Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Diagoras Zarganis"'
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
We present a case of a seven-year-old immunocompetent female patient who developed systemic symptoms mimicking an autoimmune rather than an infectious disease. The patient presented with rash, biquotidian fever, night sweats, and arthralgias. There w
Externí odkaz:
https://doaj.org/article/4441032e7cc4474aaa6398c985936dc8
Autor:
Andreas Mentis, Nikolaos Bodozoglou, Diagoras Zarganis, Giorgos Vartzelis, Elina Horefti, Ioannis Drikos, Evagelia Triantafylou, Minas Kapetanakis, Maria Tsolia, Garyfallia Syridou
Publikováno v:
The Pediatric infectious disease journal. 39(2)
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a recently described entity so far exclusively in East Asian children. AESD diagnosis is based on clinicoradiologic criteria, often without pleocytic CSF and characteriz
Autor:
Diagoras Zarganis, Christina Bothou, Maria Karantza, Anastasios Papadimitriou, Dimitrios T Papadimitriou
Publikováno v:
Hormones (Athens, Greece). 17(3)
The first and rate-limited step of steroidogenesis in all steroidogenic tissues is the conversion of cholesterol to pregnenolone, catalysed by P450scc side-chain cleavage enzyme (CYP11A1 gene—SCC). SCC deficiency has been characterised as an autoso
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2013 (2013)
Case Reports in Pediatrics, Vol 2013 (2013)
We present a case of a seven-year-old immunocompetent female patient who developed systemic symptoms mimicking an autoimmune rather than an infectious disease. The patient presented with rash, biquotidian fever, night sweats, and arthralgias. There w
Autor:
Georgia Papaioannou, Aglaia Zellos, Dimitris Chatzis, Diagoras Zarganis, Christos Bartsocas, Stelios Ypsiladis
Publikováno v:
Pediatrics. 129:e515-e518
Protein-losing enteropathy in children is caused by intestinal metabolic, inflammatory, or infectious processes, or by lymphatic obstruction (intestinal lymphangiectasia). In this report, a 17-month-old child is presented with protein-losing enteropa
Publikováno v:
Annals of the Rheumatic Diseases. 71:702.13-702
Background Although previously considered a rare cause of pyrexia of unknown origin(PUO), with the aid of new diagnostic tools the clinical spectrum of bartonella henselae infection has expanded[1]. Methods We present a case of a seven year old immun