COMPLEX THERAPY OF CHILDREN WITH MUCOVISCIDOSIS. RECOMMENDATIONS OF A PEDIATRICIAN
Педиатрическая фармакология, 2006 Treatment of children's mucoviscidosis is a multicomponent complex of medical and non medicamental types of therapy. The earlier the basic mucoviscidosis treatment has started, the more favourable the diagnosis for the patient will be.
O.I. Simonova
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Interventions for the eradication of meticillin-resistant Staphylococcus aureus (MRSA) in people with cystic fibrosis [PDF]
, 2015 Background: Cystic fibrosis is an inherited recessive disorder of chloride transport that is characterised by recurrent and persistent pulmonary infections from resistant organisms that result in lung function deterioration and early mortality in ...
Adeboyeku +70 more
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ROLE OF THE KNOWN MUCOLYTICS IN MUCOVISCIDOSIS THERAPY
Педиатрическая фармакология, 2014 The primary objective in the mucoviscidosis therapy is to ensure normal rheology of respiratory secretion for effective evacuationthereof from the bronchial tree and nasal sinuses.
O. I. Simonova, Yu. V. Gorinova
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Making It Last: Storage Time and Temperature Have Differential Impacts on Metabolite Profiles of Airway Samples from Cystic Fibrosis Patients. [PDF]
, 2017 Metabolites of human or microbial origin have the potential to be important biomarkers of the disease state in cystic fibrosis (CF). Clinical sample collection and storage conditions may impact metabolite abundances with clinical relevance.
John J. LiPuma +5 more
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VIRAL INFECTIONS IN CHILDREN SUFFERED FROM CISTIC FIBROSIS
Педиатрическая фармакология, 2011 Results of study of antiviral immunity indicators in patients with mucoviscidosis were presented. A significant antibody deficiency against a number of antigenically unrelated viruses — acute respiratory pathogens and Мycoplasma pneumonia, significantly ...
N.N. Nisevich +5 more
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Severe liver dysfunction in an infant with cystic fibrosis masquerading as metabolic liver disease
Indian Journal of Pathology and Microbiology, 2016 We present a rare presentation of cystic fibrosis with neonatal cholestasis. Histological features of mucoviscidosis were present in liver involving the biliary tract, intestinal mucosa, pancreas, and lung.
K P Srikanth +3 more
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Cystás fibrosisban szenvedő betegek életminőségének felmérése Magyarországon [PDF]
, 2013 Bevezetés: A cystás fibrosis progresszív genetikai betegség, amely korlátozhatja a betegek mindennapi életét, befolyásolja életminőségüket. Célkitűzés: A szerzők célul tűzték ki a hazai cystás fibrosisban szenvedő betegek életminőségének felmérését ...
Bodnár, Réka +9 more
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Histopathological effects of Doxorubicin on pancreas in male Albino rats [PDF]
Iraqi Journal of Veterinary Sciences, 2015 The aim of this study was to investigate the histopathological side effects of doxorubicin on pancreas tissue in male albino rats Rattus norvegicus. This study were used 55 adult rats (2.5-3.5) month of age.
I.A. Ali, H.J. Jumaa, H.Kh. Ismael
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Jornal de Pediatria, 2001 OBJETIVO: avaliar a freqüência de diabetes mellitus (DM) e de intolerância à glicose nos pacientes com fibrose cística seguidos no Serviço de Gastropediatria do HC-FMRP-USP.
Flávia A.A. de Castro +3 more
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A Multicenter Screening Study [PDF]
, 2014 Background In cystic fibrosis, highly variable glucose tolerance is suspected. However, no study provided within-patient coefficients of variation.
Ballmann, Manfred +6 more
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