neurol Sci; 2018 Jan; 384():1-6. PubMed ID: 29249364
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Functional gait measures correlate to fear of falling, and quality of life in patients with Hereditary Spastic Paraplegia: A cross-sectional study.
    Gaßner H; List J; Martindale CF; Regensburger M; Klucken J; Winkler J; Kohl Z
    Clin Neurol Neurosurg; 2021 Oct; 209():106888. PubMed ID: 34455170
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation and clinical characteristics of autosomal-dominant hereditary spastic paraplegias in China.
    Luo Y; Chen C; Zhan Z; Wang Y; Du J; Hu Z; Liao X; Zhao G; Wang J; Yan X; Jiang H; Pan Q; Xia K; Tang B; Shen L
    Neurodegener Dis; 2014; 14(4):176-83. PubMed ID: 25341883
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia.
    McMonagle P; Byrne P; Hutchinson M
    Neurology; 2004 Feb; 62(3):407-10. PubMed ID: 14872021
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hereditary spastic paraplegia type 4 (SPG4): clinical and molecular-genetic characteristics].
    Rudenskaia GE; Sermiagina IG; Illarioshkin SN; Sidorova OP; Fedotov VP; Poliakov AV
    Zh Nevrol Psikhiatr Im S S Korsakova; 2010; 110(6):12-9. PubMed ID: 20559269
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4).
    Navas-Sánchez FJ; Martín De Blas D; Fernández-Pena A; Alemán-Gómez Y; Lage-Castellanos A; Marcos-Vidal L; Guzmán-De-Villoria JA; Catalina I; Lillo L; Muñoz-Blanco JL; -Ugalde AO; Quintáns B; Sobrido MJ; Carmona S; Grandas F; Desco M
    Amyotroph Lateral Scler Frontotemporal Degener; 2022 Feb; 23(1-2):25-34. PubMed ID: 34396852
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Reduced regional cerebral blood flow in SPG4-linked hereditary spastic paraplegia.
    Scheuer KH; Nielsen JE; Krabbe K; Simonsen C; Koefoed P; Sørensen SA; Gade A; Paulson OB; Law I
    J Neurol Sci; 2005 Aug; 235(1-2):23-32. PubMed ID: 15939438
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report.
    Nagai T; Sunami Y; Kato R; Sugai M; Takahara M; Ohta K; Fujinaka H; Goto K; Okanura O; Nakajima T; Ozawa T
    Case Rep Neurol; 2021; 13(1):84-91. PubMed ID: 33708099
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Proton magnetic resonance spectroscopy and cognition in patients with spastin mutations.
    Erichsen AK; Server A; Landrø NI; Sandvik L; Tallaksen CM
    J Neurol Sci; 2009 Feb; 277(1-2):124-9. PubMed ID: 19084842
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).
    Estrada-Cuzcano A; Martin S; Chamova T; Synofzik M; Timmann D; Holemans T; Andreeva A; Reichbauer J; De Rycke R; Chang DI; van Veen S; Samuel J; Schöls L; Pöppel T; Mollerup Sørensen D; Asselbergh B; Klein C; Zuchner S; Jordanova A; Vangheluwe P; Tournev I; Schüle R
    Brain; 2017 Feb; 140(2):287-305. PubMed ID: 28137957
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Hereditary spastic paraplegia type 4 (SPG4) in Russian patients].
    Rudenskaya GE; Kadnikova VA; Sidorova OP; Beetz C; Illarioshkin SN; Dadaly EL; Proskokova TN; Ryzhkova OP
    Zh Nevrol Psikhiatr Im S S Korsakova; 2019; 119(11):11-20. PubMed ID: 31851166
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.