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Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients.
Alkhzouz C, Cabau G, Lazea C, Asavoaie C, Bucerzan S, Mirea AM, Farcas M, Miclaus Jnr M, Popp R, Miclea D. Alkhzouz C, et al. Among authors: bucerzan s. Pharmgenomics Pers Med. 2021 Mar 17;14:349-358. doi: 10.2147/PGPM.S295241. eCollection 2021. Pharmgenomics Pers Med. 2021. PMID: 33889011 Free PMC article.
Osteoarthropathy in mucopolysaccharidosis type II.
Nascu I, Grigorescu-Sido P, Al-Khzouz C, Bucerzan S, Denes C, Lazea C. Nascu I, et al. Among authors: bucerzan s. Clujul Med. 2013;86(3):270-3. Epub 2013 Aug 5. Clujul Med. 2013. PMID: 26527960 Free PMC article.
Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability.
Miclea D, Szucs A, Mirea A, Stefan DM, Nazarie F, Bucerzan S, Lazea C, Grama A, Pop TL, Farcas M, Zaharie G, Matyas M, Mager M, Vintan M, Popp R, Alkhzouz C. Miclea D, et al. Among authors: bucerzan s. Int J Gen Med. 2021 Aug 16;14:4511-4515. doi: 10.2147/IJGM.S320033. eCollection 2021. Int J Gen Med. 2021. PMID: 34429637 Free PMC article.
Diagnostic, treatment and outcome possibilities in achondroplasia.
Bucerzan S, Alkhzouz C, Crisan M, Miclea D, Asavoaie C, Ilies R, Grigorescu-Sido P. Bucerzan S, et al. Med Pharm Rep. 2021 Aug;94(Suppl No 1):S22-S24. doi: 10.15386/mpr-2222. Epub 2021 Aug 10. Med Pharm Rep. 2021. PMID: 34527903 Free PMC article.
23 results