Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ariana, Szilagyi"'
Autor:
Cristian Marinău, Andrei Csep, Cristian Sava, Alin Iuhas, Larisa Niulaș, Ariana Szilagyi, Ladislau Ritli, Andreea Balmoș, Claudia Jurca
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Treating Ewing's Sarcoma of the thorax (Askin's tumor) with antineoplastic therapy in a malnourished cystic fibrosis patient colonized with Pseudomonas aeruginosa and Staphylococcus aureus may carry a significant potential for complications. We prese
Externí odkaz:
https://doaj.org/article/c543795a157a49f2a845c2de1dedcbdd
Autor:
Christian S. Guay, Mariam Khebir, T. Shiva Shahiri, Ariana Szilagyi, Erin Elizabeth Cole, Gabrielle Simoneau, Mohamed Badawy
Publikováno v:
Intensive Care Medicine Experimental, Vol 9, Iss 1, Pp 1-13 (2021)
Abstract Background Real-time automated analysis of videos of the microvasculature is an essential step in the development of research protocols and clinical algorithms that incorporate point-of-care microvascular analysis. In response to the call fo
Externí odkaz:
https://doaj.org/article/ff80d632530340cb8657188791887d4d
Publikováno v:
Canadian Journal of Cardiology. 38:384-388
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1cc7da7a666498283a0c9c663e165f1
https://doi.org/10.1016/j.cjca.2021.12.018
https://doi.org/10.1016/j.cjca.2021.12.018
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:
Ariana Szilagyi, Erin Elizabeth Cole, Mariam Khebir, T Shiva Shahiri, Mohamed Badawy, Christian S. Guay, Gabrielle Simoneau
Publikováno v:
Intensive Care Medicine Experimental, Vol 9, Iss 1, Pp 1-13 (2021)
Intensive Care Medicine Experimental
Intensive Care Medicine Experimental
Background Real-time automated analysis of videos of the microvasculature is an essential step in the development of research protocols and clinical algorithms that incorporate point-of-care microvascular analysis. In response to the call for validat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a88344a119b55b2b7561d79f449b065
https://doi.org/10.1186/s40635-021-00380-0
https://doi.org/10.1186/s40635-021-00380-0
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:
ru Jurca, Kinga Kozma, Claudia Jurca, Alex, Ariana Szilagyi, Alfred Klausegger, Marius Bembea
Publikováno v:
Journal of Rare Disorders: Diagnosis & Therapy.
We present a rare lethal case of a dystrophic form of epidermolysis bullosa (EB) associated with type 1 diabetes mellitus in a 5-year-old boy diagnosed with EB at birth. This association has not been reported before. Two well-known mutations in the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27dde0cacb6c2fc18017c09bef09ea4a
https://doi.org/10.21767/2380-7245.100176
https://doi.org/10.21767/2380-7245.100176
Autor:
Claudia, Jurca, Bogdan, Dima, Marius, Bembea, Eniko, Bereki, Ariana, Szilagyi, Andreea, Balmos, Alexandru, Jurca
Publikováno v:
Archives of Disease in Childhood; 2017, Vol. 102 Issue: Supplement 2 pA183-A183, 1p