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Items: 26

1.

Monoamine neurotransmitters and movement disorders in children and adults.

Doummar D, Moussa F, Nougues MC, Ravelli C, Louha M, Whalen S, Burglen L, Rodriguez D, Billette de Villemeur T.

Rev Neurol (Paris). 2018 Nov;174(9):581-588. doi: 10.1016/j.neurol.2018.07.002. Epub 2018 Aug 27. Review.

PMID:
30166070
2.

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.

Int J Pediatr Otorhinolaryngol. 2018 Sep;112:1-5. doi: 10.1016/j.ijporl.2018.06.012. Epub 2018 Jun 12.

PMID:
30055715
3.

The IL-4 rs2070874 polymorphism may be associated with the severity of recurrent viral-induced wheeze.

Amat F, Louha M, Benet M, Guiddir T, Bourgoin-Heck M, Saint-Pierre P, Paluel-Marmont C, Fontaine C, Lambert N, Couderc R, Gonzalez JR, Just J.

Pediatr Pulmonol. 2017 Nov;52(11):1435-1442. doi: 10.1002/ppul.23834. Epub 2017 Sep 26.

PMID:
28950434
4.

Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.

Nattes E, Lejeune S, Carsin A, Borie R, Gibertini I, Balinotti J, Nathan N, Marchand-Adam S, Thumerelle C, Fauroux B, Bosdure E, Houdouin V, Delestrain C, Louha M, Couderc R, De Becdelievre A, Fanen P, Funalot B, Crestani B, Deschildre A, Dubus JC, Epaud R.

Respir Med. 2017 Aug;129:16-23. doi: 10.1016/j.rmed.2017.05.014. Epub 2017 May 26.

5.

A rare large mutation involving two exons of the SP-B gene in an infant with severe respiratory distress.

Takcı Ş, Anuk-İnce D, Louha M, Couderc R, Çakar N, Köseoğlu RD, Ateş Ö.

Turk J Pediatr. 2017;59(4):483-486. doi: 10.24953/turkjped.2017.04.018.

6.

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.

PLoS One. 2016 Sep 1;11(9):e0161893. doi: 10.1371/journal.pone.0161893. eCollection 2016.

7.

A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family.

Behlouli A, Bonnet C, Abdi S, Hasbellaoui M, Boudjenah F, Hardelin JP, Louha M, Makrelouf M, Ammar-Khodja F, Zenati A, Petit C.

Int J Pediatr Otorhinolaryngol. 2016 Aug;87:28-33. doi: 10.1016/j.ijporl.2016.04.040. Epub 2016 May 20.

PMID:
27368438
8.

Benign hereditary chorea, not only chorea: a family case presentation.

Koht J, Løstegaard SO, Wedding I, Vidailhet M, Louha M, Tallaksen CM.

Cerebellum Ataxias. 2016 Feb 2;3:3. doi: 10.1186/s40673-016-0041-7. eCollection 2016.

9.

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.

Mol Genet Genomic Med. 2015 May;3(3):189-96. doi: 10.1002/mgg3.131. Epub 2015 Feb 15.

10.

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.

PLoS One. 2015 Mar 23;10(3):e0120584. doi: 10.1371/journal.pone.0120584. eCollection 2015.

11.

Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?

Enaud L, Hadchouel A, Coulomb A, Berteloot L, Lacaille F, Boccon-Gibod L, Boulay V, Darcel F, Griese M, Linard M, Louha M, Renouil M, Rivière JP, Toupance B, Verkarre V, Delacourt C, de Blic J.

Orphanet J Rare Dis. 2014 Jun 14;9:85. doi: 10.1186/1750-1172-9-85.

12.

Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, Boespflug OT, Besbes G, Abdelhak S, Petit C.

PLoS One. 2014 Jun 13;9(6):e99797. doi: 10.1371/journal.pone.0099797. eCollection 2014.

13.

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.

Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C.

Orphanet J Rare Dis. 2014 Apr 17;9:55. doi: 10.1186/1750-1172-9-55.

14.

Survival of an infant with homozygous surfactant protein C (SFTPC) mutation.

Arıkan-Ayyıldız Z, Caglayan-Sozmen S, Isık S, Deterding R, Dishop MK, Couderc R, Epaud R, Louha M, Uzuner N.

Pediatr Pulmonol. 2014 Mar;49(3):E112-5. doi: 10.1002/ppul.22976. Epub 2013 Dec 17.

PMID:
24347240
15.

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.

Otol Neurotol. 2013 Dec;34(9):1590-4. doi: 10.1097/MAO.0000000000000228.

PMID:
24232061
16.

Combined pulmonary fibrosis and emphysema syndrome associated with ABCA3 mutations.

Epaud R, Delestrain C, Louha M, Simon S, Fanen P, Tazi A.

Eur Respir J. 2014 Feb;43(2):638-41. doi: 10.1183/09031936.00145213. Epub 2013 Oct 17. No abstract available.

17.

Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment.

Bonnet C, Louha M, Loundon N, Michalski N, Verpy E, Smagghe L, Hardelin JP, Rouillon I, Jonard L, Couderc R, Gherbi S, Garabedian EN, Denoyelle F, Petit C, Marlin S.

Gene. 2013 Sep 25;527(2):537-40. doi: 10.1016/j.gene.2013.06.044. Epub 2013 Jul 11.

PMID:
23850727
18.

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.

Gras D, Jonard L, Roze E, Chantot-Bastaraud S, Koht J, Motte J, Rodriguez D, Louha M, Caubel I, Kemlin I, Lion-François L, Goizet C, Guillot L, Moutard ML, Epaud R, Héron B, Charles P, Tallot M, Camuzat A, Durr A, Polak M, Devos D, Sanlaville D, Vuillaume I, Billette de Villemeur T, Vidailhet M, Doummar D.

J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):956-62. doi: 10.1136/jnnp-2012-302505. Epub 2012 Jul 24.

PMID:
22832740
19.

Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrum.

Béhin A, Jardel C, Claeys KG, Fagart J, Louha M, Romero NB, Laforêt P, Eymard B, Lombès A.

Neurology. 2012 Feb 28;78(9):644-8. doi: 10.1212/WNL.0b013e318248df2b. Epub 2012 Feb 15.

PMID:
22345218
20.

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

Couderc R, Jonard L, Louha M.

Clin Biochem. 2011 May;44(7):514-5. doi: 10.1016/j.clinbiochem.2011.02.030. No abstract available.

PMID:
22036354
21.

Molecular diagnosis of genetic deafness.

Jonard L, Marlin S, Louha M, Bonnet C, Couderc R, Garabedian N, Denoyelle F; all the team of Centre de Référence des Surdités Génétiques, Hôpital Trousseau, APHP, Paris, France.

Clin Biochem. 2011 May;44(7):510-1. doi: 10.1016/j.clinbiochem.2011.02.031. No abstract available.

PMID:
22036352
22.

Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype.

Jonard L, Couloigner V, Pierrot S, Louha M, Gherbi S, Denoyelle F, Marlin S.

Eur J Med Genet. 2012 Jan;55(1):56-8. doi: 10.1016/j.ejmg.2011.06.009. Epub 2011 Aug 23.

PMID:
21888995
23.

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.

Am J Pathol. 2000 Jan;156(1):57-63.

24.

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.

Am J Clin Pathol. 1999 Aug;112(2):171-8.

PMID:
10439796
25.

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.

Hepatology. 1999 Mar;29(3):879-82.

PMID:
10051492
26.

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.

Hepatology. 1997 Oct;26(4):998-1005.

PMID:
9328326

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