M. Louha

发表

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

K. Schütze, A. Sabile, C. Bréchot, 2000, The American journal of pathology.

Combined pulmonary fibrosis and emphysema syndrome associated with ABCA3 mutations

S. Simon, R. Epaud, M. Louha, 2013, European Respiratory Journal.

Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.

R. Epaud, R. Borie, E. Bosdure, 2017, Respiratory medicine.

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

C. Petit, J. Hardelin, M. Louha, 2018, International journal of pediatric otorhinolaryngology.

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

C. Petit, D. Weil, J. Hardelin, 2014, PloS one.

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

R. Deterding, R. Epaud, M. Dishop, 2014, Pediatric pulmonology.

Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients

C. Petit, J. Hardelin, S. Abdelhak, 2015, PloS one.

Genetic Update on Auditory Neuropathy

P. Deltenre, F. Denoyelle, M. Louha, 2011, Audiology and Neurotology Extra.

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

C. Petit, J. Hardelin, M. Louha, 2016, International journal of pediatric otorhinolaryngology.

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

Y. Chrétien, A. Sabile, C. Bréchot, 1999, American journal of clinical pathology.

Monoamine neurotransmitters and movement disorders in children and adults.

Marie-Christine Nouguès, M. Louha, T. Billette de Villemeur, 2018, Revue neurologique.

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

C. Bréchot, S. Pol, D. Franco, 1997, Hepatology.

Adult cases of mitochondrial DNA depletion due to TK2 defect

K. Claeys, P. Laforêt, B. Eymard, 2012, Neurology.

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

C. Petit, J. Hardelin, Amel Bahloul, 2016, PloS one.

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

C. Delacourt, B. Toupance, M. Griese, 2014, Orphanet Journal of Rare Diseases.

New insights into CC2D2A-related Joubert syndrome

F. Rivier, C. Garel, A. Afenjar, 2022, Journal of Medical Genetics.

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

M. Vidailhet, J. Koht, M. Louha, 2016, Cerebellum & Ataxias.

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

M. Vidailhet, A. Durr, M. Polak, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

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

J. González, M. Benet, J. Just, 2017, Pediatric pulmonology.

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

M. Louha, N. Çakar, R. Couderc, 2017, The Turkish journal of pediatrics.

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

C. Petit, D. Weil, J. Hardelin, 2015, Molecular genetics & genomic medicine.

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

C. Petit, N. Michalski, J. Hardelin, 2013, Gene.

Discovery of a Large Deletion of KAL1 in 2 Deaf Brothers

F. Denoyelle, M. Louha, S. Chantot-Bastaraud, 2013, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

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

C. Petit, J. Hardelin, M. Louha, 2014, Orphanet Journal of Rare Diseases.

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

M. Vidailhet, J. Koht, M. Louha, 2016, Cerebellum & Ataxias.

Molecular diagnosis of genetic deafness.

F. Denoyelle, M. Louha, N. Garabedian, 2011, Clinical Biochemistry.

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

C. Petit, J. Hardelin, M. Louha, 2016, International journal of pediatric otorhinolaryngology.