O. Sanal

发表

Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)

A. Fischer, L. Notarangelo, A. Plebani, 2000, Cell.

A single ataxia telangiectasia gene with a product similar to PI-3 kinase.

M. Lovett, F. Collins, S. Weissman, 1995, Science.

Toward gene therapy for human CD3 deficiencies.

O. Sanal, J. R. Regueiro, A. Pacheco-Castro, 2003, Human gene therapy.

Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease

O. Sanal, I. Tezcan, M. de Boer, 2009, European journal of clinical investigation.

Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations

O. Sanal, I. Tezcan, M. de Boer, 2009, European journal of clinical investigation.

Assessment of repeatability and reproducibility of mental and panoramic mandibular indices on digital panoramic images.

O. Sanal, M. Alkurt, I. Peker, 2007, International dental journal.

Defective lymphocyte locomotion in Chédiak-Higashi syndrome.

O. Sanal, O. Yeǧin, A. Gürgey, 1983, American journal of diseases of children.

A Case of DOCK8 Deficient Hyper-IgE Syndrome Presenting Primarily With Eczema, Food Allergy, and Asthma.

O. Sanal, D. Ayvaz, U. Sahiner, 2013, Pediatric allergy, immunology, and pulmonology.

Human CD3γ, but not CD3δ, haploinsufficiency differentially impairs γδ versus αβ surface TCR expression

E. López-Granados, H. Takada, O. Sanal, 2013, BMC Immunology.

Differential Biological Role of CD3 Chains Revealed by Human Immunodeficiencies1

O. Sanal, J. R. Regueiro, S. Kilic, 2007, The Journal of Immunology.

Isolated cutaneous response to granulocyte-monocyte colony stimulating factor in fatal idiopathic disseminated Bacillus-Calmette-Guerin infection

O. Sanal, I. Tezcan, N. Klein, 2000, European Journal of Pediatrics.

Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase

J. Palmblad, O. Sanal, M. de Boer, 2006, Human mutation.

Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency

İ. Reisli, O. Sanal, I. Tezcan, 2008, European Journal of Pediatrics.

Interleukin (IL)-12 and IL-23 are key cytokines for immunity against Salmonella in humans.

S. Dorman, J. Casanova, C. Picard, 2004, The Journal of infectious diseases.

Residual Type 1 Immunity in Patients Genetically Deficient for Interleukin 12 Receptor β1 (IL-12Rβ1)

M. Kurimoto, T. Ottenhoff, O. Sanal, 2000, The Journal of experimental medicine.

A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis.

O. Sanal, I. Tezcan, F. Ersoy, 2007, The Pediatric infectious disease journal.

Presentation of Interleukin-12/-23 Receptor β1 Deficiency with Various Clinical Symptoms of Salmonella Infections

T. Ottenhoff, O. Sanal, I. Tezcan, 2006, Journal of Clinical Immunology.

Severe Mycobacterium bovis BCG infections in a large series of novel IL–12 receptor β1 deficient patients and evidence for the existence of partial IL–12 receptor β1 deficiency

O. Sanal, I. Tezcan, F. Ersoy, 2003, European journal of immunology.

Human host defense and cytokines in mycobacterial infectious diseases: interleukin-18 cannot compensate for genetic defects in the interleukin-12 system.

M. Kurimoto, T. Ottenhoff, O. Sanal, 2002, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

A novel mutation in the interleukin-1 receptor antagonist associated with intrauterine disease onset.

O. Sanal, R. Goldbach-Mansky, E. Altiok, 2012, Clinical immunology.

Predominance of null mutations in ataxia-telangiectasia.

Y. Shiloh, S. Gilad, O. Sanal, 1996, Human molecular genetics.

Henoch-Schönlein purpura in Wiskott-Aldrich syndrome

A. Bakkaloğlu, O. Sanal, A. Duzova, 2001, Pediatric Nephrology.

Identification of ATM mutations using extended RT‐PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A‐T mutations in Israel

Y. Shiloh, S. Gilad, O. Sanal, 1998, Human mutation.

Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium.

