Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alina BELENGEANU"'
Autor:
Meszaros, Noemi1, Alina, Belengeanu2, Elena, Lazar3, Marioara, Cornianu3, Dorina, Stoicanescu1, Nicoleta, Andreescu1, Simona, Farcas1, Monica, Stoian1, Cristina, Popa1
Publikováno v:
Acta Medica Marisiensis. Dec2010, Vol. 56 Issue 6, p546-549. 4p. 8 Color Photographs, 1 Chart.
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
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
Autor:
Valerica Belengeanu, Eirik Frengen, Nicoleta Andreescu, Alina Belengeanu, Thilini H. Gamage, Doriana Misceo, Simona Farcas, Monica Stoian
Publikováno v:
Gene. 539(1)
We report a 20-month-old girl ascertained at the age of 11 months for developmental delay. She presented with hypotonia and delayed motor development. The patient had severe language impairment and showed behaviour consistent with autism spectrum dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bdf0cb9281f9311273fd7ec53e180f7
https://pubmed.ncbi.nlm.nih.gov/24508274
https://pubmed.ncbi.nlm.nih.gov/24508274
Publikováno v:
Clinical Dysmorphology. 13:265-267
We report two siblings with congenital generalized hypertrichosis and distinctive facial appearance consistent with the dysmorphic facial features described in Ambras syndrome. The patients were born to non-consanguineous, phenotypically normal paren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50c991287a3064f0b8cda6951a8288a6
https://doi.org/10.1097/00019605-200410000-00014
https://doi.org/10.1097/00019605-200410000-00014
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 51(2)
The invasive mammary cancer is the most frequent malignant tumor of women. Different inherited or acquired molecular genetic alterations have been identified in human breast cancers. A fraction of these cancers, as part of their development, undergoe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc5e551e5830f37c3ac6bbedeba239dd
https://pubmed.ncbi.nlm.nih.gov/20495751
https://pubmed.ncbi.nlm.nih.gov/20495751
Autor:
Luminita Pilat, David Chirila, Calin Popa, Doriana Misceo, Valerica Belengeanu, Ilinca Frunza, Cristina Popescu, Monica Stoian, Viorica Leordean, Alina Belengeanu
Publikováno v:
Current Opinion in Biotechnology. 24:S97-S98
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f099dbcc1071f9a8f190895ce22b63d3
https://doi.org/10.1016/j.copbio.2013.05.293
https://doi.org/10.1016/j.copbio.2013.05.293
Autor:
Valerica, Belengeanu, Kinga, Rozsnyai, Cristina, Gug, Mariana, Bănăţeanu, Simona, Farcaş, Alina, Belengeanu
Publikováno v:
Clinical dysmorphology. 13(4)
We report two siblings with congenital generalized hypertrichosis and distinctive facial appearance consistent with the dysmorphic facial features described in Ambras syndrome. The patients were born to non-consanguineous, phenotypically normal paren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7eda881443faf86be90a69bc1b9417d1
https://pubmed.ncbi.nlm.nih.gov/15365467
https://pubmed.ncbi.nlm.nih.gov/15365467