DOI: 10.1055/s-00046370

Global Medical Genetics

Issue 03 · Volume 10 · September 2023 DOI: 10.1055/s-013-57850

Review Article

133
Zhang, Yue; Dong, Xifeng; Wang, Huaquan: VEXAS Syndrome—Review
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
229
Xu, Yanmei; Chen, Yunfei; Zhang, Lei: Review: Advances in the Pathogenesis and Treatment of Immune Thrombocytopenia Associated with Viral Hepatitis

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
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
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
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
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
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
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

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
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

Letter to the Editor

188
Finsterer, Josef: Strokelike Episodes in PMM-2 Carriers Differ from Those in Mitochondrial Disorders

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
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
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