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Diana Miclea

Showing results (1-10 of 32) with videos related to

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Frontiers in Genetics|July 26, 2021
Case Report: Uncommon Association of <i>ITGB4</i> and <i>KRT10</i> Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis CongenitaMelinda Matyas, Diana Miclea, Gabriela Zaharie
Clujul Medical (1957)|November 27, 2015
Genetic testing in patients with global developmental delay / intellectual disabilities. A reviewDiana Miclea, Loredana Peca, Zina Cuzmici, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 19, 2022
Osteogenesis imperfecta and rheumatoid arthritis: connective issuesLaura Otilia Damian, Diana Miclea, Romana Vulturar, et al.
Medicine and Pharmacy Reports|September 16, 2021
Genetic testing in pediatric endocrine pathologyDiana Miclea, Camelia Alkhzouz, Simona Bucerzan, et al.
Diagnostics (Basel, Switzerland)|August 27, 2021
46,XX DSD: Developmental, Clinical and Genetic AspectsCamelia Alkhzouz, Simona Bucerzan, Maria Miclaus, et al.
Medicine and Pharmacy Reports|September 16, 2021
Early clinical signs in lysosomal diseasesCamelia Alkhzouz, Diana Miclea, Simona Bucerzan, et al.
Frontiers in Pediatrics|August 8, 2020
16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the LiteratureSimona Bucerzan, Diana Miclea, Cecilia Lazea, et al.
Medicine and Pharmacy Reports|September 16, 2021
Challenges in the diagnosis and management of urea cycle disorders in Romanian childrenTudor Lucian Pop, Alina Grama, Diana Miclea, et al.
Frontiers in Genetics|June 10, 2025
Case Report: A neurodevelopmental disorder with global developmental delay, microcephaly, eye anomalies, sweat dysregulation, and skeletal implications due to an ultra-rare <i>de novo</i> 5q14.3q15 copy number gainCostela Lacrimioara Serban, Alexandra Mihailescu, Diana Miclea, et al.
Medicine and Pharmacy Reports|September 16, 2021
Diagnostic, treatment and outcome possibilities in achondroplasiaSimona Bucerzan, Camelia Alkhzouz, Mirela Crisan, et al.
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Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Frontiers in Genetics|July 26, 2021
Case Report: Uncommon Association of <i>ITGB4</i> and <i>KRT10</i> Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis CongenitaMelinda Matyas, Diana Miclea, Gabriela Zaharie
Clujul Medical (1957)|November 27, 2015
Genetic testing in patients with global developmental delay / intellectual disabilities. A reviewDiana Miclea, Loredana Peca, Zina Cuzmici, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 19, 2022
Osteogenesis imperfecta and rheumatoid arthritis: connective issuesLaura Otilia Damian, Diana Miclea, Romana Vulturar, et al.
Medicine and Pharmacy Reports|September 16, 2021
Genetic testing in pediatric endocrine pathologyDiana Miclea, Camelia Alkhzouz, Simona Bucerzan, et al.
Diagnostics (Basel, Switzerland)|August 27, 2021
46,XX DSD: Developmental, Clinical and Genetic AspectsCamelia Alkhzouz, Simona Bucerzan, Maria Miclaus, et al.
Medicine and Pharmacy Reports|September 16, 2021
Early clinical signs in lysosomal diseasesCamelia Alkhzouz, Diana Miclea, Simona Bucerzan, et al.
Frontiers in Pediatrics|August 8, 2020
16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the LiteratureSimona Bucerzan, Diana Miclea, Cecilia Lazea, et al.
Medicine and Pharmacy Reports|September 16, 2021
Challenges in the diagnosis and management of urea cycle disorders in Romanian childrenTudor Lucian Pop, Alina Grama, Diana Miclea, et al.
Frontiers in Genetics|June 10, 2025
Case Report: A neurodevelopmental disorder with global developmental delay, microcephaly, eye anomalies, sweat dysregulation, and skeletal implications due to an ultra-rare <i>de novo</i> 5q14.3q15 copy number gainCostela Lacrimioara Serban, Alexandra Mihailescu, Diana Miclea, et al.
Medicine and Pharmacy Reports|September 16, 2021
Diagnostic, treatment and outcome possibilities in achondroplasiaSimona Bucerzan, Camelia Alkhzouz, Mirela Crisan, et al.
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