Belgin Kesim
A5016711637- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Pharmacogenetics and Drug Metabolism
- Blood Coagulation and Thrombosis Mechanisms
- Urticaria and Related Conditions
- Dermatological and Skeletal Disorders
- Ottoman and Turkish Studies
- Ubiquitin and proteasome pathways
- interferon and immune responses
- Glycosylation and Glycoproteins Research
- SARS-CoV-2 and COVID-19 Research
- Tryptophan and brain disorders
- Autoimmune Bullous Skin Diseases
- BRCA gene mutations in cancer
- Vitamin K Research Studies
- COVID-19 Clinical Research Studies
- COVID-19 diagnosis using AI
Şişli Etfal Eğitim ve Araştırma Hastanesi
2014-2020
<i>Background:</i> No published data presently exist concerning hereditary angioedema (HAE) in Turkey. The aim of the study was to initiate a preliminary multicentric evaluation about HAE and determine genetic properties Turkish patients. <i>Methods:</i> Based on records drawn from four medical centers we identified total 70 subjects, belonging 60 unrelated families, fulfilling clinical laboratory criteria for diagnosis with C1 inhibitor deficiency. Ten type I...
This article announces the recipient of 2014 inaugural Werner Kalow Responsible Innovation Prize in Global Omics and Personalized Medicine by Pacific Rim Association for Clinical Pharmacogenetics (PRACP): Bernard Lerer, professor psychiatry director Biological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. The is given to an exceptional interdisciplinary scholar who has made highly innovative enduring contributions global omics science personalized...
World Health Organization, named the disease caused by Severe Acute Respiratory syndrome-coronavirus-2 coronavirus on 11 February 2020 as Coronavirus Disease-2019 (COVID-19).A person who has clinical symptom and a history of contact with patient confirmed COVID-19 is identified ''possible case'' expected to be laboratory test.A case asymptomatic/symptomatic suspected individual positive molecular test.Specific diagnosis made specific tests respiratory samples (orafarengeal/ nasopharyngeal...
Hereditary angioedema is a rare autosomal dominantly inherited immunodeficiency disorder characterized by potentially life-threatening attacks.We aimed to investigate the clinical and genetic features of family with attacks.The medical history, C1-INH gene mutation Turkish were investigated outcomes long-term treatments described.Five members had experienced recurrent swellings on face extremities triggered trauma. They all misdiagnosed as familial Mediterranean fever (FMF) depending...
Johanson–Blizzard syndrome (JBS) is a rare autosomal recessive disorder, characterized by exocrine pancreatic deficiency and wide range of other abnormalities. Here, we present an infant with failure to thrive, deficiency, developmental delay, cutis aplasia on the scalp, alae nasi, hypospadias, hypothyroidism. Molecular studies revealed novel homozygous nonsense mutation in exon 22 ubiquitin protein ligase E3 component N-recognin 1 gene, which confirmed diagnosis JBS. In conclusion, it was...
OMICS: A Journal of Integrative BiologyVol. 24, No. 8 InterviewFree AccessCOVID-19 Interview: Dr. Belgin Eroğlu Kesim on Women in Science Advancing SARS-CoV-2 Tests—“One Health” and Changing the World for BetterBelgin Vural ÖzdemirBelgin KesimAddress correspondence to: Kesim, MD, Physician Medical Geneticist, İstanbul, Turkey E-mail Address: [email protected]Physician Turkey.Search more papers by this author ÖzdemirOMICS: Biology, New Rochelle, York.Search authorPublished Online:3 Aug...