Wissenschaftliche Arbeiten

Prof. Dr. Ferah Genel

185 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  1. Dock8 deficiency and a diagnostic score to differentiate it from other hyper-IgE syndromes

    UCL Discovery (University College London), 2012

    DOI 10.25405/ncl.34191864 Frei zugänglicher VolltextQuelle: OpenAlex

  2. DOCK8 Deficiency and Diagnostic Guidelines for Hyper-IgE Syndromes

    UCL Discovery (University College London), 2012

    Frei zugänglicher VolltextQuelle: OpenAlex

  3. Our experience in neonatal varicella

    Journal of Dr Behcet Uz Children s Hospital, 2012

    DOI 10.5222/buchd.2012.154 Quelle: OpenAlex

  4. A Case of Cd20 Positive Mediastinal Rhabdomyosarcoma

    Turkish Journal of Pathology, 2012

    DOI 10.5146/tjpath.2012.01135 PMID 23011831 Frei zugänglicher VolltextQuelle: OpenAlex

  5. Clinical Presentation and Long-Term Outcome of Dock8 Deficiency - A Survey of 134 Patients

    UCL Discovery (University College London), 2012

    Quelle: OpenAlex

  6. CLINICAL PRESENTATION AND LONG-TERM OUTCOME OF DOCK8 DEFICIENCY - A SURVEY OF 134 PATIENTS

    Bursa Uludag University - AVESIS, 2012

    Quelle: OpenAlex

  7. DOCK8 deficiency and diagnostic guidelines for hyper-IgE syndromes

    Bursa Uludag University - AVESIS, 2012

    Quelle: OpenAlex

  8. DOCK8 DEFICIENCY AND A DIAGNOSTIC SCORE TO DIFFERENTIATE IT FROM OTHER HYPER-IGE SYNDROMES

    Bursa Uludag University - AVESIS, 2012

    Quelle: OpenAlex

  9. Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations

    Genes and Immunity, 2011

    DOI 10.1038/gene.2011.39 PMID 21654842 108 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  10. Molecular characterization of two novel cases of complete complement inhibitor Factor I deficiency

    Molecular Immunology, 2011

    DOI 10.1016/j.molimm.2011.01.012 PMID 21316765 22 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  11. Molecular basis of hereditary C1q deficiency-revisited: Identification of several novel disease causing mutations

    Molecular Immunology, 2011

    DOI 10.1016/j.molimm.2011.06.401 5 Zitationen (OpenAlex) Quelle: OpenAlex

  12. Effects Of Nutritional Types Of İnfants Between 0-4 Months On The Psychomotor Development

    Journal of Dr Behcet Uz Children s Hospital, 2011

    DOI 10.5222/buchd.2011.020 3 Zitationen (OpenAlex) Quelle: OpenAlex

  13. Retinopathy Of Prematurity In Our Nenatal Intensive Care Unit, Incidence, Risk Factors And Outcome

    Journal of Dr Behcet Uz Children s Hospital, 2011

    DOI 10.5222/buchd.2011.007 1 Zitation (OpenAlex) Quelle: OpenAlex

  14. Hearing Screening Test Results Of Newborns at High Risk for Developmentel Delay

    Journal of Dr Behcet Uz Children s Hospital, 2011

    DOI 10.5222/buchd.2011.001 1 Zitation (OpenAlex) Quelle: OpenAlex

  15. Gelişimsel açıdan yüksek riskli bebeklerde işitme tarama sonuçları

    İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2011

    Quelle: OpenAlex

  16. Two Serious Complications of Organophosphate Poisoning in the Same Patient: Acute Pancreatitis and Late-Onset Polyneuropathy: Case Report

    Turkiye Klinikleri Journal of Pediatrics, 2010

    2 Zitationen (OpenAlex) Quelle: OpenAlex

  17. Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiency.