T. Goradia, E. Sobel, Y. Shiloh, 1991, American journal of human genetics.

Association of tumour necrosis factor‐alpha ‐308 G/A polymorphism with primary open‐angle glaucoma

O. Sanal, I. Tezcan, F. Ersoy, 2012, Clinical & experimental ophthalmology.

Reduced memory B cells in patients with hyper IgE syndrome.

A. Plebani, J. Franco, J. Litzman, 2008, Clinical immunology.

Epstein-Barr-virus-carrying lymphoma in a patient with ataxia-telangiectasia.

G. Klein, O. Sanal, F. Ersoy, 1981, British medical journal.

Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency

S. Tangye, O. Sanal, I. Tezcan, 2021, Journal of Clinical Immunology.

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R

O. Sanal, I. Tezcan, I. Bilic, 2015, Haematologica.

Mutations in STAT3 and IL12RB1 impair the development of human IL-17–producing T cells

A. Fischer, J. Casanova, C. Picard, 2008, The Journal of experimental medicine.

Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia.

H. Kanegane, O. Sanal, I. Tezcan, 2002, American journal of medical genetics.

Antibody Response to a Seven-Valent Pneumococcal Conjugated Vaccine in Patients with Ataxia-Telangiectasia

O. Sanal, I. Tezcan, F. Ersoy, 2004, Journal of Clinical Immunology.

A novel mutation in TAP1 gene leading to MHC class I deficiency: Report of two cases and review of the literature.

M. van der Burg, O. Sanal, I. Tezcan, 2017, Clinical immunology.

Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations.

O. Sanal, I. Tezcan, C. Meischl, 2002, Experimental hematology.

Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region.

T. Foroud, W. Salser, O. Sanal, 1990, American journal of human genetics.

Genetic Haplotyping of Ataxia-telangiectasia Families Localizes the Major Gene to an ∼ 850 kb Region on Chromosome 11q23.1.

Y. Shiloh, O. Sanal, A. Børresen, 1994, International journal of radiation biology.

Selective complete C1q deficiencyReport of two new cases

O. Sanal, O. Yeǧin, A. I. Berkel, 1981 .

Residual Type 1 Immunity in Patients Genetically Deficient for Interleukin 12 Receptor β1 (IL-12Rβ1)

M. Kurimoto, O. Sanal, T. Ottenhoff, 2000, The Journal of Experimental Medicine.

IL‐12 receptor deficiency revisited: IL‐23‐mediated signaling is also impaired in human genetic IL‐12 receptor β1 deficiency

T. Ottenhoff, O. Sanal, T. Ottenhoff, 2003, European journal of immunology.

Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication

J. Franco, Y. Lau, O. Sanal, 2017, Front. Immunol..

An allelic variant of Griscelli disease: presentation with severe hypotonia, mental-motor retardation, and hypopigmentation consistent with Elejalde syndrome (neuroectodermal melanolysosomal disorder)

O. Sanal, I. Tezcan, F. Ersoy, 2000, Journal of Neurology.

Long Term Follow-Up of the Patients with Severe Combined Immunodeficiency After Hematopoietic Stem Cell Transplantation: A Single-Center Study

O. Sanal, I. Tezcan, D. Çağdaş, 2021, Immunological investigations.

TCR Dynamics in Human Mature T Lymphocytes Lacking CD3γ1

O. Sanal, A. Alcover, J. R. Regueiro, 2003, The Journal of Immunology.

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia.

A. Borkhardt, O. Sanal, I. Tezcan, 2014, Blood.

CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome.

A. Villa, M. Vihinen, S. Giliani, 1996, Immunology today.

Acquired factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome.

O. Sanal, I. Tezcan, F. Ersoy, 2007, Journal of pediatric hematology/oncology.

Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X–linked Thrombocytopenia–A single center study

O. Sanal, I. Tezcan, D. Çağdaş, 2021, Immunological investigations.

Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly

A. Fischer, F. Deist, A. Plebani, 2006, Cell.

Cernunnos Defi ciency: A Case Report

O. Sanal, I. Tezcan, T. Turul, 2011 .

Oral findings, treatment and follow-up of a case with major aphthous stomatitis (Sutton's disease).

