Výsledky vyhledávání - "Pawaree Saisawat"

Akademický článek

Changes in Prevalence and Phenotype of Hypertension in Children Suspected of Hypertension Using the 2022 American Heart Association Guidelines

Autor: Norrarath Nimkarn MD, Kwanchai Pirojsakul MD, Songkiat Chantarogh MD, Pawaree Saisawat MD, Kanchana Tangnararatchakit MD

Publikováno v: Global Pediatric Health, Vol 11 (2024)

Objective The American Heart Association (AHA) launched the 2022 guidelines for the diagnosis of hypertension (HT) by ambulatory blood pressure monitoring (ABPM). The present study aimed to evaluate the impacts of the 2022 AHA guidelines on the chang

Externí odkaz: https://doaj.org/article/6c803f0f64b24f89816aa49639c8550e

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Akademický článek

Control of blood pressure in hypertensive children and adolescents assessed by ambulatory blood pressure monitoring

Autor: Kevalin Vigraijaroenying, Kwanchai Pirojsakul, Poomiporn Katanyuwong, Kanchana Tangnararatchakit, Pawaree Saisawat, Songkiat Chantarogh, Witchuri Paksi, Uthen Bunmee

Publikováno v: BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)

Abstract Background There have been few studies evaluating the control of hypertension (HT) in children. This study aimed to assess the control of HT using ambulatory blood pressure monitoring (ABPM) and to compare the parameters between the uncontro

Externí odkaz: https://doaj.org/article/ad378566770b49e2bc6845b9612cc296

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Akademický článek

Waist-to-height-ratio is associated with sustained hypertension in children and adolescents with high office blood pressure

Autor: Norrarath Nimkarn, Anyamanee Sewarit, Kwanchai Pirojsakul, Witchuri Paksi, Songkiat Chantarogh, Pawaree Saisawat, Kanchana Tangnararatchakit

Publikováno v: Frontiers in Cardiovascular Medicine, Vol 9 (2023)

BackgroundWaist-to-height-ratio (WHtR) has been proposed as another indicator for cardiometabolic risk factors including hypertension. Normally, hypertension can be diagnosed in the office setting by detecting high blood pressure for three occasions.

Externí odkaz: https://doaj.org/article/3fe80e7d1fdd48d3b3a7b32a56b7d4ee

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Akademický článek

Clinical Outcomes of Renal Replacement Therapy in Pediatric Acute Kidney Injury: A 10-Year Retrospective Observational Study

Autor: Chayuttra Voraruth MD, Kwanchai Pirojsakul MD, Pawaree Saisawat MD, Songkiat Chantarogh MD, Kanchana Tangnararatchakit MD

Publikováno v: Global Pediatric Health, Vol 9 (2022)

Children with severe acute kidney injury (AKI) have had a high mortality rate despite the use of advanced renal replacement therapy (RRT). This study aims to determine the clinical outcomes and the predictors of survival in pediatric AKI requiring RR

Externí odkaz: https://doaj.org/article/32a2284c39ae4caeae0a4016add01a06

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Endocapillary Proliferation was Associated with Unfavorable Outcomes in Children with Henoch-Schönlein Purpura Nephritis and IgA Nephropathy

Autor: Supatjaree Chanvitan, Kwanchai Pirojsakul, Kanchana Tangnararatchakit, Suchin Worawichawong, Songkiat Chantarogh, Pawaree Saisawat

Introduction: There are limited data on the outcomes in children with Henoch-Schönlein purpura nephritis (HSPN) and IgA nephropathy (IgAN) in limited-resource countries. This study was aimed to evaluate the outcome of HSPN and IgAN and to evaluate t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::49afbf68842f227f3eb28eca752e54d6
https://doi.org/10.21203/rs.3.rs-39010/v1

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Unusual cause of anemia in a child with end-stage renal disease: Answers

