Výsledky vyhledávání - "Udit Narayan Padhi"

Akademický článek

NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients

Autor: Udit Narayan Padhi, Madhubala Mulkalwar, Lakkakula Saikrishna, Henu Kumar Verma, LVKS Bhaskar

Publikováno v: Brazilian Journal of Nephrology (2022)

ABSTRACT Introduction: Endothelial nitric oxide synthase (eNOS) genes have been implicated in renal hemodynamics as potent regulators of vascular tone and blood pressure. It has been linked to a reduction in plasma nitric oxide levels. Several studie

Externí odkaz: https://doaj.org/article/47bf5d0ba2f94276add66dbd75c7d8ee

Zobrazit plný text záznamu

O polimorfismo intron 4 a/b do gene NOS3 está associado à DRET em pacientes com doença renal policística autossômica dominante

Autor: Udit Narayan Padhi, Madhubala Mulkalwar, Lakkakula Saikrishna, Henu Kumar Verma, LVKS Bhaskar

Publikováno v: Brazilian Journal of Nephrology (2022)
Brazilian Journal of Nephrology, Issue: ahead, Published: 31 JAN 2022
Brazilian Journal of Nephrology n.ahead 2022
Jornal Brasileiro de Nefrologia
Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
Brazilian Journal of Nephrology v.44 n.2 2022

Introduction: Endothelial nitric oxide synthase (eNOS) genes have been implicated in renal hemodynamics as potent regulators of vascular tone and blood pressure. It has been linked to a reduction in plasma nitric oxide levels. Several studies have re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72c65443c8cfe8cb9f759a58bc6ee371
https://doi.org/10.1590/2175-8239-jbn-2021-0089

Zobrazit plný text záznamu

Defining vitamin D deficiency in patients with sickle cell disease; A meta-analysis

Autor: Anupa Sahu, Udit Narayan Padhi, LVKS Bhaskar

Publikováno v: Journal of Parathyroid Disease. 10:e11154

Introduction: Sickle cell disease (SCD) is one of the hereditary blood disorders that affects the red blood cells. Several lines of evidence indicated that the vitamin D deficiency (VDD) is quite common in children with SCD and vitamin D supplementat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::486a5c63fd5a80b977a800f731fc0669
https://doi.org/10.34172/jpd.2022.11154

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání