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Is autosomal dominant polycystic kidney disease an early sweet disease?
Angélique Dachy, Jean-Paul Decuypere, Rudi Vennekens, François Jouret & Djalila Mekahli
doi : 10.1007/s00467-021-05406-z
Volume 37, issue 9, September 2022
An updated view of the pathogenesis of steroid-sensitive nephrotic syndrome
Tomoko Horinouchi, Kandai Nozu & Kazumoto Iijima
Thrombotic microangiopathy in children
Lilian Monteiro P. Palma, Maria Helena Vaisbich-Guimar?es, Meera Sridharan, Cheryl L. Tran & Sanjeev Sethi
Approach to genetic testing to optimize the safety of living donor transplantation in Alport syndrome spectrum
Yasar Caliskan & Krista L. Lentine
Scoping review of the dietary intake of children with chronic kidney disease
Erin Melhuish, Rachel Lindeback & Kelly Lambert
Rickets guidance: part I—diagnostic workup
Dieter Haffner, Maren Leifheit-Nestler, Andrea Grund & Dirk Schnabel
Acute kidney injury in pediatrics: an overview focusing on pathophysiology
Ana Fl?via Lima Ruas, Gabriel Malheiros Lébeis, Nicholas Bianco de Castro, Vit?ria Andrade Palmeira, Larissa Braga Costa, Katharina Lanza & Ana Cristi
Siblings with complement activation, thrombotic microangiopathy and gangrene: Questions
Sidharth Kumar Sethi, Maninder Dhaliwal, Veena Raghunathan, Hritik Raaj, Samit Kumar Mahato, Ananya Vadhera, Marie-Agnes Dragon-Durey, Pranaw Kumar Jh
Siblings with complement activation, thrombotic microangiopathy and gangrene: Answers
Sidharth Kumar Sethi, Maninder Dhaliwal, Veena Raghunathan, Hritik Raaj, Samit Kumar Mahato, Ananya Vadhera, Marie-Agnes Dragon-Durey, Pranaw Kumar Jh
A rare cause of oligoanuric kidney failure – a diagnosis not to miss: Questions
Benjamin L. Spector & Judith Sebestyen VanSickle
A rare cause of oligoanuric kidney failure – a diagnosis not to miss: Answers
Benjamin L. Spector & Judith Sebestyen VanSickle
Female adolescent with recurrent anemia and thrombocytopenia: Questions
Michell Lozano Chinga, Zeinab Afify, Amy Lowichik, Matthew M. Grinsell, Meredith Seamon & Jessica A. Meznarich
Female adolescent with recurrent anemia and thrombocytopenia: Answers
Michell Lozano Chinga, Zeinab Afify, Amy Lowichik, Matthew M. Grinsell, Meredith Seamon & Jessica A. Meznarich
Metabolic alkalosis in peritoneal dialysis — beyond the obvious: Questions
Neha Sharma & Abdulla M. Ehlayel
Metabolic alkalosis in peritoneal dialysis — beyond the obvious: Answers
Neha Sharma & Abdulla M. Ehlayel
Urinary metabolomics to develop predictors for pediatric acute kidney injury
Alexandra Franiek, Atul Sharma, Vedran Cockovski, David S. Wishart, Michael Zappitelli & Tom D. Blydt-Hansen
Low dose rabbit antithymocyte globulin is non-inferior to higher dose in low-risk pediatric kidney transplant recipients
Vaka K. Sigurjonsdottir, Lynn Maestretti, Anne McGrath, Waldo Concepcion, Amy Gallo, Urdur Jonsdottir, Paul C. Grimm & Abanti Chaudhuri
Major adverse kidney events after acute kidney injury in the pediatric intensive care unit: a propensity score–matched cohort study
Alexander J. Kula, Pingping Qu, Bryan Strub, Jodi M. Smith & Shina Menon
Dexamethasone to prevent kidney scarring in acute pyelonephritis: a randomized clinical trial
Neus Rius-Gordillo, Natà lia Ferré, Juan David González, Zaira Ibars, Ester Parada-Ricart, Maria Gloria Fraga, Sara Chocron, Manuel Samper, Carmen Vice
Defining kidney outcomes in children with acute lymphoblastic leukemia in the modern era
Reeti Kumar, Suzanne Reed, Joseph R. Stanek & John D. Mahan
Use of normal saline and incidence of dyselectrolytaemia in children following kidney transplantation
Samantha J. Williamson, Nicholas D. Plant & Mohan Shenoy
Glucocorticoid discontinuation in pediatric-onset systemic lupus erythematosus: a single-center experience
Kentaro Nishi, Masao Ogura, Sho Ishiwa, Toru Kanamori, Mika Okutsu, Shunsuke Yokota, Taishi Nada, Mai Sato, Koichi Kamei, Kenji Ishikura & Shuichi Ito
The effect of gender-affirming hormone treatment on serum creatinine in transgender and gender-diverse youth: implications for estimating GFR
Kate Millington, Ellis Barrera, Ankana Daga, Nina Mann, Johanna Olson-Kennedy, Robert Garofalo, Stephen M. Rosenthal & Yee-Ming Chan
Anti-factor H antibody associated hemolytic uremic syndrome following SARS-CoV-2 infection
Priyanka Khandelwal, Sudarsan Krishnasamy, Srinivasavaradan Govindarajan, Manish Kumar, Binata Marik, Aditi Sinha, Pankaj Hari & Arvind Bagga
Development and autoregulation of kidney function in children: a retrospective study using 99mTc-MAG3 renography
Xinhua Cao, Xiaoyin Xu, S. Ted Treves, Laura A. Drubach, Neha Kwatra, Min Zhang, Frederic H. Fahey, David A. Diamond & Stephan D. Voss
Hemodynamic instability during connection to continuous kidney replacement therapy in critically ill pediatric patients
Sameer Thadani, Thomas Fogarty, Theresa Mottes, Jack F. Price, Poyyapakkam Srivaths, Cynthia Bell & Ayse Akcan-Arikan
Evaluation of the relationship between serum carnitine levels and intradialytic complications in children with kidney failure
Behnaz Bazargani, Sayed Yousef Mojtahedi, Daryoosh Fahimi, Fahimeh Askarian, Mastaneh Moghtaderi, Arash Abbasi, Maryam Samimi & Maryam Bakhtiari Koohs
Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology
Claudio La Scola, Anita Ammenti, Cristina Bertulli, Monica Bodria, Milena Brugnara, Roberta Camilla, Valentina Capone, Luca Casadio, Roberto Chimenz,
Nephrogenic diabetes insipidus with new onset diabetic ketoacidosis in a child — challenges in fluid and electrolyte management
Yu-Shan Tseng, Nicole Swaney, Katherine Cashen, Amrish Jain, Nina Ma & Andrew Prout
Evaluation of the creatinine-based chronic kidney disease in children (under 25Â years) equation in healthy children and adolescents
Hans Pottel, Jonas Bj?rk, Pierre Delanaye & Ulf Nyman
Focal segmental glomerulosclerosis recurrence in a young adult with kidney transplant after mRNA COVID-19 vaccination
Rosanna Fulchiero & Sandra Amaral
Response to: Focal segmental glomerulosclerosis recurrence in a young adult with kidney transplant after mRNA COVID-19 vaccination
Clarkson Crane & Elizabeth Ingulli
Correction to: Is autosomal dominant polycystic kidney disease an early sweet disease?
Angélique Dachy, Jean-Paul Decuypere, Rudi Vennekens, François Jouret & Djalila Mekahli
