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Train Support Vector Machine Using Fuzzy C-means Without a Prior Knowledge for Hyperspectral Image Content Classification

ARO (Koya), 2022-09, Vol.10 (2), p.22-28

Taher, Akar H.

2022

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A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease

Clinical immunology (Orlando, Fla.), 2015-07, Vol.159 (1), p.58-62

2015

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Perplexing Etiology of Hyperphenylalaninemia in an Infant Referred via Newborn Screening

Clinical chemistry (Baltimore, Md.), 2021-10, Vol.67 (10), p.1428-1431

2021

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Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis

Haematologica (Roma), 2016-10, Vol.101 (10), p.1180-1189

2016

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A case of XLF deficiency presented with diffuse large B cell lymphoma in the brain

Clinical immunology (Orlando, Fla.), 2015-12, Vol.161 (2), p.394-395

2015

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The Frequency of HLA-A, HLA-B, and HLA-DRB1 Alleles in Patients with Acute Lymphoblastic Leukemia in the Turkish Population: A Case-Control Study

Turkish journal of haematology, 2016-12, Vol.33 (4), p.339-345

2016

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THE INFLUENCE OF HLA-DQ2 HETERODIMERS ON THE CLINICAL FEATURES AND LABORATORY OF PATIENTS WITH CELIAC DISEASE

Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2015-12, Vol.32 (6), p.2594-2599

2015

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Silent brain infarcts in two patients with zeta chain-associated protein 70 kDa (ZAP70) deficiency

Clinical immunology (Orlando, Fla.), 2015-05, Vol.158 (1), p.88-91

2015

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Clericuzio-type Poikiloderma with Neutropenia Syndrome in a Turkish Family: a Three Report of Siblings with Mutation in the C16orf57 gene

Iranian journal of allergy, asthma, and immunology, 2015-06, Vol.14 (3), p.331-331

2015

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Atypical Severe Combined Immunodeficiency Caused by a Novel Homozygous Mutation In Rag1 Gene in a Girl who Presented with Pyoderma Gangrenosum: A Case Report and Literature Review

Journal of clinical immunology, 2014-10, Vol.34 (7), p.792-795

2014

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X-linked agammaglobulinemia in two siblings with a novel mutation in the BTK gene who presented with polyarticular juvenile idiopathic arthritis

Scandinavian journal of rheumatology, 2015-03, Vol.44 (2), p.168-170

2015

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Increased Postexercise Lipoxin A4 Levels in Exhaled Breath Condensate in Asthmatic Children With Exercise-Induced Bronchoconstriction

Journal of investigational allergology & clinical immunology, 2016-01, Vol.26 (1), p.19-24

2016

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Relationships of Human Leukocyte Antigen-A, -B, -DRB1 Alleles, and Haplotypes in 129 Ethnic Turkish Patients With Acute Myeloblastic Leukemia

Laboratory medicine, 2015-08, Vol.46 (3), p.195-199

2015

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Exhaled breath condensate annexin A5 levels in exercise-induced bronchoconstriction in asthma: A preliminary study

Allergologia et immunopathologia, 2015-11, Vol.43 (6), p.538-542

2015

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Prurigo simplex subacuta or prurigo simplex acuta?

European annals of allergy and clinical immunology, 2014-07, Vol.46 (4), p.152

2014

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Silent brain infarcts in two patients with zeta chain-associated protein 70kDa (ZAP70) deficiency

Clinical immunology (Orlando, Fla.), 2015-05, Vol.158 (1), p.88-91

2015

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Determination of the Cricothyroid Membrane Height by Age and Sex and Optimal Tracheal Tube Size

The Laryngoscope, 2024-04, Vol.134 (4), p.1825-1830

2024

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The association of forced expiratory volume in one second and forced expiratory flow at 50% of the vital capacity, peak expiratory flow parameters, and blood eosinophil counts in exercise-induced bronchospasm in children with mild asthma

Asia Pacific allergy, 2015-04, Vol.5 (2), p.98-102

2015

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Combined immunodeficiencies: twenty years experience from a single center in Turkey

Central-European journal of immunology, 2016, Vol.41 (1), p.107-115

2016

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Hair dyes and temporary tattoos are a real hazard for adolescents?

