Padmini P. Polinati

New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies

Tiina Ojala, Padmini P. Polinati, Tuula Manninen et al. · Pediatric Research · 2012 · 97 citations · Full text

New Mutation, Mendelian Disorder, Mitochondrial Function +10

Patient-Specific Induced Pluripotent Stem Cell–Derived RPE Cells: Understanding the Pathogenesis of Retinopathy in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency

Padmini P. Polinati, Tanja Ilmarinen, Ras Trokovic et al. · Investigative Ophthalmology & Visual Science · 2014 · 36 citations · Full text

Malonyl-CoA decarboxylase deficiency: Long-term follow-up of a patient new clinical features and novel mutations

Padmini P. Polinati, Leena Valanne, Tiina Tyni · Brain and Development · 2014 · 18 citations

Mendelian Disorder, Genetic Disorder, Genetics +6