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.
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]