Madrimova A.G

4 та иш

Tashkent State Medical University, Tashkent, Uzbekistan

1. MITOCHONDRIAL MUTATION m.1555A>G IN MT-RNR1 AS A PREDICTIVE BIOMARKER OF AMINOGLYCOSIDE-INDUCED SENSORINEURAL HEARING LOSS IN CHILDREN

   Madrimova A.G

   МақолаNeonatal Respiratory Health ResearchZenodo (CERN European Organization for Nuclear Research)20260 иқтибос

   ABIABI:AkademIndex/openalex/2026.article.025822

2. MUTATIONAL SPECTRUM OF THE GJB2 GENE AS THE LEADING GENETIC CAUSE OF NON-SYNDROMIC SENSORINEURAL HEARING LOSS IN CHILDREN

   Madrimova A.G

   МақолаHearing, Cochlea, Tinnitus, GeneticsZenodo (CERN European Organization for Nuclear Research)20260 иқтибос

   ABIABI:AkademIndex/openalex/2026.article.025851

3. MITOCHONDRIAL MUTATION m.1555A>G IN MT-RNR1 AS A PREDICTIVE BIOMARKER OF AMINOGLYCOSIDE-INDUCED SENSORINEURAL HEARING LOSS IN CHILDREN

   Madrimova A.G

   МақолаNeonatal Respiratory Health ResearchZenodo (CERN European Organization for Nuclear Research)20260 иқтибос

   ABIABI:AkademIndex/openalex/2026.article.025856

4. MUTATIONAL SPECTRUM OF THE GJB2 GENE AS THE LEADING GENETIC CAUSE OF NON-SYNDROMIC SENSORINEURAL HEARING LOSS IN CHILDREN

   Madrimova A.G

   МақолаHearing, Cochlea, Tinnitus, GeneticsZenodo (CERN European Organization for Nuclear Research)20260 иқтибос

   ABIABI:AkademIndex/openalex/2026.article.025998