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Publications by Foad Taghdiri

Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports
Multidisciplinary
2016English

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Novel GRN Mutation Presenting as an Aphasic Dementia and Evolving Into Corticobasal Syndrome

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Novel Mutations in COL4A3, COL4A4, and COL4A5 in Chinese Patients With Alport Syndrome

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Numerosity Impairment in Corticobasal Syndrome.

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2010English

Novel IRF6 Mutations in Honduran Van Der Woude Syndrome Patients

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2011English

Dopamine Transporter SPECT Imaging in Corticobasal Syndrome

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391 Validating Causative Mutations in Patients With Ehlers-Danlos Syndrome Using a Novel Xenograft Model

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Novel Mutations in BCOR in Three Patients With Oculo-Facio-Cardio-Dental Syndrome, but None in Lenz Microphthalmia Syndrome

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Three Novel PAX6 Mutations in Patients With Aniridia

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Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients

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