O. Sanal, I. Tezcan, H. Hasturk, 1994, The Journal of clinical pediatric dentistry.

Twenty-year follow-up of 160 patients with ataxia-telangiectasia.

O. Sanal, A. I. Berkel, F. Ersoy, 1991, The Turkish journal of pediatrics.

Human T cell repertoire generation in the absence of MHC class II expression results in a circulating CD4+CD8- population with altered physicochemical properties of complementarity-determining region 3.

O. Sanal, F. Ersoy, P. J. van den Elsen, 1996, Journal of immunology.

The Impact of Single Amino Acid Substitutions in CD3γ on the CD3ϵγ Interaction and T-Cell Receptor–CD3 Complex Formation

J. Abrahams, O. Sanal, F. Koning, 2006 .

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene

A. Fischer, C. Griscelli, O. Sanal, 1997, Nature Genetics.

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.

A. Schäffer, E. Gertz, A. Plebani, 2010, The Journal of allergy and clinical immunology.

Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences.

Sara G. Becker-Catania, O. Sanal, L. Chessa, 1999, American journal of human genetics.

Additional Diverse Findings Expand the Clinical Presentation of DOCK8 Deficiency

O. Sanal, I. Tezcan, Dara M Strauss-Albee, 2012, Journal of Clinical Immunology.

Localization of an ataxia-telangiectasia gene to chromosome 11q22–23

M. Leppert, P. O'Connell, D. Weeks, 1988, Nature.

Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency

A. Fischer, F. Deist, O. Sanal, 2001, Cell.

CVID Associated with Systemic Amyloidosis

O. Sanal, I. Tezcan, S. Esenboğa, 2015, Case reports in immunology.

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

Clinical spectrum of X-linked hyper-IgM syndrome.

A. Fischer, L. Notarangelo, O. Sanal, 1997, The Journal of pediatrics.

A case of chronic severe neutropenia: oral findings and consequences of short-term granulocyte colony-stimulating factor treatment.

O. Sanal, I. Tezcan, N. Yamalık, 1998, Australian dental journal.

Hyper-IgE syndrome: a case report.

O. Sanal, I. Tezcan, A. Göçmen, 1990, The Turkish journal of pediatrics.

Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.

J. Casanova, J. Franco, C. Picard, 2014, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Mycobacterial Disease and Impaired IFN-γ Immunity in Humans with Inherited ISG15 Deficiency

J. Casanova, C. Rice, A. Abhyankar, 2012, Science.

Natural history and early diagnosis of LAD-1/variant syndrome.

O. Sanal, K. Seeger, T. Kuijpers, 2007, Blood.

Chronic granulomatous disease presenting with hypogammaglobulinemia.

O. Sanal, D. Ayvaz, T. T. Ozgür, 2011, Journal of investigational allergology & clinical immunology.

Early diagnosis of ataxia-telangiectasia using radiosensitivity testing.

Sara G. Becker-Catania, O. Sanal, L. Chessa, 2002, The Journal of pediatrics.

Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia

C. Doil, J. Bartek, J. Lukas, 2011, Cell Death and Differentiation.

Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

J. Casanova, L. Notarangelo, Y. Crow, 2014, Nature.

STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation.

E. Uz, O. Sanal, I. Tezcan, 2015, Clinical immunology.

Mutations of chronic granulomatous disease in Turkish families

O. Sanal, I. Tezcan, M. de Boer, 2007, European journal of clinical investigation.

Skewing of X‐chromosome inactivation in three generations of carriers with X‐linked chronic granulomatous disease within one family

O. Sanal, I. Tezcan, M. de Boer, 2006, European journal of clinical investigation.

Neutrophil chemotaxis and periodontal status in Down's syndrome patients.

