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819 results on '"Ishikura, Kenji"'

103. IPNA clinical practice recommendations for the diagnosis and management of children with steroid-sensitive nephrotic syndrome

Author

Trautmann, Agnes, Boyer, Olivia, Hodson, Elisabeth, Bagga, Arvind, Gipson, Debbie S., Samuel, Susan, Wetzels, Jack, Alhasan, Khalid, Banerjee, Sushmita, Bhimma, Rajendra, Bonilla-Felix, Melvin, Cano, Francisco, Christian, Martin, Hahn, Deirdre, Kang, Hee Gyung, Nakanishi, Koichi, Safouh, Hesham, Trachtman, Howard, Xu, Hong, Cook, Wendy, Vivarelli, Marina, Haffner, Dieter, Bouts, Antonia, Dossier, Claire, Emma, Francesco, Kemper, Markus, Topaloglu, Rezan, Waters, Aoife, Thorsten Weber, Lutz, Zurowska, Alexandra, Gibson, Keisha L., Greenbaum, Larry, Massengill, Susan, Selewski, David, Srivastava, Tarak, Wang, Chia-shi, Wenderfer, Scott, Johnstone, Lilian, Larkins, Nicholas, Wong, William, Alba, Agnes A., Ha, T. S., Mokham, Masoumeh, Zhong, Xuhui, Hamada, Riku, Iijima, Kazumoto, Ishikura, Kenji, Nozu, Kandai, Bresolin, Nilzete, de Jesus Gonzalez, Nilka, Restrepo, Jaime, Anochie, Ifeoma, McCulloch, Mignon, Pediatrics, Paediatric Nephrology, ARD - Amsterdam Reproduction and Development, and AII - Amsterdam institute for Infection and Immunity

Subjects
Steroid-sensitive nephrotic syndrome, All institutes and research themes of the Radboud University Medical Center, Frequently relapsing nephrotic syndrome, Nephrology, Steroid toxicity, Pediatrics, Perinatology and Child Health, SSNS, Steroid-dependent nephrotic syndrome, Renal disorders Radboud Institute for Health Sciences [Radboudumc 11], Children, Pediatrics, Immunosuppressive treatment
Abstract

Contains fulltext : 290812.pdf (Publisher’s version ) (Open Access) Idiopathic nephrotic syndrome is the most frequent pediatric glomerular disease, affecting from 1.15 to 16.9 per 100,000 children per year globally. It is characterized by massive proteinuria, hypoalbuminemia, and/or concomitant edema. Approximately 85-90% of patients attain complete remission of proteinuria within 4-6 weeks of treatment with glucocorticoids, and therefore, have steroid-sensitive nephrotic syndrome (SSNS). Among those patients who are steroid sensitive, 70-80% will have at least one relapse during follow-up, and up to 50% of these patients will experience frequent relapses or become dependent on glucocorticoids to maintain remission. The dose and duration of steroid treatment to prolong time between relapses remains a subject of much debate, and patients continue to experience a high prevalence of steroid-related morbidity. Various steroid-sparing immunosuppressive drugs have been used in clinical practice; however, there is marked practice variation in the selection of these drugs and timing of their introduction during the course of the disease. Therefore, international evidence-based clinical practice recommendations (CPRs) are needed to guide clinical practice and reduce practice variation. The International Pediatric Nephrology Association (IPNA) convened a team of experts including pediatric nephrologists, an adult nephrologist, and a patient representative to develop comprehensive CPRs on the diagnosis and management of SSNS in children. After performing a systematic literature review on 12 clinically relevant PICO (Patient or Population covered, Intervention, Comparator, Outcome) questions, recommendations were formulated and formally graded at several virtual consensus meetings. New definitions for treatment outcomes to help guide change of therapy and recommendations for important research questions are given.

