Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Maria Bitsori"'
Autor:
Ioannis Petrakis, Maria Sfakiotaki, Maria Bitsori, Eleni Drosataki, Kleio Dermitzaki, Christos Pleros, Ariadni Androvitsanea, Dimitrios Samonakis, Amalia Sertedaki, Paraskevi Xekouki, Emmanouil Galanakis, Kostas Stylianou
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 8, p 4552 (2024)
The evolving landscape of clinical genetics is becoming increasingly relevant in the field of nephrology. HNF1B-associated renal disease presents with a diverse array of renal and extrarenal manifestations, prominently featuring cystic kidney disease
Externí odkaz:
https://doaj.org/article/d8d26d6eb61a44848ecb0edd182d9fd2
Publikováno v:
Journal of Pediatric Urology. 19:6-18
Publikováno v:
Am J Trop Med Hyg
Acute Q fever is usually asymptomatic or is associated with a mild self-limited course and a favorable outcome. The occurrence of endocarditis during acute infection by Coxiella burnetii is an emerging clinical entity observed in adults that has been
Publikováno v:
Acta Paediatrica. 109:1260-1266
AIM We investigated the impact of any antibiotic exposure on unusual and resistant pathogens in children with a urinary tract infection (UTI). METHODS This was a retrospective cohort study of 695 children (54% female) hospitalised with 711 UTI episod
Publikováno v:
J Pediatr Genet
Dent disease is a rare X-linked renal proximal tubulopathy presenting with low-molecular-weight proteinuria (LMWP), hypercalciuria, and nephrocalcinosis, other signs of incomplete renal Fanconi syndrome, and renal failure. Early identification of pat
Autor:
Smaragdi Marinaki, Constantinos J. Stefanidis, Andromach Mitsioni, Hara Gakiopoulou, Maria Bitsori, Vasiliki Karava, Argyroula Zampetoglou, Sofia Havaki
Publikováno v:
Pediatric Transplantation. 24
Glomerular crescents in kidney transplantation are indicative of severe glomerular injury and constitute a hallmark of RPGN. Their concurrence with ABMR has been rarely described only in adult patients. We report a case of 10-year-old boy with compou
Autor:
Maria Bitsori, Emmanouil Galanakis
Publikováno v:
The Pediatric infectious disease journal. 38(12)
Publikováno v:
CEN Case Reports. 7:153-157
Cystinosis is a rare autosomal recessive lysosomal transport disorder, characterized by the accumulation of the aminoacid cystine and progressive dysfunction of several organs. Kidneys are severely affected, and the most frequent form, infantile neph
Autor:
Maria Bitsori, Emmanouil Galanakis
Publikováno v:
The Pediatric infectious disease journal. 38(6S Suppl 1)
Rickettsiae are globally encountered pathogens with foci of endemicity and epidemic exacerbations under circumstances of crowding and decline of sanitation. Diagnosis is often missed due to misconceptions about epidemiology, confusing terminology and
Autor:
Emmanouil Galanakis, Maria Bitsori, Eleni Vergadi, Maria Raissaki, Alexander D. Karatzanis, S. Velegrakis
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 141:110508
Diagnosis and management of complicated mastoiditis in childhood are still controversial. We investigated the clinical manifestations, evaluation and management of children with mastoiditis complicated with cerebral venous sinus thrombosis.Retrospect