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Publications by Howard Slater
Molecular Inconsistencies in a Fragile X Male With Early Onset Ataxia
Genes
Genetics
Linking the FMR1 Alleles With Small CGG Expansions With Neurodevelopmental Disorders: Preliminary Data Suggest an Involvement of Epigenetic Mechanisms
American Journal of Medical Genetics, Part A
Genetics
Related publications
Fragile Male, Not Fragile-X
Advances in Psychiatric Treatment
Fragile X Premutation With Atypical Symptoms at Onset
Archives of Neurology
Mouse Models of the Fragile X Premutation and the Fragile X Associated Tremor/Ataxia Syndrome
Results and Problems in Cell Differentiation
Developmental Biology
Cell Biology
Parkinsonism in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Revisited
Parkinsonism and Related Disorders
Gerontology
Geriatrics
Neurology
Dementia in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Comparison With Alzheimer's Disease
American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics
Psychiatry
Molecular Neuroscience
Mental Health
Genetics
Cellular
Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) in Grey Zone Carriers
Clinical Genetics
Genetics
Hypertension inFMR1premutation Males With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)
American Journal of Medical Genetics, Part A
Genetics
In Silico, in Vitro, and in Vivo Approaches to Identify Molecular Players in Fragile X Tremor and Ataxia Syndrome
Frontiers in Molecular Biosciences
Biochemistry
Genetics
Molecular Biology
CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome
Neuron
Neuroscience
