Glenn Lopate

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

Margaret J. Kovach, Brook Waggoner, Suzanne M. Leal et al. · Molecular Genetics and Metabolism · 2001 · 197 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +12

Exome sequencing reveals <i>DNAJB6</i> mutations in dominantly‐inherited myopathy

Matthew B. Harms, R. Brian Sommerville, Peggy Allred et al. · Annals of Neurology · 2011 · 172 citations · Full text

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

David Adams, Michael Polydefkis, Alejandra González‐Duarte et al. · The Lancet Neurology · 2020 · 154 citations · Full text

Alzheimer's Disease, Open-label Extension Study, Medicine +5

Treatment of Chronic Inflammatory Demyelinating Polyneuropathy With High-Dose Intermittent Intravenous Methylprednisolone

Glenn Lopate, Alan Pestronk, Muhammad Al‐Lozi · Archives of Neurology · 2005 · 115 citations

Sensory exam with a quantitative tuning fork

Alan Pestronk, Julaine Florence, T. Levine et al. · Neurology · 2004 · 113 citations