European annals of allergy and clinical immunology, 2014-01, Vol.46 (1), p.35

2014

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AMINO ACID LEVELS IN CHILDREN WITH CELIAC DISEASE

Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2015-07, Vol.32 (1), p.139-143

2015

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A selective IgA deficiency in a boy who presented recurrent parotitis

European journal of microbiology & immunology, 2014-06, Vol.4 (2), p.144-146

2014

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Grass pollen triggered anaphylaxis in an adolescent boy

European annals of allergy and clinical immunology, 2015-01, Vol.47 (1), p.20

2015

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Hematopoietic Stem Cell Transplant for Primary Immunodeficiency Diseases: A Single-Center Experience

Experimental and clinical transplantation, 2017-06, Vol.15 (3), p.337-343

2017

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An association of hypochondroplasia and immune deficiency

Journal of Pediatric Endocrinology and Metabolism, 2014-07, Vol.27 (7-8), p.783

2014

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Train Support Vector Machine Using Fuzzy C-means Without a Prior Knowledge for Hyperspectral Image Content Classification

A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease

Perplexing Etiology of Hyperphenylalaninemia in an Infant Referred via Newborn Screening

Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis

A case of XLF deficiency presented with diffuse large B cell lymphoma in the brain

The Frequency of HLA-A, HLA-B, and HLA-DRB1 Alleles in Patients with Acute Lymphoblastic Leukemia in the Turkish Population: A Case-Control Study

THE INFLUENCE OF HLA-DQ2 HETERODIMERS ON THE CLINICAL FEATURES AND LABORATORY OF PATIENTS WITH CELIAC DISEASE

Silent brain infarcts in two patients with zeta chain-associated protein 70 kDa (ZAP70) deficiency

Clericuzio-type Poikiloderma with Neutropenia Syndrome in a Turkish Family: a Three Report of Siblings with Mutation in the C16orf57 gene

Atypical Severe Combined Immunodeficiency Caused by a Novel Homozygous Mutation In Rag1 Gene in a Girl who Presented with Pyoderma Gangrenosum: A Case Report and Literature Review

X-linked agammaglobulinemia in two siblings with a novel mutation in the BTK gene who presented with polyarticular juvenile idiopathic arthritis

Increased Postexercise Lipoxin A4 Levels in Exhaled Breath Condensate in Asthmatic Children With Exercise-Induced Bronchoconstriction

Relationships of Human Leukocyte Antigen-A, -B, -DRB1 Alleles, and Haplotypes in 129 Ethnic Turkish Patients With Acute Myeloblastic Leukemia

Exhaled breath condensate annexin A5 levels in exercise-induced bronchoconstriction in asthma: A preliminary study

Prurigo simplex subacuta or prurigo simplex acuta?

Silent brain infarcts in two patients with zeta chain-associated protein 70kDa (ZAP70) deficiency

Determination of the Cricothyroid Membrane Height by Age and Sex and Optimal Tracheal Tube Size

The association of forced expiratory volume in one second and forced expiratory flow at 50% of the vital capacity, peak expiratory flow parameters, and blood eosinophil counts in exercise-induced bronchospasm in children with mild asthma

Combined immunodeficiencies: twenty years experience from a single center in Turkey

Hair dyes and temporary tattoos are a real hazard for adolescents?

AMINO ACID LEVELS IN CHILDREN WITH CELIAC DISEASE

A selective IgA deficiency in a boy who presented recurrent parotitis

Grass pollen triggered anaphylaxis in an adolescent boy

Hematopoietic Stem Cell Transplant for Primary Immunodeficiency Diseases: A Single-Center Experience

An association of hypochondroplasia and immune deficiency

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