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Single-Port Laparoscopic Surgery in Urology: Initial Experience

Urology (Ridgewood, N.J.), 2008, Vol.71 (1), p.3-6

2008

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Robotic Laparoendoscopic Single-Site Surgery Using GelPort as the Access Platform

European urology, 2010-01, Vol.57 (1), p.132-137

2010

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Single-Port Laparoscopic Radical Prostatectomy

Urology (Ridgewood, N.J.), 2008-12, Vol.72 (6), p.1190-1193

2008

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Robotic single port suprapubic transvesical enucleation of the prostate (R‐STEP): initial experience

BJU international, 2012-09, Vol.110 (5), p.732-737

2012

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Synthesis of Aminopyridines and Aminopyridones by Cobalt-Catalyzed [2+2+2] Cycloadditions Involving Yne-Ynamides: Scope, Limitations, and Mechanistic Insights

Chemistry : a European journal, 2012-04, Vol.18 (14), p.4337-4344

2012

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Regioselective Cobalt-Catalyzed Formation of Bicyclic 3- and 4-Aminopyridines

Organic letters, 2011-04, Vol.13 (8), p.2030-2033

2011

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Robotic salvage retropubic prostatectomy after radiation/brachytherapy: initial results

BJU international, 2008-07, Vol.102 (1), p.93-96

2008

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Identification and profiling of 3,5-dimethyl-isoxazole-4-carboxylic acid [2-methyl-4-((2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-yl)phenyl] amide as histamine H3 receptor antagonist for the treatment of depression

Bioorganic & medicinal chemistry letters, 2013-12, Vol.23 (23), p.6269-6273

2013

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Robotic Partial Nephrectomy in the Treatment of Renal Angiomyolipoma

Journal of endourology, 2016-03, Vol.30 (3), p.275

2016

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SSR180711, a Novel Selective α7 Nicotinic Receptor Partial Agonist: (1) Binding and Functional Profile

Neuropsychopharmacology (New York, N.Y.), 2006-10, Vol.32 (1), p.1-16

2006

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Urine leak in minimally invasive partial nephrectomy: analysis of risk factors and role of intraoperative ureteral catheterization

International Brazilian journal of urology, 2014-12, Vol.40 (6), p.763-771

2014

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Design and synthesis of a novel series of histamine H3 receptor antagonists through a scaffold hopping strategy

Bioorganic & medicinal chemistry, 2015-02, Vol.23 (3), p.429-438

2015

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Robotic partial nephrectomy for caliceal diverticulum: a single-center case series

Journal of endourology, 2014-08, Vol.28 (8), p.958

2014

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Discovery of a potent, selective, and orally bioavailable histamine H3 receptor antagonist SAR110068 for the treatment of sleep–wake disorders

Bioorganic & medicinal chemistry letters, 2013-11, Vol.23 (22), p.6141-6145

2013

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Discovery of aryl ureas and aryl amides as potent and selective histamine H3 receptor antagonists for the treatment of obesity (Part I)

Bioorganic & medicinal chemistry letters, 2013-06, Vol.23 (11), p.3416-3420

2013

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Discovery of aryl ureas and aryl amides as potent and selective histamine H3 receptor antagonists for the treatment of obesity (Part II)

Bioorganic & medicinal chemistry letters, 2013-06, Vol.23 (11), p.3421-3426

2013

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Comparative Efficacy and Selectivity of Pharmacological Inhibitors of DYRK and CLK Protein Kinases

Journal of medicinal chemistry, 2023-03, Vol.66 (6), p.4106-4130

2023

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SSR180575 (7-chloro-N,N,5-trimethyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-acetamide), a peripheral benzodiazepine receptor ligand, promotes neuronal survival and repair

The Journal of pharmacology and experimental therapeutics, 2002-06, Vol.301 (3), p.1067

2002

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Atlas of Laparoscopic and Robotic Single Site Surgery

1, 2017

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Leucettinibs, a Class of DYRK/CLK Kinase Inhibitors Inspired by the Marine Sponge Natural Product Leucettamine B

Journal of medicinal chemistry, 2023-08, Vol.66 (15), p.10694-10714

2023

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Phosphinic Derivatives as New Dual Enkephalin-Degrading Enzyme Inhibitors: Synthesis, Biological Properties, and Antinociceptive Activities

Journal of medicinal chemistry, 2000-04, Vol.43 (7), p.1398-1408

2000

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Chemical, Biochemical, Cellular, and Physiological Characterization of Leucettinib-21, a Down Syndrome and Alzheimer’s Disease Drug Candidate

Journal of medicinal chemistry, 2023-12, Vol.66 (23), p.15648-15670

2023

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Discovery and Optimization of Potent and Orally Available CTP Synthetase Inhibitors for Use in Treatment of Diseases Driven by Aberrant Immune Cell Proliferation

Journal of medicinal chemistry, 2022-12, Vol.65 (24), p.16640-16650

2022

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Single-Port Laparoscopic Surgery in Urology: Initial Experience

Robotic Laparoendoscopic Single-Site Surgery Using GelPort as the Access Platform

Single-Port Laparoscopic Radical Prostatectomy

Robotic single port suprapubic transvesical enucleation of the prostate (R‐STEP): initial experience

Synthesis of Aminopyridines and Aminopyridones by Cobalt-Catalyzed [2+2+2] Cycloadditions Involving Yne-Ynamides: Scope, Limitations, and Mechanistic Insights

Selective blockade of the hydrolysis of the endocannabinoid 2-arachidonoylglycerol impairs learning and memory performance while producing antinociceptive activity in rodents

Regioselective Cobalt-Catalyzed Formation of Bicyclic 3- and 4-Aminopyridines

Robotic salvage retropubic prostatectomy after radiation/brachytherapy: initial results

Identification and profiling of 3,5-dimethyl-isoxazole-4-carboxylic acid [2-methyl-4-((2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-yl)phenyl] amide as histamine H3 receptor antagonist for the treatment of depression

Robotic Partial Nephrectomy in the Treatment of Renal Angiomyolipoma

Neurochemical, Electrophysiological and Pharmacological Profiles of the Selective Inhibitor of the Glycine Transporter-1 SSR504734, a Potential New Type of Antipsychotic

SSR180711, a Novel Selective α7 Nicotinic Receptor Partial Agonist: (1) Binding and Functional Profile

Urine leak in minimally invasive partial nephrectomy: analysis of risk factors and role of intraoperative ureteral catheterization

Design and synthesis of a novel series of histamine H3 receptor antagonists through a scaffold hopping strategy

Robotic partial nephrectomy for caliceal diverticulum: a single-center case series

Discovery of a potent, selective, and orally bioavailable histamine H3 receptor antagonist SAR110068 for the treatment of sleep–wake disorders

Discovery of aryl ureas and aryl amides as potent and selective histamine H3 receptor antagonists for the treatment of obesity (Part I)

Discovery of aryl ureas and aryl amides as potent and selective histamine H3 receptor antagonists for the treatment of obesity (Part II)

Comparative Efficacy and Selectivity of Pharmacological Inhibitors of DYRK and CLK Protein Kinases

SSR180575 (7-chloro-N,N,5-trimethyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-acetamide), a peripheral benzodiazepine receptor ligand, promotes neuronal survival and repair

Atlas of Laparoscopic and Robotic Single Site Surgery

Leucettinibs, a Class of DYRK/CLK Kinase Inhibitors Inspired by the Marine Sponge Natural Product Leucettamine B

Phosphinic Derivatives as New Dual Enkephalin-Degrading Enzyme Inhibitors: Synthesis, Biological Properties, and Antinociceptive Activities

Chemical, Biochemical, Cellular, and Physiological Characterization of Leucettinib-21, a Down Syndrome and Alzheimer’s Disease Drug Candidate

Discovery and Optimization of Potent and Orally Available CTP Synthetase Inhibitors for Use in Treatment of Diseases Driven by Aberrant Immune Cell Proliferation

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