Results 81 to 90 of about 1,065 (178)

Enfermedad fibroquística del páncreas en el recién nacido

, 2009
Objective: To present cases with pancreatic cystic fibrosis (mucoviscidosis) identified in neonatal necropsies and to verify its identification clinical profile. Design: Histologic descriptive, retrospective study with analytical component.
Pereda Garay, José
core  

Mind-body and art therapies impact on emotional regulation in patients with chronic diseases: a pragmatic mixed-methods randomized controlled trial. [PDF]

BMC Complement Med Ther, 2023
Le Rhun A, Caillet P, Lebeaupin M, Duval M, Guilmault L, Anthoine E, Borghi G, Leclère B, Moret L.   +8 more
europepmc   +1 more source

The International Week of Surfactant Research: Increasing knowledge about surfactant and unexploited opportunities. [PDF]

Biomed J, 2021
De Luca D, Touqui L.
europepmc   +1 more source

Psychological outcomes and support in grandparents whose grandchildren suffer from a severe physical illness: A systematic review. [PDF]

Heliyon, 2022
Priboi C, Gantner B, Holmer P, Neves da Silva L, Tinner EM, Roser K, Michel G.   +6 more
europepmc   +1 more source

囊性纤维化伴反应性关节炎的诊断经验

Zhongguo shiyan zhenduanxue, 1997
囊性纤维化伴反应性关节炎的诊断经验王振刚高明曾昭耆作者单位：１００７３０北京医院囊性纤维化（ＣｙｓｔｉｃＦｉｂｒｏｓｉｓ）又称粘液粘稠病（Ｍｕｃｏｖｉｓｃｉｄｏｓｉｓ），是一种累及全身分泌粘液的器官和汗腺的常染色体隐性遗传性疾病，主要影响胰腺、消化道...
doaj  

Prevalência da mutação ΔF508 no gene cystic fibrosis transmembrane conductance regulator em pacientes com fibrose cística em um centro de referência no Brasil Prevalence of ΔF508 mutation in the cystic fibrosis transmembrane conductance regulator gene among cystic fibrosis patients from a Brazilian referral center

Jornal de Pediatria, 2012
OBJETIVO: Verificar a presença da mutação ΔF508 no gene cystic fibrosis transmembrane conductance regulator na população de pacientes com fibrose cística, diagnosticados pelo teste de sódio e cloro no suor, em acompanhamento no Ambulatório de ...
Andréia Marisa Bieger, Fernando Augusto de Lima Marson, Carmen Sílvia Bertuzzo   +2 more
doaj  

ВИРУСНЫЕ ИНФЕКЦИИ У ДЕТЕЙ С МУКОВИСЦИДОЗОМ

, 2015
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 ...
Н.С. Селютина, N.N. Nisevich, E.V. Sereda, I.N. Nikishtsev, N.S. Selyutina, Л.Л. Нисевич, O.V. Kriger, N.L. Agoshkova, Е.В. Середа, Н.Л. Агошкова, О.В. Кригер, И.Н. Никишцев   +11 more
core  

Edemas of the face and lymphoscintigraphic examination. [PDF]

Sci Rep, 2021
Bourgeois P, Peters E, Van Mieghem A, Vrancken A, Giacalone G, Zeltzer A.   +5 more
europepmc   +1 more source

Fibrose cística no adulto: aspectos diagnósticos e terapêuticos Cystic fibrosis in adults: diagnostic and therapeutic aspects

Jornal Brasileiro de Pneumologia, 2008
A fibrose cística, que já foi considerada uma doença da infância, é agora também uma doença do adulto. O aumento da longevidade resultou em mais problemas médicos relacionados com a idade e com a própria doença.
Paulo de Tarso Roth Dalcin, Fernando Antônio de Abreu e Silva   +1 more
doaj  

Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and Pneumonia. [PDF]

Antibiotics (Basel), 2023
Bär A, Schmitt-Grohé S, Held J, Lubig J, Hanslik G, Fahlbusch FB, Reutter H, Woelfle J, van der Donk A, Schleier M, Hepp T, Morhart P.   +11 more
europepmc   +1 more source