ataxia - Robuta Search

https://friedreichsataxianews.com/ Friedreich's Ataxia News | Community, Research & Resources May 28, 2026 - The Web's Daily Resource for Friedreich's Ataxia News community research ataxia news resources https://www.curefa.org/ FARA - Friedreich's Ataxia Research Alliance - Funding Research to Cure FA Jan 19, 2026 - The Friedreich’s Ataxia Research Alliance (FARA) is a 501(c)(3) nonprofit dedicated to curing Friedreich’s ataxia by funding research, supporting clinical... research alliance fara ataxia funding cure https://ataxiacongress.org/ International Congress for Ataxia Research – ICAR 2026 international congress ataxia research icar https://ataxia-global-initiative.net/ Ataxia Global Initiative Oct 23, 2025 - The Ataxia Global Initiative (AGI) is a worldwide research platform that has the goal to facilitate the clinical development of therapies for ataxias. ataxia global initiative https://pubmed.ncbi.nlm.nih.gov/7704559/ Mapping of Friedreich's ataxia locus by identification of recombination events in patients... The Friedreich's ataxia locus (FRDA) maps on chromosome 9q13. Genetic data, obtained from a small number of recombination events, indicated that the FRDA locus... https://disorders.eyes.arizona.edu/references/hereditary-ataxia-series-twenty-one-cases On hereditary ataxia with a series of twenty-one cases | Hereditary Ocular Diseases with a series of https://researchconnect.buffalo.edu/en/publications/iron-and-iron-responsive-proteins-in-the-cardiomyopathy-of-friedr/ Iron and iron-responsive proteins in the cardiomyopathy of Friedreich's ataxia - SUNY University at... https://medlineplus.gov/genetics/condition/autosomal-recessive-spastic-ataxia-of-charlevoix-saguenay/ Autosomal recessive spastic ataxia of Charlevoix-Saguenay: MedlinePlus Genetics Autosomal recessive spastic ataxia of Charlevoix-Saguenay, more commonly known as ARSACS, is a condition affecting muscle movement. Explore symptoms,... autosomal recessive spastic ataxia charlevoix https://species.wikimedia.org/wiki/Ataxia_variegata Ataxia variegata - Wikispecies ataxia variegata wikispecies https://www.repository.cam.ac.uk/items/4759a9ea-cf9e-4cae-b052-51bce5f6f9ce Genomic profiling of acute myeloid leukaemia associated with ataxia telangiectasia identifies a... Ataxia Telangiectasia (A-T) is an autosomal recessive disease, characterised by progressive neurodegeneration with cerebellar ataxia, oculo-cutaneous... acute myeloid leukaemia genomic profiling https://pubmed.ncbi.nlm.nih.gov/30332300/ Sacsin, mutated in the ataxia ARSACS, regulates intermediate filament assembly and dynamics Loss of sacsin, a large 520 kDa multidomain protein, causes autosomal recessive spastic ataxia of the Charlevoix-Saguenay, one of the most common... in the https://pubmed.ncbi.nlm.nih.gov/22328086/ Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy Autosomal dominant cerebellar ataxia, deafness and narcolepsy (ADCA-DN) is characterized by late onset (30-40 years old) cerebellar ataxia, sensory neuronal... cerebellar ataxia mutations cause autosomal https://brainandmind.weill.cornell.edu/adult-onset-niemann-pick-disease-type-c-masquerading-spinocerebellar-ataxia Adult-onset Niemann-Pick disease type C masquerading as spinocerebellar ataxia. | Feil Family Brain... https://pubmed.ncbi.nlm.nih.gov/41690933/ Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia Most patients with a rare movement disorder (MD) do not receive a molecular diagnosis, and the underlying genetic variants and mediating genes remain elusive.... loss of function https://research.rug.nl/nl/activities/genetics-in-dystonia-and-ataxia/ Genetics in dystonia and ataxia - de research portal van de Rijksuniversiteit Groningen research portal genetics dystonia ataxia https://rarediseases.info.nih.gov/diseases/17556/autosomal-recessive-cerebellar-ataxia-pyramidal-signs-nystagmus-oculomotor-apraxia-syndrome Autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome |... Find symptoms and other information about Autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome. cerebellar ataxia autosomal recessive pyramidal signs https://www.semanticscholar.org/topic/Spinocerebellar-ataxia-19/2314299 Spinocerebellar ataxia 19 | Semantic Scholar spinocerebellar ataxia semantic scholar https://pubmed.ncbi.nlm.nih.gov/2466555/?dopt=Abstract Ataxia-telangiectasia-like Chinese hamster V79 cell mutants with radioresistant DNA synthesis,... We have isolated three radiosensitive mutants (V-C4, V-E5, and V-G8) of the Chinese hamster V79 cell line which also show increased sensitivities to killing by... ataxia telangiectasia https://doctor.ndtv.com/faq/is-cerebral-and-cerebellar-ataxia-hereditary-4058 Is Cerebral and Cerebellar Ataxia hereditary? cerebellar ataxia cerebral hereditary https://lod.nal.usda.gov/nalt/en/page/13558?clang=es NAL Agricultural Thesaurus: NALT: ataxia nal agricultural thesaurus ataxia https://disorders.eyes.arizona.edu/references/autosomal-recessive-disorder-posterior-column-ataxia-and-retinitis-pigmentosa An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa | Hereditary... https://ub01.uni-tuebingen.de/xmlui/handle/10900/87156 A recessive ataxia diagnosis algorithm for the next generation sequencing era for the next generation recessive ataxia diagnosis algorithm https://publikationen.uni-tuebingen.de/xmlui/handle/10900/99519 Patient-reported outcomes in Friedreich's ataxia after withdrawal from idebenone patient reported outcomes https://www.news-medical.net/health/Friedreichs-Ataxia-Signs.aspx Friedreich's Ataxia Signs Jul 13, 2023 - Friedreich's ataxia is a hereditary disorder that leads to progressive and irreversible damage to the nervous system. Initial signs of the condition include... ataxia signs https://herenciageneticayenfermedad.blogspot.com/2016/02/bdnf-y-frataxina-nueva-diana-en-ataxia.html herenciageneticayenfermedad: BDNF y frataxina, nueva diana en ataxia de Friedreich -... BDNF y frataxina, nueva diana en ataxia de Friedreich - DiarioMedico.com PUBLICADO EN 'MOLECULAR THERAPY' BDNF y frataxina, nueva diana e... bdnf nueva diana en ataxia https://tobias-lib.ub.uni-tuebingen.de/xmlui/handle/10900/134287 Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17 https://pubmed.ncbi.nlm.nih.gov/37414537/ Can CANVAS due to RFC1 biallelic expansions present with pure ataxia? due to canvas https://es.wikipedia.org/wiki/Ataxia_de_Friedreich Ataxia de Friedreich - Wikipedia, la enciclopedia libre ataxia de friedreich wikipedia la enciclopedia libre https://collections.nlm.nih.gov/?f%5Bdrep2.subjectAggregate%5D%5B%5D=Ataxia&per_page=20&sort=drep3.titleSortForm+asc Subjects: Ataxia - Digital Collections - National Library of Medicine Search Results national library of medicine digital collections subjects ataxia search https://rarediseases.info.nih.gov/diseases/2600/early-onset-cerebellar-ataxia-with-retained-tendon-reflexes Early onset cerebellar ataxia with retained tendon reflexes | About the Disease | GARD Find symptoms and other information about Early onset cerebellar ataxia with retained tendon reflexes. about the disease early onset cerebellar ataxia https://pmc.ncbi.nlm.nih.gov/articles/PMC13034344/ Peripheral frataxin levels govern long-term clinical progression in Friedreich ataxia - PMC Novel therapeutics for Friedreich ataxia employ diverse strategies to increase frataxin protein levels, and a better understanding of the relation to clinical... long term https://profiles.uchicago.edu/profiles/display/8258189 Early Cerebellar Network Shifting in Spinocerebellar Ataxia Type 6. | Profiles RNS spinocerebellar ataxia early network shifting https://scholars.duke.edu/grant/297763 Scholars@Duke grant: A