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Simona Bucerzan

Showing results (11-20 of 25) with videos related to

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Medicine and Pharmacy Reports|September 16, 2021
Cardiovascular manifestations in Marfan syndromeCecilia Lazea, Simona Bucerzan, Mirela Crisan, et al.
Therapeutics and Clinical Risk Management|December 1, 2018
Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1Anca Zimmermann, Radu A Popp, Heidi Rossmann, 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.
Diagnostics (Basel, Switzerland)|November 27, 2021
Molecular and Cytogenetic Analysis of Romanian Patients with Differences in Sex DevelopmentDiana Miclea, Camelia Alkhzouz, Simona Bucerzan, et al.
Journal of Gastrointestinal and Liver Diseases : JGLD|December 17, 2016
Cholelithiasis in Patients with Gaucher Disease type 1: Risk Factors and the Role of ABCG5/ABCG8 Gene VariantsAnca Zimmermann, Radu A Popp, Camelia Al-Khzouz, 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.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 13, 2015
The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiencyCecilia Lazea, Paula Grigorescu-Sido, Radu Popp, et al.
Pharmacogenomics and Personalized Medicine|April 23, 2021
Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis PatientsCamelia Alkhzouz, Georgiana Cabau, Cecilia Lazea, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 1, 2019
Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disabilityDiana Micleaa, Camelia Al-Khzouza, Sergiu Osan, et al.
Diagnostics (Basel, Switzerland)|June 2, 2021
Cardiac Manifestations in a Group of Romanian Patients with Gaucher Disease Type 1 (a Monocentric Study)Cecilia Lazea, Simona Bucerzan, Camelia Al-Khzouz, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Medicine and Pharmacy Reports|September 16, 2021
Cardiovascular manifestations in Marfan syndromeCecilia Lazea, Simona Bucerzan, Mirela Crisan, et al.
Therapeutics and Clinical Risk Management|December 1, 2018
Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1Anca Zimmermann, Radu A Popp, Heidi Rossmann, 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.
Diagnostics (Basel, Switzerland)|November 27, 2021
Molecular and Cytogenetic Analysis of Romanian Patients with Differences in Sex DevelopmentDiana Miclea, Camelia Alkhzouz, Simona Bucerzan, et al.
Journal of Gastrointestinal and Liver Diseases : JGLD|December 17, 2016
Cholelithiasis in Patients with Gaucher Disease type 1: Risk Factors and the Role of ABCG5/ABCG8 Gene VariantsAnca Zimmermann, Radu A Popp, Camelia Al-Khzouz, 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.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 13, 2015
The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiencyCecilia Lazea, Paula Grigorescu-Sido, Radu Popp, et al.
Pharmacogenomics and Personalized Medicine|April 23, 2021
Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis PatientsCamelia Alkhzouz, Georgiana Cabau, Cecilia Lazea, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 1, 2019
Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disabilityDiana Micleaa, Camelia Al-Khzouza, Sergiu Osan, et al.
Diagnostics (Basel, Switzerland)|June 2, 2021
Cardiac Manifestations in a Group of Romanian Patients with Gaucher Disease Type 1 (a Monocentric Study)Cecilia Lazea, Simona Bucerzan, Camelia Al-Khzouz, et al.
Pageof 3