Published
2022

105. Interventions for Shiga toxin-producing Escherichia coli gastroenteritis and risk of hemolytic uremic syndrome: A population-based matched case control study

Author

Myojin, Shota, primary, Pak, Kyongsun, additional, Sako, Mayumi, additional, Kobayashi, Tohru, additional, Takahashi, Takuri, additional, Sunagawa, Tomimasa, additional, Tsuboi, Norihiko, additional, Ishikura, Kenji, additional, Kubota, Masaya, additional, Kubota, Mitsuru, additional, Igarashi, Takashi, additional, Morioka, Ichiro, additional, and Miyairi, Isao, additional

Published
2022
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107. Early and frequent development of ocular hypertension in children with nephrotic syndrome

Author

Kawaguchi, Emi, Ishikura, Kenji, Hamada, Riku, Nagaoka, Yoshinobu, Morikawa, Yoshihiko, Sakai, Tomoyuki, Hamasaki, Yuko, Hataya, Hiroshi, Noda, Eiichiro, Miura, Masaru, Ando, Takashi, and Honda, Masataka

Subjects
Corticosteroids -- Dosage and administration -- Research, Nephrotic syndrome -- Research -- Patient outcomes -- Development and progression -- Drug therapy, Health
Abstract

Background Prednisolone, the first-line treatment for children with nephrotic syndrome, causes severe side effects. One of these side effects is ocular hypertension, which can result in severe and permanent visual disturbance. However, the exact prevalence, severity and timing of development of ocular hypertension have yet to be fully explored in this pediatric patient group. Methods In this retrospective cohort study, children with nephrotic syndrome treated with prednisolone for their first episode were analyzed. Intraocular pressure was screened with an iCare® tonometer and confirmed with Goldmann applanation tonometry before the initiation of prednisolone treatment and at 1 and 4 weeks thereafter. Results A total of 26 children with nephrotic syndrome were included in this study, of whom eight (30.8%) required treatment with eye drops for ocular hypertension. The median time interval between the diagnosis of ocular hypertension and start of treatment was 9 (range 5-31) days. At relapse of nephrotic syndrome, all children who had undergone treatment for ocular hypertension in their first episode again required treatment for ocular hypertension. Conclusions Routine ophthalmologic examination should be conducted from the early phase after the start of prednisolone treatment. In addition, children with episodes of ocular hypertension may be at greater risk of its reappearance with relapse of the nephrotic syndrome. Keywords Intraocular pressure * Children * Prednisolone * Nephrotic syndrome * iCare tonometer * Goldmann applanation tonometry * Side effect, Introduction Corticosteroid medications, such as prednisolone, play a fundamental role in the treatment of children with idiopathic nephrotic syndrome. Approximately 80-90% of children respond to prednisolone [1], and its introduction [...]

Published
2014
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114. Comparison of inulin clearance with 2-h creatinine clearance in Japanese pediatric patients with renal disease: open-label phase 3 study of inulin

Author

Uemura, Osamu, primary, Ishikura, Kenji, additional, Kamei, Koichi, additional, Hamada, Riku, additional, Yamamoto, Masaki, additional, Gotoh, Yoshimitsu, additional, Fujita, Naoya, additional, Sakai, Tomoyuki, additional, Sano, Takafumi, additional, Fushimi, Masahiko, additional, and Iijima, Kazumoto, additional

Published
2021
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117. Renal Complications in 6p Duplication Syndrome: Microarray-Based Investigation of the Candidate Gene(s) for the Development of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) and Focal Segmental Glomerular Sclerosis (FSGS)

Author

Yoshimura-Furuhata, Megumi, Nishimura-Tadaki, Akira, Amano, Yoshiro, Ehara, Takashi, Hamasaki, Yuko, Muramatsu, Masaki, Shishido, Seiichiro, Aikawa, Atsushi, Hamada, Riku, Ishikura, Kenji, Hataya, Hiroshi, Hidaka, Yoshihiko, Noda, Shunsuke, Koike, Kenichi, Wakui, Keiko, Fukushima, Yoshimitsu, Matsumoto, Naomichi, Awazu, Midori, Miyake, Noriko, and Kosho, Tomoki

Published
2015
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118. Prospective 5-year follow-up of cyclosporine treatment in children with steroid-resistant nephrosis

Author

Hamasaki, Yuko, Yoshikawa, Norishige, Nakazato, Hitoshi, Sasaki, Satoshi, Iijima, Kazumoto, Nakanishi, Koichi, Matsuyama, Takeshi, Ishikura, Kenji, Ito, Shuichi, Kaneko, Tetsuji, and Honda, Masataka

