Browsing by Author Contopoulos-Ioannidis, D.

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Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IREPapanikolaou, G.; Chandrinou, H.; Bouzas, E.; Contopoulos-Ioannidis, D.; Kalotychou, V.; Prentzas, K.; Lilakos, K.; Asproudis, I.; Palaiologou, D.; Premetis, E.; Papassotiriou, I.; Sakellaropoulos, N.24-Nov-2015-
Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiencyContopoulos-Ioannidis, D.; Evangeliou, A.; ter Laak, H.; de Vries, B.; Pfundt, R.; Scheffer, H.; Smeitink, J.; Tzoufi, M.; Makis, A.; Marinos, E.; Hess, R.; Adams, D.; Huizing, M.; Morava, E.24-Nov-2015-