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Efficacy of Fidaxomicin Versus Vancomycin as Therapy for Clostridium difficile Infection in Individuals Taking Concomitant Antibiotics for Other Concurrent Infections

Clinical infectious diseases, 2011-09, Vol.53 (5), p.440-447

2011

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Effect of Age on Treatment Outcomes in Clostridium difficile Infection

Journal of the American Geriatrics Society (JAGS), 2013-02, Vol.61 (2), p.222-230

2013

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Development of Globo‑H Cancer Vaccine

Accounts of chemical research, 2015-03, Vol.48 (3), p.643-652

2015

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Fidaxomicin versus Vancomycin for Clostridium difficile Infection

The New England journal of medicine, 2011-02, Vol.364 (5), p.422-431

2011

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Novel Structures Derived from 2-[[(2-Pyridyl)methyl]thio]-1H-benzimidazole as Anti-Helicobacter pylori Agents, Part 2

Journal of medicinal chemistry, 2002-09, Vol.45 (19), p.4300-4309

2002

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An efficient entry to new sugar modified ketolide antibiotics

Tetrahedron letters, 2005-02, Vol.46 (9), p.1483-1487

2005

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Structure–activity relationships of bivalent aminoglycosides and evaluation of their microbiological activities

Bioorganic & medicinal chemistry letters, 2005-04, Vol.15 (8), p.2123-2128

2005

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Total synthesis of (±) indolmycin

Tetrahedron letters, 1996-09, Vol.37 (36), p.6447-6448

Shue, Youe-Kong

1996

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Amide bond surrogates: A general synthetic route to trans carbon-carbon double bono isosteres

Tetrahedron letters, 1987, Vol.28 (28), p.3225-3228

1987

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Randomized phase II/III trial of active immunotherapy with OPT-822/OPT-821 in patients with metastatic breast cancer

Journal of clinical oncology, 2016-05, Vol.34 (15_suppl), p.1003-1003

2016

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Effect of Age on Treatment Outcomes in C lostridium difficile Infection

Journal of the American Geriatrics Society (JAGS), 2013-02, Vol.61 (2), p.222-230

2013

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Risk of Recurrence and Time to Recurrence Following Treatment of Clostridium difficile Infection: Patient Characteristics and the Differential Effect of Fidaxomicin vs. Vancomycin

Gastroenterology (New York, N.Y. 1943), 2011, Vol.140 (5), p.S-360-S-361

2011

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A Practical Asymmetric Synthesis of A Pseudomonic Acid Precursor from D-Arabinose or D-Xylose

Synthetic communications, 1996-03, Vol.26 (5), p.935-944

1996

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751a Opt-80 Versus Vancomycin in Clostridium difficile Infection: Results of a Randomized Clinical Trial

Gastroenterology (New York, N.Y. 1943), 2009, Vol.136 (5), p.A-115-A-115

2009

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Novel methodology for the synthesis of trans-alkene dipeptide isosteres

Journal of organic chemistry, 1991-03, Vol.56 (6), p.2107-2111

1991

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Double bond isosteres of the peptide bond: Synthesis and biological activity of cholecystokinin (CCK) C-terminal hexapeptide analogs

Bioorganic & medicinal chemistry, 1993-09, Vol.1 (3), p.161-171

1993

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Synthesis and in vitro characterization of novel amino terminally modified oxotremorine derivatives for brain muscarinic receptors

Journal of medicinal chemistry, 1992-05, Vol.35 (9), p.1550-1557

1992

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ChemInform Abstract: Combinatorial Synthesis of Aminoglycoside Libraries

ChemInform, 2002-01, Vol.33 (1), p.no-no

2002

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Total synthesis of a mitosene

Journal of organic chemistry, 1984-12, Vol.49 (26), p.5164-5174

1984

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Novel Asp32-Replacement Tetrapeptide Analogs as Potent and Selective CCK-A Agonists

Journal of medicinal chemistry, 1994-05, Vol.37 (11), p.1562-1568

1994

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An efficient synthesis of 2-methyl-5,6,7,8-tetrahydro-4H-furo[2,3-d]azepines

Journal of organic chemistry, 1991-04, Vol.56 (8), p.2936-2938

1991

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Novel Structures Derived from 2-[[(2-Pyridyl)methyl]thio]-1 H -benzimidazole as Anti- Helicobacter p ylori Agents, Part 2

Journal of medicinal chemistry, 2002-09, Vol.45 (19), p.4300-4309

2002

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Tetrapeptide CCK agonists: structure-activity studies on modifications at the N-terminus

Journal of medicinal chemistry, 1994-01, Vol.37 (2), p.309-313

1994

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Amide bond surrogates: A novel alternate synthesis of the LEU-ASP carbon-carbon double bond isostere of CCK4

Tetrahedron letters, 1988-01, Vol.29 (33), p.4041-4044

1988

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Amide bond surrogates: A novel alternate synthesis of the LEU-ASP [formula omitted] carbon-carbon double bond isostere of CCK 4

Tetrahedron letters, 1988, Vol.29 (33), p.4041-4044

1988

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Efficacy of Fidaxomicin Versus Vancomycin as Therapy for Clostridium difficile Infection in Individuals Taking Concomitant Antibiotics for Other Concurrent Infections

Effect of Age on Treatment Outcomes in Clostridium difficile Infection

Development of Globo‑H Cancer Vaccine

Fidaxomicin versus Vancomycin for Clostridium difficile Infection

Novel Structures Derived from 2-[[(2-Pyridyl)methyl]thio]-1H-benzimidazole as Anti-Helicobacter pylori Agents, Part 2

An efficient entry to new sugar modified ketolide antibiotics

Structure–activity relationships of bivalent aminoglycosides and evaluation of their microbiological activities

Total synthesis of (±) indolmycin

Amide bond surrogates: A general synthetic route to trans carbon-carbon double bono isosteres

Randomized phase II/III trial of active immunotherapy with OPT-822/OPT-821 in patients with metastatic breast cancer

Effect of Age on Treatment Outcomes in C lostridium difficile Infection

Risk of Recurrence and Time to Recurrence Following Treatment of Clostridium difficile Infection: Patient Characteristics and the Differential Effect of Fidaxomicin vs. Vancomycin

A Practical Asymmetric Synthesis of A Pseudomonic Acid Precursor from D-Arabinose or D-Xylose

751a Opt-80 Versus Vancomycin in Clostridium difficile Infection: Results of a Randomized Clinical Trial

Novel methodology for the synthesis of trans-alkene dipeptide isosteres

Double bond isosteres of the peptide bond: Synthesis and biological activity of cholecystokinin (CCK) C-terminal hexapeptide analogs

Synthesis and in vitro characterization of novel amino terminally modified oxotremorine derivatives for brain muscarinic receptors

ChemInform Abstract: Combinatorial Synthesis of Aminoglycoside Libraries

Total synthesis of a mitosene

Novel Asp32-Replacement Tetrapeptide Analogs as Potent and Selective CCK-A Agonists

An efficient synthesis of 2-methyl-5,6,7,8-tetrahydro-4H-furo[2,3-d]azepines

Novel Structures Derived from 2-[[(2-Pyridyl)methyl]thio]-1 H -benzimidazole as Anti- Helicobacter p ylori Agents, Part 2

Tetrapeptide CCK agonists: structure-activity studies on modifications at the N-terminus

Amide bond surrogates: A novel alternate synthesis of the LEU-ASP carbon-carbon double bond isostere of CCK4

Amide bond surrogates: A novel alternate synthesis of the LEU-ASP [formula omitted] carbon-carbon double bond isostere of CCK 4

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