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Publications by Carmen Müllner

Familial Hemiplegic Migraine Type 1 Mutations K1336E, W1684R, and V1696I Alter Cav2.1 Ca2+Channel Gating

Journal of Biological Chemistry

Molecular Biology

English

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Divergent Sodium Channel Defects in Familial Hemiplegic Migraine

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

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Recurrent ATP1A2 Mutations in Portuguese Families With Familial Hemiplegic Migraine

Journal of Human Genetics

English

Familial Hemiplegic Migraine Type I: The Molecular Signaling Pathway

Journal of Neurology & Stroke

English

Familial Hemiplegic Migraine With Prolonged Hemiplegia

Archives of Disease in Childhood

English

Sporadic Hemiplegic Migraine With ATP1A2 and Prothrombin Gene Mutations

Case Reports in Neurological Medicine

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Respiratory Arrest in Familial Hemiplegic Migraine: A Clinical and Neuropathological Study.

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Modal Gating of Human CaV2.1 (P/Q-Type) Calcium Channels

Journal of General Physiology

English

Hypertrophic Cardiomyopathy Mutations Increase Myofilament Ca2+buffering, Alter Intracellular Ca2+handling and Stimulate Ca2+dependent Signalling

Journal of Biological Chemistry

Molecular Biology

English

Differential Modulation of Cav2.1 Channels by Calmodulin and Ca2+-Binding Protein 1

Nature Neuroscience

English