Items where Author is "Sisodiya, Sanjay M."

Up a level
Export as [feed] Atom [feed] RSS
Group by: Item Type | No Grouping
Number of items: 4.

Journal Article

Steward, Charles A. and Roovers, Jolien and Suner, Marie-Marthe and Gonzalez, Jose M. and Uszczynska-Ratajczak, Barbara and Pervouchine, Dmitri and Fitzgerald, Stephen and Viola, Margarida and Stamberger, Hannah and Hamdan, Fadi F. and Ceulemans, Berten and Leroy, Patricia and Nava, Caroline and Lepine, Anne and Tapanari, Electra and Keiller, Don and Abbs, Stephen and Sanchis-Juan, Alba and Grozeva, Detelina and Rogers, Anthony S. and Diekhans, Mark and Guigó, Roderic and Petryszak, Robert and Minassian, Berge A. and Cavalleri, Gianpiero and Vitsios, Dimitrios and Petrovski, Slavé and Harrow, Jennifer and Flicek, Paul and Raymond, F. Lucy and Lench, Nicholas J. and De Jonghe, Peter and Mudge, Jonathan M. and Weckhuysen, Sarah and Sisodiya, Sanjay M. and Frankish, Adam (2019) Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A. npj Genomic Medicine, 4 (1). p. 31. ISSN 2056-7944

Johannesen, Katrine M. and Gardella, Elena and Encinas, Alejandra C. and Lehesjoki, Anna‐Elina and Linnankivi, Tarja and Petersen, Michael B. and Lund, Ida C. B. and Blichfeldt, Susanne and Miranda, Maria J. and Pal, Deb K. and Lascelles, Karine and Procopis, Peter and Orsini, Alessandro and Bonuccelli, Alice and Giacomini, Thea and Helbig, Ingo and Fenger, Christina D. and Sisodiya, Sanjay M. and Hernandez‐Hernandez, Laura and Krithika, S. and Rumple, Melissa and Masnada, Silvia and Valente, Marialuisa and Cereda, Cristina and Giordano, Lucio and Accorsi, Patrizia and Bürki, Sarah E. and Mancardi, Margherita and Korff, Christian and Guerrini, Renzo and Spiczak, Sarah and Hoffman‐Zacharska, Dorota and Mazurczak, Tomasz and Coppola, Antonietta and Buono, Salvatore and Vecchi, Marilena and Hammer, Michael F. and Varesio, Costanza and Veggiotti, Pierangelo and Lal, Dennis and Brünger, Tobias and Zara, Federico and Striano, Pasquale and Rubboli, Guido and Møller, Rikke S. (2019) The spectrum of intermediate SCN 8A ‐related epilepsy. Epilepsia, 60 (5). pp. 830-844. ISSN 1528-1167

Zagaglia, Sara and Selch, Christina and Nisevic, Jelena R. and Mei, Davide and Michalak, Zuzanna and Hernandez-Hernandez, Laura and Krithika, S. and Vezyroglou, Katharina and Varadkar, Sophia M. and Pepler, Alexander and Biskup, Saskia and Leão, Miguel and Gärtner, Jutta and Merkenschlager, Andreas and Jaksch, Michaela and Møller, Rikke S. and Gardella, Elena and Kristiansen, Britta S. and Hansen, Lars K. and Vari, Maria S. and Helbig, Katherine L. and Desai, Sonal and Smith-Hicks, Constance L. and Hino-Fukuyo, Naomi and Talvik, Tiina and Laugesaar, Rael and Ilves, Pilvi and Õunap, Katrin and Körber, Ingrid and Hartlieb, Till and Kudernatsch, Manfred and Winkler, Peter and Schimmel, Mareike and Hasse, Anette and Knuf, Markus and Heinemeyer, Jan and Makowski, Christine and Ghedia, Sondhya and Subramanian, Gopinath M. and Striano, Pasquale and Thomas, Rhys H. and Micallef, Caroline and Thom, Maria and Werring, David J. and Kluger, Gerhard J. and Cross, J. Helen and Guerrini, Renzo and Balestrini, Simona and Sisodiya, Sanjay M. (2018) Neurologic phenotypes associated with COL4A1/2 mutations. Neurology, 91 (22). e2078-e2088. ISSN 1526-632X

Coppola, Antonietta and Morrogh, Deborah and Farrell, Fiona and Balestrini, Simona and Hernandez-Hernandez, Laura and Krithika, S. and Sander, Josemir W. and Waters, Jonathan J. and Sisodiya, Sanjay M. (2018) Ring Chromosome 17 Not Involving the Miller-Dieker Region: A Case with Drug-Resistant Epilepsy. Molecular Syndromology, 9 (1). pp. 38-44. ISSN 1661-8777

This list was generated on Thu Aug 6 02:19:11 2020 BST.