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Pediatric Clinics of North America
|
November 21, 2018
Fanconi Syndrome
John W Foreman
Pediatric Nephrology (Berlin, Germany)
|
October 14, 2006
Drug-induced granulomatous interstitial nephritis in a pediatric patient
James E Tong, David N Howell, John W Foreman
The Journal of Urology
|
September 9, 2014
Efficacy of antibiotic prophylaxis in children with vesicoureteral reflux: systematic review and meta-analysis
Hsin-Hsiao S Wang, Rasheed A Gbadegesin, John W Foreman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 17, 2012
Hypercalcemia, hypercalciuria, and elevated calcitriol concentrations with autosomal dominant transmission due to CYP24A1 mutations: effects of ketoconazole therapy
Peter J Tebben, Dawn S Milliner, Ronald L Horst, et al.
Frontiers in Pediatrics
|
April 12, 2019
Psychosocial Assessment of Candidates for Transplantation (PACT) Score Identifies High Risk Patients in Pediatric Renal Transplantation
Kyle W Freischlag, Vivian Chen, Shashi K Nagaraj, et al.
Nature Genetics
|
July 23, 2003
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Edgar A Otto, Bernhard Schermer, Tomoko Obara, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 9, 2018
Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings
Jonathan H Pelletier, Karan R Kumar, Rachel Engen, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 17, 2018
Correction to: Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings : A Midwest Pediatric Nephrology Consortium (MWPNC) study
Jonathan H Pelletier, Karan R Kumar, Rachel Engen, et al.
Nature
|
January 24, 2012
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Lynn M Boyden, Murim Choi, Keith A Choate, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Pediatric Clinics of North America
|
November 21, 2018
Fanconi Syndrome
John W Foreman
Pediatric Nephrology (Berlin, Germany)
|
October 14, 2006
Drug-induced granulomatous interstitial nephritis in a pediatric patient
James E Tong, David N Howell, John W Foreman
The Journal of Urology
|
September 9, 2014
Efficacy of antibiotic prophylaxis in children with vesicoureteral reflux: systematic review and meta-analysis
Hsin-Hsiao S Wang, Rasheed A Gbadegesin, John W Foreman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 17, 2012
Hypercalcemia, hypercalciuria, and elevated calcitriol concentrations with autosomal dominant transmission due to CYP24A1 mutations: effects of ketoconazole therapy
Peter J Tebben, Dawn S Milliner, Ronald L Horst, et al.
Frontiers in Pediatrics
|
April 12, 2019
Psychosocial Assessment of Candidates for Transplantation (PACT) Score Identifies High Risk Patients in Pediatric Renal Transplantation
Kyle W Freischlag, Vivian Chen, Shashi K Nagaraj, et al.
Nature Genetics
|
July 23, 2003
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Edgar A Otto, Bernhard Schermer, Tomoko Obara, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 9, 2018
Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings
Jonathan H Pelletier, Karan R Kumar, Rachel Engen, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 17, 2018
Correction to: Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings : A Midwest Pediatric Nephrology Consortium (MWPNC) study
Jonathan H Pelletier, Karan R Kumar, Rachel Engen, et al.
Nature
|
January 24, 2012
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Lynn M Boyden, Murim Choi, Keith A Choate, et al.
Page
of 1