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Akademický článek

Independent risk factors and long-term outcomes for acute kidney injury in pediatric patients undergoing hematopoietic stem cell transplantation: a retrospective cohort study

Autor: Daishi Hirano, Daisuke Kakegawa, Saori Miwa, Chisato Umeda, Yoichi Takemasa, Ai Tokunaga, Yuhei Kawakami, Akira Ito

Publikováno v: BMC Nephrology, Vol 21, Iss 1, Pp 1-7 (2020)

Abstract Background Acute kidney injury (AKI) remains a frequent complication in children undergoing hematopoietic stem cell transplantation (HSCT) and an independent risk factor of the patient’s survival and a prognostic factor of progression to c

Externí odkaz: https://doaj.org/article/39c88d374f75479581b008a69b76d429

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Familial juvenile hyperuricemia in early childhood in a boy with a novel gene mutation

Autor: Yoichi Takemasa, Hiroyuki Ida, Yuhei Kawakami, Saori Miwa, Ai Tokunaga, Daisuke Kakegawa, Akira Ito, Chisato Umeda, Daishi Hirano

Publikováno v: CEN Case Rep

Familial juvenile hyperuricemic nephropathy (FJHN) is a rare autosomal dominant disease caused by mutations in the uromodulin (UMOD) gene. It is characterized by the development of gout, tubulointerstitial nephropathy, and end-stage renal disease. He

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::990ea02160853045838e1213b410d81f
https://doi.org/10.1007/s13730-020-00566-7

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Glyceraldehyde-3-phosphate dehydrogenase of Mycoplasma pneumoniae induces infection-related glomerulonephritis

Autor: Norihisa Noguchi, Hidemasa Nakaminami, Akira Ito, Takeaki Wajima, Daisuke Kakegawa, Yoichi Takemasa, Daishi Hirano, Hiroyuki Ida, Takashi Oda, Ai Tokunaga, Saori Miwa, Akifumi Yamada, Chisato Umeda

Publikováno v: Clinical Nephrology. 92:263-272

Infection-related glomerulonephritis (IRGN) was previously thought to be due mostly to Streptococcus species, but is now known to be caused by a variety of other pathogens. Nephritis-associated plasmin receptor (NAPlr) was originally isolated from gr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1d97cb3082046a268c7ebcb0c0677730
https://doi.org/10.5414/cn109786

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Impact of acute kidney injury in patients prescribed angiotensin-converting enzyme inhibitors over the first two years of life

Autor: Yoichi Takemasa, Ai Tokunaga, Akira Ito, Chisato Umeda, Daishi Hirano, Daisuke Kakegawa, Kawakami Yuhei, Saori Miwa

Publikováno v: Pediatric nephrology (Berlin, Germany). 36(7)

The association of long-term acute kidney injury (AKI) risk with angiotensin-converting enzyme (ACE) inhibitor use in neonates/infants is poorly understood. We examined this association to identify potential AKI risk factors. We retrospectively evalu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8b2b2330054e669508d5236281aa752
https://pubmed.ncbi.nlm.nih.gov/33462699

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Independent risk factors and long-term outcomes for acute kidney injury in pediatric patients undergoing hematopoietic stem cell transplantation: a retrospective cohort study

Autor: Ai Tokunaga, Daisuke Kakegawa, Yuhei Kawakami, Chisato Umeda, Daishi Hirano, Akira Ito, Yoichi Takemasa, Saori Miwa

Publikováno v: BMC Nephrology, Vol 21, Iss 1, Pp 1-7 (2020)
BMC Nephrology

BackgroundAcute kidney injury (AKI) remains a frequent complication in children undergoing hematopoietic stem cell transplantation (HSCT) and an independent risk factor of the patient’s survival and a prognostic factor of progression to chronic kid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63a60400d0a25546c10f04dd347bf0f6
https://doi.org/10.1186/s12882-020-02045-8

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Efficient engraftment of genetically modified cells is necessary to ameliorate central nervous system involvement of murine model of mucopolysaccharidosis type II by hematopoietic stem cell targeted gene therapy

Autor: Takashi Higuchi, Hiroyuki Ida, Fusao Kato, Hiroshi Kobayashi, Toya Ohashi, Saori Miwa, Yohta Shimada, Ayako M. Watabe, Takahiro Fukuda

Publikováno v: Molecular genetics and metabolism. 130(4)

Mucopolysaccharidosis type II (MPS II) is a lysosomal storage disease (LSD) caused by a deficiency of the iduronate-2-sulfatase (IDS) that catabolizes glycosaminoglycans (GAGs). Abnormal accumulations of GAGs in somatic cells lead to various manifest

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b96845c27cb4c4a1ca88aadf5bdc39f8
https://pubmed.ncbi.nlm.nih.gov/32631737

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A review of clinical characteristics and genetic backgrounds in Alport syndrome

Publikováno v: Clinical and Experimental Nephrology

Alport syndrome (AS) is a progressive hereditary renal disease that is characterized by sensorineural hearing loss and ocular abnormalities. It is divided into three modes of inheritance, namely, X-linked Alport syndrome (XLAS), autosomal recessive A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c26cea3952dcf79ddcc54c32e77cda6
https://doi.org/10.1007/s10157-018-1629-4

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Independent Risk Factors and 2-Year Outcomes of Acute Kidney Injury after Surgery for Congenital Heart Disease

Autor: Akifumi Yamada, Hiroyuki Ida, Daisuke Kakegawa, Saori Miwa, Kosuke Chiba, Yoichi Takemasa, Daishi Hirano, Akira Ito, Ai Tokunaga, Chisato Umeda

Publikováno v: American Journal of Nephrology. 46:204-209

Background: Data are limited regarding risk factors for acute kidney injury (AKI) following cardiac surgery in children with congenital heart disease (CHD). This observational study was performed to examine temporal trends in AKI incidence according

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be7ff1e3a064563645cc5cd70b584b3
https://doi.org/10.1159/000480358

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