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Publications by Angelika F. Hahn
Mutation of Senataxin Alters Disease-Specific Transcriptional Networks in Patients With Ataxia With Oculomotor Apraxia Type 2
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Supportive Care for Patients With Guillain-Barré Syndrome
Archives of Neurology
Related publications
Ataxia With Oculomotor Apraxia Type 1 - New Mutation, Characteristic Phenotype
Movement Disorders Clinical Practice
Neurology
Erratum To: Ataxia With Oculomotor Apraxia Type 1 Without Oculomotor Apraxia: A Case Report
Journal of Clinical Neurology (Korea
Neurology
Ataxia-Oculomotor Apraxia Type 1
Recessive Ataxia With Ocular Apraxia
Archives of Neurology
Eyelid "Apraxia" in Patients With Motor Neuron Disease.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4
Frontiers in Neurology
Neurology
Neurofibromatosis Type 2 Presenting With Oculomotor Ophthalmoplegia and Distal Myopathy
Case Reports in Ophthalmological Medicine
Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity
American Journal of Human Genetics
Genetics
Metformin in Patients With Type 2 Diabetes and Kidney Disease
JAMA - Journal of the American Medical Association
Medicine