Subjects
Steroids (Drugs) -- Dosage and administration -- Complications and side effects, Nephrotic syndrome -- Risk factors -- Drug therapy -- Research, Cyclosporine -- Dosage and administration -- Complications and side effects, Health
Abstract

Background Cyclosporine has improved remission rates in children with steroid-resistant nephrotic syndrome (SRNS). However, little prospective long-term follow-up data is available. Methods We prospectively followed and analyzed 5-year outcomes of all 35 patients enrolled in our previous prospective multicenter trial with cyclosporine and steroids in children with SRNS. At enrollment, 23 cases were classified as minimal change (MC), five as diffuse mesangial proliferation (DMP), and seven as focal segmental glomeruloscle rosis (FSGS). Results Renal survival at 5 years (median 7.7 years) was 94.3 %. Patient status was complete remission (CR) in 31 (88.6 %) (MC/DMP, 25; FSGS, 6); partial remission in one (FSGS); and non-remission in three (MC/DMP), including chronic kidney disease and end-stage kidney disease in one each. Among 31 patients with CR, 22 (71.0 %) were receiving treatment with immunosuppressants at 5 years, including cyclosporine in 19, and seven of these 22 continued to show frequent relapse. Response to cyclosporine at 4 months predicted 5-year outcome in 31 of35 patients. Conclusions Although SRNS treatment with cyclosporine provides high renal survival and remission rates, many children require ongoing immunosuppression. Management has advanced from the prevention of end-stage kidney disease to the long-term maintenance of remission and management of relapse after induction therapy. Keywords Steroid resistance * Nephrotic syndrome * Pediatric nephrology * Cyclosporine * Long-term outcome, Introduction The use of cyclosporine has revolutionized the treatment of steroid-resistant nephrotic syndrome (SRNS) in children, and outcomes have gradually improved over the last 15 years. In particular, Waldo et [...]

Published
2013
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120. Influenza Virus Vaccination in Pediatric Nephrotic Syndrome Induces a Significant Reduction of Relapse and Influenza Virus Infection: A Nationwide Survey

Author

Ishimori, Shingo, primary, Ando, Takashi, additional, Kikunaga, Kaori, additional, Terano, Chikako, additional, Sato, Mai, additional, Komaki, Fumiyo, additional, Hamada, Riku, additional, Hamasaki, Yuko, additional, Araki, Yoshinori, additional, Gotoh, Yoshimitsu, additional, Nakanishi, Koichi, additional, Nakazato, Hitoshi, additional, Matsuyama, Takeshi, additional, Iijima, Kazumoto, additional, Yoshikawa, Norishige, additional, Ito, Shuichi, additional, Honda, Masataka, additional, and Ishikura, Kenji, additional

Published
2021
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128. Establishing core outcome domains in pediatric kidney disease: report of the Standardized Outcomes in Nephrology—Children and Adolescents (SONG-KIDS) consensus workshops

