Lack of Information on the Effects of COVID-19 on Rare Pathologies Has Further Hampered Access to Healthcare Services

por Severin, Emilia, Dan, Dorica
Publicado 2022

The impact of RAS mutation on the treatment strategy of colorectal cancer

por Pirvu, Edvina Elena, Severin, Emilia, Niţă, Irina, Toma, Ştefania Andreea
Publicado 2023

Case report: Tackling the complexities of an extremely premature newborn with intrauterine growth restriction and congenital metabolic disorders through a multidisciplinary approac...

por Roșca, Ioana, Preda, Andrei Gheorghe, Constantin, Andreea Teodora, Coroleucă, Ciprian, Severin, Emilia, Teleanu, Raluca Ioana, Turenschi, Alina
Publicado 2023

Changes in skeletal dysplasia nosology

por Jurcă, Maria Claudia, Jurcă, Sânziana Iulia, Mirodot, Filip, Bercea, Bogdan, Severin, Emilia Maria, Bembea, Marius, Jurcă, Alexandru Daniel
Publicado 2021

Correlations between Demographic, Clinical, and Paraclinical Variables and Outcomes in Patients with KRAS-Mutant or KRAS Wild-Type Metastatic Colorectal Cancer—A Retrospective Stud...

por Pîrvu, Edvina Elena, Severin, Emilia, Pătru, Raluca Ileana, Niță, Irina, Toma, Stefania Andreea, Macarie, Roxana Rodica, Cocioabă, Cristina Elena, Florescu, Ioana, Coniac, Simona
Publicado 2023

Challenging diagnoses of tetraploidy/diploidy and trisomy 12: utility of first-tier prenatal testing methods

por Iordanescu, Irina Ioana, Neacsu, Anca Teodora, Catana, Andreea, Barabas-CuzmicI, Zina, Suciu, Viorel, Dragomir, Cristina, Voicu, Diana Elena, Severin, Emilia, Militaru, Mariela Sanda
Publicado 2023

The Importance of Implementing a Transition Strategy for Patients with Muscular Dystrophy: From Child to Adult—Insights from a Tertiary Centre for Rare Neurological Diseases

por Lupu, Maria, Ioghen, Mihaela, Perjoc, Radu-Ștefan, Scarlat, Andra-Maria, Vladâcenco, Oana Aurelia, Roza, Eugenia, Epure, Diana Ana-Maria, Teleanu, Raluca Ioana, Severin, Emilia Maria
Publicado 2023

Developments in Genetics: Better Management of Ovarian Cancer Patients

por Maioru, Ovidiu-Virgil, Radoi, Viorica-Elena, Coman, Madalin-Codrut, Hotinceanu, Iulian-Andrei, Dan, Andra, Eftenoiu, Anca-Elena, Burtavel, Livia-Mălina, Bohiltea, Laurentiu-Camil, Severin, Emilia-Maria
Publicado 2023

Tuberous Sclerosis, Type II Diabetes Mellitus and the PI3K/AKT/mTOR Signaling Pathways—Case Report and Literature Review

por Jurca, Claudia Maria, Kozma, Kinga, Petchesi, Codruta Diana, Zaha, Dana Carmen, Magyar, Ioan, Munteanu, Mihai, Faur, Lucian, Jurca, Aurora, Bembea, Dan, Severin, Emilia, Jurca, Alexandru Daniel
Publicado 2023

The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients

por Budisteanu, Magdalena, Papuc, Sorina Mihaela, Streata, Ioana, Cucu, Mihai, Pirvu, Andrei, Serban-Sosoi, Simona, Erbescu, Alina, Andrei, Emanuela, Iliescu, Catrinel, Ioana, Doina, Severin, Emilia, Ioana, Mihai, Arghir, Aurora
Publicado 2021

Cardiofaciocutaneous syndrome – a longitudinal study of a case over 33 years: case report and review of the literature

por Jurcă, Maria Claudia, Iuhas, Oana Alexandra, Puiu, Maria, Chiriţă-Emandi, Adela, Andreescu, Nicoleta Ioana, Petcheşi, Codruţa Diana, Jurcă, Alexandru Daniel, Magyar, Ioan, Jurcă, Sânziana Iulia, Kozma, Kinga, Severin, Emilia Maria, Bembea, Marius
Publicado 2021