Andreescu N - Search Results

1

Lethal evolution of a newborn with consistent features of hydrolethalus syndrome--Romanian patient.

Belengeanu V, Viskari H, Tallila J, Lahtela J, Farcas S, Andreescu N, Stoian M, Bohiltea CL, Fryns JP. Belengeanu V, et al. Among authors: andreescu n. Genet Couns. 2011;22(3):293-304. Genet Couns. 2011. PMID: 22029171

2

Ichthyosis congenita, harlequin fetus type: a case report.

Belengeanu V, Stoicanescu D, Stoian M, Andreescu N, Budisan C. Belengeanu V, et al. Among authors: andreescu n. Adv Med Sci. 2009;54(1):113-5. doi: 10.2478/v10039-009-0019-2. Adv Med Sci. 2009. PMID: 19556209

3

The heterogeneity of craniofacial morphology in Prader-Willi patients.

Belengeanu D, Bratu C, Stoian M, Motoc A, Ormerod E, Podariu AC, Farcaş S, Andreescu N. Belengeanu D, et al. Among authors: andreescu n. Rom J Morphol Embryol. 2012;53(3):527-32. Rom J Morphol Embryol. 2012. PMID: 22990543 Free article.

4

A de novo 2.3 Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl.

Belengeanu V, Gamage TH, Farcas S, Stoian M, Andreescu N, Belengeanu A, Frengen E, Misceo D. Belengeanu V, et al. Among authors: andreescu n. Gene. 2014 Apr 10;539(1):168-72. doi: 10.1016/j.gene.2014.01.060. Epub 2014 Feb 4. Gene. 2014. PMID: 24508274

5

Structural chromosomal anomalies detected by prenatal genetic diagnosis: our experience.

Farcaş S, Crişan CD, Andreescu N, Stoian M, Motoc AG. Farcaş S, et al. Among authors: andreescu n. Rom J Morphol Embryol. 2013;54(2):377-83. Rom J Morphol Embryol. 2013. PMID: 23771085 Free article.

6

Assessment of chromosomal aneuploidies in sperm of infertile males by using FISH technique.

Andreescu NI, Cosma M, Farcaş SS, Stoian M, Amzăr DG, Puiu M. Andreescu NI, et al. Rom J Morphol Embryol. 2016;57(1):173-8. Rom J Morphol Embryol. 2016. PMID: 27151704 Free article.

7

-759C÷T polymorphism of the HTR2C gene is not correlated with atypical antipsychotics-induced weight gain, among Romanian psychotic patients.

Grădinaru RC, Andreescu NI, Nussbaum LA, Farcaş SS, Dumitraşcu V, Suciu L, Puiu M. Grădinaru RC, et al. Rom J Morphol Embryol. 2016;57(4):1343-1349. Rom J Morphol Embryol. 2016. PMID: 28174802 Free article.

8

A rare case of partial trisomy 8q24.12-q24.3 and partial monosomy of 8q24.3: Prenatal diagnosis and clinical findings.

Farcas S, Erdelean D, Anne-Elise Szekely F, Navolan D, Andreescu N, Cioca A. Farcas S, et al. Among authors: andreescu n. Taiwan J Obstet Gynecol. 2019 Jan;58(1):36-39. doi: 10.1016/j.tjog.2018.11.005. Taiwan J Obstet Gynecol. 2019. PMID: 30638476 Free article.

9

Chest wall deformities and their possible associations with different genetic syndromes.

Andreescu N, Sharma A, Mihailescu A, Zimbru CG, David VL, Horhat R, Kundnani NR, Puiu M, Farcas S. Andreescu N, et al. Eur Rev Med Pharmacol Sci. 2022 Jul;26(14):5107-5114. doi: 10.26355/eurrev_202207_29298. Eur Rev Med Pharmacol Sci. 2022. PMID: 35916808 Free article.

10

Does the Genetic Cause of Prader-Willi Syndrome Explain the Highly Variable Phenotype?

Dobrescu AI, Chirita-Emandi A, Andreescu N, Farcas S, Puiu M. Dobrescu AI, et al. Among authors: andreescu n. Maedica (Bucur). 2016 Sep;11(3):191-197. Maedica (Bucur). 2016. PMID: 28694852 Free PMC article.

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