Dr. Hart Lidov, MD

• Neuromuscular Medicine

• Pediatric Neurology

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• Brigham & Women's Hospital/boston Children's Hospital, Neuropathology

  Fellowship Hospital, 1991

• Brigham & Women's Hospital/boston Children's Hospital, Neuropathology|national Hospital Of London, Neuropathology

  Fellowship Hospital, 1991

• National Hospital Of London, Neuropathology

  Fellowship Hospital, 1989

• Massachusetts General Hospital, Pediatric Neurology

  Residency Hospital, 1987

• Massachusetts General Hospital, Pediatrics

  Internship Hospital, 1983

• Johns Hopkins University, Graduate School

  1982

• Johns Hopkins School Of Medicine

  Medical School, 1982

• Johns Hopkins University

  Undergraduate School, 1974

• Identification of a pathogenic mutation inATP2A1via in silico analysis of exome data for cryptic aberrant splice sites, 2019-01-28

• Disruption of GMNC-MCIDAS multiciliogenesis program is critical in choroid plexus carcinoma development, 2022-03-23

• EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy, 2016-02-17

• Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas, 2014-01-12

• A novelGIT2-BRAFfusion in pilocytic astrocytoma, 2017-11-15

• OTX2 Represses Myogenic and Neuronal Differentiation in Medulloblastoma Cells, 2012-09-17

• Inefficient dystrophin expression after cord blood transplantation in DMD, 2010-10-05

• Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations, 2016-05-20

• SomaticSLC35A2variants in the brain are associated with intractable neocortical epilepsy, 2018-05-16

• Sonic Hedgehog promotes proliferation of Notch-dependent monociliated choroid plexus tumour cells, 2016-03-21

• Differential Neuronal Vulnerability varies according to Specific Cardiopulmonary Bypass Insult in a Porcine Survival Model, 2010-04-08

• The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States, 2016-10-06

• Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation inGNE, 2011-06-28

• Mutations in the satellite cell geneMEGF10cause a recessive congenital myopathy with minicores, 2012-02-28

• The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles, 2018-07-24

• Rapid Reversal of Uremic Neuropathy Following Renal Transplantation in an Adolescent, 2011-12-21

• Aprotinin Protects the Cerebral Microcirculation during Cardiopulmonary Bypass, 2010-03-25