Showing results (171-180 of 271) with videos related to
Sort By:
Pageof 28
The Journal of Pediatrics|July 7, 1999
Familial aggregation in Behçet's disease: high frequency in siblings and parents of pediatric probandsI Koné-Paut, I Geisler, B Wechsler, et al.Archives of Disease in Childhood|October 23, 2004
Nephrolithiasis associated with ceftriaxone therapy: a prospective study in 51 childrenZ Avci, A Koktener, N Uras, et al.Transplantation Proceedings|March 29, 2011
Comparison of basiliximab and daclizumab with triple immunosuppression in renal transplantationS Aktas, T Colak, E Baskin, et al.Neuromuscular Disorders : NMD|October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB lociB Talim, A Ferreiro, B Cormand, et al.Anadolu Kardiyoloji Dergisi : AKD = the Anatolian Journal of Cardiology|July 10, 2002
[Evaluation of dynamic left ventricular outflow tract obstruction by dobutamine stress echocardiography]O Bolca, B Dağdeviren, M Eren, et al.Clinical and Experimental Rheumatology|August 29, 2003
Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean feverA Duzova, A Bakkaloglu, N Besbas, et al.Heart (British Cardiac Society)|December 17, 2003
Relation between aortic stiffness and left ventricular diastolic function in patients with hypertension, diabetes, or bothM Eren, S Gorgulu, N Uslu, et al.Clinical Rheumatology|October 25, 2003
The role of apoptosis in childhood Henoch-Schonlein purpuraF Ozaltin, N Besbas, D Uckan, et al.Clinical and Experimental Rheumatology|December 5, 2008
The analysis of interleukin-1 receptor antagonist and interleukin-1beta gene polymorphisms in Turkish FMF patients: do they predispose to secondary amyloidosis?B Balci-Peynircioğlu, Z E Taşkiran, B Türel, et al.Reproductive Biomedicine Online|March 3, 2004
Preimplantation genetic diagnosis for early-onset torsion dystoniaS Rechitsky, O Verlinsky, A Kuliev, et al.Pageof 28