Phillip L. Pearl

Murine succinate semialdehyde dehydrogenase (SSADH) deficiency, a heritable disorder of GABA metabolism with epileptic phenotype

K. Gibson, C. Jakobs, O. Snead, 2005, IUBMB life.

Phenotype of GABA-transaminase deficiency

W. Chung, P. Bonnen, J. Riviello, 2017, Neurology.

Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood

P. Chakraborty, A. Guberman, P. Pearl, 2015, Neurology.

Succinic semialdehyde dehydrogenase deficiency: a metabolic and genomic approach to diagnosis

Charul Gijavanekar, Abbhirami Rajagopal, K. Glinton, 2024, Frontiers in genetics.

Succinic Semialdehyde Dehydrogenase Deficiency: Review of the Natural History Study

C. Papadelis, E. Hanson, P. Pearl, 2021, Journal of child neurology.

Expression profiling reveals multiple myelin alterations in murine succinate semialdehyde dehydrogenase deficiency

E. A. Donarum, C. Jakobs, M. Gupta, 2006, Journal of Inherited Metabolic Disease.

Cerebellar Atrophy in Human and Murine Succinic Semialdehyde Dehydrogenase Deficiency

M. Gupta, J. Munasinghe, A. Finegersh, 2010, Journal of child neurology.