Author

Guha, Abhjit, Solarin, Adaobi, Sinha, Aditi, Platona, Adriana, Hamilton, Alexander, Woods-Barnard, Alice, Neu, Alicia, Tong, Allison, Dart, Allison, Eddy, Allison, Karathanas, Alyssa, Baumgart, Amanda, Fielding, Amelia, LePage, Amelia, Bernier-Jean, Amelie, Kelly, Amy, Teixeira, Ana, Viecelli, Andrea, Matus, Andrea, Narva, Andrew, Ju, Angela, Wang, Angela Yee-Moon, Sharma, Ankit, Fielding, Anna, Francis, Anna, Meza, Anthony, Fielding, Aria, Teixeira-Pinto, Armando, Bagga, Arvind, Jankauskienė, Augustina, Kelly, Ayano, Gillespie, Barbara, Sautenet, Benedicte, Vogt, Beth, Foster, Bethany, Warady, Bradley, Dixon, Bradley, Manns, Braden, Hemmelgarn, Brenda, Bscardark, Brittney, Romeo, Brooklyn, Hanson, Camilla, Meza, Carlos, Brockett, Carter, Guha, Chandana, Prestidge, Chanel, Logeman, Charlotte, Green, Charmaine, Sanchez-Kazi, Cheryl, Perkins, Christy, Schmitt, Claus Peter, Fielding, Craig, Settee, Craig, Sumpton, Daniel, Meza, Daniel, Karathanas, Darien, Harris, David, Wheeler, David, Hooper, David, Gipson, Debbie, Geary, Denis, Bockenhauer, Detlef, Haffner, Dieter, Mekahli, Djalila, Drozdz, Dorota, Romeo, Ed, Ku, Elaine, Urbina, Elaine, Levtchenko, Elena, Balovlenkov, Elena, Hodson, Elisabeth, Morales, Emily, O'Lone, Emma, Machuca, Emma, Carlton, Emmah, Au, Eric, Olver, Erin, Morales, Estefania, Mirza, Fatima, Mackie, Fiona, Tentori, Francesca, Schaefer, Franz, Higgins, Gail, Deschenes, Georges, Plunkett, Georgia, Yoder, Gerilyn, Wong, Germaine, Morales, Giselle, Germino, Greg, Desmond, Hailey, Perkins, Hayley, Mitchell-Smith, Harrison, Coolican, Helen, Xu, Hong, Yap, Hui-Kim, Anochie, Ifeoma, Ha, Il-Soo, Davis, Ira, Liu, Isaac, Samaniego, Israel, Groothoff, Jaap, Machuca, Jaime, Machuca, James, Kerklaan, Jasmijn, Brockett, Jeff, Norton, Jenna, Shen, Jenny, Goebel, Jens, Rao, Jia, Machuca, Jimmy, Mitchell-Smith, Jo, Watson, Jo, Gill, John, Craig, Jonathan, Flynn, Joseph T., Kausman, Joshua, Samuels, Joshua, Bacchetta, Justine, Yoder, Kaleb, Manera, Karine, Azukaitis, Karolis, Twombley, Katherine, McMichael, Kelly-Ann, Ishikura, Kenji, Romeo, Kennedy, Settee, Kevin, Van, Kim Linh, McMichael, Lachlan, Trinh, Lany, Greenbaum, Larry, Sanchez, Laura, Fielding, Leo, Rees, Lesley, Lippincott, Leslie, Mejia-Saldivar, Levi, Saldivar, Lidia, Guay-Woodford, Lisa, Samaniego, Lizett, Hamiwka, Lorraine, Bell, Lorraine, Dunn, Louese, Barry, Lucinda, Macauley, Luke, Holmes, Luke, Karathanas, Madelynn, Mitchell-Smith, Madison, Walker, Mandy, Benavides, Manuel, Tonelli, Marcello, Ferris, Maria, Vivarelli, Marina, Wolfenden, Mark, Howell, Martin, Christian, Martin, Schreiber, Martin, Moxey-Mims, Marva, Leonard, Mary, Karathanas, Matthew, Pearl, Meghan, Natatmadja, Melissa, Brockett, Melissa, Bonilla-Felix, Melvin, Atkinson, Meredith, Zappitelli, Michael, Baum, Michel, Rheault, Michelle, McCulloch, Mignon, Matsuda-Abedini, Mina, Michael, Mini, Khan, Mohammad, Salih, Mohammad, Carlton, Mycah Ann, Benador, Nadine, Plunkett, Ngairre, Webb, Nick, Scholes-Robertson, Nicki, Larkins, Nicolas, Evangelidis, Nicole, Yoder, Nigel, Meza, Norma, Olver, Paige, Carlton, Paiyton, Brophy, Patrick, Tugwell, Peter, Cochat, Pierre, Mehrotra, Rajnish, Wolfenden, Raphael, Gbadegesin, Rasheed, Benavides, Raymond, Johnson, Rebecca, Morales, Ricardo, Jr., McGee, Richard, Fish, Richard, Gardos, Robert, Pecoits-Filho, Roberto, Vargas, Rocio, Saldivar, Rodolfo, Coppo, Rosanna, Shroff, Rukshana, Raina, Rupesh, Youssouf, Sajeda, Crowe, Sally, Anumudu, Samaya, Chan, Samuel, Baldacchino, Sarah, Wenderfer, Scott, Wolfenden, Sebastian, Carlton, Selah, Sutton, Shanna, Murphy, Shannon, Teo, Sharon, Salih, Sheyma, Sahney, Shobha, Carlton, Silas, Carter, Simon, Pearson, Simone, Khan, Simra, Wilson, Skyla, Sharma, Sonia, Alexander, Stephen, Marks, Stephen, Cornish, Stephen, Goldstein, Stuart, Samuel, Susan, Furth, Susan, Mendley, Susan, Lippincott, Susan, Charles, Symone, Gutman, Talia, Mitchell-Smith, Terri, Harris, Tess, Vetter, Thorsten, Carlton, Tiffany, Carlton, Timothy, Querfeld, Uwe, Saglimbene, Valeria, Charles, Virginia, van Biesen, Wim, Winkelmayer, Wolfgang, Machuca, Yenissey, Cho, Yeoungjee, Salih, Yusuf, Anh, Yo Han, Perkins, Zachary, Salih, Zeynab, Hanson, Camilla S., Craig, Jonathan C., Eddy, Allison A., Gipson, Debbie S., Webb, Nicholas J.A., Alexander, Stephen I., Furth, Susan L., Viecelli, Andrea K., Au, Eric H., Shen, Jenny I., Manera, Karine E., Carter, Simon A., and Walker, Amanda

