Travaux scientifiques

Prof. Dr. Safa Barış

395 publications. La source de l’information est indiquée à côté de chaque publication.

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  1. A patient with mushroom allergy; a new etiological agent of Kounis syndrome.

    Tuberkuloz ve toraks, 2016

    Source : ORCID

  2. Birincil immün yetersizlikli hastalarda otoimmünite çeşitliliği, klinik özellikleri ve tedavi seçenekleri.

    Turkish Pediatrics Archive/Turk Pediatri Arsivi, 2016

    Source : ORCID

  3. Birincil immün yetmezliklerde deri altı immünglobulin kullanımı.

    Turkish Pediatrics Archive/Turk Pediatri Arsivi, 2016

    Source : ORCID

  4. DO CUT-OFF VALUES OF IgE AND EOSINOPHIL LEVELS HELP DISCRIMINATE HYPERIGE SYNDROME FROM ATOPIC DISEASES?

    JOURNAL OF CLINICAL IMMUNOLOGY, 2016

    Source : ORCID

  5. House dust mites confer a distinct immunological feature among dermatitis

    Iranian Journal of Allergy, Asthma and Immunology, 2016

    PMID 27921406 3 citations (OpenAlex) Texte intégral en libre accèsSource : ORCID

  6. House dust mites confer a distinct immunological feature among dermatitis

    Iranian Journal of Allergy, Asthma and Immunology, 2016

    Source : ORCID

  7. 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)

    JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, 2016

    Source : ORCID

  8. MONOGENIC PRIMARY IMMUNE DEFICIENCIES IDENDIFIED IN A PEDIATRIC-ONSET CVID COHORT, IS THERE A PREDICTIVE MARKER?

    JOURNAL OF CLINICAL IMMUNOLOGY, 2016

    Source : ORCID

  9. Nijmegen-Breakage Syndrome; Two Siblings Presenting with Different Phenotypes

    Asthma Allergy Immunology, 2016

    DOI 10.21911/aai.6007 Texte intégral en libre accèsSource : ORCID

  10. Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia

    Clinical Immunology, 2016

    DOI 10.1016/j.clim.2016.02.008 PMID 26916670 21 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  11. Primary catastrophic antiphospholipid syndrome in an 8 year-old-girl,Primer katastrofik antifosfolipid sendrom: 8 yaşında kız çocuk

    Marmara Medical Journal, 2016

    DOI 10.5472/mmjcr.2901.07 Texte intégral en libre accèsSource : ORCID

  12. Primary catastrophic antiphospholipid syndrome in an 8 year-old-girl.

    Marmara Medical Journal, 2016

    Source : ORCID

  13. School Board Policies on Prevention and Management of Anaphylaxis in İstanbul: Where Do We Stand?

    Balkan medical journal, 2016

    DOI 10.5152/balkanmedj.2016.15500 PMID 27761282 4 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  14. Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

    Journal of Clinical Immunology, 2016

    DOI 10.1007/s10875-016-0312-3 PMID 27379765 78 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  15. Severe early-onset combined immunodeficiency due to heterozygous gain-of-function mutations in STAT1

    Journal of clinical immunology, 2016

    Source : ORCID

  16. The effect of systemic corticosteroids on the innate and adaptive immune system in children with steroid responsive nephrotic syndrome

    European journal of pediatrics, 2016

    DOI 10.1007/s00431-016-2694-x PMID 26833050 28 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  17. The plethora, clinical manifestations and treatment options of autoimmunity in patients with primary immunodeficiency

    Turkish Archives of Pediatrics/Türk Pediatri Arşivi, 2016

    DOI 10.5152/turkpediatriars.2016.3928 PMID 28123330 11 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  18. Two patients with novel missense mutation in the purine nucleoside phosphorylase gene without serious or recurrent infections

    Clinical and Experimental Neuroimmunology, 2016

    DOI 10.1111/cen3.12254 4 citations (OpenAlex) Source : ORCID

  19. Use of subcutaneous immunoglobulin in primary immune deficiencies

    Turkish Archives of Pediatrics/Türk Pediatri Arşivi, 2016

    DOI 10.5152/turkpediatriars.2016.3058 PMID 27103859 8 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  20. Sinus pericranii: Diagnosis with contrast enhanced MRI venography

    Journal of Pediatric Neurology, 2015

    DOI 10.1055/s-0035-1557476 2 citations (OpenAlex) Source : OpenAlex

  21. Atypical presentation of Takayasu’s arteritis in an adolescent.

    Marmara Medical Journal, 2015

    DOI 10.5472/mmjcr.2803.01 1 citation (OpenAlex) Texte intégral en libre accèsSource : ORCID

  22. Dihidrorhodamin Testi ile Oksidatif Patlama: Sağlıklı Kontrollerde Referans Değerleri

    2015

    Source : ORCID

  23. Ev Tozu Akarı Duyarlı Astımlı Çocuklarda Subkutan Allerjen İmmünoterapi Üzerine Vitamin D Desteğinin Etkisi

    2015

    Source : ORCID

  24. Evaluation of Hyperimmunoglobulin M Syndrome by Flow Cytometry

    TURKISH JOURNAL OF IMMUNOLOGY, 2015

    Source : ORCID

  25. G6PC3 deficiency: Primary immune deficiency beyond just neutropenia

    Journal of Pediatric Hematology/Oncology, 2015

    DOI 10.1097/mph.0000000000000441 PMID 26479985 22 citations (Europe PMC) Source : ORCID