Cross-Species Atlas of Purkinje Cell Subtypes to Identify Ataxia-Causing... https://www.semanticscholar.org/topic/EPISODIC-ATAXIA%2C-TYPE-5/594995 EPISODIC ATAXIA, TYPE 5 | Semantic Scholar episodic ataxia type semantic scholar https://prism.northwestern.edu/records/taxfy-07b09 Hereditary Myokymia and Paroxysmal Ataxia hereditary ataxia https://about.uq.edu.au/experts/project/35101 Sleep measurements in Friedreich's ataxia, Huntington's disease patients and healthy volunteers |... https://about.uq.edu.au/experts/project/42007 Ataxia-telangiectasia: treating mitochondrial dysfunction with a novel form of anaplerosis |... ataxia telangiectasia mitochondrial dysfunction treating https://www.bigbadbikeride.com/ The Big Bad Bike Ride | Charity Bike ride for Friedreich's ataxia The Big Bad Bike Ride is a Charity Bike ride in aid of Friedreich's ataxia, set up by Graham Kennedy in 1991 the big bad bike ride charity ataxia https://refubium.fu-berlin.de/handle/fub188/34323?locale-attribute=en Refubium - Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1 optic atrophy https://pmc.ncbi.nlm.nih.gov/articles/PMC11994129/ Ataxia Telangiectasia with Giant Suprasellar Arachnoid Cyst - A Case Report and a Brief Review - PMC Ataxiatelangiectasia (A-T) is an infrequent genetic neurodegenerative disorder inherited autosomal recessively. It is mainly characterized by early-onset... https://www.semanticscholar.org/topic/Ataxia-Telangiectasia/8263 Ataxia Telangiectasia | Semantic Scholar An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA... ataxia telangiectasia semantic scholar https://cureat.org/index.php The Global Search for a Cure for A-T (Ataxia Telangiectasia) Cure A-T - A-T Global Directory search for a cure global ataxia telangiectasia https://pubmed.ncbi.nlm.nih.gov/17149738/ Case of spinocerebellar ataxia type 17 (SCA17) associated with only 41 repeats of the TATA-binding... Case of spinocerebellar ataxia type 17 (SCA17) associated with only 41 repeats of the TATA-binding protein (TBP) gene https://boris-portal.unibe.ch/entities/publication/19db9a09-ad7a-470e-8691-f5aee2d3c952 How to Detect Isolated PEX10-Related Cerebellar Ataxia? A 4-year-old boy presented with subacute onset of cerebellar ataxia. Neuroimaging revealed cerebellar atrophy. Metabolic screening tests aiming to detect... how to detect isolated related ataxia https://hsrc.himmelfarb.gwu.edu/smhs_neuro_facpubs/353/ "Neuropathology in a case of episodic ataxia type 4." by M J Merrill, D Nai et al. By M J Merrill, D Nai, Pritha Ghosh, et al., Published on 04/01/16 https://pubmed.ncbi.nlm.nih.gov/35882292/ Effects of a Supplement Containing Cannabidiol (CBD) on Sedation and Ataxia Scores and Health Supplements containing Cannabidiol (CBD) are available for horses, however, few studies have been published on their effects on behavior and health parameters.... https://structure.bmc.lu.se/idbase/RNF168base/index.php?content=bioinfor/IDbases RNF168base: Ataxia telangiectasia | Bioinformatics | ataxia telangiectasia bioinformatics https://pubmed.ncbi.nlm.nih.gov/15390180/ Cancer risk according to type and location of ATM mutation in ataxia-telangiectasia families Epidemiological studies have indicated that ataxia-telangiectasia (AT) heterozygotes in AT families have an increased risk of cancer, particularly of breast... https://ub01.uni-tuebingen.de/xmlui/handle/10900/104945 A clinical diagnostic algorithm for early onset cerebellar ataxia clinical diagnostic early onset algorithm ataxia https://aims.biokin.com.au/ Biokin | Ataxia Instrumented Measurement Systems BioKin Ataxia Instrumented Measurement Systems deliver scalable, AI-enabled tools for monitoring neurodegenerative disorders, supporting clinical trials and... ataxia measurement systems https://pan-american-hereditary-ataxia-network-pahan7.webnode.page/ Pan-american-hereditary-ataxia-network-pahan7 