Published
2020
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130. Epidemiology of biopsy-proven Henoch–Schönlein purpura nephritis in children: A nationwide survey in Japan.

Author

Terano, Chikako, Hamada, Riku, Tatsuno, Ichiro, Hamasaki, Yuko, Araki, Yoshinori, Gotoh, Yoshimitsu, Nakanishi, Koichi, Nakazato, Hitoshi, Matsuyama, Takeshi, Iijima, Kazumoto, Yoshikawa, Norishige, Kaneko, Tetsuji, Ito, Shuichi, Honda, Masataka, and Ishikura, Kenji

Subjects
RENAL biopsy, NEPHRITIS, JAPANESE people, ACUTE kidney failure, MEDICAL protocols
Abstract

Background: Little is known about the epidemiology of Henoch–Schönlein purpura nephritis (HSPN). Methods: We conducted a nationwide epidemiological survey of Japanese children aged 1 to 15 years with HSPN. Children who were newly diagnosed with HSPN by biopsy between January 2013 and December 2015 were eligible for the survey to clarify the incidence of HSPN. We also conducted an institutional survey on kidney biopsy criteria and treatment protocols. Results: A total of 353 of 412 institutions (85.7%) responded to the questionnaire. Of the 353 institutions, 174 reported to perform kidney biopsies at their institutions, and 563 children were diagnosed with HSPN. Considering the collection rate, the estimated incidence of biopsy-proven HSPN was 1.32 cases/100,000 children per year. The median age at biopsy was 7.0 years, and the male-to-female ratio was 1.2:1. The kidney biopsy criteria and treatment protocols for HSPN were as follows. Patients with acute kidney injury underwent biopsy at least one month after onset. For patients without kidney dysfunction, the timing for biopsy was determined by the amount of proteinuria. Regarding the treatment of HSPN, there were certain commonalities among the treatment protocols, they eventually differed depending on the institutions involved. Conclusions: The incidence of biopsy-proven HSPN was 1.32 cases/100,000 children per year in Japan. The male-to-female ratio and date of diagnosis of HSPN were similar to those in previous studies. The kidney biopsy criteria and treatment protocols for HSPN varied among institutions. Further studies are warranted to establish an optimal treatment policy based on the prognosis. [ABSTRACT FROM AUTHOR]

Published
2022
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136. ERK and p38 mediate high-glucose-induced hypertrophy and TGF-[beta] expression in renal tubular cells

Author

Fujita, Hisayo, Omori, Sayu, Ishikura, Kenji, Hida, Mariko, and Awazu, Midori

Subjects
Diabetes -- Research, Protein kinases -- Research, Biological sciences
Abstract

