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Koparir, Asuman and Bahena Carbajal, Paulina and Zamini, Mina and Naghinejad, Maryam and Najarzadeh Torbati, Paria and Hofrichter, Michaela A. H. and Tovornik, Stefanie and Koparir, Erkan and Dragicevic Babic, Neda and Aboulfazl, Rad and Daniel, Owrang and Kalay, Irem and Chamanrou, Niloofar and Nicolás Martínez, Luis (2026) Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics. Molecular Medicine.
Najafi, Maryam and Riedhammer, Korbinian Maria and Rad, Aboulfazl and Najarzadeh Torbati, Paria and Berutti, Riccardo and Schüle, Isabel and Schroda, Sophie and Meitinger, Thomas and Ćomić, Jasmina and Sadeghi-Bojd, Simin and Baranzehi, Tayebeh and Shojaei, Azadeh and Azarfar, Anoush and Khazaei, Mahmood Reza and Köttgen, Anna and Backofen, Rolf and Ghayoor Karimiani, Ehsan and Hoefele, Julia and Schmidts, Miriam (2022) High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases. Frontiers in Pediatrics.