  26. G6PC3 deficiency: primary immune deficiency beyond just neutropenia

    Journal of pediatric hematology/oncology, 2015

    Source : ORCID

  27. Gene therapy using a self-inactivating lentiviral vector improves clinical and laboratory manifestations of Wiskott-Aldrich syndrome

    Blood, 2015

    DOI 10.1182/blood.v126.23.260.260 14 citations (OpenAlex) Texte intégral en libre accèsSource : ORCID

  28. Hiperimmünoglobulin M Sendromunun Akan Hücre Ölçer ile Değerlendirilmesi

    2015

    Source : ORCID

  29. Hiperimmünoglobulin M Sendromunun Akan Hücre Ölçer ile Değerlendirilmesi

    2015

    Source : ORCID

  30. Is there any marker to predict target organ involvement in combined immunodeficient patients?: 900

    Allergy: European Journal of Allergy and Clinical Immunology, 2015

    Source : ORCID

  31. Işıl barlan hocamızın bilimsel zekâsı ve akademik hayatta bizlere öğrettikleri

    Turkish Journal of Immunology, 2015

    Source : ORCID

  32. JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family

    Journal of Clinical Immunology, 2015

    DOI 10.1007/s10875-015-0156-2 PMID 25851723 18 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  33. JAGN1 deficient severe congenital neutropenia: two cases from the same family

    Journal of clinical immunology, 2015

    Source : ORCID

  34. Long-term effect of sublingual and subcutaneous immunotherapy in dust mite–allergic children with asthma/rhinitis: A 3-year prospective randomized controlled trial

    Journal of Investigational Allergology and Clinical Immunology, 2015

    Source : ORCID

  35. Lymphocyte subset abnormalities in heterozygous carrier state for ataxiatelangiectasia

    Allergy: European Journal of Allergy and Clinical Immunology, 2015

    Source : ORCID

  36. Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study

    Respiratory Medicine, 2015

    DOI 10.1016/j.rmed.2015.07.007 PMID 26216378 8 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  37. Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: a double-blind, double-dummy study

    Respiratory medicine, 2015

    Source : ORCID

  38. Oxidative Burst with Dihydrorhodamine Test: Reference Values in Healthy Controls

    TURKISH JOURNAL OF IMMUNOLOGY, 2015

    Source : ORCID

  39. Potential Immunoregulatory Roles of Natural Killer Cells in Children with Atopic Dermatitis

    Journal of Allergy and Clinical Immunology, 2015

    DOI 10.1016/j.jaci.2014.12.1685 1 citation (OpenAlex) Texte intégral en libre accèsSource : ORCID

  40. Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency

    Journal of Clinical Immunology, 2015

    DOI 10.1007/s10875-015-0178-9 PMID 26233237 38 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  41. Potentially beneficial effect of hydroxychloroquine in a patient with a novel mutation in protein kinase C$δ$ deficiency

    Journal of clinical immunology, 2015

    Source : ORCID

  42. Purine nucleoside phosphorylase (PNP) deficiency presenting as combined immune deficiency with no infections

    Allergy: European Journal of Allergy and Clinical Immunology, 2015

    Source : ORCID

  43. Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population

    Meta gene, 2015

    DOI 10.1016/j.mgene.2015.06.002 PMID 26137447 3 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  44. The Association of TLR4 and NOD2 Polymorphisms and Febrile Neutropenia in Children with Burkitt Lymphoma

    International Journal of Hematology and Oncology, 2015

    Source : ORCID

  45. The Effect of Vitamin D Supplementation on Subcutaneous Allergen Immunotherapy in House Dust Mite Sensitive Asthmatic Children

    Turkish Journal of Immunology, 2015

    DOI 10.5606/tji.2015.425 1 citation (OpenAlex) Texte intégral en libre accèsSource : ORCID

  46. The effect of systemic corticosteroids on the innate and adaptive immune system: 1052

    Allergy: European Journal of Allergy and Clinical Immunology, 2015

    Source : ORCID

  47. To estimate the major allergen in multisensitized children with rhinitis: is nasal provocation really needed?: 235

    Allergy: European Journal of Allergy and Clinical Immunology, 2015

    Source : ORCID

  48. Early-onset neurolupus: A challenge for pediatricians

    Marmara Medical Journal, 2015

    DOI 10.5472/mmjcr.2802.08 Texte intégral en libre accèsSource : ORCID

  49. Alteration in humoral immunity is common among family members of patients with common variable immunodeficiency

    J Investig Allergol Clin Immunol, 2014

    Source : ORCID

  50. Alteration in humoral immunity is common among family members of patients with common variable immunodeficiency

    Journal of Investigational Allergology and Clinical Immunology, 2014

    Source : ORCID