We investigated the expression of ERK, p38 mitogen-activated protein kinase (p38), and JNK in renal tubules of diabetic rats following 3 wk after streptozotocin injection (DM). Although the expression of ERK was not different between controls and DM, phosphorylated ERK was expressed more intensely in DM. p38 And phosphorylated p38 were detected only in the diabetic kidney and were localized in all tubular segments. JNK and phosphorylated JNK were expressed similarly in controls and DM. Transforming growth factor (TGF)-[beta] was expressed in all tubular segments of DM, coinciding with the localization of p38. In LLC-P[K.sub.1] cells, phosphorylation of ERK and p38 increased after 24- to 72-h exposure to high glucose (HG). Coincubation with a p38 inhibitor SB-203580 or a MEK inhibitor, PD-98059, suppressed the HG-induced increases in protein content, [[sup.3]H]leucine incorporation, and the protein-to-DNA ratio. SB-203580 or PD-98059 also abolished the HG-stimulated expression of TGF-[beta] protein. These results demonstrate that ERK and p38 are activated in renal tubular cells of DM and may mediate HG-induced cellular hypertrophy and TGF-[beta] expression. mitogen-activated protein kinase; diabetes; kidney

Published
2004

143. Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome

Author

Jia, Xiaoyuan, primary, Yamamura, Tomohiko, additional, Gbadegesin, Rasheed, additional, McNulty, Michelle T., additional, Song, Kyuyong, additional, Nagano, China, additional, Hitomi, Yuki, additional, Lee, Dongwon, additional, Aiba, Yoshihiro, additional, Khor, Seik-Soon, additional, Ueno, Kazuko, additional, Kawai, Yosuke, additional, Nagasaki, Masao, additional, Noiri, Eisei, additional, Horinouchi, Tomoko, additional, Kaito, Hiroshi, additional, Hamada, Riku, additional, Okamoto, Takayuki, additional, Kamei, Koichi, additional, Kaku, Yoshitsugu, additional, Fujimaru, Rika, additional, Tanaka, Ryojiro, additional, Shima, Yuko, additional, Baek, Jiwon, additional, Kang, Hee Gyung, additional, Ha, Il-Soo, additional, Han, Kyoung Hee, additional, Yang, Eun Mi, additional, Abeyagunawardena, Asiri, additional, Lane, Brandon, additional, Chryst-Stangl, Megan, additional, Esezobor, Christopher, additional, Solarin, Adaobi, additional, Dossier, Claire, additional, Deschênes, Georges, additional, Vivarelli, Marina, additional, Debiec, Hanna, additional, Ishikura, Kenji, additional, Matsuo, Masafumi, additional, Nozu, Kandai, additional, Ronco, Pierre, additional, Cheong, Hae Il, additional, Sampson, Matthew G., additional, Tokunaga, Katsushi, additional, Iijima, Kazumoto, additional, Araki, Yoshinori, additional, Nagaoka, Yoshinobu, additional, Sato, Yasuyuki, additional, Hayashi, Asako, additional, Takahashi, Toshiyuki, additional, Aoyagi, Hayato, additional, Ueno, Michihiko, additional, Nakanishi, Masanori, additional, Toita, Nariaki, additional, Uetake, Kimiaki, additional, Kobayashi, Norio, additional, Fujita, Shoji, additional, Tsuruga, Kazushi, additional, Kumagai, Naonori, additional, Kudo, Hiroki, additional, Tanaka, Eriko, additional, Omori, Tae, additional, Okada, Mari, additional, Hatai, Yoshiho, additional, Udagawa, Tomohiro, additional, Motoyoshi, Yaeko, additional, Ogura, Masao, additional, Sato, Mai, additional, Kano, Yuji, additional, Hattori, Motoshi, additional, Miura, Kenichiro, additional, Harita, Yutaka, additional, Kanda, Shoichiro, additional, Sawanobori, Emi, additional, Kobayashi, Anna, additional, Kojika, Manabu, additional, Ohwada, Yoko, additional, Yan, Kunimasa, additional, Hataya, Hiroshi, additional, Terano, Chikako, additional, Harada, Ryoko, additional, Hamasaki, Yuko, additional, Hashimoto, Junya, additional, Ito, Shuichi, additional, Machida, Hiroyuki, additional, Inaba, Aya, additional, Matsuyama, Takeshi