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Camelia Alkhzouz

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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.
Medicine and Pharmacy Reports|September 16, 2021
Diagnostic, treatment and outcome possibilities in achondroplasiaSimona Bucerzan, Camelia Alkhzouz, Mirela Crisan, et al.
Molecular Neurobiology|August 1, 2025
Telomere Biology, Erosion, and Age-Related Conditions: Insights from Down Syndrome and Other Telomere-Associated DisordersEnikő Kutasi, Adina Chis, Mihaela Adela Vintan, et al.
Therapeutics and Clinical Risk Management|May 13, 2017
Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)Simona Bucerzan, Diana Miclea, Radu Popp, et al.
JIMD Reports|June 29, 2016
Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type IICamelia Alkhzouz, Cecilia Lazea, Simona Bucerzan, et al.
Biomedicines|March 28, 2025
Salivary Proteome Insights: Evaluation of Saliva Preparation Methods in Mucopolysaccharidoses ResearchMaria-Andreea Soporan, Ioana-Ecaterina Pralea, Maria Iacobescu, et al.
European Journal of Internal Medicine|March 9, 2010
Baseline characteristics and outcome in Romanian patients with Gaucher disease type 1Paula Grigorescu-Sido, Cristina Drugan, Camelia Alkhzouz, et al.
Italian Journal of Pediatrics|December 30, 2022
Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disabilityDiana Miclea, Sergiu Osan, Simona Bucerzan, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
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.
Medicine and Pharmacy Reports|September 16, 2021
Diagnostic, treatment and outcome possibilities in achondroplasiaSimona Bucerzan, Camelia Alkhzouz, Mirela Crisan, et al.
Molecular Neurobiology|August 1, 2025
Telomere Biology, Erosion, and Age-Related Conditions: Insights from Down Syndrome and Other Telomere-Associated DisordersEnikő Kutasi, Adina Chis, Mihaela Adela Vintan, et al.
Therapeutics and Clinical Risk Management|May 13, 2017
Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)Simona Bucerzan, Diana Miclea, Radu Popp, et al.
JIMD Reports|June 29, 2016
Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type IICamelia Alkhzouz, Cecilia Lazea, Simona Bucerzan, et al.
Biomedicines|March 28, 2025
Salivary Proteome Insights: Evaluation of Saliva Preparation Methods in Mucopolysaccharidoses ResearchMaria-Andreea Soporan, Ioana-Ecaterina Pralea, Maria Iacobescu, et al.
European Journal of Internal Medicine|March 9, 2010
Baseline characteristics and outcome in Romanian patients with Gaucher disease type 1Paula Grigorescu-Sido, Cristina Drugan, Camelia Alkhzouz, et al.
Italian Journal of Pediatrics|December 30, 2022
Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disabilityDiana Miclea, Sergiu Osan, Simona Bucerzan, et al.
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