Neuromelanin imaging analyses of the substantia nigra in patients with Machado-Joseph disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Neurology (clinical),Radiology, Nuclear Medicine and imaging
Link
http://link.springer.com/content/pdf/10.1007/s00234-020-02479-9.pdf
Reference36 articles.
1. Mendonça N, França MC Jr, Gonçalves AF, Januário C (2018) Clinical features of Machado-Joseph disease. Adv Exp Med Biol 1049:255–273
2. Schöls L, Bauer P, Schmidt T, Schulte T, Riess O (2004) Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol 3:291–304
3. Kawaguchi Y, Okamoto T, Taniwaki M, Aizawa M, Inoue M, Katayama S, Kawakami H, Nakamura S, Nishimura M, Akiguchi I, Kimura J, Narumiya S, Kakizuka A (1994) CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet 8:221–228
4. Dürr A, Stevanin G, Cancel G, Duyckaerts C, Abbas N, Didierjean O et al (1996) Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features. Ann Neurol 39:490–499
5. Schöls L, Reimold M, Seidel K, Globas C, Brockmann K, Hauser TK et al (2015) No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra. Brain. 138:3316–3326
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