Sarah Van Dine, DO

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Medical Specialty
Department or Group
Isabelle Rapin Division of Child Neurology, Saul R. Korey Department of Neurology
Patient Age Group(s)
Montefiore Medical Center
111 East 210 Street
Bronx, NY 10467
Fax (Medical Records)
University Affiliation
University Title
Resident Physician
Research Areas of Interest
Autoimmune Neuropathy
Congenital Myopathies
Vitamin D Deficiency in Myasthenia Gravis

Sarah Van Dine, DO, MS, is a Child Neurology Fellow at the Children's Hospital at Montefiore (Albert Einstein College of Medicine). She trained at the NYIT College of Osteopathic Medicine where she completed a year as an Academic Scholar receiving a Masters of Science in addition to her doctorate. Her prior research pursuits include studying cortical and cerebellar malformations, and the effect of hypothyroxenemia on cortical development. Currently, she is working on clinical research projects in the areas of vitamin D deficiency in myasthenia, autoimmune neuropathy, and small fiber neuropathy in children.

Spontaneous malformations of the cerebellar vermis: Prevalence, inheritance, and relationship to lobule/fissure organization in the C57BL/6 lineage.
Van Dine SE, Siu NY, Toia A, Cuoco JA, Betz AJ, Bolivar VJ, Torres G, Ramos RL.
Neuroscience. 2015 Dec 3;310:242-51.

Cellular and axonal diversity in molecular layer heterotopia of the rat cerebellar vermis.
Van Dine SE, Salem E, George E, Siu NY, Dotzler T, Ramos RL.
Biomed Res Int. 2013;2013:805467.

Axonal anatomy of molecular layer heterotopia of the cerebellar vermis.
Van Dine SE, Salem E, Patel DB, George E, Ramos RL.
J Chem Neuroanat. 2013 Jan;47:90-5.

Neurodevelopmental Malformations of the Cerebellar Vermis in Genetically Engineered Rats.
Ramos RL, Van Dine SE, Gilbert ME, Leheste JR, Torres G.
Cerebellum. 2015 Dec;14(6):624-31.

Cellular and axonal constituents of neocortical molecular layer heterotopia.
Ramos RL, Siu NY, Brunken WJ, Yee KT, Gabel LA, Van Dine SE, Hoplight BJ.
Dev Neurosci. 2014;36(6):477-89.

Molecular layer heterotopia of the cerebellar vermis in mutant and transgenic mouse models on a C57BL/6 background.
Ramos RL, Van Dine SE, George E, Patel D, Hoplight BJ, Leheste JR, Richfield EK, Torres G.
Brain Res Bull. 2013 Aug;97:63-8.

Neuronal migration defect of the developing cerebellar vermis in substrains of C57BL/6 mice: cytoarchitecture and prevalence of molecular layer heterotopia.
Mangaru Z, Salem E, Sherman M, Van Dine SE, Bhambri A, Brumberg JC, Richfield EK, Gabel LA, Ramos RL.
Dev Neurosci. 2013;35(1):28-39.