Autor: Nalinee Chongviriyapan, Uthaiwan Kongkhanin, Kwanchai Pirojsakul, Songkiat Chantarogh, Kanchana Tangnararatchakit, Surapong Lertthammakiat, Apinya Thanapinyo, Pawaree Saisawat, Kearkiat Praditpornsilpa

Publikováno v: Pediatric nephrology (Berlin, Germany). 32(12)

This is the case of a 5-year-old girl diagnosed with end-stage renal disease due to bilateral renal hypoplasia who developed anemia of unknown cause.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20142704bb25e4e796c4839b5d5f221e
https://pubmed.ncbi.nlm.nih.gov/28255803

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Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract

Autor: Radovan Bogdanovic, Daw Yang Hwang, Stefan Kohl, Alina C. Hilger, Natasa Stajic, Friedhelm Hildebrandt, Elijah O. Kehinde, Pawaree Saisawat, Velibor Tasic, Asaf Vivante, Gabriel C. Dworschak, Heiko Reutter

Publikováno v: Journal of the American Society of Nephrology. 25:1917-1922

Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately 40% of children with ESRD in the United States. Hitherto, mutations in 23 genes have been described as causing autosomal dominant isolated CAKUT in humans. However

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::531ba07b89f5fc7cca653a02dcf81360
https://doi.org/10.1681/asn.2013101103

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Rapid Detection of Monogenic Causes of Childhood-Onset Steroid-Resistant Nephrotic Syndrome

Autor: Edgar A. Otto, Jan Halbritter, Heon Yung Gee, Friedhelm Hildebrandt, Pawaree Saisawat, Neveen A. Soliman, Humphrey Fang, Virginia Vega-Warner, Carolin E. Sadowski, Shazia Ashraf, Svjetlana Lovric, Jameela A. Kari

Publikováno v: Clinical Journal of the American Society of Nephrology. 9:1109-1116

In steroid-resistant nephrotic syndrome (SRNS),21 single-gene causes are known. However, mutation analysis of all known SRNS genes is time and cost intensive. This report describes a new high-throughput method of mutation analysis using a PCR-based m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fba3b5759db756a91f153427f3924ff2
https://doi.org/10.2215/cjn.09010813

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Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract

Autor: Heiko Reutter, Friedhelm Hildebrandt, Pawaree Saisawat, Elijah O. Kehinde, Asaf Vivante, Velibor Tasic, Daw Yang Hwang, Radovan Bogdanovic, Gabriel C. Dworschak, Neveen A. Soliman, Alina C. Hilger, Stefan Kohl

Publikováno v: Kidney international

Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately half of children with chronic kidney disease. CAKUT can be caused by monogenic mutations; however, data are lacking on their frequency. Genetic diagnosis has been

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a6b8e3cf3d853be3fd67022c7cfd2ae
http://europepmc.org/articles/PMC4040148

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ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling

Publikováno v: Gee, H Y, Saisawat, P, Ashraf, S, Hurd, T W, Vega-Warner, V, Fang, H, Beck, B B, Gribouval, O, Zhou, W, Diaz, K A, Natarajan, S, Wiggins, R C, Lovric, S, Chernin, G, Schoeb, D S, Ovunc, B, Frishberg, Y, Soliman, N A, Fathy, H M, Goebel, H, Hoefele, J, Weber, L T, Innis, J W, Faul, C, Han, Z, Washburn, J, Antignac, C, Levy, S, Otto, E A & Hildebrandt, F 2013, ' ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling ', Journal of Clinical Investigation, vol. 123, no. 8, pp. 3243-53 . https://doi.org/10.1172/JCI69134

Nephrotic syndrome (NS) is divided into steroid-sensitive (SSNS) and -resistant (SRNS) variants. SRNS causes end-stage kidney disease, which cannot be cured. While the disease mechanisms of NS are not well understood, genetic mapping studies suggest

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e4c29ebf2b0e00f6b6980f0ac1cef8b
https://doi.org/10.1172/jci69134

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