465 related articles for article (PubMed ID: 24954637)
1. Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms.
Lo Giudice T; Lombardi F; Santorelli FM; Kawarai T; Orlacchio A
Exp Neurol; 2014 Nov; 261():518-39. PubMed ID: 24954637
[TBL] [Abstract][Full Text] [Related]
2. Hereditary Spastic Paraplegia Type 11-Clinical, Genetic and Neuroimaging Characteristics.
Chojdak-Łukasiewicz J; Sulima K; Zimny A; Waliszewska-Prosół M; Budrewicz S
Int J Mol Sci; 2023 Dec; 24(24):. PubMed ID: 38139357
[TBL] [Abstract][Full Text] [Related]
3. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.
Finsterer J; Löscher W; Quasthoff S; Wanschitz J; Auer-Grumbach M; Stevanin G
J Neurol Sci; 2012 Jul; 318(1-2):1-18. PubMed ID: 22554690
[TBL] [Abstract][Full Text] [Related]
4. Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation.
Fink JK; Hedera P
Semin Neurol; 1999; 19(3):301-9. PubMed ID: 12194386
[TBL] [Abstract][Full Text] [Related]
5. [AAA ATPases and hereditary spastic paraplegia].
Wang YG; Shen L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):298-301. PubMed ID: 19504443
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Molecular genetics study of hereditary spastic paraplegia accompanied by distal amyotrophy-an update].
Wang ZZ; Cen ZD; Luo W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):429-34. PubMed ID: 23926010
[TBL] [Abstract][Full Text] [Related]
8. Hereditary spastic paraplegia.
Murala S; Nagarajan E; Bollu PC
Neurol Sci; 2021 Mar; 42(3):883-894. PubMed ID: 33439395
[TBL] [Abstract][Full Text] [Related]
9. Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
Fink JK; Heiman-Patterson T; Bird T; Cambi F; Dubé MP; Figlewicz DA; Fink JK; Haines JL; Heiman-Patterson T; Hentati A; Pericak-Vance MA; Raskind W; Rouleau GA; Siddique T
Neurology; 1996 Jun; 46(6):1507-14. PubMed ID: 8649538
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex.
Parodi L; Fenu S; Barbier M; Banneau G; Duyckaerts C; Tezenas du Montcel S; Monin ML; Ait Said S; Guegan J; Tallaksen CME; Sablonniere B; Brice A; Stevanin G; Depienne C; Durr A;
Brain; 2018 Dec; 141(12):3331-3342. PubMed ID: 30476002
[TBL] [Abstract][Full Text] [Related]
12. Hereditary spastic paraplegia: Genetic heterogeneity and common pathways.
Panza E; Meyyazhagan A; Orlacchio A
Exp Neurol; 2022 Nov; 357():114203. PubMed ID: 35970204
[TBL] [Abstract][Full Text] [Related]
13. Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54).
Gonzalez M; Nampoothiri S; Kornblum C; Oteyza AC; Walter J; Konidari I; Hulme W; Speziani F; Schöls L; Züchner S; Schüle R
Eur J Hum Genet; 2013 Nov; 21(11):1214-8. PubMed ID: 23486545
[TBL] [Abstract][Full Text] [Related]
14. Hereditary spastic paraplegia: Novel insights into the pathogenesis and management.
Awuah WA; Tan JK; Shkodina AD; Ferreira T; Adebusoye FT; Mazzoleni A; Wellington J; David L; Chilcott E; Huang H; Abdul-Rahman T; Shet V; Atallah O; Kalmanovich J; Jiffry R; Madhu DE; Sikora K; Kmyta O; Delva MY
SAGE Open Med; 2024; 12():20503121231221941. PubMed ID: 38162912
[TBL] [Abstract][Full Text] [Related]
15. Update on the Genetics of Spastic Paraplegias.
Boutry M; Morais S; Stevanin G
Curr Neurol Neurosci Rep; 2019 Feb; 19(4):18. PubMed ID: 30820684
[TBL] [Abstract][Full Text] [Related]
16. Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms.
Salinas S; Proukakis C; Crosby A; Warner TT
Lancet Neurol; 2008 Dec; 7(12):1127-38. PubMed ID: 19007737
[TBL] [Abstract][Full Text] [Related]
17. Molecular aspects of hereditary spastic paraplegia.
Noreau A; Dion PA; Rouleau GA
Exp Cell Res; 2014 Jul; 325(1):18-26. PubMed ID: 24631291
[TBL] [Abstract][Full Text] [Related]
18. A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum.
Blumkin L; Lerman-Sagie T; Lev D; Yosovich K; Leshinsky-Silver E
J Neurol Sci; 2011 Jun; 305(1-2):67-70. PubMed ID: 21440262
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still counting.
Klebe S; Stevanin G; Depienne C
Rev Neurol (Paris); 2015; 171(6-7):505-30. PubMed ID: 26008818
[TBL] [Abstract][Full Text] [Related]
20. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.
Fink JK
Acta Neuropathol; 2013 Sep; 126(3):307-28. PubMed ID: 23897027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
