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au.\*:("MAAT-KIEVIT, J. A")

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Diagnosis and management of early-and late-onset cerebellar ataxiaBRUSSE, E; MAAT-KIEVIT, J. A; VAN SWIETEN, J. C et al.Clinical genetics. 2007, Vol 71, Num 1, pp 12-24, issn 0009-9163, 13 p.Article

Family history and DNA analysis in patients with suspected Huntington's diseaseSIESLING, S; DE VLIS, M. V.-V; LOSEKOOT, M et al.Journal of neurology, neurosurgery and psychiatry. 2000, Vol 69, Num 1, pp 54-59, issn 0022-3050Article

Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysisVAN DE WARRENBURG, B. P. C; SINKE, R. J; KNOERS, N. V. A. M et al.Neurology. 2002, Vol 58, Num 5, pp 702-708, issn 0028-3878Article

Distinct genetic forms of frontotemporal dementiaSEELAAR, H; KAMPHORST, W; DOOIJES, D et al.Neurology. 2008, Vol 71, Num 16, pp 1220-1226, issn 0028-3878, 7 p.Article

Monozygotic twin brothers with the fragile X syndrome : different CGG repeats and different mental capacitiesHELDERMAN-VAN DEN ENDEN, A. T. J. M; MAASWINKEL-MOOIJ, P. D; HOOGENDOORN, E et al.Journal of medical genetics. 1999, Vol 36, Num 3, pp 253-257, issn 0022-2593Article

Early-onset parkinsonism associated with PINK1 mutations : Frequency, genotypes, and phenotypesBONIFATI, V; ROHE, C. F; FINCATI, E et al.Neurology. 2005, Vol 65, Num 1, pp 87-95, issn 0028-3878, 9 p.Article

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