O. Sanal, I. Tezcan, F. Ersoy, 1993, The Journal of Nihon University School of Dentistry.

Juvenile recurrent parotitis and immunodeficiency: Report of two cases

O. Sanal, S. Saraç, T. Turul, 2007 .

Comprehensive scanning of the ATM gene with DOVAM‐S

O. Sanal, R. Gatti, S. Sommer, 2003, Human mutation.

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency.

A. Fischer, A. Plebani, J. Litzman, 2004, Clinical immunology.

Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease

J. Casanova, O. Sanal, A. Boland, 2011, Journal of Medical Genetics.

Genetics, cytokines and human infectious disease: lessons from weakly pathogenic mycobacteria and salmonellae

T. Ottenhoff, O. Sanal, F. Verreck, 2002, Nature Genetics.

Epstein-Barr virus-related antibody patterns in ataxia-telangiectasia.

G. Klein, O. Sanal, F. Ersoy, 1979, Clinical and experimental immunology.

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

J. Casanova, A. Bousfiha, F. Ailal, 2015, Immunological reviews.

Griscelli Disease: Genotype–Phenotype Correlation in an Array of Clinical Heterogeneity

O. Sanal, I. Tezcan, F. Ersoy, 2002, Journal of Clinical Immunology.

Fanconi's aplastic anemia, analysis of 18 cases.

O. Sanal, A. Çavdar, A. Arcasoy, 1980, Acta haematologica.

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).

A. Fischer, O. Sanal, I. Tezcan, 2003, The Journal of clinical investigation.

Defective anti-polysaccharide antibody response in patients with ataxia-telangiectasia.

O. Sanal, I. Tezcan, F. Ersoy, 2004, The Turkish journal of pediatrics.

Ataxia-telangiectasia: phenotype/genotype studies of ATM protein expression, mutations, and radiosensitivity.

Sara G. Becker-Catania, O. Sanal, L. Chessa, 2000, Molecular genetics and metabolism.

Thirty years of primary immunodeficiencies in Turkey

O. Sanal, I. Tezcan, 2011, Annals of the New York Academy of Sciences.

Clinical Variants of Ataxia-Telangiectasia

O. Sanal, I. Tezcan, F. Ersoy, 1993 .

Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination.

A. Fischer, A. Plebani, P. Revy, 2003, The Journal of clinical investigation.

Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.

O. Sanal, I. Tezcan, F. Ersoy, 2005, The Journal of pediatrics.

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

O. Sanal, A. Somer, O. Yeǧin, 2013 .

Griscelli's syndrome: clinical features of three siblings.

O. Sanal, T. Küçükali, K. Tınaztepe, 1993, The Turkish journal of pediatrics.

LAD-1/variant syndrome is caused by mutations in FERMT3.

Dirk Roos, Frank Baas, Arthur J Verhoeven, 2009, Blood.

Clinical and genetic features of the patients with X‐Linked agammaglobulinemia from Turkey: Single‐centre experience

O. Sanal, I. Tezcan, D. Çağdaş, 2018, Scandinavian journal of immunology.

A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair

A. Fischer, Likun Du, Q. Pan-Hammarström, 2007, The Journal of experimental medicine.

Studies on lymphocyte cell surface in ataxia-telangiectasia.

O. Sanal, O. Yeǧin, N. Ozer, 1985, Clinical and experimental immunology.

ISG15 deficiency and increased viral resistance in humans but not mice

O. Sanal, I. Tezcan, A. García-Sastre, 2016, Nature Communications.

The Effect of IVIG on Superoxide Generation in Primary Humoral Immunodeficiencies

O. Sanal, I. Tezcan, F. Ersoy, 2016, The Annals of Clinical and Analytical Medicine.

Localization of an ataxia-telangiectasia gene to an ∼500-kb interval on chromosome 11q23.1 : linkage analysis of 176 families by an international consortium

T. Goradia, E. Sobel, Y. Shiloh, 1991 .

High levels of delayed radiation-induced apoptosis observed in lymphoblastoid cell lines from ataxia-telangiectasia patients.

