Straussberg, Rachel

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

Piao, X., Hill, R. S., Bodell, A., Chang, B. S., Basel-Vanagaite, L., Straussberg, R., Dobyns, W. B., Qasrawi, B., Winter, R. M., Innes, A. M., et al. (2004) · Science

Fetal and Pediatric Neurological DisordersNeurogenesis and neuroplasticity mechanisms

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Early onset epileptic encephalopathy caused by de novo SCN 8A mutations

Ohba, C., Kato, M., Takahashi, S., Lerman‐Sagie, T., Lev, D., Terashima, H., Kubota, M., Kawawaki, H., Matsufuji, M., Kojima, Y., et al. (2014) · Epilepsia

Epilepsy research and treatmentIon channel regulation and function

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Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia

Halevy, A., Lerer, I., Cohen, R., Kornreich, L., Shuper, A., Gamliel, M., Zimerman, B.-E., Korabi, I., Meiner, V., Straussberg, R., et al. (2014) · Journal of Neurology

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

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A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder

Orenstein, N., Goldberg-Stern, H., Straussberg, R., Bazak, L., Weisz Hubshman, M., Kropach, N., Gilad, O., Scheuerman, O., Dory, Y., Kraus, D., et al. (2018) · European Journal of Paediatric Neurology

Epilepsy research and treatmentGenomics and Rare Diseases

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Phagocytic capacity and apoptosis of peripheral blood cells from patients with iron deficiency anemia

Bergman, M., Salman, H., Pinchasi, R., Straussberg, R., Djaldetti, M., & Bessler, H. (2005) · Biomedicine & Pharmacotherapy

Iron Metabolism and DisordersPhagocytosis and Immune Regulation

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