يعرض 1 - 10 نتائج من 68 نتيجة بحث عن '"CLINICAL FEATURE"', وقت الاستعلام: 1.31s تنقيح النتائج
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    المصدر: Annals of Saudi Medicine
    Annals of Saudi Medicine, Vol 41, Iss 6, Pp 318-326 (2021)

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    المساهمون: İstinye Üniversitesi, Hastane, Sirzai, Hulya, Taşkıran, Özden Özyemişçi (ORCID 0000-0002-2052-6072 & YÖK ID 133091), Külcü, D.G., Kuran, B., Karahan, A.Y., Özgirgin, N., Başaran, S., Yalıman, A., Savaş, S., Tıkız, C., Aktaş, İ., Bardak, A., Tuncer, T., Yılmaz, F., Erhan, B., Şirzai, H., Çelik, B., Durlanık, G., Doğu, B., Öncü, J., Hüner, B., Öztürk, G., Eskiyurt, N., Akpınar, F.M., Özkan, F.Ü., Paker, N., Buğdaycı, D.S., Gündüz, B., Şatır, Ö., Atalay, N.Ş., Yıldız, N., Altındağ, Ö., Demir, S.E., Kaya, E., Uçar, D., Sarı, A., Karataş, G.K, School of Medicine

    المصدر: Turkish Journal of Physical Medicine and Rehabilitation

    وصف الملف: application/pdf; pdf

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    المساهمون: DİZMAN, DİDEM

    المصدر: Australasian Journal of Dermatology. 62

    مصطلحات موضوعية: bullous pemphigoid, Male, demography, Pemphigoid, age distribution, Turkey, very elderly, preschool child, incidence study, Turkey (republic), cardiovascular disease, immune system diseases, middle aged, Pemphigoid, Bullous, Prospective Studies, Child, skin and connective tissue diseases, Aged, 80 and over, integumentary system, adult, Incidence, Incidence (epidemiology), benign mucous membrane pemphigoid, pemphigus, clinical trial, pemphigoid gestationis, neurologic disease, aged, female, Child, Preschool, histopathology, young adult, diagnostic procedure, tertiary care center, Bullous pemphigoid, acquired epidermolysis bullosa, prospective study, Epidermolysis bullosa acquisita, medicine.medical_specialty, pemphigoid, Adolescent, Dermatology, Article, turkey (bird), mucous membrane pemphigoid, Pemphigoid Gestationis, medicine, Humans, controlled study, epidermolysis bullosa, human, immunofluorescence, Sex Distribution, skin biopsy, Benign Mucous Membrane Pemphigoid, DURDU M., Bozca B. C. , ENLİ S., Yazici Ozgen Z., YAYLI S., AKTAN Ş., MUTLU D., ERTURAN İ., AYVAZ ÇELİK H. H. , MELİKOĞLU M., et al., -A multicentre prospective analysis of the incidence of pemphigoid diseases in Turkey-, AUSTRALASIAN JOURNAL OF DERMATOLOGY, 2021, business.industry, sex ratio, medicine.disease, major clinical study, human tissue, eye diseases, clinical feature, enzyme linked immunosorbent assay, Pemphigus, multicenter study, Etiology, dipeptidyl peptidase IV inhibitor, business

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    المساهمون: İstinye Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Özkaya, Ozan, Ozan Özkaya / DKK-1373-2022, Ozan Özkaya / 7003365098

