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Profil bibliographique

Minu George

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

14Publications signalées
463Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Diabetes Management and ResearchObesity, Physical Activity, DietDiabetes Treatment and ManagementPancreatic function and diabetesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Les publications récentes

Accès ouvert 2020 article OpenAlex

Comparison of Morphine and Clonidine as Adjuncts to Bupivacaine in Spinal Anaesthesia- A Double Blind Randomised Control Trial

Dattaraj Satish Sinai Sukhthanker, Yvonne Menezes, Bhagyashri Ramnath Kanekar, Minu George

Introduction: Spinal anaesthesia is a preferred choice for infraumbilical surgery. Various drugs have been added intrathecally to augment analgesia in the postoperative period. Morphine an opiate was among the first to be introduced. More recently the alpha-2 agonist Clonidine. Aim: To compare …

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0 citations JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
Accès ouvert 2018 article OpenAlex

Feasibility of Ideal Cardiovascular Health Evaluation in a Pediatric Clinic Setting

Piers R. Blackett, K P Farrell, Minh Truong, Minu George et autres

The feasibility of "point-of-care" screening for ideal cardiovascular health was explored in a pediatric specialty clinic setting. Children and adolescents aged 9-18 years (n=91) with treated and stabilized diseases were recruited at a pediatric endocrinology clinic. A table-top device was used to …

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6 citations Advances in Preventive Medicine
Accès ouvert 2014 article OpenAlex

Vitamin D supplementation in obese type 2 diabetes subjects in Ajman, UAE: a randomized controlled double-blinded clinical trial

Amena Sadiya, Solafa M. Ahmed, Martin Carlsson, Yohannes Tesfa et autres

OBJECTIVES: To study the effect of Vitamin D3 supplementation on metabolic control in an obese type 2 diabetes Emirati population. METHODS: This randomized double-blind clinical trial was conducted with 87 vitamin D-deficient obese, type 2 diabetic participants. The vitamin D-group (n=45) and …

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79 citations European Journal of Clinical Nutrition
2012 article OpenAlex

Role of 11βHSD Type 2 Enzyme Activity in Essential Hypertension and Children with Chronic Kidney Disease (CKD)

Anil Mongia, Risa Vecker, Minu George, Hanan Tawadrous et autres

BACKGROUND: The mineralocorticoid receptor is protected from excess of glucocorticoids by conversion of active cortisol to inactive cortisone by enzyme 11β-hydroxysteroid dehydrogenase type 2 present in the kidney. The metabolites of cortisol and cortisone are excreted in the urine as tetrahydrocortisol (5αTHF+5βTHF) …

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23 citations The Journal of Clinical Endocrinology & Metabolism
Accès ouvert 2012 article OpenAlex

Blood Pressure over Height Ratios: Simple and Accurate Method of Detecting Elevated Blood Pressure in Children

Ovidiu Galescu, Minu George, Sudhakar Basetty, I Predescu et autres

Background. Blood pressure (BP) percentiles in childhood are assessed according to age, gender, and height. Objective. To create a simple BP/height ratio for both systolic BP (SBP) and diastolic BP (DBP). To study the relationship between BP/height ratios and corresponding BP percentiles …

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42 citations International Journal of Pediatrics
2011 article OpenAlex

Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to17βHSD-3defect confirmed by molecular analysis

Minu George, Sunil Sinha, Irene Mamkin, Pascal Philibert et autres

AIMS: 17-β-Hydroxysteroid dehydrogenase type 3 (17βHSD-3) is expressed exclusively in the testes where it converts Δ4 androstenedione (Δ4) to testosterone (T). Here, we report a patient with a rare mutation at a critical site in HSD17B3 gene leading to deficiency of 17β …

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10 citations Gynecological Endocrinology
2010 article OpenAlex

The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency

Minu George, Maria I. New, Svetlana Ten, Charles Sultan et autres

17-β-Hydroxysteroid dehydrogenase type 3 (17βHSD-3) deficiency is a rare, but frequently misdiagnosed autosomal recessive cause of 46,XY disorder of sex development (DSD). 17βHSD-3 enzyme is present almost exclusively in the testes and converts Δ4-androstenedione (Δ4) to testosterone (T). The diagnosis can be …

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101 citations Hormone Research in Paediatrics

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