Global Medical Genetics

Issue 03 · September 2023

Review Article
133
Zhang, Yue; Dong, Xifeng; Wang, Huaquan:
VEXAS Syndrome—Review
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205
Qaed, Eskandar; Al-Hamyari, Bandar; Al-Maamari, Ahmed; Qaid, Abdullah; Alademy, Haneen; Almoiliqy, Marwan; Munyemana, Jean Claude; Al-Nusaif, Murad; Alafifi, Jameel; Alyafeai, Eman; Safi, Mohammed; Geng, Zhaohong; Tang, Zeyao; Ma, Xiaodong:
Fisetin's Promising Antitumor Effects: Uncovering Mechanisms and Targeting for Future Therapies
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229
Xu, Yanmei; Chen, Yunfei; Zhang, Lei:
Review: Advances in the Pathogenesis and Treatment of Immune Thrombocytopenia Associated with Viral Hepatitis
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Original Article
144
He, Juan; Zhang, Xin; Chen, Xi; Xu, Zongyao; Chen, Xiaoqi; Xu, Jiangyan:
Shared Genes and Molecular Mechanisms between Nonalcoholic Fatty Liver Disease and Hepatocellular Carcinoma Established by WGCNA Analysis
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164
Fakhr, Fatemeh; Shaygannejad, Vahid; Khorrami, Mehdi; Saberi, Leila; Mirmosayyeb, Omid; Sadeghi, Erfan; Kheirollahi, Majid:
ADAR Expression and Single Nucleotide Variants in Multiple Sclerosis Patients Affect the Response to Interferon Beta Therapy
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172
Pancrazzi, Alessandro; Bloise, Francesco; Moncada, Alice; Perticucci, Roberta; Vecchietti, Stefania; Pompili, Francesca; Ricciarini, Francesca; Lenzi, Silvia; Gatteschi, Cristina; Giusti, Sabrina; Rosito, Maria Pia; Del Buono, Sabrina; Belardi, Paola; Bruni, Alessandra; Borri, Filippo; Campione, Andrea; Laurini, Lorella; Occhini, Rossella; Presenti, Loretta; Viticchi, Viviana; Rossi, Maja; Bardi, Sara; D'Urso, Antonio; Dei, Simona; Venezia, Duccio; Scala, Raffaele; Bengala, Carmelo; Decarli, Nicola Libertà; Carnevali, Andrea; Milandri, Carlo; Ognibene, Agostino:
BL-MOL-AR Project, Preliminary Results about Liquid Biopsy: Molecular Approach Experience and Research Activity in Oncological Settings
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194
Zhang, Mengying; Zhang, Gaochao; Xu, Fangfang; Liu, Mengyuan; Dong, Xifeng; Qi, Weiwei; Wang, Huaquan:
Identification of Plasma Thrombopoietin Level and Its Significance in Patients with Aplastic Anemia and Myelodysplastic Syndrome
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199
Rahman, Md Arifur; Islam, Md Monirul; Ali, Md Eunus; Islam, Mohammad Ariful; Afroze, Farhana; Hossain, Mohammad Shamim; Rus'd, Ahmed Abu:
Molecular Epidemiology of HCV RNA Genotype-3 in Dhaka City, Bangladesh
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240
Tuncel, Gulten; Sanlıdag, Burcin; Dirik, Eray; Baris, Tugba; Ergoren, Mahmut Cerkez; Temel, Sehime Gulsun:
Lessons from Real Life Experience: Importance of In-House Sequencing and Smart Ratio-Based Real-Time PCR Outperform Multiplex Ligation-Dependent Probe Amplification in Prenatal Diagnosis for Spinal Muscular Atrophy: Bench to Bedside Diagnosis
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247
Zhang, Xialin; Chen, Kun; Bian, Sicheng; Wang, Gang; Qin, Xiuyu; Zhang, Ruijuan; Yang, Linhua:
Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China
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Original Research
159
Ahmadi, Saba; Surmava, Sandro; Kvaratskhelia, Eka; Abzianidze, Elene; Kankava, Ketevani:
IL-10 Polymorphism and Breast Cancer Risk in Georgian Women: A Case–Control Study
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221
Kavitha, Loganathan; Vijayashree Priyadharsini, Jayaseelan; Kattula, Deepthi; Rao, Umadevi Krishna Mohan; Balaji Srikanth, Rajabather; Kuzhalmozhi, Manogaran; Ranganathan, Kannan:
Expression of CD44 in Head and Neck Squamous Cell Carcinoma—An In-Silico Study
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Letter to the Editor
188
Finsterer, Josef:
Strokelike Episodes in PMM-2 Carriers Differ from Those in Mitochondrial Disorders
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Case Report
190
Sreedevi, N.; Swapna, N.; Maruthy, Santosh; Jayakumar, T.; Sylvester, Charles:
Molecular Evaluation of Joubert Syndrome and Hearing Impairment in a Patient with Ataxic Cerebral Palsy
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234
Pavone, Piero; Falsaperla, Raffaele; Ruggieri, Martino; Marino, Simona Domenica; Parano, Enrico; Pappalardo, Xena Giada:
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report
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263
Wang, Sumei; Liang, Minglu; Ma, Jiehui; Huang, Sheng; Fan, Lili; Zhu, Feng; Sun, Dan:
Possible Role of Mitochondrial Transfer RNA Gene 5816 A > G Genetic Polymorphism (m.5816A > G) in a 3-Year-Old Child with Dystonia: Report of a Case
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Global Medical Genetics

VEXAS Syndrome—Review

Fisetin's Promising Antitumor Effects: Uncovering Mechanisms and Targeting for Future Therapies

Review: Advances in the Pathogenesis and Treatment of Immune Thrombocytopenia Associated with Viral Hepatitis

Shared Genes and Molecular Mechanisms between Nonalcoholic Fatty Liver Disease and Hepatocellular Carcinoma Established by WGCNA Analysis

ADAR Expression and Single Nucleotide Variants in Multiple Sclerosis Patients Affect the Response to Interferon Beta Therapy

BL-MOL-AR Project, Preliminary Results about Liquid Biopsy: Molecular Approach Experience and Research Activity in Oncological Settings

Identification of Plasma Thrombopoietin Level and Its Significance in Patients with Aplastic Anemia and Myelodysplastic Syndrome

Molecular Epidemiology of HCV RNA Genotype-3 in Dhaka City, Bangladesh

Lessons from Real Life Experience: Importance of In-House Sequencing and Smart Ratio-Based Real-Time PCR Outperform Multiplex Ligation-Dependent Probe Amplification in Prenatal Diagnosis for Spinal Muscular Atrophy: Bench to Bedside Diagnosis

Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China

IL-10 Polymorphism and Breast Cancer Risk in Georgian Women: A Case–Control Study

Expression of CD44 in Head and Neck Squamous Cell Carcinoma—An In-Silico Study

Strokelike Episodes in PMM-2 Carriers Differ from Those in Mitochondrial Disorders

Molecular Evaluation of Joubert Syndrome and Hearing Impairment in a Patient with Ataxic Cerebral Palsy

A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report

Possible Role of Mitochondrial Transfer RNA Gene 5816 A > G Genetic Polymorphism (m.5816A > G) in a 3-Year-Old Child with Dystonia: Report of a Case