    المصدر: Rheumatology International. 39:911-919

    مصطلحات موضوعية: Male, Genetic testing, genetic association, lpin2 protein, autoinflammatory disease, pyrin, molecular pathology, Agammaglobulinemia, middle aged, genetics, cytoskeleton protein, Child, next generation sequencing, adult, Sequence analysis, adenosine deaminase deficiency, High-Throughput Nucleotide Sequencing, clinical trial, cryopyrin, Phosphotransferases (Alcohol Group Acceptor), priority journal, SLC29A3 protein, human, Child, Preschool, Majeed syndrome, Intercellular Signaling Peptides and Proteins, Mefv Gene, card14 protein, heredity, Immunology, DNA sequence, signal transducing adaptor protein, interleukin 10 receptor alpha, tmem173 protein, Article, Rheumatology, cross-sectional study, inheritance, Humans, human, CINCA syndrome, Genetic Testing, infancy, congenital dyserythropoietic anemia, mevalonate kinase, Calcium-Binding Proteins, Hereditary Autoinflammatory Diseases, Immunologic Deficiency Syndromes, Pyrin, major clinical study, pstpip1 protein, adenosine deaminase, Cytoskeletal Proteins, multicenter study, Severe Combined Immunodeficiency, Mevalonate Kinase Deficiency, genomic DNA, Adenosine Deaminase, systemic disease, NLRC4 protein, human, preschool child, slc29a3 protein, familial Mediterranean fever, genetic variability, hereditary periodic fever, pathogenicity, Immunology and Allergy, PSTPIP1 protein, human, Anemia, Dyserythropoietic, Congenital, nucleoside transporter, ada2 protein, osteomyelitis, vascular disease, Osteomyelitis, genetic screening, Middle Aged, unclassified drug, Familial Mediterranean Fever, female, young adult, sting associated vasculopathy, Female, caspase recruitment domain signaling protein, diagnostic value, Sequence Analysis, onset age, Adult, nlrc4 protein, Adolescent, MEFV gene, Nucleoside Transport Proteins, high throughput sequencing, Young Adult, Muckle Wells syndrome, follow up, mvk protein, signal peptide, phosphotransferase, Adaptor Proteins, Signal Transducing, MEFV protein, human, caspase recruitment domain protein 15, immune-related gene, calcium binding protein, Sequence Analysis, DNA, immune deficiency, Cryopyrin-Associated Periodic Syndromes, clinical feature, CARD Signaling Adaptor Proteins, ADA2 protein, human, protein

    وصف الملف: application/pdf

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    المصدر: Genetics in Medicine. 18:1226-1234

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    المساهمون: Ege Üniversitesi, Bursa Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları., Çekiç, Şükrü, Karalı, Yasin, Aslan, Törehan, Sevinir, Betül, Kılıç, Sara Şebnem, FFS-1974-2022, AAH-1570-2021

    المصدر: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and ImmunologyREFERENCES. 31(5)

    مصطلحات موضوعية: Male, Secondary, Hematologic malignancy, Turkey, medicine.medical_treatment, Lymphadenopathy, Diseases, Real time polymerase chain reaction, Pediatrics, Gene, 0302 clinical medicine, Squamous cell carcinoma, Guanine Nucleotide Exchange Factors, Colon adenocarcinoma, Neurilemoma, Child, Nephroblastoma, Burkitt lymphoma, Rectum carcinoma, Prognosis, Multicenter study, Clinical trial, Antineoplastic agent, Child, Preschool, Cohort, Nonhodgkin lymphoma, Cancer chemotherapy, Cohort analysis, Human, medicine.medical_specialty, Remission, Immunology, Major clinical study, Article, 03 medical and health sciences, Age, Humoral immune deficiency, Humans, Acute myeloid leukemia, Immunologic Deficiency Syndromes, Infant, Sex difference, medicine.disease, Mortality rate, B cell lymphoma, Lymphoma, DOCK8 protein, Malignant neoplasm, 030228 respiratory system, DOCK8 Deficiency, Cancer incidence, Ataxia Telangiectasia, Mutation, ATM Protein, Guanine nucleotide exchange factor, Small cell sarcoma, Allergy, DOCK8 deficiency, Immune deficiency, Hematopoietic stem cell transplantation, Turkey (republic), ataxia-telangiectasia, T cell lymphoma, Turkey (bird), Neoplasms, Immunology and Allergy, 030212 general & internal medicine, Thyroid papillary carcinoma, Priority journal, non-Hodgkin lymphoma, Middle Aged, Consanguineous marriage, Cancer radiotherapy, Bloom syndrome, Female, Hemangiopericytoma, Adult, Hodgkin disease, Adolescent, Primary Immunodeficiency Diseases, Family history, Wiskott Aldrich syndrome, lymphoma, primary immunodeficiency, Malignancy, Pathophysiology, Common variable immunodeficiency, Young Adult, Internal medicine, medicine, cancer, Hepatosplenomegaly, Chemotherapy, business.industry, Cancer, Combined immunodeficiency, Solid malignant neoplasm, Clinical feature, Preschool child, Pediatrics, Perinatology and Child Health, Primary immunodeficiency, Neoplasm, business, malignancy