Sialidosis type 1 in a Turkish family: a case report and review of literatures Mustafa Kılıç, Suzan İcil, Abdullah Sezer, Öznur Kaya-Güneş, Selim S. Comoğlu Journal of Pediatric Endocrinology and Metabolism.2025; 38(2): 176. CrossRef
Novel Pathogenic Variant in the NEU1 Gene in a Patient With Sialidosis With Progressive Myoclonus Ataxia With Cherry-Red Spot Lulup K. Sahoo, Vidyasagar Kota, Pradeep K. Panigrahi, Srimant Pattnaik, Ajit P. Mishra, Srikanta K. Sahoo Neurology.2023; 101(19): 861. CrossRef