H. Blattmann, O. Sanal, I. Tezcan, 2001, International journal of radiation oncology, biology, physics.

Altered apoptotic profiles in irradiated patients with increased toxicity.

H. Blattmann, P. Coucke, O. Sanal, 1999, International journal of radiation oncology, biology, physics.

The effect of mannose-binding protein gene polymorphisms in recurrent respiratory system infections in children and lung tuberculosis.

O. Sanal, I. Tezcan, F. Ersoy, 2003, The Turkish journal of pediatrics.

The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID).

O. Sanal, I. Tezcan, F. Ersoy, 2005, The Turkish journal of pediatrics.

Additional Diverse Findings Expand the Clinical Presentation of DOCK8 Deficiency

O. Sanal, I. Tezcan, Dara M Strauss-Albee, 2012, Journal of Clinical Immunology.

Residual type 1 immunity in patients genetically deficient for interleukin 12 receptor beta1 (IL-12Rbeta1): evidence for an IL-12Rbeta1-independent pathway of IL-12 responsiveness in human T cells.

M. Kurimoto, T. Ottenhoff, O. Sanal, 2000 .

Clinical and immunological studies in a case of selective complete C1q deficiency.

O. Sanal, O. Yeǧin, U. Ors, 1979, Clinical and experimental immunology.

A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase.

O. Sanal, I. Tezcan, F. Ersoy, 2006, The Turkish journal of pediatrics.

Corrigendum to “Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency” [Clin. Immunol. 110 (2004) 22–29]

A. Plebani, J. Litzman, O. Sanal, 2004 .

A case of selective Clq deficiency.

O. Sanal, M. Loos, R. Thesen, 1977, Turkish Journal of Pediatrics.

Homozygous C2 deficiency: association with defective alternative pathway function and immunoglobulin deficiency.

O. Sanal, I. Tezcan, L. Yel, 1996, International Archives of Allergy and Immunology.

Hereditary C1q deficiency: a new family with C1qA deficiency.

O. Sanal, S. Ersoy-Evans, R. Topaloğlu, 2010, The Turkish journal of pediatrics.

C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma

O. Sanal, R. Topaloğlu, F. Ozaltin, 2012, Clinical Rheumatology.

ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome

O. Sanal, I. Tezcan, M. Hershfield, 2018, Journal of Clinical Immunology.

Immune Dysfunctions in Ataxia-Telangiectasia

O. Sanal, F. Ersoy, O. Yeǧin, 1984 .

Gingivitis and Very High IgE Level in a Chronic Granulomatous Disease Patient with Unusual Presentation: A Case Report.

O. Sanal, S. Hakki, E. Yaprak, 2011, Pediatric allergy, immunology, and pulmonology.

Toll-Like Receptor Stimulation Induces Higher TNF-α Secretion in Peripheral Blood Mononuclear Cells from Patients with Hyper IgE Syndrome

A. Plebani, J. Franco, J. Litzman, 2008, International Archives of Allergy and Immunology.

Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.

O. Sanal, I. Tezcan, F. Ersoy, 2010, The Turkish journal of pediatrics.

The impact of single amino acid substitutions in CD3gamma on the CD3epsilongamma interaction and T-cell receptor-CD3 complex formation.

J. Abrahams, O. Sanal, F. Koning, 2006, Human immunology.

Erratum: Human intracellular ISG15 prevents interferon-α±/β 2 over-amplification and auto-inflammation (Nature 517 (2015) (89-93) 10.1038/nature13801))

J. Casanova, L. Notarangelo, Y. Crow, 2015 .

Cernunnos deficiency: a case report.

O. Sanal, I. Tezcan, T. Turul, 2011, Journal of investigational allergology & clinical immunology.

Progressive neurodegenerative syndrome in a patient with X-linked agammaglobulinemia receiving intravenous immunoglobulin therapy.

O. Sanal, A. Kurne, E. Saka, 2014, Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology.

Clinical and immunological aspects of hyper-IgM syndrome.

