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Subject: Clinical genetics
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Case Report
Triple synchronous malignancies of the stomach, bladder and thyroid in a previously treated prostate cancer patient: A Case Report
    Oliver Oey, Siaw Sze Tiong, Sze Ling Wong, Suresh Navadgi, Yasir Khan
10.3897/folmed.65.e96012
 31-08-2023
 Unique: 972 | Total: 1369  | Access Period:
 Reprint: € 5,00
 693-698
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Original Article
Analysis and evaluation of correlation between DNA polymorphism in the genes MTHFR, PAI-1 and serum creatinine, creatinine clearance and albumin/creatinine ratio in morning urine of patients with type 2 diabetes mellitus and diabetic nephropathy
Dimitar Nikolov, Vili K. Stoyanova, Ludmila Vladimirova-Kitova, Alexander Linev,     Georgi Nikolov, Spas Kitov
10.3897/folmed.64.e67912
 31-12-2022
 Unique: 1420 | Total: 2147  | Access Period:
 Reprint: € 6,00
 896-904
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Case Report
New deletion in LAMP2 causing familial Danon disease. Effect of the X-chromosome inactivation
    Larysa Sivitskaya,     Tatiyana Vaikhanskaya, Nina Danilenko, Aleh Liaudanski, Oleg Davydenko,     Nikolai Zhelev
10.3897/folmed.64.e66292
 31-10-2022
 Unique: 1289 | Total: 2095  | Access Period:
 Reprint: € 6,00
 853-862
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Original Article
Assessment of the methylene blue mediated photodynamic therapy on BCL2 and BAX genes expression at mRNA level and apoptosis of head and neck squamous cell carcinoma cell line
Shadi Kahalian,     Maryam Koopaie, Neda Hakimiha, Sajad Kolahdooz
10.3897/folmed.64.e60825
 30-04-2022
 Unique: 1401 | Total: 2400  | Access Period:
 Reprint: € 5,00
 221-228
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Original Article
Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour
    Milena Stoyanova, Mari Hachmeriyan,     Mariya Levkova, Stoyan Bichev, Miglena Georgieva, Vilhelm Mladenov, Lyudmila Angelova
10.3897/folmed.64.e60518
 28-02-2022
 Unique: 1443 | Total: 2582  | Access Period:
 27-32
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Original Article
Genetic heterogeneity of beta thalassemia mutations in Kahramanmaraş province in Southern Turkey: preliminary report
    Ergul Belge Kurutaş, Mehmet Emrah Aksan, Petek Curuk, Mehmet Akif Curuk
10.3897/folmed.63.e55627
 31-10-2021
 Unique: 1899 | Total: 3708  | Access Period:
 697-703
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Original Article
Exploring pharmacogenetic variation in a Bulgarian psychiatric cohort
    Hristo Y. Ivanov, Branimir Velinov, Gergana Kyosovksa, Denitsa Grigorova, Peter Shopov
10.3897/folmed.63.e61484
 30-06-2021
 Unique: 1666 | Total: 3069  | Access Period:
 365-371
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Case Report
16p11.2 Duplication Syndrome - a Case Report
    Mariya Levkova, Milena Stoyanova, Rada Staneva, Mari Hachmeriyan, Lyudmila Angelova
10.3897/folmed.63.e52763
 28-02-2021
 Unique: 2194 | Total: 4412  | Access Period:
 138-141
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Review
Vitamin D: a Review of its Effects on Epigenetics and Gene Regulation
Violeta Snegarova, Darina Naydenova
10.3897/folmed.62.e50204.
 31-12-2020
 Unique: 3619 | Total: 6807  | Access Period:
 662-667
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Review
Presence of IL-8 Gene Polymorphism and IL-8 Serum Levels in Patients with Chronic Periodontitis - Literature Review
Antoaneta Mlachkova, Christina Popova, Velichka Doseva
10.3897/folmed.62.e47722
 30-06-2020
 Unique: 2455 | Total: 5422  | Access Period:
 253-257
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Original Article
Evaluation of the Immune Response Against Helicobacter pylori in Infused BALB/c Mice by pcDNA3.1(+)-ureA 
Maryam Nasr-Esfahani, Abbas Doosti, Hossein Sazegar
10.3897/folmed.62.e47932
 31-03-2020
 Unique: 2303 | Total: 5557  | Access Period:
 37-45
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Review
Review of Potential Significance of Mutations of ADAMTS20, NF1 and PKHD1 Detected Using Next Generation Sequencing (NGS) in Dermal Fibrosarcoma Arising in Dermatofibrosarcoma Protuberans
Artur Kowalik, Andrzej Wincewicz, Sebastian Zięba, Janusz Kopczynski, Mariusz Koda, Stanisław Sulkowski, Luiza Kańczuga-Koda, Stanisław Góźdź
10.3897/folmed.62.e48003
 31-03-2020
 Unique: 2602 | Total: 5633  | Access Period:
 17-22
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