Prevention of Neurocognitive Impairment in Children Through Newborn Screening for Congenital Hypothyroidism von N Menon, P S

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Fetal Hyperthyroidism: Intrauterine Treatment with Carbimazole in Two Siblings von Batra, Chandar Mohan, Gupta, Vidya, Gupta, Nomeeta, Menon, P. S. N.

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Prevention of Iodine Deficiency Disorders in Children in India – the Way Forward von Menon, P. S. N.

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Precocious Puberty—Perspectives on Diagnosis and Management von Menon, P. S. N., Vijayakumar, M.

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Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function von Griffith, Andrew J, Kurima, Kiyoto, Peters, Linda M, Yang, Yandan, Riazuddin, Saima, Ahmed, Zubair M, Naz, Sadaf, Arnaud, Deidre, Drury, Stacy, Mo, Jianhong, Makishima, Tomoko, Ghosh, Manju, Menon, P.S.N, Deshmukh, Dilip, Oddoux, Carole, Ostrer, Harry, Khan, Shaheen, Riazuddin, Sheikh, Deininger, Prescott L, Hampton, Lori L, Sullivan, Susan L, Battey, James F, Keats, Bronya J.B, Wilcox, Edward R, Friedman, Thomas B

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Physical growth in children with reflux nephropathy with normal or mildly impaired renal function von Das, Sankar Kumar, Menon, P. S. N., Bagga, A., Bhatnagar, V., Rajalakshmi, M., Gupta, A. K.

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Pituitary Size and Response of Growth Hormone Deficient Children to Growth Hormone Therapy von Menon, P. S. N.

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Childhood Obesity, Metabolic Syndrome and Pentraxin-3 von Menon, P. S. N.

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Insulin like growth factors axis and growth disorders von BAJPAI, Anurag, MENON, P. S. N

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Current Issues in Pediatric Endocrinology von Menon, P. S. N., Jain, Vandana, Varma, Surendra K.

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New Paradigms in the Diagnosis and Management of Pediatric Endocrine Disorders von Menon, P. S. N., Jain, Vandana, Varma, Surendra K.

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Adiponectin and type 1 diabetes mellitus in children von Menon, P S N

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Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India von Shastri, Shivaram S, Kabra, Madhulika, Kabra, Sushil Kumar, Pandey, Ravindra M, Menon, P.S.N

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Central diabetes insipidus: clinical profile and factors indicating organic etiology in children von Bajpai, Anurag, Kabra, Madhulika, Menon, P S N

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Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism: Indian experience von CHOWDHURY, M. R, TIWARI, M, KABRA, M, MENNN, P. S. N

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Familial combined hyperlipidemia in a North Indian kindred von SRIRAM, C. S, GULATI, Sheffali, CHOPRA, Vikas, VASHIST, Suman, MENON, P. S. N

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Familial hypercholesterolemia von RACHNA KAPOOR SETH, GULATI, Sheffali, SETH, Sandeep, MENON, P. S. N, KALRA, Veena

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Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario von Maheshwari, Manjula, Vijaya, R., Ghosh, Manju, Shastri, Shivaram, Kabra, Madhulika, Menon, P.S.N.

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Contemporary issues in precocious puberty von Bajpai, Anurag, Menon, P S N

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