Phenotype variability in patients with infantile spinal muscular atrophy: Distal muscle weakness and peripheral neuropathy in compound heterozygotes with SMN1 gene deletions
Barisic, N, Grdjan, P, Lehman, I, Sertic, J, Cvitanovic-Sojat, L.J, Jakovcevic, A, Rudnik-Schöneborn, S
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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Journal Article
74PPromoter hypermethylation of Wnt pathway inhibitor SFRP1 gene and its expression levels in human astrocytomas
Kafka, A, Karin, V, Serman, L, Bukovac, A, Njirić, N, Jakovcevic, A, Pecina-Slaus, N
Published in Annals of oncology (01.03.2018)
Published in Annals of oncology (01.03.2018)
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Journal Article
Promoter hypermethylation of Wnt pathway inhibitor SFRP1 gene and its expression levels in human astrocytomas
Kafka, A., Karin, V., Serman, L., Bukovac, A., Njirić, N., Jakovcevic, A., Pecina-Slaus, N.
Published in Annals of oncology (01.03.2018)
Published in Annals of oncology (01.03.2018)
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Journal Article
Warthin-Like Tumor Variant of Papillary Thyroid Carcinoma: Case Report
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Conference Proceeding
Mesenchymal Chondrosarcoma of the Suboccipital Region: Case Report
Košuta, I, Jakovčević, A, Hutinec, Z, Potočki, K, Rožanković, M
Published in Acta clinica Croatica (30.03.2012)
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Published in Acta clinica Croatica (30.03.2012)
Conference Proceeding
Primary Intracranial Pleomorphic Leiomyosarcoma with Rhabdoid Features: A Case Report
Jakovčević, A., Dotlić, S., Žarković, K., Paladino, J.
Published in Acta clinica Croatica (01.07.2009)
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Published in Acta clinica Croatica (01.07.2009)
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