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COVID-19 Interview: Dr. Belgin Eroğlu Kesim on Women in Science Advancing SARS-CoV-2 Tests—“One Health” and Changing the World for the Better

Omics (Larchmont, N.Y.), 2020-08, Vol.24 (8), p.454-456

2020

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Bernard Lerer: recipient of the 2014 inaugural Werner Kalow Responsible Innovation Prize in Global Omics and Personalized Medicine (Pacific Rim Association for Clinical Pharmacogenetics)

Omics (Larchmont, N.Y.), 2014-04, Vol.18 (4), p.211-221

2014

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A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene

Journal of allergy and clinical immunology, 2009-04, Vol.123 (4), p.962-964

2009

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The Characteristics of SARS-CoV-2 Virus and Microbiological Diagnosis

European Archives of Medical Research, 2020-09, Vol.36 (1), p.10-20

2020

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Gene symbol: SERPING1. Disease: Angioneurotic oedema

Human genetics, 2008-10, Vol.124 (3), p.308-308

2008

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Gene symbol: SERPING1. Disease: Angioneurotic oedema

Human genetics, 2008-10, Vol.124 (3), p.309-309

2008

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Gene symbol: SERPING1. Disease: Angioneurotic oedema

Human genetics, 2008-10, Vol.124 (3), p.310-310

2008

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Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (1), p.1

2017

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Molecular Analysis of Factor V Leiden, Factor V Hong Kong, Factor II G20210A, Methylenetetrahydrofolate Reductase C677T, and A1298C Mutations Related to Turkish Thrombosis Patients

Clinical and applied thrombosis/hemostasis, 2007-10, Vol.13 (4), p.435-438

2007

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An Appeal to the Global Health Community for a Tripartite Innovation: An “Essential Diagnostics List,” “Health in All Policies,” and “See-Through 21 st Century Science and Ethics”

Omics (Larchmont, N.Y.), 2015-08, Vol.19 (8), p.435-442

2015

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Gene symbol: SERPING1. Disease: Angioneurotic oedema

Human genetics, 2008-10, Vol.124 (3), p.309

2008

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Gene symbol: SERPING1. Disease: Angioneurotic oedema

Human genetics, 2008-10, Vol.124 (3), p.309

2008

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Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.1

2017

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Letter to the editor: A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene

Journal of allergy and clinical immunology, 2009-04, Vol.123 (4), p.962-964

2009

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A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene

The Journal of allergy and clinical immunology, 2009, Vol.123 (4), p.962-964

2009

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An Appeal to the Global Health Community for a Tripartite Innovation: An "Essential Diagnostics List," "Health in All Policies," and "See-Through 21(st) Century Science and Ethics"

Omics (Larchmont, N.Y.), 2015-08, Vol.19 (8), p.435

2015

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COVID-19 Interview: Dr. Belgin Eroğlu Kesim on Women in Science Advancing SARS-CoV-2 Tests—“One Health” and Changing the World for the Better

Bernard Lerer: recipient of the 2014 inaugural Werner Kalow Responsible Innovation Prize in Global Omics and Personalized Medicine (Pacific Rim Association for Clinical Pharmacogenetics)

A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene

The Characteristics of SARS-CoV-2 Virus and Microbiological Diagnosis

Gene symbol: SERPING1. Disease: Angioneurotic oedema

Gene symbol: SERPING1. Disease: Angioneurotic oedema

Gene symbol: SERPING1. Disease: Angioneurotic oedema

Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age

Molecular Analysis of Factor V Leiden, Factor V Hong Kong, Factor II G20210A, Methylenetetrahydrofolate Reductase C677T, and A1298C Mutations Related to Turkish Thrombosis Patients

An Appeal to the Global Health Community for a Tripartite Innovation: An “Essential Diagnostics List,” “Health in All Policies,” and “See-Through 21 st Century Science and Ethics”

Gene symbol: SERPING1. Disease: Angioneurotic oedema

Gene symbol: SERPING1. Disease: Angioneurotic oedema

Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age

Letter to the editor: A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene

A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene

An Appeal to the Global Health Community for a Tripartite Innovation: An "Essential Diagnostics List," "Health in All Policies," and "See-Through 21(st) Century Science and Ethics"

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