Megarbane A - Search Results

1

Feeding problems and gastrointestinal diseases in Down syndrome.

Ravel A, Mircher C, Rebillat AS, Cieuta-Walti C, Megarbane A. Ravel A, et al. Among authors: megarbane a. Arch Pediatr. 2020 Jan;27(1):53-60. doi: 10.1016/j.arcped.2019.11.008. Epub 2019 Nov 26. Arch Pediatr. 2020. PMID: 31784293 Review.

2

[Amino acids and trisomy 21].

Lejeune J, Rethoré MO, de Blois MC, Peeters M, Naffah J, Megarbane A, Cattaneo F, Mircher C, Rabier D, Parvy P, et al. Lejeune J, et al. Among authors: megarbane a. Ann Genet. 1992;35(1):8-13. Ann Genet. 1992. PMID: 1535189 French.

3

The 50th anniversary of the discovery of trisomy 21: the past, present, and future of research and treatment of Down syndrome.

Mégarbané A, Ravel A, Mircher C, Sturtz F, Grattau Y, Rethoré MO, Delabar JM, Mobley WC. Mégarbané A, et al. Genet Med. 2009 Sep;11(9):611-6. doi: 10.1097/GIM.0b013e3181b2e34c. Genet Med. 2009. PMID: 19636252 Free article. Review.

4

How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?

Ravel A, Chouery E, Stora S, Jalkh N, Villard L, Temtamy S, Mégarbané A. Ravel A, et al. Among authors: megarbane a. Am J Med Genet A. 2011 Apr;155A(4):880-4. doi: 10.1002/ajmg.a.33879. Epub 2011 Mar 17. Am J Med Genet A. 2011. PMID: 21416592

5

Lack of anti-citrullinated fibrinogen and anti-CCP antibodies in adult patients with Down syndrome.

Berthelot JM, Nogueira L, Mircher C, Megarbane A, Maugars Y, Serre G. Berthelot JM, et al. Among authors: megarbane a. Joint Bone Spine. 2012 Oct;79(5):526-7. doi: 10.1016/j.jbspin.2012.03.002. Epub 2012 May 4. Joint Bone Spine. 2012. PMID: 22560845 No abstract available.

6

Molecular signatures of cardiac defects in Down syndrome lymphoblastoid cell lines suggest altered ciliome and Hedgehog pathways.

Ripoll C, Rivals I, Ait Yahya-Graison E, Dauphinot L, Paly E, Mircher C, Ravel A, Grattau Y, Bléhaut H, Mégarbane A, Dembour G, de Fréminville B, Touraine R, Créau N, Potier MC, Delabar JM. Ripoll C, et al. Among authors: megarbane a. PLoS One. 2012;7(8):e41616. doi: 10.1371/journal.pone.0041616. Epub 2012 Aug 9. PLoS One. 2012. PMID: 22912673 Free PMC article.

7

The intellectual disability of trisomy 21: differences in gene expression in a case series of patients with lower and higher IQ.

Mégarbané A, Noguier F, Stora S, Manchon L, Mircher C, Bruno R, Dorison N, Pierrat F, Rethoré MO, Trentin B, Ravel A, Morent M, Lefranc G, Piquemal D. Mégarbané A, et al. Eur J Hum Genet. 2013 Nov;21(11):1253-9. doi: 10.1038/ejhg.2013.24. Epub 2013 Feb 20. Eur J Hum Genet. 2013. PMID: 23422941 Free PMC article.

8

Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulation.

Haertle L, Müller T, Lardenoije R, Maierhofer A, Dittrich M, Riemens RJM, Stora S, Roche M, Leber M, Riedel-Heller S, Wagner M, Scherer M, Ravel A, Mircher C, Cieuta-Walti C, Durand S, van de Hove DLA, Hoffmann P, Ramirez A, Haaf T, El Hajj N, Mégarbané A. Haertle L, et al. Among authors: megarbane a. Clin Epigenetics. 2019 Dec 16;11(1):195. doi: 10.1186/s13148-019-0787-x. Clin Epigenetics. 2019. PMID: 31843015 Free PMC article.

9

Transcriptomic study in women with trisomy 21 identifies a possible role of the GTPases of the immunity-associated proteins (GIMAP) in the protection of breast cancer.

Mégarbané A, Piquemal D, Rebillat AS, Stora S, Pierrat F, Bruno R, Noguier F, Mircher C, Ravel A, Vilaire-Meunier M, Durand S, Lefranc G. Mégarbané A, et al. Sci Rep. 2020 Jun 10;10(1):9447. doi: 10.1038/s41598-020-66469-w. Sci Rep. 2020. PMID: 32523132 Free PMC article.

10

Efficacy and safety of methylphenidate on attention deficit hyperactivity disorder in children with Down syndrome.

Roche M, Mircher C, Toulas J, Prioux E, Conte M, Ravel A, Falquero S, Labidi A, Stora S, Durand S, Mégarbané A, Cieuta-Walti C. Roche M, et al. Among authors: megarbane a. J Intellect Disabil Res. 2021 Aug;65(8):795-800. doi: 10.1111/jir.12832. Epub 2021 Apr 20. J Intellect Disabil Res. 2021. PMID: 33880800

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