Hanna, M. G.

The primary periodic paralyses: diagnosis, pathogenesis and treatment

Venance, S. L., Cannon, S. C., Fialho, D., Fontaine, B., Hanna, M. G., Ptacek, L. J., Tristani-Firouzi, M., Tawil, R., & Griggs, R. C. (2006) · Brain

Ion channel regulation and functionCardiac electrophysiology and arrhythmias

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Cardiolipin, Mitochondria, and Neurological Disease

Falabella, M., Vernon, H. J., Hanna, M. G., Claypool, S. M., & Pitceathly, R. D. S. (2021) · Trends in Endocrinology & Metabolism

Mitochondrial Function and PathologyLipid metabolism and biosynthesis

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Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

Matthews, E., Labrum, R., Sweeney, M. G., Sud, R., Haworth, A., Chinnery, P. F., Meola, G., Schorge, S., Kullmann, D. M., Davis, M. B., et al. (2009) · Neurology

Ion channel regulation and functionCardiac electrophysiology and arrhythmias

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Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment

Salpietro, V., Malintan, N. T., Llano-Rivas, I., Spaeth, C. G., Efthymiou, S., Striano, P., Vandrovcova, J., Cutrupi, M. C., Chimenz, R., David, E., et al. (2019) · The American Journal of Human Genetics

Cellular transport and secretionGenetics and Neurodevelopmental Disorders

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Climate change and disorders of the nervous system

Sisodiya, S. M., Gulcebi, M. I., Fortunato, F., Mills, J. D., Haynes, E., Bramon, E., Chadwick, P., Ciccarelli, O., David, A. S., De Meyer, K., et al. (2024) · The Lancet Neurology

Climate Change and Health ImpactsHealth, Environment, Cognitive Aging

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Muscle and not neuronal biomarkers correlate with severity in spinal and bulbar muscular atrophy

Lombardi, V., Querin, G., Ziff, O. J., Zampedri, L., Martinelli, I., Heller, C., Foiani, M., Bertolin, C., Lu, C.-H., Malik, B., et al. (2019) · Neurology

Genetic Neurodegenerative DiseasesAmyotrophic Lateral Sclerosis Research

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An interactive voice response diary for patients with non‐dystrophic myotonia

Statland, J. M., Wang, Y., Richesson, R., Bundy, B., Herbelin, L., Gomes, J., Trivedi, J., Venance, S., Amato, A., Hanna, M., et al. (2011) · Muscle & Nerve

Ion channel regulation and functionDeep Brain Stimulation and Movement Disorders

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Mutations in XRCC1 cause cerebellar ataxia and peripheral neuropathy

O’Connor, E., Vandrovcova, J., Bugiardini, E., Chelban, V., Manole, A., Davagnanam, I., Wiethoff, S., Pittman, A., Lynch, D. S., Efthymiou, S., et al. (2018) · Journal of Neurology, Neurosurgery & Psychiatry

Genetic Neurodegenerative DiseasesHereditary Neurological Disorders

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Muscle disease: THE BARE ESSENTIALS

Merrison, A. F. A., & Hanna, M. G. (2009) · Practical Neurology

Inflammatory Myopathies and DermatomyositisMuscle Physiology and Disorders

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