    PubMed, 2010

    PMID 20635792 10 Zitationen (OpenAlex) Quelle: OpenAlex

  18. DOCK8 Deletions and Mutations Are Associated With The Autosomal Recessive Hyper-IgE Phenotype

    Journal of Allergy and Clinical Immunology, 2010

    DOI 10.1016/j.jaci.2010.01.006 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  19. PP-327. Evaluation of breast milk sodium and neonatal hypernatremic dehydration

    Early Human Development, 2010

    DOI 10.1016/j.earlhumdev.2010.09.390 1 Zitation (OpenAlex) Quelle: OpenAlex

  20. PP-79. The role of alloimmunization to irregular erythrocyte antigens in neonatal hyperbilirubinemia

    Early Human Development, 2010

    DOI 10.1016/j.earlhumdev.2010.09.132 1 Zitation (OpenAlex) Quelle: OpenAlex

  21. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome (vol 124, pg 1289, 2009)

    UCL Discovery (University College London), 2010

    1 Zitation (OpenAlex) Quelle: OpenAlex

  22. PP-172. Prospective analysis of 109 term cases of breast-feeding associated hypernatremia

    Early Human Development, 2010

    DOI 10.1016/j.earlhumdev.2010.09.227 Quelle: OpenAlex

  23. PP-156. Evaluation of 40 cases with symptomatic cytomegalovirus infection

    Early Human Development, 2010

    DOI 10.1016/j.earlhumdev.2010.09.210 Quelle: OpenAlex

  24. 851 Hereditary Angioedema and Long-Term Prophylaxis

    Pediatric Research, 2010

    DOI 10.1203/00006450-201011001-00851 Quelle: OpenAlex

  25. Thirty-eight of 47 patients with autosomal-recessive hyper-IgE syndrome carry deletions and point mutations in Dock8

    2010

    Quelle: OpenAlex

  26. PP-158. Etiology of fever in 103 neonates hospitalized at Dr. Behcet Uz Children's Hospital, İzmir

    Early Human Development, 2010

    DOI 10.1016/j.earlhumdev.2010.09.212 Quelle: OpenAlex

  27. A Case of Autoimmune Lymphoproliferative Syndrome with Kimura's Disease Like Histopathology

    Turkiye Klinikleri Journal of Pediatrics, 2009

    1 Zitation (OpenAlex) Quelle: OpenAlex

  28. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

    Journal of Allergy and Clinical Immunology, 2009

    DOI 10.1016/j.jaci.2009.10.038 PMID 20004785 526 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  29. Defects along the TH17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

    Journal of Allergy and Clinical Immunology, 2009

    DOI 10.1016/j.jaci.2009.05.004 PMID 19577286 107 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  30. Monocyte HLA-DR expression as predictor of poor outcome in neonates with late onset neonatal sepsis

    Journal of Infection, 2009

    DOI 10.1016/j.jinf.2009.12.004 PMID 20025903 65 Zitationen (OpenAlex) Quelle: OpenAlex

  31. Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID

    Clinical and Experimental Medicine, 2009

    DOI 10.1007/s10238-009-0053-1 PMID 19458910 19 Zitationen (OpenAlex) Quelle: OpenAlex

  32. Interleukin‐12/‐23 receptor beta 1 deficiency in an infant with draining BCG lymphadenitis

    Pediatrics International, 2009

    DOI 10.1111/j.1442-200x.2009.02818.x PMID 19379268 9 Zitationen (OpenAlex) Quelle: OpenAlex

  33. Risk factors for vancomycin-resistant enteroccocci colonization in infants in neonatal intensive care unit

    Open Medicine, 2009

    DOI 10.2478/s11536-009-0073-y 4 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  34. Antikor eksikliği olan çocuklarda allerji sikliği

    2009

    1 Zitation (OpenAlex) Quelle: OpenAlex

  35. EVALUATION OF ADHESION MOLECULES ON PERIPHERAL BLOOD NEUTROPHILS AND MONOCYTES FOR EARLY DIAGNOSIS OF NEONATAL SEPSIS

