Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Viorica Radoi"'
Autor:
Sebastian Militaru, Robert Adam, Lucian Dorobantu, Paolo Ferrazzi, Maria Iascone, Viorica Radoi, Gener Ismail, Bogdan A. Popescu, Ruxandra Jurcut
Publikováno v:
Anatolian Journal of Cardiology, Vol 22, Iss 3, Pp 154-158 (2019)
Externí odkaz:
https://doaj.org/article/0b783f89eb1043378399e2523e72ccc6
Autor:
Viorica Radoi, Andrei Kozma, Vasilica Toma, Horia Lăzărescu, Radu Ursu, Agnes Katherine Lackner, Laurențiu Camil Bohîlțea, Norina Forna
Publikováno v:
Romanian Journal of Oral Rehabilitation, Vol 11, Iss 2, Pp 90-95 (2019)
Progress in genetics and molecular biology has resulted in the emergence of new concepts to explain the etiology and pathogenesis of many human disease processes including oro-dental diseases. Recent advances in molecular aspects of odontogenesis ind
Externí odkaz:
https://doaj.org/article/a105987f9bd84a04a46f9d6944db98ec
Autor:
Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Radu Ursu, Agnes Katalin Lackner, Laurentiu Camil Bohiltea, Horia Lazarescu
Publikováno v:
Romanian Journal of Stomatology, Vol 65, Iss 2, Pp 97-100 (2019)
Defective enamel formation may result either from factors of environmental origin or from genetic abnormality. Such genetically determined enamel malformations have been described in patients with chromosomal anomalies and with inherited single gene
Externí odkaz:
https://doaj.org/article/27904ada8362456e92183ec672e5b106
Publikováno v:
Diagnostics, Vol 12, Iss 4, p 985 (2022)
Twin pregnancy contributes to perinatal mortality, particularly monochorionic diamniotic twin pregnancy. Placental abnormalities are much more common in twin pregnancies than in singletons. In MCDA pregnancy, vascular anastomoses are always present a
Externí odkaz:
https://doaj.org/article/2cf4117d4d604be3a71ebb6e9ae2d1b7
Autor:
Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Ana Maria Alexandra Stanescu, Radu Ursu, Laurentiu Camil Bohaltea
Publikováno v:
Romanian Medical Journal, Vol 65, Iss 4, Pp 258-260 (2018)
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic neural crest cells, continuing with their movement towards the first pharyngeal arch and leading to the development of many elements of the craniof
Externí odkaz:
https://doaj.org/article/fba0f8e2083f4878a2565c746d2abe48
Autor:
Tiberiu Georgescu, Viorica Radoi, Micaela Radulescu, Aurora Ilian, Oana Daniela Toader, Lucian G. Pop, Nicolae Bacalbasa
Publikováno v:
Medicina, Vol 57, Iss 11, p 1253 (2021)
Tracheal atresia is an extremely rare condition whereby a partial or total obstruction of the trachea is seen. It is almost always lethal, with just a handful of cases that ended with a good outcome. In this study we report on a 15-week male fetus, d
Externí odkaz:
https://doaj.org/article/633e9447a94c429ebb2a90c939095f82
Autor:
Viorica Radoi, Lucian Gheorghe Pop, Nicolae Bacalbasa, Anca Maria Panaitescu, Anca Marina Ciobanu, Dragos Cretoiu, Oana Daniela Toader
Publikováno v:
Medicina, Vol 57, Iss 10, p 1031 (2021)
Mirror syndrome (MS) or Ballantyne’s syndrome is a rare maternal condition that can be life-threatening for both mother and fetus. The condition is characterized by maternal signs and symptoms similar to those seen in preeclampsia in the setting of
Externí odkaz:
https://doaj.org/article/17adea478ac44f4e917b5540d56ed5b5
Autor:
Viorica Radoi, Nadejda Birladeanu
Publikováno v:
Romanian Journal of Cardiology. 31:831-835
The expanding appreciation of genetics by researchers, by clinicians and the general population goes hand in hand with the acknowledgement of its role in a multitude of diseases. However, each newly developed genetic test raises conflictual concerns
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acc4537041420c403b9376837d811a72
https://doi.org/10.47803/rjc.2020.31.4.831
https://doi.org/10.47803/rjc.2020.31.4.831
Autor:
Viorica Radoi, Florentina Gherghiceanu, Dragos Cretoiu, Irina Balescu, Radu Ursu, Nicolae Bacalbasa, Daniela Oana Toader, Florentina Furtunescu, Lucian Pop, Daniel Radavoi
Publikováno v:
Cancer Diagn Progn
Background/Aim: The aim of the study was to report the case of a 5-month-old boy with a complex prenatal and neonatal symptomatology diagnosed with a “de novo" pathogenic variant of PUF60 gene. Case Report: Our hospital, undertook the antenatal and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b06a886ac73c788ef93dcff77ded291
https://doi.org/10.21873/cdp.10029
https://doi.org/10.21873/cdp.10029
Autor:
Răzvan Capşa, Adriana Mursă, Alexandra Bastian, Viorica Radoi, Ruxandra Jurcuţ, Bogdan A. Popescu, Bogdan Ovidiu Popescu, Cristina Mitu, Adrian Giucă
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Hypertrophic cardiomyopathy (HCM) is a genetic disorder mostly caused by sarcomeric gene mutations, but almost 10% of cases are attributed to inherited metabolic and neuromuscular disorders. First described in 2008 in an American-Italian f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ca8812234dc0ffd1365ae4639456e0e
http://link.springer.com/article/10.1186/s12881-020-01131-w
http://link.springer.com/article/10.1186/s12881-020-01131-w