Hachicha M - Search Results

1

Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.

Bougacha-Elleuch N, Charfi N, Miled N, Bouhajja H, Belguith N, Mnif M, Jorge P, Chikhrouhou N, Ayadi H, Hachicha M, Abid M. Bougacha-Elleuch N, et al. Among authors: hachicha m. Eur J Pediatr. 2015 Dec;174(12):1703. doi: 10.1007/s00431-015-2669-3. Eur J Pediatr. 2015. PMID: 26567037 No abstract available.

2

Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.

Bougacha-Elleuch N, Charfi N, Miled N, Bouhajja H, Belguith N, Mnif M, Jaurge P, Chikhrouhou N, Ayadi H, Hachicha M, Abid M. Bougacha-Elleuch N, et al. Among authors: hachicha m. Eur J Pediatr. 2015 Nov;174(11):1491-501. doi: 10.1007/s00431-015-2550-4. Epub 2015 May 13. Eur J Pediatr. 2015. PMID: 25968604

3

A novel nonsense mutation in HSD17B3 gene in a Tunisian patient with sexual ambiguity.

Ben Rhouma B, Belguith N, Mnif MF, Kamoun T, Charfi N, Kamoun M, Abdelhedi F, Hachicha M, Kamoun H, Abid M, Fakhfakh F. Ben Rhouma B, et al. Among authors: hachicha m. J Sex Med. 2013 Oct;10(10):2586-9. doi: 10.1111/j.1743-6109.2012.02763.x. Epub 2012 May 17. J Sex Med. 2013. PMID: 22594312

4

Ganglioneuroma of adrenal gland in a patient with Turner syndrome.

Kamoun M, Mnif MF, Rekik N, Belguith N, Charfi N, Mnif L, Elleuch M, Mnif F, Kamoun T, Mnif Z, Kamoun H, Sellami-Boudawara T, Hachicha M, Abid M. Kamoun M, et al. Among authors: hachicha m. Ann Diagn Pathol. 2010 Apr;14(2):133-6. doi: 10.1016/j.anndiagpath.2009.06.007. Epub 2009 Sep 8. Ann Diagn Pathol. 2010. PMID: 20227019

5

Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Mnif MF, Kamoun M, Mnif F, Charfi N, Naceur BB, Kallel N, Rekik N, Mnif Z, Sfar MH, Sfar MT, Hachicha M, Abid M. Mnif MF, et al. Among authors: hachicha m. Indian J Endocrinol Metab. 2012 Nov;16(6):939-46. doi: 10.4103/2230-8210.102995. Indian J Endocrinol Metab. 2012. PMID: 23226639 Free PMC article.

6

Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Mnif MF, Kamoun M, Mnif F, Charfi N, Kallel N, Ben Naceur B, Rekik N, Mnif Z, Sfar MH, Sfar MT, Hachicha M, Keskes LA, Abid M. Mnif MF, et al. Among authors: hachicha m. Am J Med Sci. 2012 Nov;344(5):363-73. doi: 10.1097/MAJ.0b013e31824369e4. Am J Med Sci. 2012. PMID: 22270393

7

Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis.

Mnif MF, Kamoun M, Mnif F, Charfi N, Kallel N, Rekik N, Naceur BB, Fourati H, Daoud E, Mnif Z, Sfar MH, Younes-Mhenni S, Sfar MT, Hachicha M, Abid M. Mnif MF, et al. Among authors: hachicha m. Indian J Endocrinol Metab. 2013 Jan;17(1):121-7. doi: 10.4103/2230-8210.107833. Indian J Endocrinol Metab. 2013. PMID: 23776864 Free PMC article.

8

Mutations in GAA Gene in Tunisian Families with Infantile Onset Pompe Disease: Novel Mutation and Structural Modeling Investigations.

Alila-Fersi O, Aloulou H, Werteni I, Mahfoudh N, Chabchoub I, Kammoun H, Keskes L, Hachicha M, Belguith N, Fakhfakh F. Alila-Fersi O, et al. Among authors: hachicha m. J Mol Neurosci. 2020 Jul;70(7):1100-1109. doi: 10.1007/s12031-020-01516-9. Epub 2020 Mar 3. J Mol Neurosci. 2020. PMID: 32125626

9

[Bardet - Biedl syndrome in the child. A study of 11 cases].

Aloulou H, Cheikhrouhou H, Belguith N, Ben Ameur S, Ben Mansour L, Chabchoub I, Kammoun T, Hachicha M. Aloulou H, et al. Among authors: hachicha m. Tunis Med. 2011 Jan;89(1):31-6. Tunis Med. 2011. PMID: 21267825 Free article. French.

10

Thyroid Hypoplasia in Congenital Hypothyroidism Associated with Thyroid Peroxidase Mutations.

Stoupa A, Chaabane R, Guériouz M, Raynaud-Ravni C, Nitschke P, Bole-Feysot C, Mnif M, Ammar Keskes L, Hachicha M, Belguith N, Polak M, Carré A. Stoupa A, et al. Among authors: hachicha m. Thyroid. 2018 Jul;28(7):941-944. doi: 10.1089/thy.2017.0502. Thyroid. 2018. PMID: 29790453

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