, additional, Goto, Miwa, additional, Shimizu, Masaki, additional, Ohta, Kazuhide, additional, Ikezumi, Yohei, additional, Yamada, Takeshi, additional, Suzuki, Toshiaki, additional, Tamamura, Soichi, additional, Mori, Yukiko, additional, Hidaka, Yoshihiko, additional, Matsuoka, Daisuke, additional, Kinoshita, Tatsuya, additional, Noda, Shunsuke, additional, Kitahara, Masashi, additional, Fujita, Naoya, additional, Hibino, Satoshi, additional, Minamikawa, Shogo, additional, Nakanishi, Keita, additional, Fujimura, Junya, additional, Sakakibara, Nana, additional, Aoto, Yuya, additional, Ishiko, Shinya, additional, Kanda, Kyoko, additional, Inaguma, Yosuke, additional, Hashimura, Yuya, additional, Ishimori, Shingo, additional, Kamiyoshi, Naohiro, additional, Shibano, Takayuki, additional, Takeshima, Yasuhiro, additional, Ueda, Hiroaki, additional, Ashida, Akira, additional, Matsumura, Hideki, additional, Kubota, Takuo, additional, Kitaoka, Taichi, additional, Okuda, Yusuke, additional, Sawai, Toshihiro, additional, Sakai, Tomoyuki, additional, Hama, Taketsugu, additional, Fujieda, Mikiya, additional, Ishihara, Masayuki, additional, Itoh, Shigeru, additional, Iwaki, Takuma, additional, Shimizu, Maki, additional, Nagatani, Koji, additional, Kagami, Shoji, additional, Urushihara, Maki, additional, Nishimura, Manao, additional, Yoshino, Miwa, additional, Hatae, Ken, additional, Hinokiyama, Maiko, additional, Kuroki, Rie, additional, Ohtsuka, Yasufumi, additional, Oka, Masafumi, additional, Nishimura, Shinji, additional, Sato, Tadashi, additional, Tanaka, Seiji, additional, Zaitsu, Ayuko, additional, Nakazato, Hitoshi, additional, Tamura, Hiroshi, additional, Nakanishi, Koichi, additional, Cho, Min Hyun, additional, Ha, Tae-Sun, additional, Kim, Ji Hyun, additional, Park, Peong Gang, additional, Cho, Myung Hyun, additional, Quiroga, Alejandro, additional, Moudgil, Asha, additional, Chavers, Blanche, additional, Kwon, Charles, additional, Bowers, Corinna, additional, Gipson, Deb, additional, Chand, Deepa, additional, Weaver, Donald Jack, additional, Abraham, Elizabeth, additional, Janjua, Halima, additional, Lin, Jen-Jar, additional, Greenbaum, Larry, additional, Kallash, Mahmoud, additional, Rheault, Michelle, additional, De Jeus Gonzalez, Nilka, additional, Brophy, Patrick, additional, Nagaraj, Shashi, additional, Massengill, Susan, additional, Srivastava, Tarak, additional, Hunley, Tray, additional, Cai, Yi, additional, Omoloja, Abiodun, additional, Silva, Cynthia, additional, Adeyemo, Adebowale, additional, Thalgahagoda, Shenal, additional, Kari, Jameela A., additional, El Desoky, Sherif, additional, Abdelhadi, Mohammed, additional, Akil, Rachida, additional, Azib, Sonia, additional, Basmaci, Romain, additional, Benoist, Gregoire, additional, Bensaid, Philippe, additional, Blanc, Philippe, additional, Boyer, Olivia, additional, Bucher, Julie, additional, Chace, Anne, additional, Chalvon, Arnaud, additional, Cheminee, Marion, additional, Chendjou, Sandrine, additional, Daoud, Patrick, additional, Elias, Ossam, additional, Gagliadone, Chantal, additional, Gajdos, Vincent, additional, Galerne, Aurélien, additional, Aigrain, Evelyne Jacqz, additional, Sanchez, Lydie Joly, additional, Khaled, Mohamed, additional, Khelfaoui, Fatima, additional, Laoudi, Yacine, additional, Larakeb, Anis, additional, Limani, Tarek, additional, Mahdi, Fouad, additional, Mandelcwaijg, Alexis, additional, Muller, Stephanie, additional, Nacer, Kacem, additional, Nathanson, Sylvie, additional, Pellegrino, Béatrice, additional, Pharaon, Isabelle, additional, Roudault, Véronica, additional, Rouget, Sébastien, additional, Saf, Marc, additional, Simon, Tabassom, additional, Tahiri, Cedric, additional, Ulinski, Tim, additional, and Zenkhri, Férielle, additional

