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Pediatric Nephrology (Berlin, Germany)|March 21, 1998
Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndromeM Vollmer, M Koehrer, R Topaloglu, et al.
Genetic Counseling (Geneva, Switzerland)|April 25, 2013
Mucolipidosis type III in an adolescent presenting with atypical facial features and skeletal deformitiesP O Simsek-Kiper, R Topaloglu, Y Sahin, et al.
Clinical Rheumatology|September 1, 2001
Survey of factor V leiden and prothrombin gene mutations in systemic lupus erythematosusR Topaloglu, C Akierli, A Bakkaloglu, et al.
Clinical Rheumatology|September 1, 2001
Pulmonary haemorrhage in a 6-year-old boy with Henoch-Schönlein purpuraN Besbas, A Duzova, R Topaloglu, et al.
European Journal of Pediatrics|August 1, 1997
Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosisU Saatçi, S Ozen, S Ozdemir, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 7, 2019
Psychiatric morbidity and different treatment modalities in children with chronic kidney diseaseG Senses Dinc, T Cak, E Cengel Kultur, et al.
Clinical Rheumatology|September 1, 1999
Antineutrophil cytoplasmic antibodies in juvenile chronic arthritisA Bakkaloglu, S Ozen, U Saatci, et al.
Pediatric Nephrology (Berlin, Germany)|June 26, 2001
Henoch-Schönlein purpura in Wiskott-Aldrich syndromeA Duzova, R Topaloglu, O Sanal, et al.
Clinical and Experimental Rheumatology|April 17, 1998
Thrombomodulin, tissue plasminogen activator and plasminogen activator inhibitor-1 in Henoch-Schönlein purpuraN Besbas, A Erbay, U Saatçi, et al.
Annals of the Rheumatic Diseases|October 2, 2004
E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean feverR Topaloglu, F Ozaltin, E Yilmaz, et al.
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