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THE STORY BEHIND THE SMILE: JEREMIAH'S JOURNEY WITH SPINOCEREBELLAR ATAXIA TYPE 10.

• Authors : OCASIO, HAILEY¹

• Source: Exceptional Parent; Dec2024, Vol. 54 Issue 12, p17-19, 3p

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The dawning age of therapy for Friedreich ataxia: The first therapy to target the underlying pathology of Friedreich ataxia was approved in 2023. Other drug and genetic therapies are in the pipeline.

• Authors : OSTERWEIL, NEIL

• Source: Neurology Reviews. 2023 Special Issue, Vol. 31, p25-28. 4p.

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FDA OKs first treatment for Friedreich ataxia.

• Source: Neurology Reviews. 2023 Special Issue, Vol. 31, p4-5. 2p.

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Recurrent Ataxia and Dystonia with Anti-Neurochondrin Autoantibodies

• Authors : BARREA, Christophe; DEPIERREUX, Frédérique

Subjects: movement disorders; autoimmunity; child

• Source: Neuropediatrics (2021)

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Vestibular impact of Friedreich ataxia in early onset patients.

• Authors : MAUDOUX, Audrey; Teissier, Natacha; Francois, Martine

Subjects: Human health sciences; Otolaryngology; Sciences de la santé humaine

• Source: Cerebellum and Ataxias (2020)

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Cerebellum & ataxias. [electronic resource].

Subjects: Cerebellum -- Periodicals; Cerebellum -- Diseases -- Periodicals; Cerebellar ataxia -- Periodicals

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Breaking the silence in Friedreich's ataxia.

• Authors : Festenstein R

Subjects: Histone Deacetylase Inhibitors*; Enzyme Inhibitors/Enzyme Inhibitors/Enzyme Inhibitors/*pharmacology ; Friedreich Ataxia/Friedreich Ataxia/Friedreich Ataxia/*genetics

• Source: Nature chemical biology [Nat Chem Biol] 2006 Oct; Vol. 2 (10), pp. 512-3.Publisher: Nature Pub. Group Country of Publication: United States NLM ID: 101231976 Publication Model: Print Cited Medium: Print ISSN: 1552-4450

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‘I’m in a Race Against Time ’.

• Authors : PFEFFER, STEPHANIE EMMA (AUTHOR); ESKIND, AMY (AUTHOR)

• Source: People. 12/13/2021, Vol. 96 Issue 24, p108-111. 4p. 6 Color Photographs.

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Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.

• Authors : Scholl, Ute I; Choi, Murim; Liu, Tiewen

Subjects: Abnormalities, Multiple/etiology/genetics; Animals; Ataxia

• Source: Proceedings of the National Academy of Sciences of the United States of America, 106 (14), 5842-7 (2009)

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POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonism.

• Authors : Van Maldergem, Lionel; Besse, Arnaud; De Paepe, Boel

Subjects: Life sciences; Genetics & genetic processes; Sciences du vivant

• Source: Annals of Clinical and Translational Neurology, 4 (1), 4-14 (2017)

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