Sandesh C.S. Nagamani

Author

Also Known As

Sandesh C S Nagamani, Sandesh C. Nagamani, Sandesh C. S. Nagamani, Sandesh C. Sreenath Nagamani, Sandesh C.S. Nagamani, Sandesh CS Nagamani, Sandesh Nagamani, Sandesh C.S. Nagamani

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine Children's National Texas Children's Hospital Case Western Reserve University Heidelberg University

About

Sandesh C.S. Nagamani is an author at Baylor College of Medicine specializing in medicine, urology, and chronic kidney disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	419
2	Allergy	2	2	111
3	Engineering	1	1	221
4	Health Sciences	1	1	69
5	Clinical Nutrition	1	1	69

Sandesh C.S. Nagamani

Publications

829

Citations

H-Index

Page 1

	Year	Citations
Requirement of argininosuccinate lyase for systemic nitric oxide production Ayelet Erez, Sandesh C.S. Nagamani, Oleg A. Shchelochkov, Nature Medicine BiosynthesisEngineeringArgininosuccinate LyaseReactive Nitrogen SpecieBiotechnology	2011	221
Nitric-Oxide Supplementation for Treatment of Long-Term Complications in Argininosuccinic Aciduria Sandesh C.S. Nagamani, Philippe M. Campeau, Oleg A. Shchelochkov, The American Journal of Human Genetics UrologyReactive Nitrogen SpecieMedicineNitrosative StressChronic Kidney Disease	2012	82
Sodium phenylbutyrate decreases plasma branched-chain amino acids in patients with urea cycle disorders Lindsay C. Burrage, Mahim Jain, Laura Gandolfo, Molecular Genetics and Metabolism UrologyRenal FunctionHealth SciencesSodium HomeostasisMedicine	2014	69
Impact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders Roland Posset, Andrea Gropman, Sandesh C.S. Nagamani, Annals of Neurology	2019	67
Arginase I deficiency: Severe infantile presentation with hyperammonemia: More common than reported? Shailly Jain‐Ghai, Sandesh C.S. Nagamani, Susan Blasér, Molecular Genetics and Metabolism AllergyMedicinePediatricsSclerodermaSevere Infantile Presentation	2011	61
Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency Lindsay C. Burrage, Qin Sun, Sarah H. Elsea, Human Molecular Genetics Translational MedicineUrologyNeurodegenerative DiseasesAutoimmune DiseaseAllergy	2015	50
Glycerol phenylbutyrate treatment in children with urea cycle disorders: Pooled analysis of short and long-term ammonia control and outcomes Susan A. Berry, Uta Lichter‐Konecki, George A. Díaz, Molecular Genetics and Metabolism Glycerol Phenylbutyrate TreatmentMedicineInherited Metabolic DiseasePediatricsGeriatric Urology	2014	47
A randomized controlled trial to evaluate the effects of high-dose versus low-dose of arginine therapy on hepatic function tests in argininosuccinic aciduria Sandesh C.S. Nagamani, Oleg A. Shchelochkov, Mary A. Mullins, Molecular Genetics and Metabolism UrologyHepatologyMedicineLiver PhysiologyHepatic Function Tests	2012	45
Early prediction of phenotypic severity in Citrullinemia Type 1 Matthias Zielonka, Stefan Kölker, Florian Gleich, Annals of Clinical and Translational Neurology	2019	45
Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder Brendan Lee, George A. Díaz, William J. Rhead, Genetics in Medicine	2014	40

Page 1