Prof. Dr. Nesrin Gülez

SKIG kullanım ilkeleri nelerdir? SKIG dozu ve sıklığı nasıl belirlenmelidir?

2019

Quelle: OpenAlex

Characteristics of the patients followed with the diagnosis of common variable immunodeficiency and the complications

Central European Journal of Immunology, 2019

DOI 10.5114/ceji.2019.87060 PMID 31530980 9 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Analysis of the CD40 and CD40LG in Turkish Hyper IgM Syndrome: Mutation profile and description of six novel mutations

European Journal of Human Genetics, 2019

Quelle: ORCID

DOCK8 deficiency; two patients with large deletions detected by Next-generation sequencing

European Journal of Human Genetics, 2019

Quelle: ORCID

Evaluation of the effects of miRNAs in familial Mediterranean fever

Clinical Rheumatology, 2019

DOI 10.1007/s10067-017-3914-0 PMID 29442258 32 Zitationen (OpenAlex) Quelle: ORCID

Hematopoietic stem cell transplantation in pediatric DOCK8 deficiency related hiper ige syndrome

Bone Marrow Transplantation, 2019

Quelle: ORCID

LATENT TUBERCULOSIS INFECTION IN CHILDREN WITH PEDIATRIC RHEUMATOLOGIC DISEASES TREATED WITH CANAKINUMAB

Annals of the Rheumatic Diseases, 2019

DOI 10.1136/annrheumdis-2019-eular.5368 Frei zugänglicher VolltextQuelle: ORCID

Mutations affecting the actin regulator WD repeat–containing protein 1 lead to aberrant lymphoid immunity

Journal of Allergy and Clinical Immunology, 2018

DOI 10.1016/j.jaci.2018.04.023 PMID 29751004 79 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients

International Journal of Immunopathology and Pharmacology, 2018

DOI 10.1177/2058738418779458 PMID 29978731 19 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

The Significance of B-cell Subsets in Patients with Unclassified Hypogammaglobulinemia and Association with Intravenous Immunoglobulin Replacement Requirement.

PubMed, 2018

DOI 10.22034/iji.2018.39336 PMID 29549228 6 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Inherited Classical and Alternative Pathway Complement Deficiencies in Children: A Single Center Experience.

PubMed, 2018

DOI 10.22034/iji.2018.39400 PMID 30593745 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

A comparative evaluation of clinical and laboratory findings and treatment costs for sublingual and subcutaneous immunotherapy in children with allergic rhinitis and asthma

Allergy, 2018

Quelle: ORCID

Long-term follow-up of paediatric MEFV carriers

Clinical Rheumatology, 2018

DOI 10.1007/s10067-017-3883-3 PMID 29101676 9 Zitationen (OpenAlex) Quelle: ORCID

Tuberculosis masked by immunodeficiency: a review of two cases diagnosed with chronic granulomatous disease

Tuberkuloz ve Toraks, 2017

DOI 10.5578/tt.22093 PMID 28621249 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

A child with subcorneal pustular dermatosis responded to IVIG treatment (Sneddon-Wilkinson disease)

Reumatologia/Rheumatology, 2017

DOI 10.5114/reum.2017.72631 PMID 29491542 6 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

NUCLEAR FACTOR KAPPA B1 (NFKB1) MUTATION İN A PATIENT WITH COMMON VARIABLE IMMUNODEFICIENCY.

2017

DOI 10.26226/morressier.594a7d45d462b8028d8933ae Quelle: OpenAlex

PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY PRESENTING AS SEVERE COMBINED IMMUNE DEFICIENCY, NEURODEVELOPMENTAL DELAY AND AUTOIMMUNE HEMOLYTIC ANEMIA

2017

DOI 10.26226/morressier.594a7d46d462b8028d893762 Quelle: OpenAlex

Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation

Journal of Allergy and Clinical Immunology, 2016

DOI 10.1016/j.jaci.2016.04.023 PMID 27350570 96 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases

Case Reports in Immunology, 2016

DOI 10.1155/2016/5459029 PMID 27699073 26 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Five years of experience in transient hypogammaglobulinemia of infancy

Journal of Dr Behcet Uz Children s Hospital, 2016

DOI 10.5222/buchd.2016.209 Frei zugänglicher VolltextQuelle: OpenAlex

Clinical, Laboratory and Molecular Approach to Ten Children with Congenital Neutropenia

The Journal of Pediatric Research, 2016

DOI 10.4274/jpr.19480 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

Comparison of the efficacy of once- and twice-daily colchicine dosage in pediatric patients with familial Mediterranean fever - a randomized controlled noninferiority trial

Arthritis Research & Therapy, 2016

DOI 10.1186/s13075-016-0980-7 PMID 27055417 26 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

The experience of canakinumab in renal amyloidosis secondary to Familial Mediterranean fever

Molecular and Cellular Pediatrics, 2016

DOI 10.1186/s40348-016-0058-2 PMID 27590627 25 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

DRESS Syndrome Induced by Sulfasalazine with Amoxicillin: Case Report

Turkiye Klinikleri Journal of Dermatology, 2016

DOI 10.5336/dermato.2015-49144 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

