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Clinical Therapeutics
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April 12, 2022
A Phase I, Open-label, Randomized, Crossover Study of the Relative Bioavailability of Capsule and Granule Formulations of Selumetinib
Sarit Cohen-Rabbie, Alexandra Mattinson, Karen So, et al.
International Journal of Pharmaceutics
|
March 12, 2015
Inter-subject variability in intestinal drug solubility
Sarit Cohen Rabbie, Talia Flanagan, Paul D Martin, et al.
Clinical and Translational Science
|
February 16, 2022
Effect of food on capsule and granule formulations of selumetinib
Sarit Cohen-Rabbie, Alexandra Mattinson, Karen So, et al.
Journal of the Neurological Sciences
|
July 27, 2010
MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions
Sharon Aharoni, Teres A Traves, Eldad Melamed, et al.
Nucleic Acids Research
|
May 3, 2019
Nonsense mutation-dependent reinitiation of translation in mammalian cells
Sarit Cohen, Lior Kramarski, Shahar Levi, et al.
Lasers in Medical Science
|
March 16, 2013
Telangiectasis in CREST syndrome and systemic sclerosis: correlation of clinical and pathological features with response to pulsed dye laser treatment
Shlomit Halachmi, Osama Gabari, Sarit Cohen, et al.
Journal of Nanobiotechnology
|
July 9, 2016
Synthesis and characterization of crosslinked polyisothiouronium methylstyrene nanoparticles of narrow size distribution for antibacterial and antibiofilm applications
Sarit Cohen, Chen Gelber, Michal Natan, et al.
Journal of Gastroenterology and Hepatology
|
August 6, 2014
Differential stimulation of peripheral blood mononuclear cells in Crohn's disease by fungal glycans
Liran Baram, Sarit Cohen-Kedar, Lior Spektor, et al.
Journal of Child Neurology
|
January 4, 2011
Juvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: a mitochondrial syndrome presenting from birth to adolescence
Esther Leshinsky-Silver, Ruslan Shuvalov, Shani Inbar, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
April 14, 2016
Estimating the variability in fraction absorbed as a paradigm for informing formulation development in early clinical drug development
Sarit Cohen Rabbie, Paul D Martin, Talia Flanagan, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 59) with videos related to
Sort By:
Page
of 6
Clinical Therapeutics
|
April 12, 2022
A Phase I, Open-label, Randomized, Crossover Study of the Relative Bioavailability of Capsule and Granule Formulations of Selumetinib
Sarit Cohen-Rabbie, Alexandra Mattinson, Karen So, et al.
International Journal of Pharmaceutics
|
March 12, 2015
Inter-subject variability in intestinal drug solubility
Sarit Cohen Rabbie, Talia Flanagan, Paul D Martin, et al.
Clinical and Translational Science
|
February 16, 2022
Effect of food on capsule and granule formulations of selumetinib
Sarit Cohen-Rabbie, Alexandra Mattinson, Karen So, et al.
Journal of the Neurological Sciences
|
July 27, 2010
MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions
Sharon Aharoni, Teres A Traves, Eldad Melamed, et al.
Nucleic Acids Research
|
May 3, 2019
Nonsense mutation-dependent reinitiation of translation in mammalian cells
Sarit Cohen, Lior Kramarski, Shahar Levi, et al.
Lasers in Medical Science
|
March 16, 2013
Telangiectasis in CREST syndrome and systemic sclerosis: correlation of clinical and pathological features with response to pulsed dye laser treatment
Shlomit Halachmi, Osama Gabari, Sarit Cohen, et al.
Journal of Nanobiotechnology
|
July 9, 2016
Synthesis and characterization of crosslinked polyisothiouronium methylstyrene nanoparticles of narrow size distribution for antibacterial and antibiofilm applications
Sarit Cohen, Chen Gelber, Michal Natan, et al.
Journal of Gastroenterology and Hepatology
|
August 6, 2014
Differential stimulation of peripheral blood mononuclear cells in Crohn's disease by fungal glycans
Liran Baram, Sarit Cohen-Kedar, Lior Spektor, et al.
Journal of Child Neurology
|
January 4, 2011
Juvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: a mitochondrial syndrome presenting from birth to adolescence
Esther Leshinsky-Silver, Ruslan Shuvalov, Shani Inbar, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
April 14, 2016
Estimating the variability in fraction absorbed as a paradigm for informing formulation development in early clinical drug development
Sarit Cohen Rabbie, Paul D Martin, Talia Flanagan, et al.
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of 6