A new COL1A1 mutation in a Greek patient with osteogenesis imperfecta: Response to a low-dose protocol of zoledronic acid and two-year follow-up
Sarantis, Michail, Kollia, Panagoula, Samara, Stavroula, Athanasopoulou, Helen, Gyftodimou, Yolanda, Lianou, Dimitra, Mpourazani, Evdoxia, Doulgeraki, Artemis
Published in Journal of research and practice on the musculoskeletal system (01.09.2018)
Published in Journal of research and practice on the musculoskeletal system (01.09.2018)
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Journal Article
Functional analysis of a novel mutation in the PCCA gene identified in a late-infantile onset propionic acidemia patient
Lianou, Dimitra, Gallego, Lorena, Michelakakis, Helen, Pérez-Cerdá, Celia, Pérez, Belén, Ginis, Stavroula, Jakobs, Cornelis, Ugarte, Magdalena, Desviat, Lourdes R.
Published in Clinica chimica acta (06.09.2010)
Published in Clinica chimica acta (06.09.2010)
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Journal Article
An interesting case of primary autoimmune neutropenia
Doulgeraki, Artemis, Kotsonis, Kosmas, Lianou, Dimitra, Cassiou, Korina
Published in Clinical pediatrics (01.04.2007)
Published in Clinical pediatrics (01.04.2007)
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Journal Article
Neurologic maturation in early treated children with congenital hypothyroidism
Makaronis, G., Lianou, Dimitra, Mengreli, Chrysanthy, Pantelakis, S.
Published in Pediatric neurology (01.09.1992)
Published in Pediatric neurology (01.09.1992)
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Journal Article
Functional analysis of a novel mutation in the PCCA gene identified in a late-infantile onset propionic acidemia patient
Lianou, Dimitra, Gallego, Lorena, Michelakakis, Helen, Pérez-Cerdá, Celia, Pérez, Belén, Ginis, Stavroula, Jakobs, Cornelis, Ugarte, Magdalena, Desviat, Lourdes R
Published in Clinica chimica acta; international journal of clinical chemistry (06.09.2010)
Published in Clinica chimica acta; international journal of clinical chemistry (06.09.2010)
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