Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Vasiliki Dermentzoglou"'
Autor:
Maria Antonietta D'Agostino, Esperanza Naredo, Alice Leahy, Hans de Graaf, Rosa Bou, Estibaliz Iglesias, Consuelo Modesto, Karin Palmblad, Giorgia Martini, Séverine Guillaume, Troels Herlin, Dragana Lazarevic, Clara Malattia, Lampros Fotis, Marite Rygg, Denise Pires Marafon, Giovanni Filocamo, Silvia Magni-Manzoni, Sorina Boiu, Nikolay Tzaribachev, Jelena Vojinovic, Lucia Campos, Valentina Muratore, Stefano Lanni, Miroslav Harjacek, Ellen Nordal, Mandica Vidović, Angela Aquilani, Francesca Ardenti Morini, Ellen Dalen Arnstad, Stefan Blazina, Vasiliki Dermentzoglou, Gry Børmark Hoftun, Christian Høst, Emilio Inarejos, Hanan Jadoun, Damjana Ključevšek, Manuela Krumrey, Rolf-Michael Küster, Hartwig Lehmann, Mirea Lopez Corbeto, Anette Lundestad, Marta Mazzoni, Rebecca Nicolai, Soley Omarsdottir, Linda Rossi Semerano, Nina Sande, Betul Sozeri, Giusyda Tarantino, Samar Tharwat, Ralph Trauzeddel, Maria Tsinti, Andrea Uva, Philomine Van Pelt, Marion Van Rossum, Annette von-Scheven-Gete, Daniel Windschall
Publikováno v:
RMD Open, Vol 8, Iss 2 (2022)
Background Despite the worldwide increasing request of education on paediatric musculoskeletal ultrasound (PedMSUS), content, conduct and format of PedMSUS courses have never been internationally agreed.Objectives To produce educational procedures fo
Externí odkaz:
https://doaj.org/article/463bf5e197c342f0a67f5a0aec7bf3be
Publikováno v:
Case Reports in Rheumatology, Vol 2011 (2011)
We report a case of a 13-year-old girl with chronic recurrent multifocal osteomyelitis (CRMO) who developed severe arthritis in four different joints within the first year from the onset of the disease. Her multiple vertebrae lesions showed significa
Externí odkaz:
https://doaj.org/article/70ec03a5b28f4a708ac491f6737372e6
Autor:
Tania Siahanidou, Irini Nikaina, Christina Kanaka-Gantenbein, Vasiliki Dermentzoglou, Margarita Pesmatzoglou, Antonis Voutetakis, Anna-Venetia Skiathitou
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 32:70-73
Background A rare disorder of sex development is 45,X/46,XY mosaicism, which is phenotypically very heterogenous, ranging from normal male (or female) to that of genital ambiguity of varying degrees. Case We report a case of a neonate with 45,X/46,XY
Autor:
Vasiliki Dermentzoglou, Christina Kanaka-Gantenbein, Athanasia Stelianidi, Elissavet Georgiadou, John Anastasopoulos, Artemis Doulgeraki, Lilia Lykopoulou
Publikováno v:
Bone Abstracts.
Autor:
Tania Siahanidou, Christina Giannakopoulou, Anna-Venetia Skiathitou, Alexandra Gkourogianni, Euthymia Tsina, Vasiliki Dermentzoglou
Publikováno v:
Clinical Dysmorphology. 25:41-43
Publikováno v:
Poster Presentations.
Background Musculoskeletal (MS) involvement and clinically evident arthritis occurs in up to 65% of patients with Juvenile Systemic or localized Scleroderma (JSc). It may be the first manifestation preceding even the onset of Raynaud or skin manifest
Publikováno v:
Pediatric radiology. 45(11)
Little attention has been given to the sonographic appearances of the epididymis in testicular torsion. To describe the position and morphology of the epididymis in childhood acute testicular torsion when testicular flow is present on color Doppler s
Publikováno v:
Case Reports in Rheumatology, Vol 2011 (2011)
Case Reports in Rheumatology
Case Reports in Rheumatology
We report a case of a 13-year-old girl with chronic recurrent multifocal osteomyelitis (CRMO) who developed severe arthritis in four different joints within the first year from the onset of the disease. Her multiple vertebrae lesions showed significa
Publikováno v:
Journal of child neurology. 23(1)
Hypoxic-ischemic brain injury is a very important neurological problem of the perinatal period and a major cause of chronic disability later in childhood. The subsequent neurological deficits are a variety of motor defects—especially spasticity but
Publikováno v:
Pediatric Rheumatology Online Journal
NOMID/CINCA is the most severe phenotype of cryopyrin-associated periodic syndrome (CAPS), characterized by persistence of inflammation-mediated symptoms and overproduction of interleukin (IL)-1β, associated with significant morbidity, if untreated.