Louha M - Search Results

1

Efficiency of Ber-EP4 antibody for isolating circulating epithelial tumor cells before RT-PCR detection.

Sabile A, Louha M, Bonte E, Poussin K, Vona G, Mejean A, Chretien Y, Bougas L, Lacour B, Capron F, Roseto A, Bréchot C, Paterlini-Bréchot P. Sabile A, et al. Among authors: louha m. Am J Clin Pathol. 1999 Aug;112(2):171-8. doi: 10.1093/ajcp/112.2.171. Am J Clin Pathol. 1999. PMID: 10439796

2

Liver resection and needle liver biopsy cause hematogenous dissemination of liver cells.

Louha M, Nicolet J, Zylberberg H, Sabile A, Vons C, Vona G, Poussin K, Tournebize M, Capron F, Pol S, Franco D, Lacour B, Bréchot C, Paterlini-Bréchot P. Louha M, et al. Hepatology. 1999 Mar;29(3):879-82. doi: 10.1002/hep.510290348. Hepatology. 1999. PMID: 10051492

3

Isolation by size of epithelial tumor cells : a new method for the immunomorphological and molecular characterization of circulatingtumor cells.

Vona G, Sabile A, Louha M, Sitruk V, Romana S, Schütze K, Capron F, Franco D, Pazzagli M, Vekemans M, Lacour B, Bréchot C, Paterlini-Bréchot P. Vona G, et al. Among authors: louha m. Am J Pathol. 2000 Jan;156(1):57-63. doi: 10.1016/S0002-9440(10)64706-2. Am J Pathol. 2000. PMID: 10623654 Free PMC article.

4

Spontaneous and iatrogenic spreading of liver-derived cells into peripheral blood of patients with primary liver cancer.

Louha M, Poussin K, Ganne N, Zylberberg H, Nalpas B, Nicolet J, Capron F, Soubrane O, Vons C, Pol S, Beaugrand M, Berthelot P, Franco D, Trinchet JC, Bréchot C, Paterlini P. Louha M, et al. Hepatology. 1997 Oct;26(4):998-1005. doi: 10.1002/hep.510260430. Hepatology. 1997. PMID: 9328326

5

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.

Abdi S, Bahloul A, Behlouli A, Hardelin JP, Makrelouf M, Boudjelida K, Louha M, Cheknene A, Belouni R, Rous Y, Merad Z, Selmane D, Hasbelaoui M, Bonnet C, Zenati A, Petit C. Abdi S, et al. Among authors: louha m. PLoS One. 2016 Sep 1;11(9):e0161893. doi: 10.1371/journal.pone.0161893. eCollection 2016. PLoS One. 2016. PMID: 27583663 Free PMC article.

6

Discovery of a large deletion of KAL1 in 2 deaf brothers.

Marlin S, Chantot-Bastaraud S, David A, Loundon N, Jonard L, Portnoï MF, Bonnet C, Louha M, Gherbi S, Garabedian EN, Couderc R, Denoyelle F. Marlin S, et al. Among authors: louha m. Otol Neurotol. 2013 Dec;34(9):1590-4. doi: 10.1097/MAO.0000000000000228. Otol Neurotol. 2013. PMID: 24232061

7

Next generation sequencing: the technology we need in pediatric laboratories?

Couderc R, Jonard L, Louha M. Couderc R, et al. Among authors: louha m. Clin Biochem. 2011 May;44(7):514-515. doi: 10.1016/j.clinbiochem.2011.02.030. Clin Biochem. 2011. PMID: 22036354 No abstract available.

8

Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.

Riahi Z, Bonnet C, Zainine R, Lahbib S, Bouyacoub Y, Bechraoui R, Marrakchi J, Hardelin JP, Louha M, Largueche L, Ben Yahia S, Kheirallah M, Elmatri L, Besbes G, Abdelhak S, Petit C. Riahi Z, et al. Among authors: louha m. PLoS One. 2015 Mar 23;10(3):e0120584. doi: 10.1371/journal.pone.0120584. eCollection 2015. PLoS One. 2015. PMID: 25798947 Free PMC article.

9

Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province.

Talbi S, Bonnet C, Riahi Z, Boudjenah F, Dahmani M, Hardelin JP, Wong Jun Tai F, Louha M, Ammar-Khodja F, Petit C. Talbi S, et al. Among authors: louha m. Int J Pediatr Otorhinolaryngol. 2018 Sep;112:1-5. doi: 10.1016/j.ijporl.2018.06.012. Epub 2018 Jun 12. Int J Pediatr Otorhinolaryngol. 2018. PMID: 30055715

10

Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.

Ammar-Khodja F, Bonnet C, Dahmani M, Ouhab S, Lefèvre GM, Ibrahim H, Hardelin JP, Weil D, Louha M, Petit C. Ammar-Khodja F, et al. Among authors: louha m. Mol Genet Genomic Med. 2015 May;3(3):189-96. doi: 10.1002/mgg3.131. Epub 2015 Feb 15. Mol Genet Genomic Med. 2015. PMID: 26029705 Free PMC article.

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