Clinical Features and Outcome of Infective Endocarditis in a University Hospital in Romania von Babeș, Emilia Elena, Lucuța, Diana Anca, Petcheși, Codruța Diana, Zaha, Andreea Atena, Ilyes, Cristian, Jurca, Alexandru Daniel, Vesa, Cosmin Mihai, Zaha, Dana Carmen, Babeș, Vlad Victor

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Clinical Challenges in Diagnosing Primordial Dwarfism: Insights from a MOPD II Case Study von Jurca, Alexandru Daniel, Petchesi, Codruța Diana, Jurca, Sânziana, Severin, Emilia, Jurca, Aurora Alexandra, Jurca, Claudia Maria

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Bioethical aspects in type I neurofibromatosis von Petchesi, Codruța Diana, Ciavoi, Gabriela, Jurca, Claudia, Vulturar, Romana, Bembea, Marius

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A rare but treatable inborn error of metabolism: Arginine glycine amidinotransferase (AGAT) deficiency von Pintilie, Sebastian Romeo, Fodor, Adriana, Bembea, Marius, Petchesi, Codruța Diana, Grad, Simona, Damian, Laura, Vulturar, Romana

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DOWN SYNDROME – LONGITUDINAL STUDY OF CLINICAL EVOLUTION AND PSYCHO-SOCIAL IMPLICATIONS von Petchesi, Codruța Diana, Ciavoi, Gabriela, Feier, Florentina, Iuhas, Oana Alexandra, Kozma, Kinga, Jurca, Claudia, Bembea, Marius

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CURRENT DATA ABOUT THE AETIOLOGY AND TREATMENT OF INFECTIVE ENDOCARDITIS von ZAHA, DANA CARMEN

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Wolfram Syndrome Type I Case Report and Review-Focus on Early Diagnosis and Genetic Variants von Jurca, Alexandru Daniel, Galea-Holhos, Larisa Bianca, Jurca, Aurora Alexandra, Atasie, Diter, Petchesi, Codruta Diana, Severin, Emilia, Jurca, Claudia Maria

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Effects of Burosumab Treatment on Two Siblings with X-Linked Hypophosphatemia. Case Report and Literature Review von Jurca, Claudia Maria, Iuhas, Oana, Kozma, Kinga, Petchesi, Codruta Diana, Zaha, Dana Carmen, Bembea, Marius, Jurca, Sanziana, Paul, Corina, Jurca, Alexandru Daniel

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

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Long-term Outcome in Patients with Turner Syndrome--Retrospective Study von Petchesi, Codruta Diana, Iuhas, Alin Remus, Hodisan, Ramona, Zaha, Dana Carmen, Jurca, Alexandru Daniel

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When Bad Luck Strikes Twice: Beckwith Wiedemann Syndrome Associated with Familial Long QT Syndrome Type I von Petchesi, Codruta Diana, Kozma, Kinga, Iuhas, Alin Remus, Hodisan, Ramona, Jurca, Alexandru Daniel

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Congenital Myasthenic Syndrome-4C in a Consanguineous Romani Family: Genetic Insights and Clinical Implications von Petchesi, Codruta Diana, Jurca, Aurora Alexandra, Jurca, Alexandru Daniel, Dorobantu, Florica Ramona, Iuhas, Alin Remus, Severin, Emilia, Jurca, Claudia Maria

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

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Genetics of congenital solid tumors von Jurcă, Maria Claudia, Ivaşcu, Marius Evelin, Jurcă, Aurora Alexandra, Kozma, Kinga, Magyar, Ioan, Şandor, Mircea Ioan, Jurcă, Alexandru Daniel, Zaha, Dana Carmen, Albu, Cristina-Crenguţa, Pantiş, Carmen, Bembea, Marius, Petcheşi, Codruţa Diana

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Empty sella associated with growth hormone deficiency and polydactyly von Jurcă, Maria Claudia, Bembea, Marius, Kozma, Kinga, Şandor, Mircea Ioan, Negrean, Rodica Anamaria, Dobjanschi, Luciana, Cuc, Emilia Albiniţa, Petcheşi, Codruţa Diana, Jurcă, Alexandru Daniel

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Anatomic variants in Dandy-Walker complex von Jurcă, Maria Claudia, Kozma, Kinga, Petcheşi, CodruŢa Diana, Bembea, Marius, Pop, Ovidiu Laurean, MuŢiu, Gabriela, Coroi, Mihaela Cristiana, Jurcă, Alexandru Daniel, Dobjanschi, Luciana

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Double autosomal trisomy with mosaicism 47,XY(+8)∕47,XY(+21). Morphological and genetic changes of a rare case von Jurcă, Maria Claudia, Bembea, Marius, Iuhas, Oana Alexandra, Kozma, Kinga, Petcheşi, Codruţa Diana, Jurcă, Alexandru Daniel, Szilágyi, Ariana, Dubău, Diana Luminiţa, Sava, Cristian Nicolae, Zaha, Dana Carmen, Cuc, Emilia Albiniţa

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Morphological and genetic abnormalities in a Jacobsen syndrome von Jurcă, Alexandru Daniel, Kozma, Kinga, Ioana, Mihai, Streaţă, Ioana, Petcheşi, Codruţa Diana, Bembea, Marius, Jurcă, Maria Claudia, Cuc, Emilia Albiniţa, Vesa, Cosmin Mihai, Buhaş, Camelia Liana

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Clinical-Epidemiological Study of a Cohort of 35 Patients with Craniosynostosis von Somolan, Claudia-Victoria, Petchesi, Codruta Diana, Jurca, Claudia, Bembea, Marius

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