Delphine Feldmann
Hôpital Armand-Trousseau(FR)Assistance Publique – Hôpitaux de Paris(FR)Institut Supérieur de Biotechnologie de Sfax(TN)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Neonatal Respiratory Health Research, Cystic Fibrosis Research Advances, Connexins and lens biology, Mitochondrial Function and Pathology
Most-Cited Works
- → GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study(2005)551 cited
- → Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure(2001)530 cited
- → Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome(2000)288 cited
- → Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France(2000)250 cited
- → SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations(2006)241 cited
- → Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650](1997)