Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Codruţa Diana Petcheşi"'
Autor:
Maria Claudia, Jurcă, Oana Alexandra, Iuhas, Maria, Puiu, Adela, Chiriţă-Emandi, Nicoleta Ioana, Andreescu, Codruţa Diana, Petcheşi, Alexandru Daniel, Jurcă, Ioan, Magyar, Sânziana Iulia, Jurcă, Kinga, Kozma, Emilia Maria, Severin, Marius, Bembea
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 62(2)
Cardiofaciocutaneous (CFC) syndrome [Online Mendelian Inheritance in Man (OMIM) #115150] is characterized by craniofacial dysmorphism, heart malformation, ectodermal abnormalities, neuromotor delay and intellectual disability. It is not a frequent di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77c8346cb2b152c0ead80cb2cc7bb0a
https://pubmed.ncbi.nlm.nih.gov/35024745
https://pubmed.ncbi.nlm.nih.gov/35024745
Autor:
Aurora Alexandra Jurcă, Marius Evelin Ivaşcu, Cristina Crenguţa Albu, Alexandru Daniel Jurcă, Ioan Magyar, Codruţa Diana Petcheşi, Marius Bembea, Maria Claudia Jurcă, Kinga Kozma, Mircea Sandor, Carmen Pantis, Dana Carmen Zaha
Publikováno v:
Romanian Journal of Morphology and Embryology
When we discuss the genetics of tumors, we cannot fail to remember that in the second decade of the twentieth century, more precisely in 1914, Theodore Boveri defined for the first time the chromosomal bases of cancer. In the last 30 years, progresse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5d16e75a9ed21998239f33e9d6d83f8
https://pubmed.ncbi.nlm.nih.gov/34171053
https://pubmed.ncbi.nlm.nih.gov/34171053
Autor:
Maria Claudia, Jurcă, Marius, Bembea, Oana Alexandra, Iuhas, Kinga, Kozma, Codruţa Diana, Petcheşi, Alexandru Daniel, Jurcă, Ariana, Szilágyi, Diana Luminiţa, Dubău, Cristian Nicolae, Sava, Dana Carmen, Zaha, Emilia Albiniţa, Cuc
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 59(3)
The co-occurrence in the same individual of two numerical chromosomal abnormalities (double aneuploidy) is a very rare condition, especially for autosomes. Clinical presentations are variable depending on the predominating aneuploidy. The authors pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f8667758be85e787d2b2043e0eba57e2
https://pubmed.ncbi.nlm.nih.gov/30534844
https://pubmed.ncbi.nlm.nih.gov/30534844
Autor:
Maria Claudia, Jurcă, Marius, Bembea, Kinga, Kozma, Mircea Ioan, Şandor, Rodica Anamaria, Negrean, Luciana, Dobjanschi, Emilia Albiniţa, Cuc, Codruţa Diana, Petcheşi, Alexandru Daniel, Jurcă
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 59(1)
Empty sella means the absence of the pituitary gland on cranial computed tomography or magnetic resonance imaging. Empty sella syndrome is the pathological variant of the imaging-described empty sella. We present the case of a male Caucasian child, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ad3a378a062a1e1904b232a287ff686
https://pubmed.ncbi.nlm.nih.gov/29940653
https://pubmed.ncbi.nlm.nih.gov/29940653
Autor:
Alexandru Daniel, Jurcă, Kinga, Kozma, Mihai, Ioana, Ioana, Streaţă, Codruţa Diana, Petcheşi, Marius, Bembea, Maria Claudia, Jurcă, Emilia Albiniţa, Cuc, Cosmin Mihai, Vesa, Camelia Liana, Buhaş
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 58(4)
Jacobsen syndrome (JS) is a contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11. The syndrome is rare and there are very few observations regarding the pubertal period of the affected individuals. We report the case o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c2b926fa07a12d91cd195a19fb83197
https://pubmed.ncbi.nlm.nih.gov/29556653
https://pubmed.ncbi.nlm.nih.gov/29556653
Autor:
Maria Claudia, Jurcă, Kinga, Kozma, CodruŢa Diana, Petcheşi, Marius, Bembea, Ovidiu Laurean, Pop, Gabriela, MuŢiu, Mihaela Cristiana, Coroi, Alexandru Daniel, Jurcă, Luciana, Dobjanschi
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 58(3)
Dandy-Walker complex (DWC) is a malformative association of the central nervous system. DWC includes four different types: Dandy-Walker malformation (vermis agenesis or hypoplasia, cystic dilatation of the fourth ventricle and a large posterior fossa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad8a90d623281972c7e9ff4311a6f5a4
https://pubmed.ncbi.nlm.nih.gov/29250689
https://pubmed.ncbi.nlm.nih.gov/29250689