Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Monica-Cristina Panzaru"'
Autor:
Monica-Cristina Pânzaru, Setalia Popa, Ancuta Lupu, Cristina Gavrilovici, Vasile Valeriu Lupu, Eusebiu Vlad Gorduza
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
The corpus callosum is the largest white matter structure connecting the two cerebral hemispheres. Agenesis of the corpus callosum (ACC), complete or partial, is one of the most common cerebral malformations in humans with a reported incidence rangin
Externí odkaz:
https://doaj.org/article/2ce992ed2f1f432fb10d12e6be44bfbe
Autor:
Monica-Cristina Pânzaru, Lavinia Caba, Laura Florea, Elena Emanuela Braha, Eusebiu Vlad Gorduza
Publikováno v:
Diagnostics, Vol 12, Iss 6, p 1325 (2022)
Epidermolysis bullosa is a heterogeneous group of rare genetic disorders characterized by mucocutaneous fragility and blister formation after minor friction or trauma. There are four major epidermolysis bullosa types based on the ultrastructural leve
Externí odkaz:
https://doaj.org/article/beb061c65c124e748f5186162d2f56fe
Autor:
Cristina Antohi, Danisia Haba, Lavinia Caba, Mihai Liviu Ciofu, Vasile-Liviu Drug, Oana-Bogdana Bărboi, Bogdan Ionuț Dobrovăț, Monica-Cristina Pânzaru, Nicoleta Carmen Gorduza, Vasile Valeriu Lupu, Doina Dimofte, Cristina Gug, Eusebiu Vlad Gorduza
Publikováno v:
Diagnostics, Vol 11, Iss 9, p 1560 (2021)
Gardner syndrome is a neoplasic disease that associates intestinal polyposis and colorectal adenocarcinoma with osteomas and soft tissue tumors determined by germline mutations in the APC gene. The early diagnosis and identification of high-risk indi
Externí odkaz:
https://doaj.org/article/8057221fe1d14810b7908c03ec1c3483
Autor:
Ioana Balinisteanu, Monica-Cristina Panzaru, Lavinia Caba, Maria-Christina Ungureanu, Andreea Florea, Ana Maria Grigore, Eusebiu Vlad Gorduza
Publikováno v:
Biomedicines, Vol 11, Iss 8, p 2143 (2023)
Cancer predisposition syndromes are entities determined especially by germinal pathogenic variants, with most of them autosomal dominantly inherited. The risk of a form of cancer is variable throughout life and affects various organs, including the t
Externí odkaz:
https://doaj.org/article/e51aa494f3ff4db68dabbebdc9aa386a
Autor:
Daniela Luminita Zob, Iolanda Augustin, Lavinia Caba, Monica-Cristina Panzaru, Setalia Popa, Alina Delia Popa, Laura Florea, Eusebiu Vlad Gorduza
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 1, p 716 (2022)
Melanoma is a common and aggressive tumor originating from melanocytes. The increasing incidence of cutaneous melanoma in recent last decades highlights the need for predictive biomarkers studies. Melanoma development is a complex process, involving
Externí odkaz:
https://doaj.org/article/a639d78e1eca4699b9f93dee269f0a45
Publikováno v:
World Journal of Clinical Cases. 11:2604-2620
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77b3aba7b686206ebbcf7e6f0bd4b130
https://doi.org/10.12998/wjcc.v11.i12.2604
https://doi.org/10.12998/wjcc.v11.i12.2604
Autor:
Lăcramioara Ionela Butnariu, Eusebiu Vlad Gorduza, Elena Țarcă, Monica-Cristina Pânzaru, Setalia Popa, Simona Stoleriu, Vasile Valeriu Lupu, Ancuta Lupu, Elena Cojocaru, Laura Mihaela Trandafir, Ștefana Maria Moisă, Andreea Florea, Laura Stătescu, Minerva Codruța Bădescu
Publikováno v:
Diagnostics, Vol 13, Iss 14, p 2348 (2023)
Atherogenic dyslipidemia plays a critical role in the development of metabolic syndrome (MetS), being one of its major components, along with central obesity, insulin resistance, and hypertension. In recent years, the development of molecular genetic
Externí odkaz:
https://doaj.org/article/ad39512519eb42e49cb6ba48b811cb05
Autor:
Cristian-Gabriel Ciobanu, Irina Nucă, Roxana Popescu, Lucian-Mihai Antoci, Lavinia Caba, Anca Viorica Ivanov, Karina-Alexandra Cojocaru, Cristina Rusu, Cosmin-Teodor Mihai, Monica-Cristina Pânzaru
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 11, p 9206 (2023)
The diagnosis and management of fragile X syndrome (FXS) have significantly improved in the last three decades, although the current diagnostic techniques are not yet able to precisely identify the number of repeats, methylation status, level of mosa
Externí odkaz:
https://doaj.org/article/7fc0b93f179e4e00ba775bf445ad2975
Autor:
Eva-Cristiana Gavril, Alina Costina Luca, Alexandrina-Stefania Curpan, Roxana Popescu, Irina Resmerita, Monica Cristina Panzaru, Lacramioara Ionela Butnariu, Eusebiu Vlad Gorduza, Mihaela Gramescu, Cristina Rusu
Publikováno v:
Children, Vol 8, Iss 9, p 751 (2021)
Wolf–Hirschhorn syndrome (WHS), a rare disorder determined by distal 4p deletion, is characterized by a pre and postnatal growth retardation, hypotonia, intellectual disability, epilepsy, craniofacial dysmorphism, and congenital fusion anomalies. T
Externí odkaz:
https://doaj.org/article/0ba04f2e8a2647d3b76fd9a44eb131ec