O'Donnel‑Luria‑Rodan Syndrome: New gene variant identified in Romania (A case report) von Catana, Andreea, Kutasi, Eniko, Cuzmici-Barabas, Zina, Militaru, Diana, Iordanescu, Irina, Militaru, Mariela Sanda

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First documented case of Myhre syndrome in Romania: A case report von Catana, Andreea, Simonescu-Colan, Ruxandra, Cuzmici-Barabas, Zina, Militaru, Diana, Iordanescu, Irina, Militaru, Mariela Sanda

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Hereditary Breast Cancer in Romania-Molecular Particularities and Genetic Counseling Challenges in an Eastern European Country von Cătană, Andreea, Trifa, Adrian P, Achimas-Cadariu, Patriciu A, Bolba-Morar, Gabriela, Lisencu, Carmen, Kutasi, Eniko, Chelaru, Vlad F, Muntean, Maximilian, Martin, Daniela L, Antone, Nicoleta Z, Fetica, Bogdan, Pop, Florina, Militaru, Mariela S

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Lateral sinus thrombosis in a young patient with sudden neurosensorial hearing loss and genetic thrombophilia: A case report von Cuzmici-Barabas, Zina, Catana, Andreea, Militaru, Mariela Sanda, Garbea, Oana, Catana, Iuliu Vlad, Pop, Ioan Victor

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Antibiotic Resistance in Helicobacter pylori Isolates from Northwestern and Central Romania Detected by Culture-Based and PCR-Based Methods von Costache, Carmen, Colosi, Horațiu Alexandru, Grad, Simona, Paștiu, Anamaria Ioana, Militaru, Mariela, Hădărean, Anca Paula, Țoc, Dan Alexandru, Neculicioiu, Vlad Sever, Baciu, Alina Mihaela, Opris, Razvan Vlad, Dumitrașcu, Dan Lucian, Colosi, Ioana Alina

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Molecular basis and therapeutic targets in prostate cancer: A comprehensive review von Militaru, Florentina Claudia, Militaru, Valentin, Crisan, Nicolae, Bocsan, Ioana Corina, Udrea, Anghel Adrian, Catana, Andreea, Kutasi, Eniko, Militaru, Mariela Sanda

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Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array von Iordănescu, Irina Ioana, Catana, Andreea, Cuzmici, Zina Barabas, Chelu, Iuliana, Dragomir, Cristina, Militaru, Maria, Severin, Emilia, Militaru, Mariela Sanda

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Insights into Clinical Disorders in Cowden Syndrome: A Comprehensive Review von Pîrlog, Lorin-Manuel, Pătrășcanu, Andrada-Adelaida, Militaru, Mariela Sanda, Cătană, Andreea

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Challenging diagnoses of tetraploidy/diploidy and trisomy 12: utility of first-tier prenatal testing methods von Iordanescu, Irina Ioana, Neacsu, Anca Teodora, Catana, Andreea, Barabas-CuzmicI, Zina, Suciu, Viorel, Dragomir, Cristina, Voicu, Diana Elena, Severin, Emilia, Militaru, Mariela Sanda

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Breast Cancer Screening and Prophylactic Mastectomy for High-Risk Women in Romania von Filip, Claudiu Ioan, Cătană, Andreea, Kutasi, Eniko, Roman, Sara Alexia, Militaru, Mariela Sanda, Risteiu, Giulia Andreea, Dindelengan, George Călin

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The Impact of Chromosomal Mosaicisms on Prenatal Diagnosis and Genetic Counseling-A Narrative Review von Militaru, Mariela Sanda, Babliuc, Ioana-Mădălina, Bloaje-Florică, Vanesa-Larisa, Danci, Valentin-Adrian, Filip-Deac, Iulia, Kutasi, Enikő, Simon, Vasile, Militaru, Mihai, Cătană, Andreea

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Novel Mutation in GALT Gene in Galactosemia Patient with Group B Streptococcus Meningitis and Acute Liver Failure von Grama, Alina, Blaga, Ligia, Nicolescu, Alina, Deleanu, Călin, Militaru, Mariela, Căinap, Simona Sorana, Pop, Irina, Tita, Georgia, Sîrbe, Claudia, Fufezan, Otilia, Vințan, Mihaela Adela, Vulturar, Romana, Pop, Tudor Lucian

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The relationship between factor V Leiden, prothrombin G20210A, and MTHFR mutations and the first major thrombotic episode in polycythemia vera and essential thrombocythemia von Trifa, Adrian P., Cucuianu, Andrei, Popp, Radu A., Coadă, Camelia A., Costache, Roxana M., Militaru, Mariela S., Vesa, Ştefan C., Pop, Ioan V.

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Cytogenetic and fragile X testing in a group of Romanian autistic children von Dronca, Eleonora, Militaru, Mariela S, Ciumărnean, Lorena, Pop, Ioan V

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G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms von Trifa, Adrian P, Cucuianu, Andrei, Petrov, Ljubomir, Urian, Laura, Militaru, Mariela S, Dima, Delia, Pop, Ioan V, Popp, Radu A

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CALR versus JAK2 mutated essential thrombocythaemia - a report on 141 patients von Trifa, Adrian P, Popp, Radu A, Cucuianu, Andrei, Bănescu, Claudia, Tevet, Mihaela, Martin, Bianca, Murat, Meilin, Vesa, Stefan C, Dima, Delia, Cândea, Marcela, Militaru, Mariela S, Pop, Ioan V

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TLR1 polymorphisms in Europeans and spontaneous pregnancy loss von Crişan, Tania O., Farcaş, Marius F., Trifa, Adrian P., Plantinga, Theo S., Militaru, Mariela S., Pop, Ioan V., Netea, Mihai G., Popp, Radu A.

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No association between the STAT5b rs6503691 (C>T) SNP and myeloproliferative neoplasms von Trifa, Adrian P., Cucuianu, Andrei, Popp, Radu A., Coadă, Camelia A., Costache, Roxana M., Sarca, Anamaria D., Farcaş, Marius F., Militaru, Mariela S., Pop, Ioan V.

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Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report von Militaru, Mariela S, Popp, Radu A, Trifa, Adrian P

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Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review von Trifa, Adrian P., Cucuianu, Andrei, Popp, Radu A., Paţiu, Mariana, Selicean, Cristina, Militaru, Mariela S., Pop, Ioan V.

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