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Publications by Vichithra R. B. Liyanage

Rett Syndrome and MeCP2

NeuroMolecular Medicine

Molecular Neuroscience

Molecular Medicine

English

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MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

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Bisphosphonates and MeCP2 Deficiency: Cellular Studies and Clinical Application in Rett Syndrome

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MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome

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The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders

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MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

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Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome

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Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome

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Mosaic MECP2 Variants in Males With Classical Rett Syndrome Features, Including Stereotypical Hand Movements

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