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.
44. Clinical features and management of hereditary spastic paraplegia. Faber I; Servelhere KR; Martinez AR; D'Abreu A; Lopes-Cendes I; França MC Arq Neuropsiquiatr; 2014 Mar; 72(3):219-26. PubMed ID: 24676440 [TBL] [Abstract][Full Text] [Related]
45. A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1. Meijer IA; Cossette P; Roussel J; Benard M; Toupin S; Rouleau GA Ann Neurol; 2004 Oct; 56(4):579-82. PubMed ID: 15455396 [TBL] [Abstract][Full Text] [Related]
47. Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family. Chan KY; Ching CK; Mak CM; Lam CW; Chan AY Hong Kong Med J; 2009 Aug; 15(4):304-7. PubMed ID: 19652243 [TBL] [Abstract][Full Text] [Related]
48. Converging cellular themes for the hereditary spastic paraplegias. Blackstone C Curr Opin Neurobiol; 2018 Aug; 51():139-146. PubMed ID: 29753924 [TBL] [Abstract][Full Text] [Related]
49. A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23. Dick KJ; Al-Mjeni R; Baskir W; Koul R; Simpson MA; Patton MA; Raeburn S; Crosby AH Neurology; 2008 Jul; 71(4):248-52. PubMed ID: 18463364 [TBL] [Abstract][Full Text] [Related]
50. Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases. Tang BS; Chen X; Zhao GH; Shen L; Yan XX; Jiang H; Luo W Chin Med J (Engl); 2004 Jul; 117(7):1002-5. PubMed ID: 15265372 [TBL] [Abstract][Full Text] [Related]
51. [Recent advances of study on hereditary spastic paraplegia type 11]. Du J; Shen L; Tang B Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):670-3. PubMed ID: 19953491 [TBL] [Abstract][Full Text] [Related]
52. A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Helbig KL; Hedrich UB; Shinde DN; Krey I; Teichmann AC; Hentschel J; Schubert J; Chamberlin AC; Huether R; Lu HM; Alcaraz WA; Tang S; Jungbluth C; Dugan SL; Vainionpää L; Karle KN; Synofzik M; Schöls L; Schüle R; Lehesjoki AE; Helbig I; Lerche H; Lemke JR Ann Neurol; 2016 Oct; 80(4):638-42. PubMed ID: 27543892 [TBL] [Abstract][Full Text] [Related]
53. Clinical and genetic aspects of spinocerebellar degeneration. Durr A; Brice A Curr Opin Neurol; 2000 Aug; 13(4):407-13. PubMed ID: 10970057 [TBL] [Abstract][Full Text] [Related]
55. Subtle Imaging Findings Aid the Diagnosis of Adolescent Hereditary Spastic Paraplegia and Ataxia. Wagner F; Titelbaum DS; Engisch R; Coskun EK; Waugh JL Clin Neuroradiol; 2019 Jun; 29(2):215-221. PubMed ID: 29379980 [TBL] [Abstract][Full Text] [Related]
56. Prevalence of hereditary ataxias and paraplegias in the province of Torino, Italy. Brignolio F; Leone M; Tribolo A; Rosso MG; Meineri P; Schiffer D Ital J Neurol Sci; 1986 Aug; 7(4):431-5. PubMed ID: 3759416 [TBL] [Abstract][Full Text] [Related]
57. Striatal dopaminergic functioning in patients with sporadic and hereditary spastic paraplegias with parkinsonism. Kim JS; Kim JM; Kim YK; Kim SE; Yun JY; Jeon BS J Korean Med Sci; 2013 Nov; 28(11):1661-6. PubMed ID: 24265532 [TBL] [Abstract][Full Text] [Related]