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The staff team at JSciMed Central offered a strongest support through a series of transitions, and continue putting a high level of energy and commitment into developing the journal. From the beginning of the journal fostering process, JSciMed Central assigned an excellent editorial officer, Mr. Ricky Martin, who frequently give advice and help ...
https://www.bbb.org/us/nv/henderson/profile/trade-publications/j-scimed-central-llc-1086-90040802
It was never indicated that authors should pay them fr this, but they are charging me $760 I submitted an article to be published in a journal owned …
https://www.zoominfo.com/c/jscimed-central-llc/356943376
J SciMed Central. JSciMed Central LLC. JSciMed Central. jscimedcentral.org. j-scimedcentral.net
https://www.jscimedcentral.com/EnvironmentalScience/Articles/environmentalscience-1-1005.php
Batch experiments were conducted for 8 hours using 0.5 g fine fraction and 30 mL of OC solutions, and the supernatants were collected after centrifuging the mixtures. Shaking time of 8 hours was chosen because preliminary kinetic tests ranging from 1 to 24 hours revealed that the equilibrium sorption was reached after 8 h of shaking for all the ...
https://www.jscimedcentral.com/Pediatrics/pediatrics-8-1196.pdf
Central Prodeus AP, et al. (2020) Ann Pediatr Child Health 8(7): 1196 (2020) 2/7 MATERIALS AND METHODS Study design This was a controlled, open-label, non-blinded, parallel-group study evaluating the efficacy and safety of racecadotril in infants, children and adolescents with acute diarrhea and was conducted
https://www.jscimedcentral.com/Pharmacology/pharmacology-5-1077.pdf
j (0.05 mg/kg subcutaneously) and meloxicam. k (5 mg/kg subcutaneously) 12 hours prior to receiving each treatment and every 12 hours after until they died or were euthanized. All mice still surviving at 48 hours after treatment were euthanized using a CO. 2. chamber. Each lyophilized venom [Western Diamondback Rattlesnake
https://www.jscimedcentral.com/Cardiology/cardiology-2-1017.php
Laboratory studies revealed an ATIII level of 51%, and an anti-factor Xa level of 0.25 IU/mL, and repeated value was 30% and 0.03 IU/mL, respectively. 2500 units of ATIII were given intravenously in addition to the continuously administered intravenous heparin therapy. Within 48 hours, the clots in the VAD completely resolved.
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