Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Bunyong, Phakdeekitcharoen"'
Autor:
Praopilad Srisuwarn, Napun Sutharattanapong, Sinee Disthabanchong, Surasak Kantachuvesiri, Chagriya Kitiyakara, Bunyong Phakdeekitcharoen, Atiporn Ingsathit, Vasant Sumethkul
Publikováno v:
Transplant International, Vol 37 (2024)
Kidney transplant recipients (KTRs) are at increased risk of developing de novo post-transplant malignancies (PTMs), with regional differences in types with excess risk compared to the general population. A single-center, population-controlled, retro
Externí odkaz:
https://doaj.org/article/b13e24140eab485688a81b8c57f93565
Autor:
Chadapa Sevamontree, Supreeya Jintajirapan, Pran Phakdeekitcharoen, Bunyong Phakdeekitcharoen
Publikováno v:
International Journal of Nephrology, Vol 2024 (2024)
Background. Hyperkalemia is a life-threatening condition in outpatient and emergency departments. Hyperkalemia is associated with more events of major adverse cardiovascular diseases, hospitalization, and death. The aim of this study is to study and
Externí odkaz:
https://doaj.org/article/28ae47f74d5547c7930f9da7d3c4eb5f
Autor:
Bunyong Phakdeekitcharoen, Watcharapong Treesinchai, Pornphan Wibulpolprasert, Sarinya Boongird, Pinkael Klytrayong
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder that leads to end stage renal disease (ESRD). Cyst expansion in ADPKD is strongly associated with the decline in renal function. Ho
Externí odkaz:
https://doaj.org/article/c288d32acb6745f38b0965b4f8d7280e
Autor:
Warun Maneepitasut, Wasinee Wongkummool, Pirut Tong-ngam, Kornkanok Promthep, Alisa Tubsuwan, Aung Khine Linn, Bunyong Phakdeekitcharoen, Suparerk Borwornpinyo, Narisorn Kitiyanant, Phetcharat Phanthong, Suradej Hongeng
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102306- (2021)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the common genetic kidney disorders that are caused by mutations in PKD1 or PKD2 gene. In this report, the MUi026-A human induced pluripotent stem cell (hiPSC) line was established from t
Externí odkaz:
https://doaj.org/article/de85bf9e20904b65a2365d17cb6e45f4
Autor:
Aung Khine Linn, Warun Maneepitasut, Alisa Tubsuwan, Narisorn Kitiyanant, Bunyong Phakdeekitcharoen, Suparerk Borwornpinyo, Suradej Hongeng, Phetcharat Phanthong
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 5, p 766 (2022)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most prevalent genetic diseases affecting the kidneys. A genetically specific mutation model is required to comprehend its pathophysiology and to develop a drug treatment. In this stu
Externí odkaz:
https://doaj.org/article/560803d11e4245c9b524c93d52341814
Autor:
Suchin Worawichawong, Sirithep Plumworasawat, Wisit Liwlompaisan, Vasant Sumethkul, Bunyong Phakdeekitcharoen, Umaporn Udomsubpayakul, Panus Chalermsanyakorn, Chagriya Kitiyakara
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0252638 (2021)
Mesangial C4d deposits have been associated with worse outcomes in Western patients with IgA nephropathy (IgAN), but there is limited data in Asians. Previously, a high proportion of stained glomeruli was often required for the classification of C4d
Externí odkaz:
https://doaj.org/article/6d3102b080a7423e8ca1d0452ef9ef0a
Autor:
Abhasnee Sobhonslidsuk, Jirachaya Wanichanuwat, Pawin Numthavaj, Areepan Sophonsritsuk, Supanna Petraksa, Alongkorn Pugasub, Paisan Jittorntam, Anucha Kongsomgan, Sittiruk Roytrakul, Bunyong Phakdeekitcharoen
Publikováno v:
Gastroenterology Research and Practice, Vol 2016 (2016)
Background. There have been few reports of nucleotide analogue-related renal tubular dysfunction (RTD) in CHB patients. We assessed the prevalence and presentation of nucleotide analogue-related proximal RTD. Methods. A cross-sectional study was perf
Externí odkaz:
https://doaj.org/article/b14e86c4a3764d9cb493736ed4f40996
Autor:
Amnuay Sirisopha, Somlak Vanavanan, Anchalee Chittamma, Bunyong Phakdeekitcharoen, Ammarin Thakkinstian, Amornpan Lertrit, Nuankanya Sathirapongsasuti, Chagriya Kitiyakara
Publikováno v:
International Journal of Nephrology, Vol 2016 (2016)
Urine neutrophil gelatinase-associated lipocalin (NGAL) is widely used as a biomarker for acute kidney injury. Cross-sectional studies have shown that NGAL may be elevated in glomerular diseases, but there is limited information on the value of NGAL
Externí odkaz:
https://doaj.org/article/69164286139c4537907faf8164a0fab6
Autor:
Pinkael Klytrayong, Pornphan Wibulpolprasert, Sarinya Boongird, Watcharapong Treesinchai, Bunyong Phakdeekitcharoen
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 22, Iss 1, Pp 1-12 (2021)
BMC Nephrology, Vol 22, Iss 1, Pp 1-12 (2021)
Background Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder that leads to end stage renal disease (ESRD). Cyst expansion in ADPKD is strongly associated with the decline in renal function. However, th
Autor:
Panus Chalermsanyakorn, Vasant Sumethkul, Bunyong Phakdeekitcharoen, Chagriya Kitiyakara, Umaporn Udomsubpayakul, Sirithep Plumworasawat, Suchin Worawichawong, Wisit Liwlompaisan
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0252638 (2021)
PLoS ONE
PLoS ONE
Mesangial C4d deposits have been associated with worse outcomes in Western patients with IgA nephropathy (IgAN), but there is limited data in Asians. Previously, a high proportion of stained glomeruli was often required for the classification of C4d