strong>Chapters in Scholarly Books

strong>Sunil K Sinha Rohan K Henry, Manmohan K Kamboj. Diabetes mellitus in children and adolescents. Int J Child Health Hum Dev Vol. 13, Iss.1, (2020) 33-49

strong>Sunil K Sinha Alicia Diaz-Thomas. Endocrinopathies associated with Noonan syndrome. Noonan Syndrome: Characteristics and Interventions. June 2019. Publisher: Elsevier Science. Editor. Amrit Bhangoo.li>

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strong>Refereed Journal articles Peer Reviewed

John Anthonypillai, Sunil K Sinha Andrey Mamkin, Svetlana Ten, Qing Dong, Amrit Bhangoo. Experience with cinacalcet in familial hypocalciuric hypercalcemia resulting from inactivating mutations in calcium sensing receptor CaSR) Endocrinol Metab Int J. 2018;6(2)137‒ DOI:li>
Nouhad Raissouni, Andrey Kolesnikov, Radhika Purushothaman, strong>Sunil Sinha Sonal Bhandari, Amrit Bhangoo, Shahid Malik, Revi Mathew, Jean-Patrice Baillargeon, Isabel M Hernandez, Michael Rosenbaum, Svetlana Ten and David Geller. Altered Glucose Disposition and Insulin Sensitivity in Peri-pubertal First-Degree Relatives of Women with Polycystic Ovary Syndrome. Int J Pediatr Endocrinol. 2012; 2012:14.li>
Philibert P, Paris F, Audran F, Kalfa N, Polak M, Thibaud E, Pinto G, Houang M, Zenaty D, Leger J, Mas JC, Pienkowski C, Einaudi S, Damiani D, Ten S, strong>Sinha S Poulat F, Sultan C. Phenotypic Variation of SF1 Gene Mutations. Adv ExMed Biol. 2011;707:67-72.li>
strong>Sinha SK Pascal Philibert, Charles Sultan^{sup>and Svetlana Ten: Inguinal hernia in a phenotypic female infant may reveal a 46XY sex reversal, supported by the identification of a novel SF1 gene mutation. Adv ExMed Biol. 2011;707:149-50.li>}
strong>Sinha SK Amrit Bhangoo, Svetlana Ten, and Joerg Gromoll. Leydig Cell Hypoplasia due to Inactivating Luteinizing Hormone/Chorionic Gonadotropin Receptor Gene Mutation Presenting as a 46,XY DSD. Adv ExMed Biol. 2011;707:147-8.li>
Bhangoo A, strong>Sinha SK Ten S. Pubertal Advancement Improves Endothelial Function as Measured by Peripheral Arterial Tonometry PAT) Horm Res Paediatrics: 2011;76(4)226-33.li>
George M, strong>Sinha S Mamkin I, Philibert P, New M, Wilson RC, Sultan C, Ten S, Bhangoo, A. Isolated Mild Clitoral Hypertrophy May Reveal 46,XY disorders of sex development in Infancy due to 17βHSD-3 Defect Confirmed by Molecular Analysis. Gynecological Endocrinology 2011;27:890-4.li>
Derr MA, Fang P, strong>Sinha SK Ten S, Hwa V, Rosenfeld RG. A novel Y332C missense mutation in the intracellular domain of the human growth hormone receptor does not alter STAT5b signaling: redundancy of GHR intracellular tyrosines involved in STAT5b signaling. Horm Res Paediatr. 2011;75(3)187-99

Alatzoglou KS, Turton JP, Kelberman D, Clayton PE, Mehta A, Buchanan C, Aylwin S, Crowne EC, Christesen HT, Hertel NT, Trainer PJ, Savage MO, Raza J, Banerjee K, strong>Sinha SK Ten S, Mushtaq T, Brauner R, Cheetham TD, Hindmarsh PC, Mullis PE, Dattani MT. Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency. JCEM. 2009 Sep;94(9)3191-9

Zhou P, Ten S, strong>Sinha S Ramchandani N, Vogiatzi M, Maclaren N. Insulin receptor autoimmunity and insulin resistance. JPEM. 2008 Apr;21(4)369-75.li>
strong>Sinha SK Amrit Bhangoo, Henry Anhalt, Noel Maclaren, Jan D. Marshall, Gayle B.Collin, Jurgen K Naggert and Svetlana Effect of Metformin and Rosiglitazone in a Prepubertal Boy with Alström Syndrome. JPEM 2007 Sep;20(9)1045-52.li>
Motaghedi R, Gujral S, strong>Sinha S Sison C, Ten S, Maclaren NK. Insulin-like growth factor binding protein-1 to screen for insulin resistance in children. Diabetes Technol Ther. 2007 Feb;9(1)43-51.li>
Ramchandani N, Ten S, Anhalt H, strong>Sinha S Ching J, Finkelstein A, Maclaren NK. Insulin pumtherapy from the time of diagnosis of type 1 diabetes. Diabetes Technol Ther. 2006 Dec;8(6) 663-70.li>
Anjli Kukerja, Guilia Costi, John Marker, Chen Hui Zhang, strong>Sinha S and Noel Maclaren. NKT Cell defects in NOD Mice suggest therapeutic opportunities. J Autoimmunity 2002) 19, 117-128.li>