Safa Baris
0000-0002-4730-9422
Marmara Universitesi Tip Fakultesi
198 papers found
Refreshing results…
Use of subcutaneous immunoglobulin in primary immune deficiencies
Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia
The effect of systemic corticosteroids on the innate and adaptive immune system in children with steroid responsive nephrotic syndrome
Birincil immün yetersizlikli hastalarda otoimmünite çeşitliliği, klinik özellikleri ve tedavi seçenekleri.
Long-Term Effect of Sublingual and Subcutaneous Immunotherapy in Dust Mite-Allergic Children With Asthma/Rhinitis: A 3-Year Prospective Randomized Controlled Trial (vol 25, pg 334, 2015)
Monogenic Primary Immune Deficiencies Idendified in a Pediatric-Onset Cvid Cohort, Is There a Predictive Marker?
DO CUT-OFF VALUES OF IgE AND EOSINOPHIL LEVELS HELP DISCRIMINATE HYPERIGE SYNDROME FROM ATOPIC DISEASES?
Birincil immün yetmezliklerde deri altı immünglobulin kullanımı.
A Patient With a Mutation in Cd40l Presenting With Panhypogammaglobulinemia and Natural Killer Cell Lymphopenia
G6PC3 Deficiency
Two patients with novel missense mutation in the purine nucleoside phosphorylase gene without serious or recurrent infections
Oxidative Burst with Dihydrorhodamine Test: Reference Values in Healthy Controls
Evaluation of Hyperimmunoglobulin M Syndrome by Flow Cytometry
The Effect of Vitamin D Supplementation on Subcutaneous Allergen Immunotherapy in House Dust Mite Sensitive Asthmatic Children
Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population
Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study
Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency
Sinus pericranii: Diagnosis with contrast enhanced MRI venography
JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family
The Association of TLR4 and NOD2 Polymorphisms and Febrile Neutropenia in Children with Burkitt Lymphoma
Missing publications? Search for publications with a matching author name.