Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Alexandru Daniel, Jurcă"'
Autor:
Romania Pharmacy 'Carol Davila' Bucharest, Dorina Galusca, Dana Carmen Zaha, Codruța Diana Petchesi, Alina Sklerniacof, Amorin Remus Popa, Emilia Severin, Kinga Kozma, Sânziana Jurca, Cristian Daina, Marius Bembea, Claudia Jurca, Cosmin Mihai Vesa, Alexandru Daniel Jurcă
Publikováno v:
Romanian Biotechnological Letters. 26:2671-2678
Congenital diaphragmatic hernia is an abnormality of embryologic development characterized by the persistence of communication between the thoracic and abdominal cavities, followed by an extremely high death rate despite medical progress. In Bihor co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64bfd83bff77f43fb2ca50e12d041491
https://doi.org/10.25083/rbl/26.3/2671-2678
https://doi.org/10.25083/rbl/26.3/2671-2678
Autor:
Maria Claudia, Jurcă, Sânziana Iulia, Jurcă, Filip, Mirodot, Bogdan, Bercea, Emilia Maria, Severin, Marius, Bembea, Alexandru Daniel, Jurcă
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 62(3)
Skeletal dysplasia (SD), also called osteochondrodysplasia (OCD), is a large group of skeletal disorders (over 400 distinct entities) caused by abnormalities in bone development and growth. SDs varies according to different natural histories, prognos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422f30249afc825fd5d1a363c1dc54d7
https://pubmed.ncbi.nlm.nih.gov/35263396
https://pubmed.ncbi.nlm.nih.gov/35263396
Autor:
Aurora Arghir, Dan Riga, Magdalena Budisteanu, Alexandru Daniel Jurcă, Ina Ofelia Focsa, Sorina Mihaela Papuc, Sorin Riga, Claudia Jurca
Publikováno v:
Open Life Sciences
Open Life Sciences, Vol 15, Iss 1, Pp 21-29 (2020)
Open Life Sciences, Vol 15, Iss 1, Pp 21-29 (2020)
Chromosomal diseases are heterogeneous conditions with complex phenotypes, which include also epileptic seizures. Each chromosomal syndrome has a range of specific characteristics regarding the type of seizures, EEG findings and specific response to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e502b35670e91756d3a78518ff0bb90
http://europepmc.org/articles/PMC8114617
http://europepmc.org/articles/PMC8114617
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:
Mihai Ioana, Claudia Jurca, Katalin Szakszon, Ariana Szilagyi, Anikó Ujfalusi, Cristian Sava, Marius Bembea, Kinga Kozma, Simona Sosoi, Andrei Pirvu, Codruța Diana Petchesi, Alexandru Daniel Jurcă, Ioana Streața, Zsuzsanna Szűcs
Publikováno v:
Genes, Vol 12, Iss 1674, p 1674 (2021)
Genes
Genes
Greig cephalopolysyndactyly syndrome (GCPS) is a rare genetic disorder (about 200 cases reported), characterized by macrocephaly, hypertelorism, and polysyndactyly. Most of the reported GCPS cases are the results of heterozygous loss of function muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cfb6a9ca3053adb30178e98a9b03324
https://www.mdpi.com/2073-4425/12/11/1674
https://www.mdpi.com/2073-4425/12/11/1674
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:
Diana Anca Lucuța, Alexandru Daniel Jurcă, Emilia Elena Babeș, Andreea Atena Zaha, Dana Carmen Zaha, Vlad Victor Babeș, Cosmin Mihai Vesa, Codruța Diana Petcheși, Cristian Ilyes
Publikováno v:
Medicina, Vol 57, Iss 158, p 158 (2021)
Medicina
Medicina; Volume 57; Issue 2; Pages: 158
Volume 57
Issue 2
Medicina
Medicina; Volume 57; Issue 2; Pages: 158
Volume 57
Issue 2
Background and Objectives: Characterization of patients with endocarditis regarding demographic, clinical, biological and imagistic data, blood culture results and possible correlation between different etiologic factors and host status characteristi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b37d43913409308d927f15235922fd3c
https://www.mdpi.com/1010-660X/57/2/158
https://www.mdpi.com/1010-660X/57/2/158
Autor:
Mircea Tamas, Éva Brigitta Patay, Alexandru Daniel Jurcă, Mihaela Zdrinca, Claudia Jurca, Luminiţa Fritea, Luciana Dobjanschi
Publikováno v:
Pakistan Journal of Botany. 53
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79647bce8f03885fb92cb4b94c51d81a
https://doi.org/10.30848/pjb2021-1(24)
https://doi.org/10.30848/pjb2021-1(24)
Autor:
Maria Claudia, Jurcă, Marius, Bembea, Mircea Ioan, Şandor, Dana Carmen, Zaha, Rodica Anamaria, Negrean, Cosmin Mihai, Vesa, Aurora Alexandra, Jurcă, Florentina Corina, Moisa, Laura Graţiela, Vicaş, Corina, Paul, Simona Diana, Cheregi, Ariana, Szilagyi, Camelia Liana, Buhaş, Alexandru Daniel, Jurcă
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 60(4)
Congenital anomalies of digits (CAD) can occur as isolated malformations, in combination with other malformation of the limbs, or as part of a genetic syndrome. The purpose of this work is to provide an overview of CAD, on morphological, genetic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::77b348fea305af69fdbd569cb048c93a
https://pubmed.ncbi.nlm.nih.gov/32239098
https://pubmed.ncbi.nlm.nih.gov/32239098
Autor:
Mihaela Cristiana, Coroi, Amine, Bakraoui, Cristian, Sala, Ovidiu, Ţica, Otilia Anca, Ţica, Maria Claudia, Jurcă, Alexandru Daniel, Jurcă, Larisa Bianca, Holhoş, Andrei Theodor, Bălăşoiu, Liana, Todor
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 60(2)
Uveal melanoma is the most common intraocular tumor characterized by increased metastatic potential. The tumor develops from uveal melanocytes that, from an embryological point of view, derive from the cells of the anterior neural crest. The risk fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00ecfb9ce55647739d697bb3f5aa593e
https://pubmed.ncbi.nlm.nih.gov/31658343
https://pubmed.ncbi.nlm.nih.gov/31658343