Lemari Pendingin Minuman # Showcase dari Polytron SCN-141X…

27. 8. 2021540 zhlédnutí#SinarJakartaPutra #scn-141 #showcase #Polytron #Limbangan #Garut

SCN Webinar: The Rise of Electrification - YouTube

► 46:00
Před 4 měsíci36 zhlédnutíSCN Webinar: The Rise of Electrification - YouTube

Let's Talk Todes: You Can Successfully Manage SCN - YouTube

11. 11. 202021 zhlédnutíSoybean Cyst Nenmatode (SCN) reduces soybean yields year in and year out. Iowa State University Nematologist Greg Tylka discusses how it’s possible to succes...

Let's Talk Todes: Scouting for SCN During the Growing Season…

11. 11. 202017 zhlédnutíIs it possible to scout for Soybean Cyst Nematode (SCN) during the growing season? North Dakota State University Plant Pathologist Sam Markell demonstrates h...

Early Diagnosis of SCN1A-Related Epilepsies - Dravet Syndrome…

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6. 7. 2022569 zhlédnutíPresented as part of the the 2022 Dravet Syndrome Foundation (DSF) Conference, Dr. Andreas Brunklaus of the Royal Hospital for Children discusses more about ...

SCN History told via the Shirts we gave out! - YouTube

27. 9. 2013186 zhlédnutíSAP Community Netowrk history told with the help of all shirts we ever gave out.

Science Center Noord (SCN) - De Glasharp van Jan Paul - YouTube

28. 2. 20091 290 zhlédnutíDe glasharp van Jan Paul (vrijwilliger bij SCN) staat sinds zaterdag 28 februari op SCN. Het instrument is gemaakt van glazen die met een bepaalde hoeveelhei...

Mercury Chemistry: Co[Hg(SCN)4] - YouTube

3. 1. 20183 771 zhlédnutíIn this video, we make an interesting compound Co[Hg(SCN)4]. It is prepared by mixing a Hg solution with NH4SCN and adding some CoCl2. The compound does not ...

Neuropeptides as a Treatment for SCN1A-derived Epilepsy…

► 37:07
6. 7. 2022346 zhlédnutíPresented as part of the the 2022 Dravet Syndrome Foundation (DSF) Conference, Dr. Andrew Escayg of Emory University describes experiments using a mouse mode...

Mioclonias en sueño, despertares (mutación en el gen SCN1A) I…

23. 5. 201691 tis. zhlédnutíEncefalopatia epiléptica de inicio temprano secundaria a mutación en el gen SCN1A
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