Zobrazeno 1 - 10 of 10 pro vyhledávání: '"T S, Fuller"'
2
When the morning after is Sunday: pharmacist prescribing of emergency contraceptive pills
Autor: J, Hutchings, J L, Winkler, T S, Fuller, J S, Gardner, E S, Wells, D, Downing, R, Shafer
Publikováno v: Journal of the American Medical Women's Association (1972). 53(5 Suppl 2)
Pharmacists are well positioned to play a major role in increasing access to emergency contraceptive pills (ECPs). A pilot project in Washington State is testing direct pharmacist prescribing. Through a collaborative drug therapy agreement, a license
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::12f49d13ae1c1af46e33f5577ae43123
https://pubmed.ncbi.nlm.nih.gov/9859629
Zobrazit plný text záznamu
3
Using pharmacies in Washington state to expand access to emergency contraception
Autor: E S, Wells, J, Hutchings, J S, Gardner, J L, Winkler, T S, Fuller, D, Downing, R, Shafer
Publikováno v: Family planning perspectives. 30(6)
The authors describe preliminary results from a 2-year demonstration project launched in July 1997 in Washington State to expand access to emergency contraceptive pills by promoting collaboration between pharmacists and independent prescribers in pro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::84314c44732eb01eb782c6c024d1dcff
https://pubmed.ncbi.nlm.nih.gov/9859020
Zobrazit plný text záznamu
7
ChemInform Abstract: FURTHER STEREOSELECTIVE REDUCTIONS OF 3-O-HEXOFURANOSYL S-METHYL DITHIOCARBONATES WITH TRIBUTYLTIN DEUTERIDE. A COMMENT ON MECHANISM
Autor: R. V. Stick, T. S. Fuller
Publikováno v: Chemischer Informationsdienst. 12
The reduction of 1,2:5,6-di-O-isopropylidene-3-O- (methylthio)thiocarbonyl-β-D-altrose, -mannose and -(3-2H)mannose with tributyltin deuteride and hydride leads to highly stereoselective syntheses of 3-deoxy-1,2:5,6-di-O-isopropylidene-β-D-(3-2H)al
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b7dbccc5afaa959a3763f0d60fe71462
https://doi.org/10.1002/chin.198115160
Zobrazit plný text záznamu
8
Further stereoselective reductions of 3-O-hexofuranosyl S-methyl dithiocarbonates with tributyltin deuteride. A comment on mechanism
Autor: R. V. Stick, T. S. Fuller
Publikováno v: Australian Journal of Chemistry. 33:2509
The reduction of 1,2:5,6-di-O-isopropylidene-3-O- (methylthio)thiocarbonyl-β-D-altrose, -mannose and -(3-2H)mannose with tributyltin deuteride and hydride leads to highly stereoselective syntheses of 3-deoxy-1,2:5,6-di-O-isopropylidene-β-D-(3-2H)al
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c8dcd2efc7c541052c3dfaff72a9e569
https://doi.org/10.1071/ch9802509
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje