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Papers published by Dr Camelia Al-Khzouz:


Diagnosis and Management of Genetic Causes of Middle Aortic Syndrome in Children: A Comprehensive Literature Review

Lazea C, Al-Khzouz C, Sufana C, Miclea D, Asavoaie C, Filimon I, Fufezan O

Therapeutics and Clinical Risk Management 2022, 18:233-248

Published Date: 16 March 2022

Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability

Miclea D, Szucs A, Mirea AM, Stefan DM, Nazarie F, Bucerzan S, Lazea C, Grama A, Pop TL, Farcas M, Zaharie G, Matyas M, Mager Snr M, Vintan M, Popp R, Alkhzouz C

International Journal of General Medicine 2021, 14:4511-4515

Published Date: 16 August 2021

Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients

Alkhzouz C, Cabau G, Lazea C, Asavoaie C, Bucerzan S, Mirea AM, Farcas M, Miclaus M Jnr, Popp R, Miclea D

Pharmacogenomics and Personalized Medicine 2021, 14:349-358

Published Date: 17 March 2021

Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)

Bucerzan S, Miclea D, Popp R, Alkhzouz C, Lazea C, Pop IV, Grigorescu-Sido P

Therapeutics and Clinical Risk Management 2017, 13:613-622

Published Date: 4 May 2017