Published
2020
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144. Perinatal factors contributing to chronic kidney disease in a cohort of Japanese children with very low birth weight

Author

Uemura, Osamu, primary, Ishikura, Kenji, additional, Kaneko, Tetsuji, additional, Hirano, Daishi, additional, Hamasaki, Yuko, additional, Ogura, Masao, additional, Mikami, Naoaki, additional, Gotoh, Yoshimitsu, additional, Sahashi, Takeshi, additional, Fujita, Naoya, additional, Yamamoto, Masaki, additional, Hibino, Satoshi, additional, Nakano, Masaru, additional, Wakano, Yasuhiro, additional, and Honda, Masataka, additional

Published
2020
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146. Establishing core outcome domains in pediatric kidney disease: report of the Standardized Outcomes in Nephrology—Children and Adolescents (SONG-KIDS) consensus workshops

Author

Hanson, Camilla S., primary, Craig, Jonathan C., additional, Logeman, Charlotte, additional, Sinha, Aditi, additional, Dart, Allison, additional, Eddy, Allison A., additional, Guha, Chandana, additional, Gipson, Debbie S., additional, Bockenhauer, Detlef, additional, Yap, Hui-Kim, additional, Groothoff, Jaap, additional, Zappitelli, Michael, additional, Webb, Nicholas J.A., additional, Alexander, Stephen I., additional, Furth, Susan L., additional, Samuel, Susan, additional, Neu, Alicia, additional, Viecelli, Andrea K., additional, Ju, Angela, additional, Sharma, Ankit, additional, Au, Eric H., additional, Desmond, Hailey, additional, Shen, Jenny I., additional, Manera, Karine E., additional, Azukaitis, Karolis, additional, Dunn, Louese, additional, Carter, Simon A., additional, Gutman, Talia, additional, Cho, Yeoungjee, additional, Walker, Amanda, additional, Francis, Anna, additional, Sanchez-Kazi, Cheryl, additional, Kausman, Joshua, additional, Pearl, Meghan, additional, Benador, Nadine, additional, Sahney, Shobha, additional, Tong, Allison, additional, Guha, Abhjit, additional, Solarin, Adaobi, additional, Platona, Adriana, additional, Hamilton, Alexander, additional, Woods-Barnard, Alice, additional, Eddy, Allison, additional, Karathanas, Alyssa, additional, Baumgart, Amanda, additional, Fielding, Amelia, additional, LePage, Amelia, additional, Bernier-Jean, Amelie, additional, Kelly, Amy, additional, Teixeira, Ana, additional, Viecelli, Andrea, additional, Matus, Andrea, additional, Narva, Andrew, additional, Wang, Angela Yee-Moon, additional, Fielding, Anna, additional, Meza, Anthony, additional, Fielding, Aria, additional, Teixeira-Pinto, Armando, additional, Bagga, Arvind, additional, Jankauskienė, Augustina, additional, Kelly, Ayano, additional, Gillespie, Barbara, additional, Sautenet, Benedicte, additional, Vogt, Beth, additional, Foster, Bethany, additional, Warady, Bradley, additional, Dixon, Bradley, additional, Manns, Braden, additional, 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Published
2020
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150. A simple, refined approach to diagnosing renovascular hypertension in children: A 10‐year study

Author

Saida, Ken, primary, Kamei, Koichi, additional, Hamada, Riku, additional, Yoshikawa, Takahisa, additional, Kano, Yuji, additional, Nagata, Hiroko, additional, Sato, Mai, additional, Ogura, Masao, additional, Harada, Ryoko, additional, Hataya, Hiroshi, additional, Miyazaki, Osamu, additional, Nosaka, Shunsuke, additional, Ito, Shuichi, additional, and Ishikura, Kenji, additional

Published
2020
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