141 related articles for article (PubMed ID: 34162189)
1. Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Cho H; Lyoo CH; Park SE; Seo Y; Han SH; Han J
Korean J Ophthalmol; 2021 Aug; 35(4):330-331. PubMed ID: 34162189
[No Abstract] [Full Text] [Related]
2. Optical coherence tomography in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Parkinson MH; Bartmann AP; Clayton LMS; Nethisinghe S; Pfundt R; Chapple JP; Reilly MM; Manji H; Wood NJ; Bremner F; Giunti P
Brain; 2018 Apr; 141(4):989-999. PubMed ID: 29538656
[TBL] [Abstract][Full Text] [Related]
3. Two cases of early-onset autosomal recessive spastic ataxia of Charlevoix-Saguenay diagnosed in adulthood.
Sahin T; Karaarslan FT; Yilmaz R; Tekgül Ş; Başak AN; Akbostanci MC
Clin Neurol Neurosurg; 2021 Feb; 201():106423. PubMed ID: 33348119
[No Abstract] [Full Text] [Related]
4. Retinal and pontine striations: neurodiagnostic signs of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Leavitt JA; Singer W; Brown WL; Pulido JS; Brodsky MC
J Neuroophthalmol; 2014 Dec; 34(4):369-71. PubMed ID: 25237835
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Foveal hypoplasia in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Shah CT; Ward TS; Matsumoto JA; Shildkrot Y
J AAPOS; 2016 Feb; 20(1):81-3. PubMed ID: 26917082
[TBL] [Abstract][Full Text] [Related]
7. [Spastic ataxia of Charlevoix-Saguenay: Diagnosis made on fundus examination].
Smirnov V; Marks C; Debruyne P; Riquet A; Defoort-Dhellemmes S
J Fr Ophtalmol; 2020 Sep; 43(7):676-677. PubMed ID: 32591161
[No Abstract] [Full Text] [Related]
8. Absent Foveal Avascular Zone in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Douglas VP; Douglas KAA; Miller JB; Gaier ED
J Neuroophthalmol; 2021 Jun; 41(2):e166-e168. PubMed ID: 32991389
[No Abstract] [Full Text] [Related]
9. Spastic ataxias.
Bereznyakova O; Dupré N
Handb Clin Neurol; 2018; 155():191-203. PubMed ID: 29891058
[TBL] [Abstract][Full Text] [Related]
10. Diagnostic Optic Nerve Features in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Hepschke JL; Rajabally YA; Mollan SP
JAMA Neurol; 2023 Jan; 80(1):104-106. PubMed ID: 36374509
[TBL] [Abstract][Full Text] [Related]
11. Coexistence of autosomal recessive spastic ataxia of Charlevoix Saguenay and spondyloepiphyseal dysplasia in a Turkish patient.
Kurt S; Kartal E; Aksoy D; Cevik B; Eken AG; Sahbaz I; Nazli Basak A
J Neurol Sci; 2015 Oct; 357(1-2):290-1. PubMed ID: 26142023
[No Abstract] [Full Text] [Related]
12. Novel SACS mutation in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Sánchez MG; Pérez JE; Pérez MR; Redondo AG
J Neurol Sci; 2015 Nov; 358(1-2):475-6. PubMed ID: 26344561
[No Abstract] [Full Text] [Related]
13. Teaching NeuroImages: Autosomal recessive spastic ataxia of Charlevoix-Saguenay: Typical MRI findings.
Biswas A; Varman M; Yoganathan S; Subhash PK; Mani S
Neurology; 2018 Apr; 90(14):e1271-e1272. PubMed ID: 29610238
[No Abstract] [Full Text] [Related]
14. 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]
15. Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS.
Rezende Filho FM; Parkinson MH; Pedroso JL; Poh R; Faber I; Lourenço CM; Júnior WM; França Junior MC; Kok F; Sallum JMF; Giunti P; Barsottini OGP
Parkinsonism Relat Disord; 2019 May; 62():148-155. PubMed ID: 30638817
[TBL] [Abstract][Full Text] [Related]
16. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): typical clinical and neuroimaging features in a Brazilian family.
Pedroso JL; Braga-Neto P; Abrahão A; Rivero RL; Abdalla C; Abdala N; Barsottini OG
Arq Neuropsiquiatr; 2011; 69(2B):288-91. PubMed ID: 21625752
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: compound heterozygotes for nonsense mutations of the SACS gene.
Narayanan V; Rice SG; Olfers SS; Sivakumar K
J Child Neurol; 2011 Dec; 26(12):1585-9. PubMed ID: 21745802
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
