Lazea C - Search Results

1

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: lazea c. 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.

2

MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism.

Zimmermann A, Schenk JP, Grigorescu Sido P, Pfaffle R, Lazea C, Zimmermann T, Heinrich U, Weber MM, Bettendorf M. Zimmermann A, et al. Among authors: lazea c. J Pediatr Endocrinol Metab. 2007 May;20(5):587-96. doi: 10.1515/jpem.2007.20.5.587. J Pediatr Endocrinol Metab. 2007. PMID: 17642419

3

Bone mineral density and bone turnover in Romanian children and young adults with classical 21-hydroxylase deficiency are influenced by glucocorticoid replacement therapy.

Zimmermann A, Sido PG, Schulze E, Al Khzouz C, Lazea C, Coldea C, Weber MM. Zimmermann A, et al. Among authors: lazea c. Clin Endocrinol (Oxf). 2009 Oct;71(4):477-84. doi: 10.1111/j.1365-2265.2008.03518.x. Epub 2008 Dec 22. Clin Endocrinol (Oxf). 2009. PMID: 19170706

4

The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiency.

Lazea C, Grigorescu-Sido P, Popp R, Legendre M, Amselem S, Al-Khzouz C, Bucerzan S, Creţ V, Crişan M, Brad C. Lazea C, et al. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):993-8. doi: 10.1515/jpem-2014-0289. J Pediatr Endocrinol Metab. 2015. PMID: 25581745

5

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: lazea c. Clujul Med. 2013;86(3):270-3. Epub 2013 Aug 5. Clujul Med. 2013. PMID: 26527960 Free PMC article.

6

Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type II.

Alkhzouz C, Lazea C, Bucerzan S, Nascu I, Kiss E, Denes CL, Grigorescu-Sido P. Alkhzouz C, et al. Among authors: lazea c. JIMD Rep. 2017;33:19-25. doi: 10.1007/8904_2016_535. Epub 2016 Jun 29. JIMD Rep. 2017. PMID: 27351199 Free PMC article.

7

Rare complications of neurofibromatosis 1 diagnosed incidentally in two children.

Lazea C, Asavoaie C, Al-Khzouz C, Popa L. Lazea C, et al. Ther Clin Risk Manag. 2018 Aug 31;14:1547-1552. doi: 10.2147/TCRM.S173237. eCollection 2018. Ther Clin Risk Manag. 2018. PMID: 30214218 Free PMC article.

8

Unusual Presentation Of Kawasaki Disease With Gastrointestinal And Renal Manifestations.

Lazea C, Man O, Sur LM, Serban R, Lazar C. Lazea C, et al. Ther Clin Risk Manag. 2019 Dec 5;15:1411-1416. doi: 10.2147/TCRM.S226624. eCollection 2019. Ther Clin Risk Manag. 2019. PMID: 31824164 Free PMC article.

9

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: lazea c. Front Pediatr. 2020 Jul 15;8:390. doi: 10.3389/fped.2020.00390. eCollection 2020. Front Pediatr. 2020. PMID: 32760686 Free PMC article.

10

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: lazea c. 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.

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