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Publications by Ylmar Correa Neto

Frequency of the Different Mutations Causing Spinocerebellar Ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a Large Group of Brazilian Patients

Arquivos de Neuro-Psiquiatria
Biological PsychiatryNeurology
1997English

Related publications

264. Translating RNAi Therapy for Spinocerebellar Ataxia 1 (SCA1) to the Clinic

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2014English

A Common Disease Haplotype Segregating in Spinocerebellar Ataxia 2 (SCA2) Pedigrees of Diverse Ethnic Origin

European Journal of Human Genetics
Genetics
1999English

Mutations inKCND3cause Spinocerebellar Ataxia Type 22

Annals of Neurology
Neurology
2012English

Brain MRI, Lumbar CSF Monoamine Concentrations, and Clinical Descriptors of Patients With Spinocerebellar Ataxia Mutations.

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
1996English

Brain Derived Neurotrophic Factor (BDNF) Delays Onset of Pathogenesis in Transgenic Mouse Model of Spinocerebellar Ataxia Type 1 (SCA1)

Frontiers in Cellular Neuroscience
Molecular NeuroscienceCellular
2019English

Frequency of KCNC3 DNA Variants as Causes of Spinocerebellar Ataxia 13 (SCA13)

PLoS ONE
Multidisciplinary
2011English

Spinocerebellar Ataxia Type 13

2020English

Spinocerebellar Ataxia Type 3

2020English

Spinocerebellar Ataxia Type 8

2020English

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