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Argirios Dinopoulos
Researcher at National and Kapodistrian University of Athens
Publications - 30
Citations - 360
Argirios Dinopoulos is an academic researcher from National and Kapodistrian University of Athens. The author has contributed to research in topics: Epilepsy & Levetiracetam. The author has an hindex of 7, co-authored 30 publications receiving 260 citations.
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Journal ArticleDOI
Genetic spectrum of hereditary neuropathies with onset in the first year of life
Jonathan Baets,Tine Deconinck,Els De Vriendt,Magdalena Zimoń,Laetitia Yperzeele,Kim Van Hoorenbeeck,K. Peeters,Ronen Spiegel,Yesim Parman,Berten Ceulemans,Patrick Van Bogaert,A. Pou-Serradell,Günther Bernert,Argirios Dinopoulos,Michaela Auer-Grumbach,Satu-Leena Sallinen,Gian Maria Fabrizi,Fernand Pauly,Peter Van den Bergh,Birdal Bilir,Esra Battaloglu,Ricardo E. Madrid,Dagmara Kabzińska,Andrzej Kochański,Haluk Topaloglu,Geoffrey P. Miller,Albena Jordanova,Vincent Timmerman,Peter De Jonghe +28 more
TL;DR: The genetic heterogeneity underlying hereditary neuropathies with infantile onset is illustrated by a heterogeneous cohort of 77 unrelated patients who presented with symptoms of peripheral neuropathy within the first year of life.
Journal ArticleDOI
De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy
Inès Mademan,Tine Deconinck,Argirios Dinopoulos,Thomas Voit,Ulrike Schara,Koenraad Devriendt,Björn Meijers,Evelyne Lerut,Peter De Jonghe,Jonathan Baets +9 more
TL;DR: This study confirms that INF2 mutations are a major cause of disease in patients with CMT disease and early signs of nephropathy and identifies 3 novel mutations that likely affect the protein structure and function.
Journal ArticleDOI
Postherpes simplex encephalitis: a case series of viral-triggered autoimmunity, synaptic autoantibodies and response to therapy.
Harry Alexopoulos,Sofia Akrivou,Sotiria Mastroyanni,Maria Antonopoulou,Argirios Dinopoulos,Melpo Giorgi,Kostas Konstantinou,Evangelos Kouremenos,Maria Lariou,Dimitrios Naoumis,Efterpi Pavlidou,Evaggelos Pavlou,Konstantinos A. Voudris,P.G. Vlachoyiannopoulos,Marinos C. Dalakas +14 more
TL;DR: A case series of post-HSV relapsing encephalopathy associated with antibodies to central nervous system (CNS) synaptic antigens and the infants had an incomplete recovery with severe psychomotor deficits probably due to the interference of anti-NMDAR antibodies with neuro-developmental processes.
Journal ArticleDOI
A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings
Alexandros A Polymeris,Alessandra Tessa,Katherine Anagnostopoulou,Anna Rubegni,Daniele Galatolo,Argirios Dinopoulos,Artemis Gika,Sotiris Youroukos,Eleni Skouteli,Filippo M. Santorelli,Roser Pons +10 more
TL;DR: The data confirm the genetic heterogeneity of childhood-onset pure HSP, with SPG4/SPAST and SPG3A/ATL1 being the most frequent forms.
Journal ArticleDOI
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C
Félixe Pelletier,Stefanie Perrier,Stefanie Perrier,Ferdy K. Cayami,Ferdy K. Cayami,Amytice Mirchi,Stephan Saikali,Luan T. Tran,Nicole Ulrick,Kether Guerrero,Emmanouil Rampakakis,Rosalina M. L. van Spaendonk,Sakkubai Naidu,Daniela Pohl,William T. Gibson,Michelle Demos,Cyril Goizet,Ingrid Tejera-Martin,Ana Potic,Brent L. Fogel,Bernard Brais,Bernard Brais,Michel Sylvain,Guillaume Sébire,Guillaume Sébire,Charles Marques Lourenço,Joshua L. Bonkowsky,Coriene E. Catsman-Berrevoets,Pedro S Pinto,Sandya Tirupathi,Petter Strømme,Ton J. de Grauw,Dorota Gieruszczak-Białek,Ingeborg Krägeloh-Mann,Hanna Mierzewska,Heike Philippi,Julia Rankin,Tahir Atik,Brenda Banwell,William S. Benko,A. Blaschek,Annette Bley,Eugen Boltshauser,Drago Bratkovic,Klara Brozova,Icíar Cimas,Christopher Clough,Bernard Corenblum,Argirios Dinopoulos,Gail Dolan,Flavio Faletra,Raymond Fernandez,Janice M. Fletcher,Maria Eugenia Garcia Garcia,Paolo Gasparini,Janina Gburek-Augustat,Dolores Gonzalez Moron,Aline Hamati,Inga Harting,Christoph Hertzberg,Alan Hill,Grace M. Hobson,A. Micheil Innes,Marcelo Andrés Kauffman,Susan M. Kirwin,Gerhard Kluger,Petra Kolditz,Urania Kotzaeridou,Roberta La Piana,Eriskay Liston,William McClintock,Meriel McEntagart,Fiona Haslam McKenzie,Serge Melançon,Anjum Misbahuddin,Mohnish Suri,Fernando I Monton,Sebastien Moutton,Raymond P J Murphy,Miriam Nickel,Hüseyin Onay,Simona Orcesi,Ferda Ozkinay,Steffi Patzer,Helio Pedro,Sandra Pekic,Mercedes Pineda Marfa,Amy Pizzino,Barbara Plecko,Bwee Tien Poll-The,Vera Popovic,Dietz Rating,Marie-France Rioux,Norberto Rodriguez Espinosa,Anne Ronan,John R. Østergaard,Elsa Rossignol,Rocío Sánchez-Carpintero,Anna Schossig,Nesrin Senbil,Laura Roos,Cathy A. Stevens,Matthis Synofzik,László Sztriha,Daniel Tibussek,Dagmar Timmann,Davide Tonduti,Bart P.C. van de Warrenburg,Maria Vázquez-López,Sunita Venkateswaran,Pontus Wasling,Evangeline Wassmer,Richard Webster,Gert Wiegand,Grace Yoon,Joost Rotteveel,Raphael Schiffmann,Marjo S. van der Knaap,Adeline Vanderver,Adeline Vanderver,Gabriel Á. Martos-Moreno,Gabriel Á. Martos-Moreno,Constantin Polychronakos,Nicole I. Wolf,Geneviève Bernard +124 more
TL;DR: Pubertal abnormalities and short stature are the most common endocrine features seen in 4H leukodystrophy, and it is noted that endocrine abnormalities are typically underinvestigated in this patient population.