O. Sanal, I. Tezcan, F. Ersoy, 1990, The Turkish journal of pediatrics.

The relationship between periodontal status and peripheral levels of neutrophils in two consanguineous siblings with severe congenital neutropenia: case reports.

O. Sanal, F. Ersoy, T. Tözüm, 2003, Quintessence international.

Periodical gingival bleeding as a presenting symptom of periodontitis due to underlying cyclic neutropenia. Case report.

O. Sanal, I. Tezcan, F. Ersoy, 1993, Australian dental journal.

Impaired IgG Antibody Production to Pneumococcal Polysaccharides in Patients with Ataxia–Telangiectasia

O. Sanal, I. Tezcan, F. Ersoy, 1999, Journal of Clinical Immunology.

Serum IgD Concentrations in Patients with Ataxia Telangiectasia and with Selective IgA Deficiency

O. Sanal, I. Tezcan, F. Ozaltin, 1998, International Archives of Allergy and Immunology.

HLA antigens in subacute sclerosing panencephalitis.

O. Sanal, S. Aysun, A. I. Berkel, 1983, Archives of neurology.

Diversity in STK4 Deficiency and Review of the Literature.

S. Özen, O. Sanal, I. Tezcan, 2021, The journal of allergy and clinical immunology. In practice.

Subpopulations of T lymphocytes in subacute sclerosing panencephalitis (SSPE).

O. Sanal, S. Aysun, O. Yeǧin, 1986, The Turkish journal of pediatrics.

Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing

O. Sanal, I. Tezcan, I. Bilic, 2017, Scandinavian journal of immunology.

FERMT3 LAD-1/variant syndrome is caused by mutations in

F. Baas, O. Sanal, K. Seeger, 2013 .

Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1.

Y. Shiloh, O. Sanal, A. Børresen, 1994, International journal of radiation biology.

Human T-cell receptor CD3- ε (CD3D) / TaqI DNA polymorphism

O. Sanal, R. Gatti, P. Charmley, 1989 .

Human T-cell receptor CD3-gamma (CD3G)/MspI DNA polymorphism.

O. Sanal, R. Gatti, P. Charmley, 1989, Nucleic Acids Research.

Human T-cell receptor CD3-epsilon (CD3E)/TaqI DNA polymorphism.

O. Sanal, R. Gatti, P. Charmley, 1989, Nucleic Acids Research.

Ataxia‐telangiectasia: linkage analysis of chromosome 11q22‐23 markers in Turkish families

E. Sobel, O. Sanal, F. Ersoy, 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Ataxia-telangiectasia: linkage evidence for genetic heterogeneity.

E. Sobel, Y. Shiloh, A. Taylor, 1992, American journal of human genetics.

ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome

O. Sanal, I. Tezcan, M. Hershfield, 2018, Journal of Clinical Immunology.

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

Toll-Like Receptor Stimulation Induces Higher TNF-α Secretion in Peripheral Blood Mononuclear Cells from Patients with Hyper IgE Syndrome

A. Plebani, J. Franco, J. Litzman, 2008, International Archives of Allergy and Immunology.

Recurrent Salmonella bacteremia in interleukin-12 receptor beta1 deficiency.

O. Sanal, M. Ceyhan, M. Bayraktar, 2006, Journal of tropical pediatrics.

Subcutaneous nodules as presenting sign of disseminated BCG infection in a SCID patient.

O. Sanal, G. Uysal, Güven Ma, 1999, Infection.

IgG subclass deficiency in children with recurrent infections.

O. Sanal, I. Tezcan, A. Göçmen, 1991, The Turkish journal of pediatrics.

Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre

M. van der Burg, O. Sanal, I. Tezcan, 2023, Clinical and experimental immunology.

Antioxidant enzymes in red blood cells and lymphocytes of ataxia-telangiectasia patients.

Y. Aksoy, O. Sanal, I. Tezcan, 2004, The Turkish journal of pediatrics.