Page last updated: 2024-08-22

n-methylaspartate and Cerebral Micropolygyria

n-methylaspartate has been researched along with Cerebral Micropolygyria in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bahi-Buisson, N; Banne, E; Brueton, LA; Chen, W; Chung, SK; Cushion, TD; Dobyns, WB; Fawcett, KA; Fry, AE; Giuliano, F; Helbig, KL; Hu, C; Iago, HF; Kannan, V; Kerr, MP; Knight, KM; Kofman, LH; Kusumoto, H; Layet, V; Lemke, JR; Lerman-Sagie, T; Mackenzie, AB; Mefford, HC; Meiner, V; Mirzaa, GM; Mugalaasi, H; Muir, AM; Mullins, JGL; Patel, CV; Pilz, DT; Rees, MI; Shaulsky, GH; Shemer-Meiri, L; Sims, D; Stoodley, N; Swanger, SA; Thompson, BAN; Traynelis, SF; Yuan, H; Zelnik, N; Zhang, J	1

Studies

Bahi-Buisson, N; Banne, E; Brueton, LA; Chen, W; Chung, SK; Cushion, TD; Dobyns, WB; Fawcett, KA; Fry, AE; Giuliano, F; Helbig, KL; Hu, C; Iago, HF; Kannan, V; Kerr, MP; Knight, KM; Kofman, LH; Kusumoto, H; Layet, V; Lemke, JR; Lerman-Sagie, T; Mackenzie, AB; Mefford, HC; Meiner, V; Mirzaa, GM; Mugalaasi, H; Muir, AM; Mullins, JGL; Patel, CV; Pilz, DT; Rees, MI; Shaulsky, GH; Shemer-Meiri, L; Sims, D; Stoodley, N; Swanger, SA; Thompson, BAN; Traynelis, SF; Yuan, H; Zelnik, N; Zhang, J

Other Studies

1 other study(ies) available for n-methylaspartate and Cerebral Micropolygyria

Article	Year
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : a journal of neurology, 2018, 03-01, Volume: 141, Issue:3 Topics: Animals; Child; Child, Preschool; DNA Mutational Analysis; Excitatory Amino Acid Agonists; Family Health; Female; Glutamic Acid; Glycine; HEK293 Cells; Humans; Infant; Magnetic Resonance Imaging; Male; Membrane Potentials; Models, Molecular; Mutagenesis; Mutation; N-Methylaspartate; Nerve Tissue Proteins; Patch-Clamp Techniques; Polymicrogyria; Rats; Receptors, N-Methyl-D-Aspartate; Transfection	2018

Article

Year

De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.

Brain : a journal of neurology, 2018, 03-01, Volume: 141, Issue:3

Topics: Animals; Child; Child, Preschool; DNA Mutational Analysis; Excitatory Amino Acid Agonists; Family Health; Female; Glutamic Acid; Glycine; HEK293 Cells; Humans; Infant; Magnetic Resonance Imaging; Male; Membrane Potentials; Models, Molecular; Mutagenesis; Mutation; N-Methylaspartate; Nerve Tissue Proteins; Patch-Clamp Techniques; Polymicrogyria; Rats; Receptors, N-Methyl-D-Aspartate; Transfection

2018