Prof. Dr. Ferah Genel

CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis

Blood, 2019

DOI 10.1182/blood.2019000644 PMID 31501153 66 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

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

2019

Quelle: OpenAlex

Bax Gene Polymorphism in Childhood Acute Lymphoblastic Leukemia and Evaluation of Apoptosis with Conventional Dose-Prednisolone Treatment

Acta Oncologica Turcica, 2019

DOI 10.5505/aot.2019.29981 Frei zugänglicher VolltextQuelle: OpenAlex

Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report

Central European Journal of Immunology, 2019

DOI 10.5114/ceji.2019.87073 PMID 31530991 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13

Journal of Pediatric Endocrinology and Metabolism, 2019

DOI 10.1515/jpem-2019-0377 PMID 31809266 12 Zitationen (OpenAlex) 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

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

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

Proceedings of the National Academy of Sciences, 2018

DOI 10.1073/pnas.1805437115 PMID 30072435 45 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages

Scandinavian Journal of Immunology, 2018

DOI 10.1111/sji.12737 PMID 30506560 23 Zitationen (OpenAlex) Quelle: 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

Neurodevelopmental evaluation of children with cyanotic congenital heart disease

Minerva Pediatrics, 2018

DOI 10.23736/s0026-4946.17.04265-7 PMID 26041003 6 Zitationen (OpenAlex) Quelle: 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

The relationship between hypernatremia and breast milk sodium levels in newborns with hypernatremic dehydration

The European Research Journal, 2018

DOI 10.18621/eurj.373386 3 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

Evaluation of symptomatic cytomegalovirus infections in our hospital between 2004 and 2009

Journal of Dr Behcet Uz Children s Hospital, 2018

DOI 10.5222/buchd.2018.15010 Frei zugänglicher VolltextQuelle: OpenAlex

Neurodevelopmental outcome of children with congenital hypothyroidism diagnosed in a national screening program in Turkey

Indian Pediatrics, 2017

DOI 10.1007/s13312-017-1111-5 PMID 28368265 14 Zitationen (OpenAlex) Quelle: OpenAlex

A harmless clinical condition presenting with dramatic elevation of alkaline phosphatase: bening transient hyperphosphatasemia of childhood

The Anatolian Journal of General Medical Research, 2017

DOI 10.5222/terh.2017.061 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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

SIDE EFFECTS AND CONTRIBUTING FACTORS OF INTRAVENOUS IMMUNOGLOBULIN REPLACEMENT THERAPY IN PATIENTS WITH PRIMARY IMMUNODEFICIENCIES

2017

DOI 10.26226/morressier.594a7d48d462b8028d893983 Quelle: OpenAlex

Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression

Jornal de Pediatria, 2016

DOI 10.1016/j.jped.2016.01.013 PMID 27553592 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression

Jornal de Pediatria (Versão em Português), 2016

DOI 10.1016/j.jpedp.2016.08.014 Frei zugänglicher VolltextQuelle: 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

STAT3 mutation presenting with atopic dermatitis

Journal of Clinical & Cellular Immunology, 2016

DOI 10.4172/2155-9899.c1.028 4 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

PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY WITH TUBERCULOSIS AND CLINICAL OUTCOME AFTER HEMATOPOIETIC STEM CELL TRANSPLANTATION

2016

DOI 10.26226/morressier.57bc1757d462b80290b4ced2 Quelle: OpenAlex

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

Journal of Clinical Immunology, 2015

DOI 10.1007/s10875-014-0126-0 PMID 25627830 320 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

Journal of Allergy and Clinical Immunology, 2015

DOI 10.1016/j.jaci.2014.12.1945 PMID 25724123 200 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency

Journal of Autoimmunity, 2015

DOI 10.1016/j.jaut.2015.06.002 PMID 26119135 46 Zitationen (OpenAlex) 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

