Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Dorina STOICANESCU"'
Autor:
Cristina Gug, Dorina Stoicanescu, Ioana Mozos, Laura Nussbaum, Mariana Cevei, Danae Stambouli, Anca Gabriela Pavel, Gabriela Doros
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Duplications of chromosome 8p lead to rare genetic conditions characterized by variable phenotypes. 8p21 and 8p23 duplications were associated with mental retardation but only 8p23 duplication was associated with heart defects. 8p22→ p21.3 duplicat
Externí odkaz:
https://doaj.org/article/dc958de5cc2547c0b0fb672431fd82bf
Autor:
Cristina Gug, Ioana Mozos, Adrian Ratiu, Anca Tudor, Eusebiu Vlad Gorduza, Lavinia Caba, Miruna Gug, Catalina Cojocariu, Cristian Furau, Gheorghe Furau, Monica Adriana Vaida, Dorina Stoicanescu
Publikováno v:
Medicina, Vol 58, Iss 1, p 79 (2022)
Background and Objectives: Non-invasive prenatal testing (NIPT) has been confirmed as the most accurate screening test for trisomies 21, 18, 13, sex chromosomes aneuploidies and several microdeletions. This study aimed to assess the accuracy of cell
Externí odkaz:
https://doaj.org/article/b6aee0f6c64f42ee97a1786dafe3a028
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 19; Issue 22; Pages: 15350
The musculoskeletal system is affected in over 40% of patients with Coronavirus disease 2019 (COVID-19). There is an increased need for post-acute rehabilitation after COVID-19, especially in elderly people with underlying health problems. The aim of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78af60935adbeabf06fdcff472adf662
Autor:
Eusebiu Vlad Gorduza, Dorina Stoicanescu, Monica Adriana Vaida, Cristina Gug, Florin Bîrsăşteanu, Adrian Lacatusu, Maria Puiu
Publikováno v:
Experimental and Therapeutic Medicine
CHARGE syndrome is an autosomal dominant condition caused by mutations in the chromodomain helicase DNA binding protein 7 (CHD7) gene. The present study reported on the case of a 16-month-old female with plurimalformative syndrome, whose etiology was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33bd15701b5f34480dc63525bd48fa8d
http://europepmc.org/articles/PMC7271729
http://europepmc.org/articles/PMC7271729
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 2
Journal of Clinical Medicine, Vol 9, Iss 2, p 441 (2020)
Volume 9
Issue 2
Journal of Clinical Medicine, Vol 9, Iss 2, p 441 (2020)
(1) Background: both sarcopenia and osteoporosis are major health problems in postmenopausal women. The aim of the study was to evaluate the quality of life (QoL) and the associated factors for sarcopenia in osteoporotic postmenopausal women, diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51951c53980fb3b42dae8e1d0c320865
Autor:
Nicoleta ANDREESCU, Dorina STOICANESCU, Alina BELENGEANU, Simona FARCAS, Cristina POPA, Monica STOIAN, Valerica BELENGEANU
Publikováno v:
Analele Universitatii din Oradea: Fascicula Biologie, Vol TOM XVII, Iss 1, Pp 9-13 (2010)
Breast cancer is among the most common forms of cancer. The molecular mechanisms involved in hormone dependence of breast cancer have been largely investigated. The role of the estrogen and progesterone receptors has been documented, but the role of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::26235fbde288f8e6f603fa9e20692d5c
Autor:
Mariana CEVEI, Dorina STOICANESCU
Publikováno v:
Analele Universitatii din Oradea: Fascicula Biologie, Vol TOM XVI, Iss 2, Pp 49-52 (2009)
Neural tube defects are a group of developmental abnormalities that results from failure of fusion of the caudal neural tube, representing one of the most common group of malformations of human structure. The etiology is thought to be multifactorial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::6b1487eaa49efa79afd16c6701b24008
Publikováno v:
Analele Universitatii din Oradea: Fascicula Biologie, Vol TOM XVI, Iss 2, Pp 138-141 (2009)
Rare disorders are defined as diseases, including those of genetic origin, which are life-threatening or chronically debilitating, which are of such low prevalence that special combined efforts are needed to address them. We present a case with a rar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::810d3ebac7df3e29e04c594d8fe9b330
Publikováno v:
Analele Universitatii din Oradea: Fascicula Biologie, Vol TOM XVI, Iss 2, Pp 20-24 (2009)
Breast cancer is among the most common forms of cancer. The molecular mechanisms involved in hormone dependence of breast cancer have been largely investigated. The role of the estrogen and progesterone receptors has been documented, but the role of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::b65ee8f054012f3758a3de3b4c1d4048
Early rehabilitation in a case of plurimalformative syndrome with deletions of chromosomes 13 and 18
Publikováno v:
Analele Universitatii din Oradea: Fascicula Biologie, Vol TOM XVI, Iss 1, Pp 42-45 (2009)
Deletion of long arm of chromosome 13 is characterized by malformations of the craniofacial region, skeletal abnormalities, other physical abnormalities and intellectual disability. Deletion of the long arm of chromosome 18 is a rare chromosomal diso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::af4af0b09be2cf885b9237c1a033a457
http://www.bioresearch.ro/bioresearch/2009-1/042-45-CEVEI.M.-An.U.O.Bio.2009.1.pdf
http://www.bioresearch.ro/bioresearch/2009-1/042-45-CEVEI.M.-An.U.O.Bio.2009.1.pdf