Pan American Hereditary Ataxia pan american hereditary ataxia network https://pubmed.ncbi.nlm.nih.gov/5687489/?dopt=Abstract Radiation reaction in ataxia telangiectasia Radiation reaction in ataxia telangiectasia radiation reaction ataxia telangiectasia https://pubmed.ncbi.nlm.nih.gov/33151022/ Electrocardiogram in Friedreich's ataxia: A short-term surrogate endpoint for treatment efficacy Friedreich's ataxia is a rare degenerative neuromuscular disorder, caused by a homozygous GAA triplet repeat expansion in the frataxin (FXN) gene, with a broad... https://www.med.unc.edu/mhi/the-schisler-lab-links-specific-protein-mutations-to-ataxia-disease-symptoms/ The Schisler Lab Links Specific Protein Mutations to Ataxia Disease Symptoms | UNC McAllister Heart... Nov 19, 2019 - Congratulations to the lab of Jonathan Schisler, MS, PhD, Assistant Professor, Department of Pharmacology, for linking the specific biochemical changes to a... https://bibliographie.uni-tuebingen.de/xmlui/handle/10900/85056?show=full Identifying Niemann-Pick type C in early-onset ataxia: two quick clinical screening tools https://www.justgiving.com/team/connorssuperheroes Connor's Superheroes! is fundraising for Ataxia Telangiectasia Children's Project, Inc. Help Michelle and Dan Graban raise money to support Ataxia Telangiectasia Children's Project, Inc. ataxia telangiectasia connor superheroes fundraising https://experts.umn.edu/en/projects/prevalence-of-gluten-sensitivity-in-hereditary-ataxia/ Prevalence of Gluten Sensitivity in Hereditary Ataxia - Experts@Minnesota gluten sensitivity prevalence hereditary ataxia experts https://boris-portal.unibe.ch/entities/publication/69dd3423-e14f-491a-91a9-f590ec085a51 Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs. We investigated a hereditary cerebellar ataxia in Belgian Shepherd dogs. Affected dogs developed uncoordinated movements and intention tremor at two weeks of... https://disorders.eyes.arizona.edu/references/2-bp-deletion-mitochondrial-atp-6-gene-responsible-narp-neuropathy-ataxia-and-retinitis A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and... https://ub01.uni-tuebingen.de/xmlui/handle/10900/105923 Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage... https://www.ucl.ac.uk/brain-sciences/ion/research/research-centres/ataxia-centre/ataxia-centre-news Ataxia Centre news | UCL Faculty of Brain Sciences centre news ataxia ucl faculty brain https://tobias-lib.uni-tuebingen.de/xmlui/handle/10900/163426 Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type... https://publikationen.uni-tuebingen.de/xmlui/handle/10900/88307 Dysphagia in Friedreich Ataxia dysphagia ataxia https://scholarworks.uvm.edu/items/58ac36e3-f475-47ac-aa98-4bda85b585ce Distinguishing Episodic Ataxia from Vestibular Migraine in Two Patients with History of Headache Cases of episodic ataxia in patients with a history of migraine/headache are likely under-recognized, as the initial presentation may favor vestibular... https://pubmed.ncbi.nlm.nih.gov/30926972/ Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia Late-onset ataxia is common, often idiopathic, and can result from cerebellar, proprioceptive, or vestibular impairment; when in combination, it is also termed... https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0268337 Detection and differentiation of ataxic and hypokinetic dysarthria in cerebellar ataxia and... Dysarthria may present during the natural course of many degenerative neurological conditions. Hypokinetic and ataxic dysarthria are common in movement... detection differentiation ataxic dysarthria ataxia https://pubmed.ncbi.nlm.nih.gov/35395209/ De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy de novo variants https://about.uq.edu.au/experts/project/28813 Investigation of the role of oxidative stress in pulmonary disease in