129 related articles for article (PubMed ID: 38847051)
1. MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study.
Scaravilli A; Negroni D; Senatore C; Ugga L; Cosottini M; Ricca I; Bender B; Traschütz A; Başak AN; Vural A; van de Warrenburg BP; Durr A; La Piana R; Timmann D; ; Schüle R; Synofzik M; Santorelli FM; Cocozza S
Mov Disord; 2024 Jun; ():. PubMed ID: 38847051
[TBL] [Abstract][Full Text] [Related]
2. An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX study.
Scaravilli A; Gabusi I; Mari G; Battocchio M; Bosticardo S; Schiavi S; Bender B; Kessler C; Brais B; La Piana R; van de Warrenburg BP; Cosottini M; Timmann D; ; Daducci A; Schüle R; Synofzik M; Santorelli FM; Cocozza S
J Neurol; 2024 Jun; ():. PubMed ID: 38880819
[TBL] [Abstract][Full Text] [Related]
3. Digital Gait Outcomes for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Discriminative, Convergent, and Ecological Validity in a Multicenter Study (PROSPAX).
Beichert L; Ilg W; Kessler C; Traschütz A; Reich S; Santorelli FM; Başak AN; Gagnon C; ; Schüle R; Synofzik M
Mov Disord; 2024 Jun; ():. PubMed ID: 38847438
[TBL] [Abstract][Full Text] [Related]
4. Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.
Ashrafi MR; Mohammadi P; Tavasoli AR; Heidari M; Hosseinpour S; Rasulinejad M; Rohani M; Akbari MG; Malamiri RA; Badv RS; Fathi D; Dehnavi AZ; Savad S; Rabbani A; Synofzik M; Mahdieh N; Rezaei Z
Cerebellum; 2023 Aug; 22(4):640-650. PubMed ID: 35731353
[TBL] [Abstract][Full Text] [Related]
5. Retinal Architecture in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Insights into Disease Pathogenesis and Biomarkers.
Rezende Filho FM; Bremner F; Pedroso JL; de Andrade JBC; Marianelli BF; Lourenço CM; Marques-Júnior W; França MC; Kok F; Sallum JMF; Parkinson MH; Barsottini OG; Giunti P
Mov Disord; 2021 Sep; 36(9):2027-2035. PubMed ID: 33893680
[TBL] [Abstract][Full Text] [Related]
6. Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum.
Synofzik M; Soehn AS; Gburek-Augustat J; Schicks J; Karle KN; Schüle R; Haack TB; Schöning M; Biskup S; Rudnik-Schöneborn S; Senderek J; Hoffmann KT; MacLeod P; Schwarz J; Bender B; Krüger S; Kreuz F; Bauer P; Schöls L
Orphanet J Rare Dis; 2013 Mar; 8():41. PubMed ID: 23497566
[TBL] [Abstract][Full Text] [Related]
7. Widening the clinical, radiological and genetic spectrum of autosomal recessive ataxia of Charlevoix-Saguenay in Indian patients.
Divya KP; Cherian A; Dhing HK; Kumar S; Thomas B; Faruq M
Acta Neurol Belg; 2024 Apr; 124(2):475-484. PubMed ID: 37898963
[TBL] [Abstract][Full Text] [Related]
8. Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) in a Thai Patient: The Classic Clinical Manifestations, Funduscopic Feature, and Brain Imaging Findings with a Novel Mutation in the
Srikajon J; Pitakpatapee Y; Limwongse C; Chirapapaisan N; Srivanitchapoom P
Tremor Other Hyperkinet Mov (N Y); 2020 Jun; 10():1. PubMed ID: 32775015
[TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - A Polish family with novel SACS mutations.
Krygier M; Konkel A; Schinwelski M; Rydzanicz M; Walczak A; Sildatke-Bauer M; Płoski R; Sławek J
Neurol Neurochir Pol; 2017; 51(6):481-485. PubMed ID: 28843771
[TBL] [Abstract][Full Text] [Related]
10. Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child.
Incecik F; Hergüner OM; Bisgin A
J Pediatr Neurosci; 2018; 13(3):355-357. PubMed ID: 30271475
[TBL] [Abstract][Full Text] [Related]
11. A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Samanci B; Gokalp EE; Bilgic B; Gurvit H; Artan S; Hanagasi HA
Neurol Sci; 2021 Jul; 42(7):2969-2973. PubMed ID: 33559790
[TBL] [Abstract][Full Text] [Related]
12. Novel Variants in
Zaman Q; Khan MA; Sahar K; Rehman G; Khan H; Rehman M; Najumuddin ; Ahmad I; Tariq M; Muthaffar OY; Abdulkareem AA; Bibi F; Naseer MI; Faisal MS; Wasif N; Jelani M
Genes (Basel); 2023 Jan; 14(2):. PubMed ID: 36833258
[TBL] [Abstract][Full Text] [Related]
13. ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
Vermeer S; Meijer RP; Pijl BJ; Timmermans J; Cruysberg JR; Bos MM; Schelhaas HJ; van de Warrenburg BP; Knoers NV; Scheffer H; Kremer B
Neurogenetics; 2008 Jul; 9(3):207-14. PubMed ID: 18465152
[TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a family report from South Brazil.
Burguêz D; Oliveira CM; Rockenbach MABC; Fussiger H; Vedolin LM; Winckler PB; Maestri MK; Finkelsztejn A; Santorelli FM; Jardim LB; Saute JAM
Arq Neuropsiquiatr; 2017 Jun; 75(6):339-344. PubMed ID: 28658401
[TBL] [Abstract][Full Text] [Related]
15. Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay due to Novel Mutations in the
Sharma R; Aravindhan A; Puente C; Veerapandiyan A
J Investig Med High Impact Case Rep; 2022; 10():23247096221139670. PubMed ID: 36458808
[TBL] [Abstract][Full Text] [Related]
16. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a report of MR imaging in 5 patients.
Martin MH; Bouchard JP; Sylvain M; St-Onge O; Truchon S
AJNR Am J Neuroradiol; 2007 Sep; 28(8):1606-8. PubMed ID: 17846221
[TBL] [Abstract][Full Text] [Related]
17. Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay without Spasticity.
Aida I; Ozawa T; Fujinaka H; Goto K; Ohta K; Nakajima T
Intern Med; 2021 Dec; 60(24):3963-3967. PubMed ID: 34121011
[TBL] [Abstract][Full Text] [Related]
18. Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series.
Prodi E; Grisoli M; Panzeri M; Minati L; Fattori F; Erbetta A; Uziel G; D'Arrigo S; Tessa A; Ciano C; Santorelli FM; Savoiardo M; Mariotti C
Eur J Neurol; 2013 Jan; 20(1):138-46. PubMed ID: 22816526
[TBL] [Abstract][Full Text] [Related]
19. Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Habibzadeh P; Tabatabaei Z; Inaloo S; Nashatizadeh MM; Synofzik M; Ostovan VR; Faghihi MA
Front Genet; 2020; 11():585136. PubMed ID: 33414805
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]