[HTML][HTML] Adalimumab with or without methotrexate in juvenile rheumatoid arthritis

…, HI Huppertz, NY Olson, JR Medich… - … England Journal of …, 2008 - Mass Medical Soc
Background Tumor necrosis factor (TNF) has a pathogenic role in juvenile rheumatoid
arthritis. We evaluated the efficacy and safety of adalimumab, a fully human monoclonal anti-TNF …

Safety and efficacy of adalimumab in treatment of patients with psoriatic arthritis who had failed disease modifying antirheumatic drug therapy.

…, AJ Kivitz, RJ Perdok, MA Weinberg, J Medich… - The Journal of …, 2007 - jrheum.org
OBJECTIVE: To demonstrate the safety and efficacy of adalimumab for the treatment of
active psoriatic arthritis (PsA) in patients with an inadequate response to disease modifying …

Adalimumab improves joint-related and skin-related functional impairment in patients with psoriatic arthritis: patient-reported outcomes of the Adalimumab …

…, MA Cifaldi, RJ Perdok, E Sasso, J Medich - Annals of the …, 2007 - ard.bmj.com
Objective: To evaluate the effects of adalimumab on patient-reported outcomes of joint-related
and skin-related functional impairment, health-related quality of life, fatigue and pain in …

An efficient synthesis of the antisecretory prostaglandin enisoprost

…, KA Babiak, JR Behling, JR Medich… - The Journal of …, 1991 - ACS Publications
An efficient 11-step synthesis of the antisecretory prostaglandin enisoproststarting with (Z, Z)-l,
5-cyclooctadiene has been developed. The key steps in thesynthesis are a selective …

Efficient preparation of [(methoxymethoxy) methyl] tributylstannane, a convenient hydroxymethyl anion equivalent

CR Johnson, JR Medich - The Journal of Organic Chemistry, 1988 - ACS Publications
The utility of-alkoxy organostannanes as precursors to-alkoxy organolithiums has been
demonstrated by several groups. 1 Recently Macdonald, McGarvey, and co-workers published a …

A short and practical synthesis of 1-deoxynojirimycin

J Behling, P Farid, JR Medich, MG Scaros… - Synthetic …, 1991 - Taylor & Francis
The potent glucosidase inhibitor 1-deoxynojirimycin was synthesized from L-sorbose using
a short synthesis and only one protecting group. The last step, which constituted the removal …

Enantioselective conjugate addition to cyclic enones with (S)-mapp-cuprates.

BE Rossiter, M Eguchi, AE Herna, D Vickers, J Medich… - Tetrahedron letters, 1991 - Elsevier
Chiral amidocuprates, formed from CuI, n-butyl or methyl lithium and (S)-N-methyl-1-phenyl-2-(1-piperidinyl)ethanamine,
(S)-MAPP, react enantioselectively with 5, 6, 7 and 8-…

Applications of enzymes in the synthesis of bioactive polyols

…, RL De Jong, A Golebiowski, JR Medich… - Pure and applied …, 1992 - degruyter.com
… De Jong, Adam Golebiowski, John R. Medich, Thomas D. Penning, Chrisantha H.
Senanayake, Darryl H. … JR Medich. K. Kunnen. …

[CITATION][C] Synthesis of the carbocyclic nucleoside (−)-Neplanocin A

JR Medich, KB Kunnen, CR Johnson - Tetrahedron letters, 1987 - Elsevier
The recent attention directed at the synthesis of compounds for the treatment of viral
infections has resulted in a large number of nucleoside analogues displaying antiviral activity. …

[CITATION][C] A Hydroxymethyl Anion Equivalent: Tributyl [(Methoxymethoxy) Methyl] Stannane: Stannane, tributyl [(methoxymethoxy) methyl]‐

…, SK Gee, CR Johnson, JR Medich - Organic …, 2003 - Wiley Online Library
A hydroxymethyl anion equivalent: tributyl [(methoxymethoxy) methyl] stannane
intermediate:(tributylstannyl) methanol reactant: Boron trifluoride etherate (13.0 mL, 0.106 …