Sarnat, Harvey B.

Infantile tauopathies: Hemimegalencephaly; tuberous sclerosis complex; focal cortical dysplasia 2; ganglioglioma

Sarnat, H. B., & Flores-Sarnat, L. (2015) · Brain and Development

Epilepsy research and treatmentFetal and Pediatric Neurological Disorders

Cited by 73

Updated clinical recommendations for the management of tuberous sclerosis complex associated epilepsy

Specchio, N., Nabbout, R., Aronica, E., Auvin, S., Benvenuto, A., de Palma, L., Feucht, M., Jansen, F., Kotulska, K., Sarnat, H., et al. (2023) · European Journal of Paediatric Neurology

Tuberous Sclerosis Complex ResearchEpilepsy research and treatment

Cited by 58

MicroRNA expression patterns in human astrocytes in relation to anatomical location and age.

Rao, V. T. S., Ludwin, S. K., Fuh, S.-C., Sawaya, R., Moore, C. S., Ho, M.-K., Bedell, B. J., Sarnat, H. B., Bar-Or, A., & Antel, J. P. (2016) · Journal of Neuropathology & Experimental Neurology

MicroRNA in disease regulationNeuroinflammation and Neurodegeneration Mechanisms

Cited by 50

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria

Akula, S. K., Chen, A. Y., Neil, J. E., Shao, D. D., Mo, A., Hylton, N. K., DiTroia, S., Ganesh, V. S., Smith, R. S., O’Kane, K., et al. (2023) · JAMA Neurology

Fetal and Pediatric Neurological DisordersGenomics and Rare Diseases

Cited by 37

Mitochondrial Myopathy of Cerebro-Hepato-Renal (Zellweger) Syndrome

Sarnat, H. B., Machin, G., Darwish, H. Z., & Rubin, S. Z. (1983) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Metabolism and Genetic DisordersMitochondrial Function and Pathology

Cited by 37