Hellin AC - Search Results

1

Pattern of congenital heart diseases in Rwandan children with genetic defects.

Teteli R, Uwineza A, Butera Y, Hitayezu J, Murorunkwere S, Umurerwa L, Ndinkabandi J, Hellin AC, Jamar M, Caberg JH, Muganga N, Mucumbitsi J, Rusingiza EK, Mutesa L. Teteli R, et al. Among authors: hellin ac. Pan Afr Med J. 2014 Sep 25;19:85. doi: 10.11604/pamj.2014.19.85.3428. eCollection 2014. Pan Afr Med J. 2014. PMID: 25722758 Free PMC article.

2

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.

Uwineza A, Caberg JH, Hitayezu J, Hellin AC, Jamar M, Dideberg V, Rusingiza EK, Bours V, Mutesa L. Uwineza A, et al. Among authors: hellin ac. BMC Med Genet. 2014 Jul 12;15:79. doi: 10.1186/1471-2350-15-79. BMC Med Genet. 2014. PMID: 25016475 Free PMC article.

3

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.

Vanakker O, Vilain C, Janssens K, Van der Aa N, Smits G, Bandelier C, Blaumeiser B, Bulk S, Caberg JH, De Leener A, De Rademaeker M, de Ravel T, Desir J, Destree A, Dheedene A, Gaillez S, Grisart B, Hellin AC, Janssens S, Keymolen K, Menten B, Pichon B, Ravoet M, Revencu N, Rombout S, Staessens C, Van Den Bogaert A, Van Den Bogaert K, Vermeesch JR, Kooy F, Sznajer Y, Devriendt K. Vanakker O, et al. Among authors: hellin ac. Eur J Med Genet. 2014 Mar;57(4):151-6. doi: 10.1016/j.ejmg.2014.02.002. Epub 2014 Feb 15. Eur J Med Genet. 2014. PMID: 24534801 Review.

4

Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13.

Uwineza A, Pierquin G, Gaillez S, Jamar M, Hellin AC, Caberg JH, Bours V. Uwineza A, et al. Among authors: hellin ac. Genet Couns. 2013;24(2):193-200. Genet Couns. 2013. PMID: 24032290 Free article.

5

A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation.

Mutesa L, Jamar M, Hellin AC, Pierquin G, Bours V. Mutesa L, et al. Among authors: hellin ac. Indian J Hum Genet. 2012 Sep;18(3):352-5. doi: 10.4103/0971-6866.108033. Indian J Hum Genet. 2012. PMID: 23716947 Free PMC article.

6

Systematic chromosomal aberrations found in murine bone marrow-derived mesenchymal stem cells.

Josse C, Schoemans R, Niessen NA, Delgaudine M, Hellin AC, Herens C, Delvenne P, Bours V. Josse C, et al. Among authors: hellin ac. Stem Cells Dev. 2010 Aug;19(8):1167-73. doi: 10.1089/scd.2009.0264. Stem Cells Dev. 2010. PMID: 20109032

7

Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.

Mutesa L, Vanbellinghen JF, Hellin AC, Segers K, Jamar M, Pierquin G, Bours V. Mutesa L, et al. Among authors: hellin ac. Genet Couns. 2009;20(1):9-17. Genet Couns. 2009. PMID: 19400538

8

Precocious puberty associated with partial trisomy 18q and monosomy 11q.

Mutesa L, Hellin AC, Jamar M, Pierquin G, Bours V, Verloes A. Mutesa L, et al. Among authors: hellin ac. Genet Couns. 2007;18(2):201-7. Genet Couns. 2007. PMID: 17710872

9

Roles of nuclear factor-kappaB, p53, and p21/WAF1 in daunomycin-induced cell cycle arrest and apoptosis.

Hellin AC, Bentires-Alj M, Verlaet M, Benoit V, Gielen J, Bours V, Merville MP. Hellin AC, et al. J Pharmacol Exp Ther. 2000 Dec;295(3):870-8. J Pharmacol Exp Ther. 2000. PMID: 11082419

10

Additive effect between NF-kappaB subunits and p53 protein for transcriptional activation of human p53 promoter.

Benoit V, Hellin AC, Huygen S, Gielen J, Bours V, Merville MP. Benoit V, et al. Among authors: hellin ac. Oncogene. 2000 Sep 28;19(41):4787-94. doi: 10.1038/sj.onc.1203831. Oncogene. 2000. PMID: 11032029

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