Roky R - Search Results

1

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.

Bakhchane A, Bousfiha A, Charoute H, Salime S, Detsouli M, Snoussi K, Nadifi S, Kabine M, Rouba H, Dehbi H, Roky R, Charif M, Barakat A. Bakhchane A, et al. Among authors: roky r. Eur J Med Genet. 2016 Jun;59(6-7):325-9. doi: 10.1016/j.ejmg.2016.05.002. Epub 2016 May 8. Eur J Med Genet. 2016. PMID: 27169813

2

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.

Charif M, Bakhchane A, Abidi O, Boulouiz R, Eloualid A, Roky R, Rouba H, Kandil M, Lenaers G, Barakat A. Charif M, et al. Among authors: roky r. Gene. 2013 Jul 1;523(1):103-5. doi: 10.1016/j.gene.2013.03.123. Epub 2013 Apr 13. Gene. 2013. PMID: 23590985 Free article.

3

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

Bakhchane A, Charoute H, Nahili H, Roky R, Rouba H, Charif M, Lenaers G, Barakat A. Bakhchane A, et al. Among authors: roky r. Gene. 2015 Dec 10;574(1):28-33. doi: 10.1016/j.gene.2015.07.075. Epub 2015 Jul 28. Gene. 2015. PMID: 26226225

4

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees.

Bakhchane A, Charif M, Salime S, Boulouiz R, Nahili H, Roky R, Lenaers G, Barakat A. Bakhchane A, et al. Among authors: roky r. PLoS One. 2015 Sep 15;10(9):e0138072. doi: 10.1371/journal.pone.0138072. eCollection 2015. PLoS One. 2015. PMID: 26371875 Free PMC article.

5

Compound heterozygous SLC29A3 mutation causes H syndrome in a Moroccan patient: A case report.

Bakhchane A, Kindil Z, Charoute H, Benchikhi K, Khadir K, Nadifi S, Baline K, Roky R, Barakat A. Bakhchane A, et al. Among authors: roky r. Curr Res Transl Med. 2016 Apr-Jun;64(2):65-8. doi: 10.1016/j.retram.2016.01.008. Epub 2016 Jun 1. Curr Res Transl Med. 2016. PMID: 27316388 Review.

6

A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability.

Krami AM, Bouzidi A, Charif M, Amalou G, Charoute H, Rouba H, Roky R, Lenaers G, Barakat A, Nahili H. Krami AM, et al. Among authors: roky r. Eur J Med Genet. 2022 Jun;65(6):104515. doi: 10.1016/j.ejmg.2022.104515. Epub 2022 Apr 27. Eur J Med Genet. 2022. PMID: 35487419

7

Association between G2677T/A polymorphism in ABCB1 gene and the risk of drug resistance epilepsy: An updated systematic review and meta-analysis.

Krami AM, Ratib C, Charoute H, Rouba H, Roky R, Barakat A, Nahili H. Krami AM, et al. Among authors: roky r. Epilepsy Res. 2022 Sep;185:106977. doi: 10.1016/j.eplepsyres.2022.106977. Epub 2022 Jul 8. Epilepsy Res. 2022. PMID: 35853334

8

Sex as a Biological Factor in the Changes in Disease Patients During Ramadan Intermittent Fasting: A Systematic Review.

Roky R, Aadil N, Krami AM, Benaji B, Errabih I, Abdelrahim DN, Faris ME. Roky R, et al. Front Nutr. 2022 Jul 1;9:908674. doi: 10.3389/fnut.2022.908674. eCollection 2022. Front Nutr. 2022. PMID: 35845800 Free PMC article.

9

Physiological and chronobiological changes during Ramadan intermittent fasting.

Roky R, Houti I, Moussamih S, Qotbi S, Aadil N. Roky R, et al. Ann Nutr Metab. 2004;48(4):296-303. doi: 10.1159/000081076. Epub 2004 Sep 24. Ann Nutr Metab. 2004. PMID: 15452402 Review.

10

Daytime sleepiness during Ramadan intermittent fasting: polysomnographic and quantitative waking EEG study.

Roky R, Chapotot F, Benchekroun MT, Benaji B, Hakkou F, Elkhalifi H, Buguet A. Roky R, et al. J Sleep Res. 2003 Jun;12(2):95-101. doi: 10.1046/j.1365-2869.2003.00341.x. J Sleep Res. 2003. PMID: 12753346

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