Kết quả tìm kiếm - Nathanel Zelnik
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Delayed language development due to infantile thiamine deficiency Bằng Aviva Fattal‐Valevski, IRIS AZOURI‐FATTAL, Yoram Greenstein, Michal Guindy, Ayala Blau, Nathanel Zelnik
Được phát hành 2009Artigo -
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De novo mutations in GRIN1 cause extensive bilateral polymicrogyria Bằng Andrew E. Fry, Katherine A. Fawcett, Nathanel Zelnik, Hongjie Yuan, Belinda A.N. Thompson, Lilach Shemer-Meiri, Thomas D. Cushion, Hood Mugalaasi, David Sims, Neil Stoodley, Seo‐Kyung Chung, Mark I. Rees, Chirag Patel, Louise Brueton, Valérie Layet, Fabienne Giuliano, Michael Kerr, Ehud Banne, Vardiella Meiner, Tally Lerman‐Sagie, Katherine L. Helbig, Laura H. Kofman, Kristin Knight, Wenjuan Chen, Varun Kannan, Chun Hu, Hirofumi Kusumoto, Jin Zhang, Sharon A. Swanger, Gil Shaulsky, Ghayda Mirzaa, Alison M. Muir, Heather C. Mefford, William B. Dobyns, Amanda B. Mackenzie, Jonathan G.L. Mullins, Johannes R. Lemke, Nadia Bahi‐Buisson, Stephen F. Traynelis, Heledd F Iago, Daniela T. Pilz
Được phát hành 2017Artigo
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Các môn học liên quan
Medicine
Epilepsy
Internal medicine
Neuroscience
Pediatrics
Psychiatry
Psychology
Bayley Scales of Infant Development
Biology
Brain development
Child development
Cognition
Comprehension
Computer science
Developmental psychology
Endocrinology
Expressive language
Gene
Genetics
Language development
Linguistics
Missense mutation
Mutation
Operating system
Philosophy
Polymicrogyria
Psychomotor learning
Receptive language
Sleep (system call)
Status epilepticus