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期刊名:Pediatric reports

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ISSN:2036-7503

e-ISSN:2036-7503

IF/分区:1.9/Q2

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共收录本刊相关文章索引93条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Philip A Bernard,Hubert Ballard,Douglas Schneider Philip A Bernard
Sedation for pediatric cardiac catheterization is a common requirement in many institutions. As the field of cardiac catheterization has evolved, the provision of sedation for these procedures has been varied. Increasingly the demand is for...
Katerina Kambouri,Stefanos Gardikis,Alexandra Giatromanolaki et al. Katerina Kambouri et al.
Primary omental infarction (POI) has a low incidence worldwide, with most cases occurring in adults. This condition is rarely considered in the differential diagnosis of acute abdominal pain in childhood. Herein, we present a case of omenta...
Paula Catarino Costa,Celeste Canha Barreto,Luisa Pereira et al. Paula Catarino Costa et al.
Prospective studies concerning liver disease in pediatric cystic fibrosis patients are scarce. The present study aimed to describe the prevalence and clinical expression of cystic fibrosis - related liver disease, in a cohort of 62 pediatri...
Kuniko Takanashi,Yashuto Suzuki,Ayumu Noro et al. Kuniko Takanashi et al.
The clinical phenotype of congenital pituitary hormone deficiency is variable and can be associated with a number of structural abnormalities of the central nervous system. We report three Japanese patients with congenital pituitary hormone...
Ali Ertug Arslankoylu,Meryem Ozlem Kutuk,Cetin Okuyaz et al. Ali Ertug Arslankoylu et al.
Neuroleptic malignant syndrome (NMS) is a rare but potentially fatal disease characterized by fever, muscle rigidity, delirium and autonomic instability. Here we report a child, with NMS due to the risperidone misdiagnosed as status epilept...
Simone Cesaro,Marta Pillon,Elisabetta Calore et al. Simone Cesaro et al.
An 8-year old boy, affected by severe aplastic anemia, developed a probable pulmonary invasive aspergillosis (IA) early after a second unrelated allogeneic hematopoietic stem cell transplant (HSCT). He was treated promptly with the combinat...
Antonio Cao,Paolo Moi,Renzo Galanello Antonio Cao
β-thalassemias are heterogeneous hereditary anemias characterized by a reduced output of β-globin chains. The disease is most frequent in the temperate regions of the world, where it represents an important health problem. In the last dec...
Peter R Donald Peter R Donald
Recent increases in the dosages of the essential antituberculosis agents isoniazid (INH), rifampicin (RMP), pyrazinamide (PZA) for use in children recommended by World Health Organization have raised concerns regarding the risk of hepatotox...
Piero Farruggia,Alessandra Macaluso,Serena Tropia et al. Piero Farruggia et al.
Evans Syndrome is a rare autoimmune disease consisting of hemolytic anemia, thrombocytopenia and/or neutropenia. It may be associated with other autoimmune or lymphoproliferative diseases. Its course can be extremely serious and, rarely, ev...
Cheryl Anne Mackay,Daynia Elizabeth Ballot,Olga Perovic Cheryl Anne Mackay
Invasive fungal disease is a significant cause of morbidity and mortality in the neonate. The current study aims to assess the 1, 3-βD-Glucan (BG) assay in a prospective analysis in neonates with suspected fungaemia. A multicentre, prospec...