Gene therapy for spinal muscular atrophy: Solomon's consensus in Covid times

por Zafeiriou, Dimitrios
Publicado 2020

Benign epilepsy with centrotemporal spikes: Relationship between type of seizures and response to medication in a Greek population

por Gkampeta, Anastasia, Fidani, Liana, Zafeiriou, Dimitrios, Pavlou, Evangelos
Publicado 2015

Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth

por VERVERI, Athina, VARGIAMI, Euthymia, PAPADOPOULOU, Vassiliki, TRYFONAS, Dimitrios, ZAFEIRIOU, Dimitrios
Publicado 2015

Response to “Leigh-like syndrome with mild mtDNA depletion due to the SUCLG1 variant c.626C>A”

por Chinopoulos, Christos, Wevers, Ron A., Waterham, Hans R., Zafeiriou, Dimitrios
Publicado 2018

Premonitory Urges and Their Link With Tic Severity in Children and Adolescents With Tic Disorders

por Kyriazi, Maria, Kalyva, Efrosini, Vargiami, Efthymia, Krikonis, Konstantinos, Zafeiriou, Dimitrios
Publicado 2019

Clinical course and seizure outcome of idiopathic childhood epilepsy: determinants of early and long-term prognosis

por Dragoumi, Pinelopi, Tzetzi, Olga, Vargiami, Efthimia, Pavlou, Evangelos, Krikonis, Konstantinos, Kontopoulos, Eleftherios, Zafeiriou, Dimitrios I
Publicado 2013

Moyamoya syndrome and neurofibromatosis type 1

por Vargiami, Euthymia, Sapountzi, Evdoxia, Samakovitis, Dimitris, Batzios, Spyros, Kyriazi, Maria, Anastasiou, Athanasia, Zafeiriou, Dimitrios I
Publicado 2014

Arterial Stiffness in a Toddler with Neurofibromatosis Type 1 and Refractory Hypertension

por Stabouli, Stella, Vargiami, Euthymia, Maliachova, Olga, Printza, Nikoleta, Dotis, John, Kyriazi, Maria, Papazoglou, Konstantinos O., Zafeiriou, Dimitrios
Publicado 2018

Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome

por Vargiami, Euthymia, Ververi, Athina, Al-Mutawa, Hamda, Gioula, Georgia, Gerou, Spyridon, Rouvalis, Fotios, Kambouris, Marios, Zafeiriou, Dimitrios I.
Publicado 2016

Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in TK2 gene

por Papadimas, George K., Vargiami, Efthimia, Dragoumi, Pinelopi, Van Coster, Rudy, Smet, Joel, Seneca, Sara, Papadopoulos, Constantinos, Kararizou, Evangelia, Zafeiriou, Dimitrios
Publicado 2020

Matrix metalloproteinase −2, −9 and arterial stiffness in children and adolescents: The role of chronic kidney disease, diabetes, and hypertension

por Stabouli, Stella, Kotsis, Vasilios, Maliachova, Olga, Printza, Nikoleta, Chainoglou, Athanasia, Christoforidis, Athanasios, Taparkou, Anna, Dotis, John, Farmaki, Evangelia, Zafeiriou, Dimitrios
Publicado 2020

Hemolytic Uremic Syndrome Due to Methylmalonic Acidemia and Homocystinuria in an Infant: A Case Report and Literature Review

por Karava, Vasiliki, Kondou, Antonia, Dotis, John, Sotiriou, Georgia, Gerou, Spyridon, Michelakakis, Helen, Vargiami, Euthymia, Economou, Marina, Zafeiriou, Dimitrios, Printza, Nikoleta
Publicado 2021

Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countries

por Magner, Martin, Almássy, Zsuzsanna, Gucev, Zoran, Kieć-Wilk, Beata, Plaiasu, Vasilica, Tylki-Szymańska, Anna, Zafeiriou, Dimitrios, Zaganas, Ioannis, Lampe, Christina
Publicado 2022

Blood pressure in children with sickle cell disease is higher than in the general pediatric population

por Kupferman, Juan C., Rosenbaum, Janet E., Lande, Marc B., Stabouli, Stella, Wang, Yongsheng, Forman, Daniella, Zafeiriou, Dimitrios I., Pavlakis, Steven G.
Publicado 2022

The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers

por Tylki-Szymańska, Anna, Almássy, Zsuzsanna, Christophidou-Anastasiadou, Violetta, Avdjieva-Tzavella, Daniela, Barisic, Ingeborg, Cerkauskiene, Rimante, Cuturilo, Goran, Djiordjevic, Maja, Gucev, Zoran, Hlavata, Anna, Kieć-Wilk, Beata, Magner, Martin, Pecin, Ivan, Plaiasu, Vasilica, Samardzic, Mira, Zafeiriou, Dimitrios, Zaganas, Ioannis, Lampe, Christina
Publicado 2022

Identification of Complement-Related Missense Variants in Pediatric Patients with Acute and Post COVID-19 Syndromes

por Gavriilaki, Eleni, Touloumenidou, Tasoula, Tsiftsoglou, Stefanos, Tragiannidis, Athanasios, Farmaki, Evangelia, Panagopoulou, Paraskevi, Michailidou, Elisavet, Koravou, Evdoxia, Koutra, Maria, Iosifidis, Ilias, Papadimitriou, Eleni, Papadopoulou-Alataki, Efimia, Papayanni, Penelope Georgia, Varelas, Christos, Papalexandri, Apostolia, Evangeliou, Athanasios, Galli-Tsinopoulou, Assimina, Zafeiriou, Dimitrios, Roilides, Emmanuel, Sakellari, Ioanna, Anagnostopoulos, Achilles
Publicado 2021

Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection

por Gavriilaki, Eleni, Tsiftsoglou, Stefanos A., Touloumenidou, Tasoula, Farmaki, Evangelia, Panagopoulou, Paraskevi, Michailidou, Elissavet, Koravou, Evaggelia-Evdoxia, Mavrikou, Ioulia, Iosifidis, Elias, Tsiatsiou, Olga, Papadimitriou, Eleni, Papadopoulou-Alataki, Efimia, Papayanni, Penelope Georgia, Varelas, Christos, Kokkoris, Styliani, Papalexandri, Apostolia, Fotoulaki, Maria, Galli-Tsinopoulou, Assimina, Zafeiriou, Dimitrios, Roilides, Emmanuel, Sakellari, Ioanna, Anagnostopoulos, Achilles, Tragiannidis, Athanasios
Publicado 2022

Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines

por Kuseyri Hübschmann, Oya, Horvath, Gabriella, Cortès-Saladelafont, Elisenda, Yıldız, Yılmaz, Mastrangelo, Mario, Pons, Roser, Friedman, Jennifer, Mercimek-Andrews, Saadet, Wong, Suet-Na, Pearson, Toni S., Zafeiriou, Dimitrios I., Kulhánek, Jan, Kurian, Manju A., López-Laso, Eduardo, Oppebøen, Mari, Kılavuz, Sebile, Wassenberg, Tessa, Goez, Helly, Scholl-Bürgi, Sabine, Porta, Francesco, Honzík, Tomáš, Santer, René, Burlina, Alberto, Sivri, H. Serap, Leuzzi, Vincenzo, Hoffmann, Georg F., Jeltsch, Kathrin, Hübschmann, Daniel, Garbade, Sven F., García-Cazorla, Angeles, Opladen, Thomas
Publicado 2021