Sidney M. Gospe, M.D., Ph.D.
Affiliations: | Neurology and Pediatrics | University of Washington, Seattle, Seattle, WA |
Area:
child neurology, neurotoxicology, neurogeneticsWebsite:
http://depts.washington.edu/neurolog/directory/faculty/facultypage.php?id=30Google:
"Sidney Gospe"Bio:
Head, Division of Pediatric Neurology
Professor, Neurology and Pediatrics
Herman and Faye Sarkowsky Endowed Chair
Mean distance: 14.29 (cluster 6) | S | N | B | C | P |
Cross-listing: BCM Tree
Parents
Sign in to add mentor| Craig Heller | grad student | 1974-1975 | Stanford |
| Wilkie Wilson | grad student | 1977-1980 | Duke |
| Marvin A. Fishman | post-doc | 1983-1986 | Baylor College of Medicine |
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Publications
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| Coughlin CR, Tseng LA, Abdenur JE, et al. (2020) Consensus guidelines for the diagnosis and management of pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency. Journal of Inherited Metabolic Disease |
| Coughlin CR, Swanson MA, Spector E, et al. (2018) The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: a common epileptic encephalopathy. Journal of Inherited Metabolic Disease |
| Gospe SM. (2018) Developmental outcome in pyridoxine-dependent epilepsy: Better late (onset) than early. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 22: 575-576 |
| Oesch G, Maga AM, Friedman SD, et al. (2018) Geometric morphometrics reveal altered corpus callosum shape in pyridoxine-dependent epilepsy. Neurology |
| Mefford HC, Zemel M, Geraghty E, et al. (2015) Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombination. Neurology. 85: 756-62 |
| Friedman SD, Ishak GE, Poliachik SL, et al. (2014) Callosal alterations in pyridoxine-dependent epilepsy. Developmental Medicine and Child Neurology. 56: 1106-10 |
| Pearl PL, Gospe SM. (2014) Pyridoxine or pyridoxal-5'-phosphate for neonatal epilepsy: the distinction just got murkier. Neurology. 82: 1392-4 |
| Tully HM, Dempsey JC, Ishak GE, et al. (2013) Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsis. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 2019-23 |
| Tuschl K, Clayton P, Gospe S, et al. (2013) The first inborn error of manganese metabolism caused by mutations in SLC30A10, a newly identified manganese transporter The Lancet. 381 |
| Mefford HC, Cook J, Gospe SM. (2012) Epilepsy due to 20q13.33 subtelomere deletion masquerading as pyridoxine-dependent epilepsy. American Journal of Medical Genetics. Part A. 158: 3190-5 |