    Archives of Disease in Childhood, 2008

    Quelle: OpenAlex

  36. Genetic, molecular and functional analyses of complement factor I deficiency

    European Journal of Immunology, 2008

    DOI 10.1002/eji.200838702 PMID 19065647 58 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  37. EFFICACY OF ENZYME REPLACEMENT THERAPY IN ADENOSINE DEAMINASE-DEFICIENT SEVERE COMBINED IMMUNE DEFICIENCY

    Archives of Disease in Childhood, 2008

    Quelle: OpenAlex

  38. İzmir Dr.Behçet Uz Çocuk Hastanesine status epileptikus kliniği ile başvuran hastaların etyoloji, klinik bulgular ve risk faktörleri yönünden değerlendirilmesi

    The Anatolian Journal of General Medical Research, 2007

    Quelle: OpenAlex

  39. Çocuklarda metoklopramid kullanımına bağlı distonik reaksiyonlar

    2007

    Quelle: OpenAlex

  40. Evatuation of the Etiology, Clinical Findings and Risk Factors in Patients with Status Epilepticus Admitted in Dr. Behçet Uz Children's Hospital

    The Anatolian Journal of General Medical Research, 2007

    DOI 10.5222/terh.2007.00579 Frei zugänglicher VolltextQuelle: OpenAlex

  41. BCG-osis and tuberculosis in a child with chronic granulomatous disease

    Journal of Allergy and Clinical Immunology, 2007

    DOI 10.1016/j.jaci.2007.04.034 PMID 17544093 134 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  42. Genetic, molecular and functional analysis of complement factor I deficiency

    Molecular Immunology, 2007

    DOI 10.1016/j.molimm.2007.06.033 Quelle: OpenAlex

  43. Acute Isoniazid Poisoning Presenting with Status Epilepticus

    The Anatolian Journal of General Medical Research, 2006

    DOI 10.5222/terh.2006.01729 Frei zugänglicher VolltextQuelle: OpenAlex

  44. Serum immunoglobulin (IgG, IgM, IgA) and IgG subclass concentrations in healthy children: a study using nephelometric technique

    The Turkish Journal of Pediatrics, 2006

    DOI 10.24953/turkjpediatr.2006.2590 PMID 16562781 146 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  45. Hypercoagulability: interaction between inflammation and coagulation in familial Mediterranean fever

    Clinical Rheumatology, 2006

    DOI 10.1007/s10067-006-0334-y PMID 16721492 43 Zitationen (OpenAlex) Quelle: OpenAlex

  46. Cutaneous leukocytoclastic vasculitis in a child with interleukin-12 receptor beta-1 deficiency

    The Journal of Pediatrics, 2006

    DOI 10.1016/j.jpeds.2005.10.003 PMID 16615980 27 Zitationen (OpenAlex) Quelle: OpenAlex

  47. Properdin deficiency in a boy with fulminant meningococcal septic shock

    Acta Paediatrica, 2006

    DOI 10.1080/08035250600603008 PMID 17062484 13 Zitationen (OpenAlex) Quelle: OpenAlex

  48. Prognostic Validation of Niclasson Scoring in Patients with Meningococcemia

    The Anatolian Journal of General Medical Research, 2006

    DOI 10.5222/terh.2006.00268 Frei zugänglicher VolltextQuelle: OpenAlex

  49. IgA and/or IgG subclass deficiency in children with recurrent respiratory infections and its relationship with chronic pulmonary damage.

    PubMed, 2005

    PMID 15864886 70 Zitationen (OpenAlex) Quelle: OpenAlex

  50. Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis

    Scandinavian Journal of Infectious Diseases, 2005

    DOI 10.1080/00365540510034536 PMID 16138437 43 Zitationen (OpenAlex) Quelle: OpenAlex