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You searched for: Author/Creator Ozretić, David

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1. 106 Diversity of clinical phenotype of patients with pyruvate dehydrogenase deficiency due to PDHA1 gene mutations. (11th October 2021)

2. 123 Kaposiform hemangioendothelioma with Kasabach-Merritt phenomenon in a neonate: Successful treatment with sirolimus. (11th October 2021)

3. 336 Thromboembolic event and it's management in a girl with restrictive cardiomyopathy and implanted Berlin Heart Excor device. (11th October 2021)

4. Early initiation of ambroxol treatment diminishes neurological manifestations of type 3 Gaucher disease: A long-term outcome of two siblings. (May 2021)