Search Results - "Menon, P. S. N."

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

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Precocious Puberty, GnRH Stimulation Test and Monitoring GnRH Analog Therapy by Menon, P. S. N.

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

“…Hyperthyroidism can manifest very early in fetal life (fetal thyrotoxicosis) or immediately after birth (neonatal thyrotoxicosis). The authors describe outcome…”
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Prevention of Iodine Deficiency Disorders in Children in India – the Way Forward by Menon, P. S. N.

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

“…Ten children aged 11 months to 10 years (means 5.7 years) with reflux nephropathy, vesicoureteric reflux (VUR) and normal or mildly impaired renal function…”
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Precocious Puberty—Perspectives on Diagnosis and Management by Menon, P. S. N., Vijayakumar, M.

“…The term ‘precocious puberty’ signifies the onset of secondary sexual characters before the age of 9 y in boys and 8 y in girls. Menarche before 9.5 y is also…”
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Insulin like growth factors axis and growth disorders by BAJPAI, Anurag, MENON, P. S. N

“…The growth hormone-insulin like growth factor (GH-IGF) axis plays a crucial role in the regulation of growth. Initially considered to be a mediator of growth…”
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Pituitary Size and Response of Growth Hormone Deficient Children to Growth Hormone Therapy by Menon, P. S. N.

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

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Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function by 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

“…Positional cloning of hereditary deafness genes is a direct approach to identify molecules and mechanisms underlying auditory function. Here we report a locus…”
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Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism: Indian experience by CHOWDHURY, M. R, TIWARI, M, KABRA, M, MENNN, P. S. N

“…The heterogeneous nature of the mutations, the size, and the complexity of the factor VIII gene makes direct mutation analysis in hemophilia A families in…”
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Familial combined hyperlipidemia in a North Indian kindred by SRIRAM, C. S, GULATI, Sheffali, CHOPRA, Vikas, VASHIST, Suman, MENON, P. S. N

“…Familial combined hyperlipidemia is the most common genetic hyperlipidemia and is responsible for premature coronary artery disease. It is genetically…”
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Familial hypercholesterolemia by RACHNA KAPOOR SETH, GULATI, Sheffali, SETH, Sandeep, MENON, P. S. N, KALRA, Veena

“…Abnormalities in the lipid profile though uncommon in pediatric practice pose an increased risk for developing heart disease. Studies suggest that adult…”
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Current Issues in Pediatric Endocrinology by Menon, P. S. N., Jain, Vandana, Varma, Surendra K.

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

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

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

“…To evaluate the profile of children with central diabetes insipidus (DI) and identify factors indicating organic etiology. Retrospective chart review. Tertiary…”
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Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India by Shastri, Shivaram S, Kabra, Madhulika, Kabra, Sushil Kumar, Pandey, Ravindra M, Menon, P.S.N

“…Abstract Background Very little is known about the genetics of cystic fibrosis (CF) from the Indian subcontinent. The aims of the study were to identify the…”
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Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario by Maheshwari, Manjula, Vijaya, R., Ghosh, Manju, Shastri, Shivaram, Kabra, Madhulika, Menon, P.S.N.

“…Several studies have reported that mutations in the GJB2 gene (coding for connexin26) are a common cause of recessive non‐syndromic hearing impairment. A GJB2…”
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Contemporary issues in precocious puberty by Bajpai, Anurag, Menon, P S N

“…Precocious puberty poses significant diagnostic and therapeutic challenge to the physician. Recent advances in the understanding of pathophysiology of…”
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