Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kanakasabapathi Ramadevi"'
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 2, Pp 260-264 (2013)
Aim and Objectives: 1. To assess the iodine nutritional status in patients with goiter by measuring urinary iodine excretion. 2. To compare the iodine nutritional status with the thyroid function and correlate with the type of thyroid disease. Study
Externí odkaz:
https://doaj.org/article/fee98e4a0fde4310bb2aacb43e2750c9
Akademický článek
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Autor:
Karunakaran, Poongkodi, Abraham, Deepak, Devadas, Geetha, Hussain, Zahir, Kanakasabapathi, Ramadevi
Publikováno v:
Indian Journal of Endocrinology & Metabolism; Nov/Dec2020, Vol. 24 Issue 6, p518-524, 7p
Publikováno v:
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 2, Pp 260-264 (2013)
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 2, Pp 260-264 (2013)
Aim and Objectives: 1. To assess the iodine nutritional status in patients with goiter by measuring urinary iodine excretion. 2. To compare the iodine nutritional status with the thyroid function and correlate with the type of thyroid disease. Study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83364e69cdb33ccc95954a7f14a8f560
http://europepmc.org/articles/PMC3683201
http://europepmc.org/articles/PMC3683201
Autor:
Richard Imrich, Shruthi K Bharadwaj, Hana Ayoob, Nicolas Sireau, Birgitta Olsson, G. Biolcati, Tom L. Blundell, Lakshminarayan R. Ranganath, Rangan Srinivasaraghavan, Anthony K Hall, Andrea Zatkova, Oliver Timmis, Kim Hanh Le Quan Sang, Fiammetta Sorge, Ludevit Kadasi, Charles Marques Lourenço, Caterina Aurizi, Mohammed Alsbou, Douglas E. V. Pires, Ronen Spiegel, Jan Radvanszky, Martina Nemethova, Kanakasabapathi Ramadevi, Annalisa Santucci, Robert Aquaron, Lia Milucci, Jozef Rovensky, Alessandro Mannoni, Berardino Porfirio, Silvia Sestini, Federica Genovese, David B. Ascher, James A. Gallagher, Christa van Kan
Publikováno v:
European journal of human genetics : EJHG. 24(1)
Alkaptonuria (AKU) is an autosomal recessive disorder caused by mutations in homogentisate-1,2-dioxygenase (HGD) gene leading to the deficiency of HGD enzyme activity. The DevelopAKUre project is underway to test nitisinone as a specific treatment to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7059e86f4e9c2904f6be81afbf73d6b1
https://pubmed.ncbi.nlm.nih.gov/25804398
https://pubmed.ncbi.nlm.nih.gov/25804398