AUTOSOMAL RECESSIVE CHRONIC GRANULOMATOUS DISEASE, HYPERINFLAMMATORY STATE AND HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; CASE REPORT

2016

DOI 10.26226/morressier.57bc1755d462b80290b4d812 Quelle: OpenAlex

Case report Asplenia in children with congenital heart disease as a cause of poor outcome

Central European Journal of Immunology, 2015

DOI 10.5114/ceji.2015.52841 PMID 26557043 8 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Case report Coexistence of hereditary angioedema in a case of familial Mediterranean fever with partial response to colchicine

Central European Journal of Immunology, 2015

DOI 10.5114/ceji.2015.50843 PMID 26155193 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

INTRAKRANİAL HEMORAJİ İLE İLİŞKİLİ CANDİDA MENENJİTİ

DergiPark (Istanbul University), 2015

Frei zugänglicher VolltextQuelle: OpenAlex

Delay in Diagnosis in Children with Visceral Leishmaniasis: A Single-Center Experience

Çocuk Enfeksiyon Dergisi/Journal of Pediatric Infection, 2015

DOI 10.5152/ced.2015.1906 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

Pulmonary complications in patients with common variable immunodeficiency

Allergy, 2015

Quelle: ORCID

Successful Hematopoietic Stem Cell Transplantation In Autosomal Recessive Hyper-IgE Syndrome Due To DOCK8 Deficiency: Single Center Experience

Bone Marrow Transplantation, 2015

Quelle: ORCID

Our experience of anti-interleukin 1 therapy

Pediatric Rheumatology, 2015

DOI 10.1186/1546-0096-13-s1-p210 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Evaluation of familial mediterranean fever patients: a single center experience

Pediatric Rheumatology, 2015

DOI 10.1186/1546-0096-13-s1-p111 Frei zugänglicher VolltextQuelle: OpenAlex

Do Elevated Serum IgM Levels Have to Be Included in Probable Diagnosis Criteria of Patients with Ataxia-Telangiectasia?

International Journal of Immunopathology and Pharmacology, 2014

DOI 10.1177/039463201402700312 PMID 25280033 16 Zitationen (OpenAlex) Quelle: OpenAlex

A Rare Cause of Bacterial Meningitis and Recurrent Pneumonia: Congenital Asplenia

Journal of Clinical Immunology, 2014

Quelle: ORCID

ASSOCIATION BETWEEN IMMUNOPHENOTYPING AND PROGNOSIS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA

Pediatric Blood and Cancer, 2014

Quelle: ORCID

AUTOSOMAL RECESSIVE HIPERIGE SYNDROME: SINGLE CENTRE EXPERIENCE

Journal of Clinical Immunology, 2014

Quelle: ORCID

C8 DEFICIENCY WITH OR WITHOUT RECURRENT MENINGITIS IN A TURKISH FAMILY

Journal of Clinical Immunology, 2014

Quelle: ORCID

Clinical and Immunological Characterizations in Eleven Turkish Patients with Autosomal Recessive Hyper Ige Syndrome Caused by DOCK8 Mutation

Journal of Clinical Immunology, 2014

Quelle: ORCID

Clinical and Immunological Correction of DOCK8 Deficient Patient by Allogeneic Hematopoietic Stem Cell Transplantation

Journal of Clinical Immunology, 2014

Quelle: ORCID

Clinical and Immunological Features of Patients with Complement Deficiencies: A Single Centre Experience

Journal of Clinical Immunology, 2014

Quelle: ORCID

Complement Deficiencies: A Single Centre Experience

Journal of Clinical Immunology, 2014

Quelle: ORCID

GRANULOMATOUS AND LYMPHOCYTIC INTERSTITIAL LUNG DISEASE IN A PATIENT WITH COMMON VARIABL IMMUNODEFICIENCY

Pediatric Pulmonology, 2014

Quelle: ORCID

Granulomatous and Lymphocytic Interstitial Lung Disease in a Patient with Common Variable Immunodeficiency

Journal of Clinical Immunology, 2014

Quelle: ORCID

Recurrent Salmonella Infections Associated with Cutaneous Vasculitis and Abdominal Tuberculosis in Interleukin-12 Receptor Beta 1 Deficiency: Two Case Reports

Journal of Clinical Immunology, 2014

Quelle: ORCID

Recurrent Salmonella Infections Associated with Cutaneous Vasculitis in Interleukin-12 Receptor Beta 1 Deficiency: Two Case Reports

Journal of Clinical Immunology, 2014

Quelle: ORCID

Hyper IgE syndrome in the differential diagnosis of atopic eczema

Allergy, 2013

Quelle: ORCID

Recurrent Peripheral Facial Palsy in a Child With Familial Mediterranean Fever

Pediatric Neurology, 2013

DOI 10.1016/j.pediatrneurol.2013.05.003 PMID 23838413 10 Zitationen (OpenAlex) Quelle: ORCID

SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE DEAMINASE DEFICIENCY: EVIDENCE FROM THREE CASE REPORTS

Journal of Clinical Immunology, 2013

Quelle: ORCID

Severe combined immunodeficiency: clinical and immunological features of six patients from a single center within a year

Allergy, 2013

Quelle: ORCID