Miclea D - Search Results

1

Genetic testing in patients with global developmental delay / intellectual disabilities. A review.

Miclea D, Peca L, Cuzmici Z, Pop IV. Miclea D, et al. Clujul Med. 2015;88(3):288-92. doi: 10.15386/cjmed-461. Epub 2015 Jul 1. Clujul Med. 2015. PMID: 26609258 Free PMC article. Review.

2

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. Bucerzan S, et al. Among authors: miclea d. Ther Clin Risk Manag. 2017 May 4;13:613-622. doi: 10.2147/TCRM.S126301. eCollection 2017. Ther Clin Risk Manag. 2017. PMID: 28496331 Free PMC article.

3

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. 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.

4

Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability.

Miclea D, Osan S, Bucerzan S, Stefan D, Popp R, Mager M, Puiu M, Zimbru C, Chirita-Emandi A, Alkhzouz C. Miclea D, et al. Ital J Pediatr. 2022 Dec 30;48(1):207. doi: 10.1186/s13052-022-01397-1. Ital J Pediatr. 2022. PMID: 36585697 Free PMC article.

5

16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the Literature.

Bucerzan S, Miclea D, Lazea C, Asavoaie C, Kulcsar A, Grigorescu-Sido P. Bucerzan S, et al. Among authors: miclea d. Front Pediatr. 2020 Jul 15;8:390. doi: 10.3389/fped.2020.00390. eCollection 2020. Front Pediatr. 2020. PMID: 32760686 Free PMC article.

6

46,XX DSD: Developmental, Clinical and Genetic Aspects.

Alkhzouz C, Bucerzan S, Miclaus M, Mirea AM, Miclea D. Alkhzouz C, et al. Among authors: miclea d. Diagnostics (Basel). 2021 Jul 30;11(8):1379. doi: 10.3390/diagnostics11081379. Diagnostics (Basel). 2021. PMID: 34441313 Free PMC article. Review.

7

Genetic testing in pediatric endocrine pathology.

Miclea D, Alkhzouz C, Bucerzan S, Grigorescu-Sido P. Miclea D, et al. Med Pharm Rep. 2021 Aug;94(Suppl No 1):S15-S18. doi: 10.15386/mpr-2220. Epub 2021 Aug 10. Med Pharm Rep. 2021. PMID: 34527901 Free PMC article.

8

A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation-Case Report With Literature Review.

Chirita Emandi A, Dobrescu AI, Doros G, Hyon C, Miclea D, Popoiu C, Puiu M, Arghirescu S. Chirita Emandi A, et al. Among authors: miclea d. Front Pediatr. 2019 Jul 8;7:270. doi: 10.3389/fped.2019.00270. eCollection 2019. Front Pediatr. 2019. PMID: 31338352 Free PMC article.

9

Case Report: Potocki-Lupski Syndrome in Five Siblings.

Grama A, Sîrbe C, Miclea D, Cǎinap SS, Huniadi D, Bulata B, Pop TL. Grama A, et al. Among authors: miclea d. Front Pediatr. 2021 Nov 8;9:698629. doi: 10.3389/fped.2021.698629. eCollection 2021. Front Pediatr. 2021. PMID: 34820340 Free PMC article.

10

Molecular and Cytogenetic Analysis of Romanian Patients with Differences in Sex Development.

Miclea D, Alkhzouz C, Bucerzan S, Grigorescu-Sido P, Popp RA, Pascanu IM, Cret V, Ghervan C, Blaga L, Zaharie G. Miclea D, et al. Diagnostics (Basel). 2021 Nov 14;11(11):2107. doi: 10.3390/diagnostics11112107. Diagnostics (Basel). 2021. PMID: 34829455 Free PMC article.

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