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Original Article
Investigation of APC, MLH1 and MSH2 Mutations in Patients with Hereditary Colorectal Carcinoma: A Single Center Experience
Mehmet Buğrahan Düz
Med Bull Haseki 2021; 59: 17-24
DOI: 10.4274/haseki.galenos.2020.6258
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Evaluation of the Relationship between Janus Kinase 2 Mutational Burden and Clinical Findings in Adult Myeloproliferative Neoplasm Patients
Cigdem Yuce Kahraman
Gulden Sincan
Abdulgani Tatar
Med Bull Haseki 2022; 60: 26-32
DOI: 10.4274/haseki.galenos.2021.7530
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Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene
Ender Coşkunpınar
Ayla Özvarnalı
Kıvanç Çefle
Ayşe Palanduz
Ahmet Gül
Derya Öztürk
Şükrü Öztürk
Şükrü Palanduz
Med Bull Haseki 2018; 56: 42-49
DOI: 10.4274/haseki.42714
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Relationship Among Clinical, Laboratory Findings, Disease Severity Scores and Genetic Mutations in Patient with Familial Mediterranean Fever
Selda Yavuz
Nilgün Selçuk Duru
Murat Elevli
Med Bull Haseki 2018; 56: 58-64
DOI: 10.4274/haseki.68077
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MEFV
Gene Mutation Analysis in Children with Immunoglobulin A Vasculitis and Its Effects on Clinical Manifestations: A Big Series from a Tertiary Center
Sema Yildirim
Zeynep Karakaya
Ozlem Ozcay
Muferet Erguven
Med Bull Haseki 2024; 62: 82-91
DOI: 10.4274/haseki.galenos.2024.9578
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Aberrant Activation-Induced Cytidine Deaminase Gene Expression Links BCR/ABL1-Negative Classical Myeloproliferative Neoplasms
Hasan Dermenci
Aynur Daglar Aday
Aysegul Basak Akadam Teker
Veysel Sabri Hancer
Metin Yusuf Gelmez
Meliha Nalcaci
Akif Selim Yavuz
Med Bull Haseki 2022; 60: 228-233
DOI: 10.4274/haseki.galenos.2022.8133
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Case Report
Portal Vein Thrombosis Related to Factor V Leiden Mutation
Kerim Çayır
Kenan Çadırcı
Mehmet Bilici
Salim Başol Tekin
Mustafa Keleş
Habip Emre
Med Bull Haseki 2009; 47: 181-182
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Case Report
A Novel Frameshift Mutation in Two Siblings with Merosin-deficient Congenital Muscular Dystrophy
Senem Ayça
Hamide Betül Gerik Çelebi
Sırrı Çam
Muzaffer Polat
Med Bull Haseki 2020; 58: 208-210
DOI: 10.4274/haseki.galenos.2019.5177
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Early Diagnosis of Fanconi-Bickel Syndrome and a Novel Mutation in
SLC2A2
Gene
Ezgi Çelikboya
Mehmet Şerif Cansever
Tanyel Zübarioğlu
Gözde Yeşil
Nurver Akıncı
Med Bull Haseki 2019; 57: 328-331
DOI: 10.4274/haseki.galenos.2018.4504
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