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.
129 related articles for article (PubMed ID: 33222977)
1. Homozygous frameshift mutation of SPG11 as a cause of progressive flaccid paralysis, ataxia and dysphagia. Lilley K; Bhuta S; Sabet A; Broadley SA J Clin Neurosci; 2020 Nov; 81():90-91. PubMed ID: 33222977 [TBL] [Abstract][Full Text] [Related]
2. SPG11: a consistent clinical phenotype in a family with homozygous spatacsin truncating mutation. Del Bo R; Di Fonzo A; Ghezzi S; Locatelli F; Stevanin G; Costa A; Corti S; Bresolin N; Comi GP Neurogenetics; 2007 Nov; 8(4):301-5. PubMed ID: 17717710 [TBL] [Abstract][Full Text] [Related]
3. Identification of a Mutation in SPG11 in an Iranian Patient with Spastic Paraplegia and Ears of the Lynx Sign. Sayad A; Akbari MT; Hesami O; Ghafouri-Fard S; Taheri M J Mol Neurosci; 2020 Jun; 70(6):959-961. PubMed ID: 32040826 [TBL] [Abstract][Full Text] [Related]
4. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum. Abdel Aleem A; Abu-Shahba N; Swistun D; Silhavy J; Bielas SL; Sattar S; Gleeson JG; Zaki MS Eur J Med Genet; 2011; 54(1):82-5. PubMed ID: 20971220 [TBL] [Abstract][Full Text] [Related]
5. A case report of SPG11 mutations in a Chinese ARHSP-TCC family. Zhang L; McFarland KN; Jiao J; Jiao Y BMC Neurol; 2016 Jun; 16():87. PubMed ID: 27256065 [TBL] [Abstract][Full Text] [Related]
6. Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia. Schüle R; Schlipf N; Synofzik M; Klebe S; Klimpe S; Hehr U; Winner B; Lindig T; Dotzer A; Riess O; Winkler J; Schöls L; Bauer P J Neurol Neurosurg Psychiatry; 2009 Dec; 80(12):1402-4. PubMed ID: 19917823 [TBL] [Abstract][Full Text] [Related]
8. Mild cognitive impairment in novel SPG11 mutation-related sporadic hereditary spastic paraplegia with thin corpus callosum: case series. Li C; Yan Q; Duan FJ; Zhao C; Zhang Z; Du Y; Zhang W BMC Neurol; 2021 Jan; 21(1):12. PubMed ID: 33430805 [TBL] [Abstract][Full Text] [Related]
9. Identification of novel SPG11 mutations in a cohort of Chinese families with hereditary spastic paraplegia. Du J; Hu YC; Tang BS; Jiang H; Shen L Int J Neurosci; 2018 Feb; 128(2):146-150. PubMed ID: 28933964 [TBL] [Abstract][Full Text] [Related]
10. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum. Olmez A; Uyanik G; Ozgül RK; Gross C; Cirak S; Elibol B; Anlar B; Winner B; Hehr U; Topaloglu H; Winkler J Neuropediatrics; 2006 Apr; 37(2):59-66. PubMed ID: 16773502 [TBL] [Abstract][Full Text] [Related]
11. Janus-faced spatacsin (SPG11): involvement in neurodevelopment and multisystem neurodegeneration. Pozner T; Regensburger M; Engelhorn T; Winkler J; Winner B Brain; 2020 Aug; 143(8):2369-2379. PubMed ID: 32355960 [TBL] [Abstract][Full Text] [Related]
12. SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. Orlén H; Melberg A; Raininko R; Kumlien E; Entesarian M; Söderberg P; Påhlman M; Darin N; Kyllerman M; Holmberg E; Engler H; Eriksson U; Dahl N Am J Med Genet B Neuropsychiatr Genet; 2009 Oct; 150B(7):984-92. PubMed ID: 19194956 [TBL] [Abstract][Full Text] [Related]
13. [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]