日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Early-Start Versus Late-Start Icodextrin for Children Receiving Chronic Peritoneal Dialysis: Findings from the International Pediatric Peritoneal Dialysis Network

早期开始与晚期开始使用艾考糊精治疗慢性腹膜透析患儿:国际儿科腹膜透析网络的研究结果

Khandelwal, Priyanka; Borzych-Dużałka, Dagmara; Hofstetter, Jonas; Ranchin, Bruno; Vondrak, Karel; Ahn, Yo Han; Yap, Hui Kim; Awad, Hazem Subhi; Hooman, Nakysa; Erickson, Robin; Rebori, Anabella; Kaur, Amrit; Yuruk Yildirim, Zeynep Nagehan; Zhai, Yihui; Kari, Jameela A; Consolo, Silvia; Chan, Eugene Yu-Hin; Yap, Yok-Chin; Szczepańska, Maria; Kang, Hee Gyung; Ng, Kar Hui; Zaloszyc, Ariane; Warady, Bradley A; Schaefer, Franz; Shroff, Rukshana

Efficacy of Calcineurin Inhibition in Children With Steroid-Resistant Nephrotic Syndrome

钙调磷酸酶抑制剂治疗儿童类固醇抵抗性肾病综合征的疗效

Trautmann, Agnes; Hofstetter, Jonas; Lipska-Ziętkiewicz, Beata; Tsygin, Alexey; Ogarek, Iwona; Saeed, Bassam; Szczepanska, Maria; Azocar, Marta; Emma, Francesco; Ozaltin, Fatih; Caliskan, Salim; Bodria, Monica; Paripovic, Dusan; Tkaczyk, Marcin; Oh, Jun; Boutaba, Mounia; Jardim, Helena; Yilmaz, Alev; Csaicsich, Dagmar; Ranchin, Bruno; Jankauskiene, Augustina; Pasini, Andrea; Bitzan, Martin; Nigmatullina, Nazym; Tory, Kalman; Zieg, Jakub; Camilla, Roberta; Hooman, Nakysa; Schaefer, Franz

Prospective Study of Modifiable Risk Factors of Arterial Hypertension and Left Ventricular Hypertrophy in Pediatric Patients on Hemodialysis

前瞻性研究血液透析患儿动脉高血压和左心室肥厚的可改变危险因素

Borzych-Dużałka, Dagmara; Shroff, Rukshana; Ranchin, Bruno; Zhai, Yihui; Paglialonga, Fabio; Kari, Jameela A; Ahn, Yo H; Awad, Hazem S; Loza, Reyner; Hooman, Nakysa; Ericson, Robin; Drożdz, Dorota; Kaur, Amrit; Bakkaloglu, Sevcan A; Samaille, Charlotte; Lee, Marsha; Tellier, Stephanie; Thumfart, Julia; Fila, Marc; Warady, Bradley A; Schaefer, Franz; Schmitt, Claus P

Hemolytic Uremic Syndrome Secondary to Scorpion Envenomation in a 7-Year-Old Boy from Southwestern Iran

伊朗西南部一名7岁男孩因蝎子蜇伤继发溶血性尿毒综合征

Mortazavi, Nafiseh; Hooman, Nakysa; Mehrazma, Mitra; Moradi, Yasaman; Aghavali, Parvin

Investigation of the current situation regarding diagnosis and treatment of Alport syndrome in Asian countries: results of survey of the Asian Paediatric Nephrology association (AsPNA) tubular and inherited working group

亚洲国家Alport综合征诊断和治疗现状调查:亚洲儿科肾脏病学会(AsPNA)肾小管和遗传性工作组调查结果

Nozu, Kandai; Resontoc, Lourdes Paula Real; Hooman, Nakysa; Vasudevan, Anil; Ding, Jie; Kang, Hee Gyung

Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

巴特综合征和吉特曼综合征患者的甲状旁腺激素和磷酸盐稳态:一项国际横断面研究

Verploegen, Maartje F A; Vargas-Poussou, Rosa; Walsh, Stephen B; Alpay, Harika; Amouzegar, Atefeh; Ariceta, Gema; Atmis, Bahriye; Bacchetta, Justine; Bárány, Peter; Baron, Stéphanie; Bayrakci, Umut Selda; Belge, Hendrica; Besouw, Martine; Blanchard, Anne; Bökenkamp, Arend; Boyer, Olivia; Burgmaier, Kathrin; Calò, Lorenzo A; Decramer, Stéphane; Devuyst, Olivier; van Dyck, Maria; Ferraro, Pietro Manuel; Fila, Marc; Francisco, Telma; Ghiggeri, Gian Marco; Gondra, Leire; Guarino, Stefano; Hooman, Nakysa; Hoorn, Ewout J; Houillier, Pascal; Kamperis, Konstantinos; Kari, Jameela A; Konrad, Martin; Levtchenko, Elena; Lucchetti, Laura; Lugani, Francesca; Marzuillo, Pierluigi; Mohidin, Barian; Neuhaus, Thomas J; Osman, Abdaldafae; Papizh, Svetlana; Perelló, Manel; Rookmaaker, Maarten B; Conti, Valerie Said; Santos, Fernando; Sawaf, Ghalia; Serdaroglu, Erkin; Szczepanska, Maria; Taroni, Francesca; Topaloglu, Rezan; Trepiccione, Francesco; Vidal, Enrico; Wan, Elizabeth R; Weber, Lutz; Yildirim, Zeynep Yuruk; Yüksel, Selçuk; Zlatanova, Galia; Bockenhauer, Detlef; Emma, Francesco; Nijenhuis, Tom

Development and pilot implementation of Iranian Hemolytic Uremic Syndrome Registry

伊朗溶血性尿毒综合征登记系统的建立和试点实施

Lazem, Mina; Hooman, Nakysa; Sheikhtaheri, Abbas

Prevalence of reflux nephropathy in Iranian children with solitary kidney: results of a multi-center study

伊朗单肾儿童反流性肾病患病率:一项多中心研究的结果

Esteghamati, Maryam; Sorkhi, Hadi; Mohammadjafari, Hamid; Derakhshan, Ali; Sadeghi-Bojd, Simin; Momtaz, Hossein Emad; Mohkam, Masoumeh; Safaeian, Baranak; Hooman, Nakysa; Safaeiasl, Afshin; Sepahi, Mohsen Akhavan; Ghasemi, Khadijeh; Bazargani, Zahra; Emami, Elham

Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation

对伊朗患者进行巴特综合征的基因诊断并检测到一种新的纯合CLCNKB突变

Nojehdeh, Somayeh Takrim; Mojbafan, Marzieh; Hooman, Nakysa; Hoseini, Rozita; Otukesh, Hasan

Lessons learned from hemolytic uremic syndrome registries: recommendations for implementation

从溶血性尿毒综合征登记研究中汲取的经验教训:实施建议

Lazem, Mina; Sheikhtaheri, Abbas; Hooman, Nakysa