1.
Urine biomarkers of chronic kidney damage and renal functional decline in childhood-onset systemic lupus erythematosus
by Brunner, Hermine I
Pediatric nephrology (Berlin, West), 2018-08-29, Vol.34 (1), p.117-128
2.
Validation of the systemic lupus erythematosus responder index for use in juvenile-onset systemic lupus erythematosus
by Mina, Rina
Annals of the rheumatic diseases, 2014-02, Vol.73 (2), p.401-406
3.
Pharmacokinetics of Prednisolone at Steady State in Young Patients With Systemic Lupus Erythematosus on Prednisone Therapy: An Open-Label, Single-Dose Study
by Sagcal-Gironella, Anna Carmela P., MD
Clinical therapeutics, 2011, Vol.33 (10), p.1524-1536
4.
Efficacy and safety of tocilizumab in patients with polyarticular-course juvenile idiopathic arthritis: results from a phase 3, randomised, double-blind withdrawal trial
by Brunner, Hermine I
Annals of the rheumatic diseases, 2015-06, Vol.74 (6), p.1110-1117
5.
Secondary analysis of APPLE study suggests atorvastatin may reduce atherosclerosis progression in pubertal lupus patients with higher C reactive protein
by Ardoin, Stacy P
Annals of the rheumatic diseases, 2014-03, Vol.73 (3), p.557-566
6.
Open-label, single dose pharmacokinetic study of prednisolone at steady state in young patients with SLE on prednisone therapy
by Sagcal-Gironella, Anna Carmela P Anna Carmela P
Clinical therapeutics, 2011-10-01, Vol.33 (10), p.1524-1536
7.
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
by Reijnders, Margot R.F
American journal of human genetics, 2016-02-04, Vol.98 (2), p.373-381
8.
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
by Reijnders, Margot R. F
American journal of human genetics, 2016-02-04, Vol.98 (2), p.373-381
9.
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
by Reijnders, Margot R. F
American journal of human genetics, 2016-02-04, Vol.98 (2), p.373-381
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