Arghir A - Search Results

1

Diagnostic approach of angelman syndrome.

Duca DG, Craiu D, Boer M, Chirieac SM, Arghir A, Tutulan-Cunita A, Barca D, Iliescu C, Lungeanu A, Magureanu S, Budisteanu M. Duca DG, et al. Among authors: arghir a. Maedica (Bucur). 2013 Sep;8(4):321-7. Maedica (Bucur). 2013. PMID: 24790661 Free PMC article.

2

Relationship between chromosomal changes complexity and disease aggressiveness in myeloid and lymphoid disorders.

Lungeanu A, Arghir A, Lupu A, Mut Popescu D. Lungeanu A, et al. Among authors: arghir a. J Cell Mol Med. 2002 Jul-Sep;6(3):389-98. doi: 10.1111/j.1582-4934.2002.tb00517.x. J Cell Mol Med. 2002. PMID: 12417055 Free PMC article.

3

Oculocutaneous albinism associated with multiple malformations and psychomotor retardation.

Budisteanu M, Arghir A, Chirieac SM, Cardos G, Lungeanu A. Budisteanu M, et al. Among authors: arghir a. Pediatr Dermatol. 2010 Mar-Apr;27(2):212-4. doi: 10.1111/j.1525-1470.2010.01115.x. Pediatr Dermatol. 2010. PMID: 20537085

4

Novel clinical finding in MECP2 duplication syndrome.

Budisteanu M, Papuc SM, Tutulan-Cunita A, Budisteanu B, Arghir A. Budisteanu M, et al. Among authors: arghir a. Eur Child Adolesc Psychiatry. 2011 Jul;20(7):373-5. doi: 10.1007/s00787-011-0184-2. Epub 2011 May 18. Eur Child Adolesc Psychiatry. 2011. PMID: 21590509 No abstract available.

5

18q deletion syndrome - A case report.

Budisteanu M, Arghir A, Chirieac SM, Tutulan-Cunita A, Lungeanu A. Budisteanu M, et al. Among authors: arghir a. Maedica (Bucur). 2010 Apr;5(2):135-8. Maedica (Bucur). 2010. PMID: 21977138 Free PMC article.

6

Variant e19a2 BCR-ABL1 fusion transcript in typical chronic myeloid leukemia.

Tutulan-Cunita AC, Chirieac SM, Mocanu G, Luca C, Costache M, Lungeanu A, Arghir A. Tutulan-Cunita AC, et al. Among authors: arghir a. Clin Lab. 2011;57(9-10):785-8. Clin Lab. 2011. PMID: 22029197

7

3p interstitial deletion: novel case report and review.

Ţuţulan-Cunită AC, Papuc SM, Arghir A, Rötzer KM, Deshpande C, Lungeanu A, Budişteanu M. Ţuţulan-Cunită AC, et al. Among authors: arghir a. J Child Neurol. 2012 Aug;27(8):1062-6. doi: 10.1177/0883073811431016. Epub 2012 Jan 30. J Child Neurol. 2012. PMID: 22290856 Review.

8

Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture.

Tuţulan-Cuniţă AC, Budişteanu M, Papuc SM, Dupont JM, Blancho D, Lebbar A, Viot G, Lungeanu A, Arghir A. Tuţulan-Cuniţă AC, et al. Among authors: arghir a. Psychiatry Res. 2012 May 30;197(3):356-7. doi: 10.1016/j.psychres.2011.11.016. Epub 2012 Feb 22. Psychiatry Res. 2012. PMID: 22365273

9

Genetic technologies in cancer investigation - applications in aggresive lymphoid malignancies.

Berbec NM, Arghir A, Vitcu A, Angelescu S, Colita Amd A, Ciobanu A, Papuc SM, Tutlan-Cunita AC, Lupu AR. Berbec NM, et al. Among authors: arghir a. Maedica (Bucur). 2012 Jan;7(1):75-9. Maedica (Bucur). 2012. PMID: 23118825 Free PMC article. No abstract available.

10

Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalities.

Papuc SM, Hackmann K, Andrieux J, Vincent-Delorme C, Budişteanu M, Arghir A, Schrock E, Ţuţulan-Cuniţă AC, Di Donato N. Papuc SM, et al. Among authors: arghir a. Eur J Med Genet. 2015 May;58(5):319-23. doi: 10.1016/j.ejmg.2015.03.005. Epub 2015 Apr 6. Eur J Med Genet. 2015. PMID: 25858704

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