Search details
1.
Epidemiology and Risk Factors for Hemodialysis Access-Associated Infections in Children: A Prospective Cohort Study From the SCOPE Collaborative.
Am J Kidney Dis
; 80(2): 186-195.e1, 2022 08.
Article
in English
| MEDLINE | ID: mdl-34979159
2.
An initiative to improve pneumococcal immunization counseling in children with nephrotic syndrome.
Pediatr Nephrol
; 37(6): 1333-1338, 2022 06.
Article
in English
| MEDLINE | ID: mdl-34734331
3.
The scope of treatment of pediatric IgA vasculitis nephritis and its outcome: a Pediatric Nephrology Research Consortium study.
Pediatr Nephrol
; 37(11): 2687-2697, 2022 Nov.
Article
in English
| MEDLINE | ID: mdl-35233641
4.
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
J Am Soc Nephrol
; 30(2): 201-215, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30655312
5.
Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
Nephrol Dial Transplant
; 34(3): 485-493, 2019 03 01.
Article
in English
| MEDLINE | ID: mdl-29534211
6.
Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children.
Nephrol Dial Transplant
; 34(3): 474-485, 2019 03 01.
Article
in English
| MEDLINE | ID: mdl-30295827
7.
Identification of novel mutations and phenotype in the steroid resistant nephrotic syndrome gene NUP93: a case report.
BMC Nephrol
; 20(1): 271, 2019 07 17.
Article
in English
| MEDLINE | ID: mdl-31315584
8.
GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome.
J Am Soc Nephrol
; 29(8): 2123-2138, 2018 08.
Article
in English
| MEDLINE | ID: mdl-29959197
9.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
J Am Soc Nephrol
; 29(9): 2348-2361, 2018 09.
Article
in English
| MEDLINE | ID: mdl-30143558
10.
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.
Kidney Int
; 93(1): 204-213, 2018 01.
Article
in English
| MEDLINE | ID: mdl-28893421
11.
Mutations in WDR4 as a new cause of Galloway-Mowat syndrome.
Am J Med Genet A
; 176(11): 2460-2465, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30079490
12.
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.
Pediatr Nephrol
; 33(2): 305-314, 2018 02.
Article
in English
| MEDLINE | ID: mdl-28921387
13.
An unusual cause of relapsing peritonitis in a patient on peritoneal dialysis.
Semin Dial
; 35(6): 561-562, 2022 11.
Article
in English
| MEDLINE | ID: mdl-35460112
14.
Fanconi syndrome, nephrotic-range proteinuria, and hypoalbuminemia in a newborn-Occam's razor or Hickam's dictum? Questions.
Pediatr Nephrol
; 37(1): 127-128, 2022 Jan.
Article
in English
| MEDLINE | ID: mdl-34633531
15.
Fanconi syndrome, nephrotic-range proteinuria, and hypoalbuminemia in a newborn-Occam's razor or Hickam's dictum? Answers.
Pediatr Nephrol
; 37(1): 129-132, 2022 Jan.
Article
in English
| MEDLINE | ID: mdl-34633532
16.
Single-center experience in pediatric renal transplantation using thymoglobulin induction and steroid minimization.
Pediatr Transplant
; 18(8): 816-21, 2014 Dec.
Article
in English
| MEDLINE | ID: mdl-25311592
17.
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.
Hypertension
; 71(4): 691-699, 2018 04.
Article
in English
| MEDLINE | ID: mdl-29483232
18.
Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome.
J Clin Invest
; 128(10): 4313-4328, 2018 10 01.
Article
in English
| MEDLINE | ID: mdl-30179222
19.
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.
Nat Commun
; 9(1): 1960, 2018 05 17.
Article
in English
| MEDLINE | ID: mdl-29773874
20.
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Clin J Am Soc Nephrol
; 13(1): 53-62, 2018 01 06.
Article
in English
| MEDLINE | ID: mdl-29127259