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Virtual Grand Rounds
Athena Diagnostics, Inc. is proud to present a series of independently created Virtual Grand Rounds. Please browse the educational opportunities presented below. COL4A1 Mutations and Hereditary Small Vessel Diseases of the Brain
Anand Viswanathan, MD, Ph.D.
Memor Disorders Unit and Stroke Service
Massachusetts General Hospital
Boston, MA Alpers Disease: Recognition, Evaluation, and Prognosis of POLG1 Mutations M. Scott Perry, MD
Medical Director, Epilepsy Monitoring Unit
Comprehensive Epilepsy Program
Cook Children's Medical Center
Fort Worth, TX
Diagnosis and Management of Myasthenia Gravis
by Jonathan Goldstein, MD
Associate Professor of Neurology and
Director of Neuromuscular Medicine,
Yale University School of Medicine Congenital Hyperinsulunism: Disease, Diagnosis, and Appropriate Treatments
by Paul S. Thornton, M.B., B.Ch., M.R.C.P.I.
Medical Director of Endocrinology,
Cook Children's Medical Center
Fort Worth, TX Spinal Muscular Atrophy (SMA)
by Basil T. Darras, MA
Associate Neurologist-in-Chief
Joseph J. Volpe Professor of Neurology (Pediatrics) Harvard Medical School Director, Division of Clinical Neurology Director, Neuromuscular Program Department of Neurology Children’s Hospital Boston Epilepsy Limited to Females with Mental Retardation
Director of Pediatrics
University of Melbourne,
Melbourne, Australia
Dravet Syndrome
by Ingrid Scheffer, MD
Director of Pediatrics
University of Melbourne,
Melbourne, Australia CADASIL: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
by Stephen Salloway, MD, MS
Director of Neurology and the Memory and Aging Program
Butler Hospital
Professor of Clinical Neurosciences and Psychiatry, The Warren Alpine Medical School of Brown University
Providence, RI Tuberous Sclerosis Update
by Mustafa Sahin, M.D., Ph.D.
Director, Multi-Disciplinary TSC Program
Children's Hospital, Boston
Harvard Medical School
Boston, MA ALS: Perspectives in Genetics
by Thomas Kwiatkowski, Jr., M.D., Ph.D.
Instructor of Neurology
Massachusetts General Hospital,
Harvard Medical School
Boston, MA Evidence for the Utility of IFN NAbs in Multiple Sclerosis
by Elliott M. Frohman, MD, Ph.D.
Professor of Neurology and Ophthalmology
Director, Multiple Sclerosis Program
University of Texas Southwestern The Genetic and Molecular Basis of Epilepsy
by John Mulley, PhD FHGSA
Department of Genetic Medicine, SA Pathology
Women's and Children's Hospital Campus
Adelaide, Australia Myasthenia Gravis
by Dr. Donald B. Sanders
Professor of Medicine, Division of Neurology
Duke University Medical Center
Durham, NC Hemiplegic Migraine
by Dr. Jonathan Gladstone
Director, Gladstone Headache Clinic
Director of Neurology & Headache Medicine, Cleveland Clinic Canada
Headache Specialist, Sunnybrook Health Sciences Centre
Co-Director, Headache Clinic, The Hospital for Sick Children, Toronto, Ontario, Canada Overview of Charcot-Marie-Tooth Disease
by Dr. Michael Shy
Professor of Neurology, Member of Center for Molecular Medicine and Genetics,
Wayne State University School of Medicine Disorders of the Calcium Sensing Receptor
(Familial Hypocalciuric Hypercalcemia)
by Dr. Ed Brown
Chief of Calcium & Bone Section-Endocrine Hypertensionb Division
Brigham and Women's Hospital - Boston, MA Maturity-Onset Diabetes of Youth
Monogenic Diabetes Syndromes
by Dr. William E. Winter
Department of Pathology and Pediatrics, University of Florida - Gainesville
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