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Simona Bucerzan

Showing results (1-10 of 25) with videos related to

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Medicine and Pharmacy Reports|September 16, 2021
Genetic testing in pediatric endocrine pathologyDiana Miclea, Camelia Alkhzouz, Simona Bucerzan, et al.
Case Reports in Genetics|February 18, 2016
A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIaAnca Zimmermann, Heidi Rossmann, 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.
Clujul Medical (1957)|November 4, 2015
Osteoarthropathy in mucopolysaccharidosis type IIIoana Nascu, Paula Grigorescu-Sido, Camelia Al-Khzouz, et al.
Medical Ultrasonography|March 11, 2016
Ultrasonographic evaluation of the median nerve at the level of the carpal tunnel outlet and mid forearm in patients with type II MucopolysaccharidosisCorina Bocsa, Carmen Asavoaie, Simona Bucerzan, 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
Diagnostic, treatment and outcome possibilities in achondroplasiaSimona Bucerzan, Camelia Alkhzouz, Mirela Crisan, 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.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Medicine and Pharmacy Reports|September 16, 2021
Genetic testing in pediatric endocrine pathologyDiana Miclea, Camelia Alkhzouz, Simona Bucerzan, et al.
Case Reports in Genetics|February 18, 2016
A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIaAnca Zimmermann, Heidi Rossmann, 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.
Clujul Medical (1957)|November 4, 2015
Osteoarthropathy in mucopolysaccharidosis type IIIoana Nascu, Paula Grigorescu-Sido, Camelia Al-Khzouz, et al.
Medical Ultrasonography|March 11, 2016
Ultrasonographic evaluation of the median nerve at the level of the carpal tunnel outlet and mid forearm in patients with type II MucopolysaccharidosisCorina Bocsa, Carmen Asavoaie, Simona Bucerzan, 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
Diagnostic, treatment and outcome possibilities in achondroplasiaSimona Bucerzan, Camelia Alkhzouz, Mirela Crisan, 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.
Pageof 3