Adenosine Deaminase-Deficient Severe Combined Immunodeficiency and Diffuse Large B-Cell Lymphoma

Pediatric Allergy Immunology and Pulmonology, 2015

DOI 10.1089/ped.2014.0478 6 Zitationen (OpenAlex) Quelle: 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

Abdominal Tuberculosis in a Child With Interleukin-12 Receptor Beta 1 Deficiency

Infectious Diseases in Clinical Practice, 2015

DOI 10.1097/ipc.0000000000000304 1 Zitation (OpenAlex) Quelle: OpenAlex

INTRAKRANİAL HEMORAJİ İLE İLİŞKİLİ CANDİDA MENENJİTİ

DergiPark (Istanbul University), 2015

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

The Extended Clinical Phenotype of 58 Patients with Dock8 Deficiency

UCL Discovery (University College London), 2014

DOI 10.25405/ncl.34244802 4 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Two Cases with Pseudohypoaldosteronism

Güncel Pediatri, 2014

DOI 10.4274/jcp.66376 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

An infant presenting with acute gastroenteritis and intestinal edema and diagnosed as Kawasaki disease: Case report

Journal of Dr Behcet Uz Children s Hospital, 2014

DOI 10.5222/buchd.2014.148 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

PS-024 Neurodevelopmental Examination By Bayley Scale Of Infant Development-ii In Children With Cyanotic Congenital Heart Disease

Congenital Heart Disease, 2014

DOI 10.1136/archdischild-2014-307384.319 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

C1q deficient individuals have a wide variety of clinical presentation, quality of life and life expectancy

Data Archiving and Networked Services (DANS), 2014

Quelle: OpenAlex

The Extended Clinical Phenotype of 58 Patients with Dock8 Deficiency

Bursa Uludag University - AVESIS, 2014

Quelle: OpenAlex

The clinical importance of myeloid antigen coexpression and TEL-AML1 mutation in patients with childhood acute lymphoblastic leukemia

Journal of Clinical and Experimental Investigations, 2013

DOI 10.5799/ahinjs.01.2013.01.0240 Frei zugänglicher VolltextQuelle: OpenAlex

Transfusion reactions in neonates

Journal of Dr Behcet Uz Children s Hospital, 2013

DOI 10.5222/buchd.2013.117 Quelle: OpenAlex

The demographic datas of chronic granulomatous disease patients and the comparation of the clinical datas before and after interferon-gamma treatment in our country

Bursa Uludag University - AVESIS, 2013

2 Zitationen (OpenAlex) Quelle: OpenAlex

Diagnostic value of platelet parameters in neonatal sepsis

Journal of Dr Behcet Uz Children s Hospital, 2013

DOI 10.5222/buchd.2012.010 1 Zitation (OpenAlex) Quelle: OpenAlex

Developmental problems in infants diagnosed as congenital cytomegalovirus infection

Journal of Dr Behcet Uz Children s Hospital, 2013

DOI 10.5222/buchd.2013.049 Quelle: OpenAlex

Ülkemizde kronik granülomatöz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi öncesi ve sonrası klinik verilerinin karşılaştırılması

Bursa Uludag University - AVESIS, 2013

Quelle: OpenAlex

Evaluation of adhesion molecules CD64, CD11b and CD62L in neutrophils and monocytes of peripheral blood for early diagnosis of neonatal infection

World Journal of Pediatrics, 2012

DOI 10.1007/s12519-011-0304-6 PMID 21874613 33 Zitationen (Europe PMC) Quelle: ORCID

Case of purine nucleoside phosphorylase deficiency presented with hematuria

Open Journal of Pediatrics, 2012

DOI 10.4236/ojped.2012.24044 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Molecular Analysis and Clinical Findings of Griscelli Syndrome Patients

Journal of Pediatric Hematology/Oncology, 2012

DOI 10.1097/mph.0b013e31826781ad PMID 22983416 15 Zitationen (OpenAlex) Quelle: OpenAlex