ouabain and Catastrophic Illness

ouabain has been researched along with Catastrophic Illness 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
Brashear, A; Dobyns, WB; Ghoneim, DH; Gunter, SA; Hahn, S; Jansen, LA; Liu, YB; McDaniel, SS; Ozelius, LJ; Paciorkowski, AR; Sweadner, KJ; Tran, T; Tully, H; Tupal, S; Tuttle, E; Vasta, V; Zhang, Q	1

Other Studies

1 other study(ies) available for ouabain and Catastrophic Illness

Article	Year
Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly. Epilepsia, 2015, Volume: 56, Issue:3 Topics: Brain; Catastrophic Illness; Child, Preschool; DNA Mutational Analysis; Electroencephalography; Enzyme Inhibitors; Epilepsy; Female; Glutamate Decarboxylase; HEK293 Cells; Humans; Infant; Male; Models, Molecular; Mutation; Nervous System Diseases; Ouabain; Sodium-Potassium-Exchanging ATPase; Transfection	2015

Article

Year

Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly.

Epilepsia, 2015, Volume: 56, Issue:3

Topics: Brain; Catastrophic Illness; Child, Preschool; DNA Mutational Analysis; Electroencephalography; Enzyme Inhibitors; Epilepsy; Female; Glutamate Decarboxylase; HEK293 Cells; Humans; Infant; Male; Models, Molecular; Mutation; Nervous System Diseases; Ouabain; Sodium-Potassium-Exchanging ATPase; Transfection

2015