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Autor:
Kuloglu, Z, Kansu, A, Selbuz, S, Kalayci, AG, Sahin, G, Kirsaclioglu, CT, Demiroren, K, Dalgic, B, Kasirga, E, Onal, Z, Islek, A, Eren, E, Hosnut, FO, Urganci, N, Yaman, A, Ozkan, T, Bozbulut, E, Dogan, G, Eksi Bozbulut, N, Durmaz Ugurcan, O, Usta, AM, Arslan, D, Akcam, M, Isik, IA, Ecevit, CO, Usta, Y, Ozgur, T, Ozcay, F, Balamtekin, N, Ozturk, Y, Cantez, S, Gulerman, F, Ustundag, GH, Emiroglu, HH, Karacabey, N, Comba, A, Erdemir, G, Aydogan, AU, Gokce, S, Kuyum, P, Gulsan, M, Tosun, MS, Tokgoz, Y, Guven, B, Yuksekkaya, H, Tumgor, G, Eren, M, Baran, M, Gumus, M, Canan, O, Kocamaz, H, Gerenli, N, Cakir, M, Agin, M, Hizli, S, Dogan, Y, Celtik, C, Deveci, U, Balci Sezer, O
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed because symptoms may be nonspecific. We aimed to investigate the prevalence of LAL-D in children with unexplained liver disease and to identify demogr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::dfc07becf6405b576c231a7fde2cbfdd