ataxia-telangiectasia |... of the oxidative stress pulmonary disease investigation role https://publikationen.uni-tuebingen.de/xmlui/handle/10900/91874 Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of... https://www.commondataelements.ninds.nih.gov/Friedreich%27s%20Ataxia Friedreich's Ataxia | NINDS CDE ataxia ninds cde https://dptcapstone.web.unc.edu/tag/cerebellar-ataxia/ cerebellar ataxia | DPT Capstone cerebellar ataxia dpt capstone https://id.wikipedia.org/wiki/Ataxia_illita Ataxia illita - Wikipedia bahasa Indonesia, ensiklopedia bebas bahasa indonesia ataxia wikipedia ensiklopedia bebas https://publikationen.uni-tuebingen.de/xmlui/handle/10900/117116?show=full Real-life gait assessment in degenerative cerebellar ataxia. Toward ecologically valid biomarkers real life https://bmcdev-e2b2a6gdfff3f6d0.uaenorth-01.azurewebsites.net/diseases/ataxia/ Ataxia - Burjeel Medical City ataxia medical city https://fine-arts-for-friedreich-s-ataxia.webnode.page/ Fine-arts-for-friedreich-s-ataxia Fine Arts For Friedreich's Ataxia fine arts ataxia https://ub01.uni-tuebingen.de/xmlui/handle/10900/151621 Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia https://pubmed.ncbi.nlm.nih.gov/28746835/ Genetic ataxia telangiectasia porcine model phenocopies the multisystemic features of the human... Ataxia telangiectasia (AT) is a progressive multisystem autosomal recessive disorder caused by mutations in the AT-mutated (ATM) gene. Early onset AT in... ataxia telangiectasia genetic porcine model https://researchportal.helsinki.fi/en/publications/autosomal-recessive-progressive-myoclonus-epilepsy-with-ataxia-an/ Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation - University... mental retardation autosomal recessive progressive myoclonus https://www.balancecrutch.com/ Ataxia Balance Crutch - Helping people with balance challenges walk with confidence The first Balance Crutch. Unlike any other assistive mobility device on the market the patented Ataxia Balance Crutch is designed for people with balance... helping people ataxia balance crutch challenges https://neuromuscular.wustl.edu/ataxia/recatax.html Ataxia: Recessive ataxia recessive https://rarediseases.info.nih.gov/diseases/17209/ataxia-telangiectasia-like-disorder-1 Ataxia-telangiectasia-like disorder 1 | About the Disease | GARD Find symptoms and other information about Ataxia-telangiectasia-like disorder 1. about the disease ataxia telangiectasia like disorder gard https://podcastdx.libsyn.com/website/friedreichs-ataxia-with-alexia-baker PodcastDX: Friedreich's Ataxia with Alexia Baker This week we talk with Alexis, 25, was diagnosed with Friedreich ataxia (FA) five years ago and since then, has been using her voice and social media platforms... ataxia alexia baker https://pmc.ncbi.nlm.nih.gov/articles/PMC20004/ The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not... The product of the ataxia-telangiectasia gene (ATM) was identified by using an antiserum developed to a peptide corresponding to the deduced amino acid... https://pubmed.ncbi.nlm.nih.gov/18319072/ CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures Coenzyme Q(10) (CoQ(10)) plays a pivotal role in oxidative phosphorylation (OXPHOS) in that it distributes electrons between the various dehydrogenases and the... cerebellar ataxia gene mutations cause ubiquinone https://medlineplus.gov/genetics/condition/ataxia-pancytopenia-syndrome/ Ataxia-pancytopenia syndrome: MedlinePlus Genetics Ataxia-pancytopenia syndrome is a rare condition that affects the part of the brain that coordinates movement (the cerebellum) and blood-forming cells in the... ataxia pancytopenia syndrome medlineplus genetics https://www3.sbs.cuhk.edu.hk/en/achievements/vincent-cheng-yin-chun-bsc-graduate-awarded-prestigious-fellowship-from-the-national-ataxia-foundationvincent-cheng-yin-chun-a-2021-bsc-graduate-in-biomedical-sciences-is-currently-pursuing-his-d-p/ Vincent Cheng Yin Chun, BSc graduate awarded prestigious fellowship from the National Ataxia... https://pmc.ncbi.nlm.nih.gov/articles/PMC21549/ Isolation of full-length ATM cDNA and correction of the ataxia-telangiectasia cellular phenotype -... A gene mutated in the human genetic disorder ataxia-telangiectasia (A-T), ATM, was recently identified by positional cloning. ATM is a member of the... https://cordis.europa.eu/project/id/QLG1-CT-1999-00584/results/de Molecular and biochemical pathogenesis of friedreich's ataxia: search for treatments. |... Deliverables, publications, datasets, software, exploitable results search for molecular biochemical pathogenesis https://news.med.miami.edu/tag/late-onset-ataxia/ late onset ataxia Archives - InventUM late onset ataxia archives inventum https://healthcare.utah.edu/neurosciences/neurology/movement-disorders/ataxia Ataxia | University of Utah Health May 1, 2026 - Ataxia happens when parts of the nervous system that control how you move are damaged. People with ataxia can't control their muscles in their arms and legs.... university of utah ataxia health https://www.nhs.uk/services/service-directory/ataxia-telangiectasia-society/N10965655 Overview - Ataxia-Telangiectasia Society - NHS Official information from NHS about Ataxia-Telangiectasia Society including contact, directions and service details ataxia telangiectasia overview society nhs https://www.nichd.nih.gov/health/topics/fxtas/conditioninfo/treatments What are the treatments for Fragile X-Associated Tremor and Ataxia Syndrome (FXTAS)? | NICHD -... Certain medications and therapies are helpful for treating symptoms of FXTAS and may help slow its progression. However, no treatment can stop FXTAS from... https://scholars.duke.edu/publication/1600754 Scholars@Duke publication: Restless legs syndrome in Friedreich ataxia: a polysomnographic study. restless legs syndrome https://pubmed.ncbi.nlm.nih.gov/16080118/ Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with... Mutations in the catalytic subunit of the mitochondrial DNA polymerase gamma (POLG) have been found to be an important cause of neurological disease. Recently,... https://pubmed.ncbi.nlm.nih.gov/38261944/ Perspectives of the Friedreich ataxia community on gene therapy clinical trials Gene therapy is a potential treatment for Friedreich ataxia, with multiple programs on the horizon. The purpose of this study was to collect opinions about... of the friedreich ataxia gene therapy perspectives https://pure.psu.edu/en/publications/replication-stalling-at-friedreichs-ataxia-gaasubnsub-repeats-in-/ Replication Stalling at Friedreich's Ataxia (GAA)n Repeats In Vivo - Penn State https://academiccommons.columbia.edu/doi/10.7916/d8-hgfd-t291 Familial Spinocerebellar Ataxia Type 2 Parkinsonism Presenting as Intractable Oromandibular... We have previously described a Korean family afflicted with spinocerebellar ataxia type 2 (SCA2) parkinsonism in which genetic analysis revealed CAG expansion... spinocerebellar ataxia familial type parkinsonism presenting https://pubmed.ncbi.nlm.nih.gov/12562765/ Ataxia telangiectasia mutated proteins, MAPKs, and RSK2 are involved in the phosphorylation of STAT3 Phosphorylation at Ser(727) is known to be required for complete activation of STAT3 by diverse stimuli including UV irradiation, but the kinase(s) responsible... https://prism.northwestern.edu/records/zbwpv-11h80 Migraine and Cerebellar Ataxia migraine ataxia https://medlineplus.gov/genetics/condition/spinocerebellar-ataxia-type-6/ Spinocerebellar ataxia type 6: MedlinePlus Genetics Spinocerebellar ataxia type 6 (SCA6) is a condition characterized by progressive problems with movement. Explore symptoms, inheritance, genetics of this... spinocerebellar ataxia type medlineplus genetics