Do pulmonary and extrapulmonary features differ among cystic fibrosis, primary ciliary dyskinesia, and healthy children?

Denizoglu Kulli, Hilal; Gurses, Hulya Nilgun; Zeren, Melih; Ucgun, Hikmet; Cakir, Erkan

Denizoglu Kulli, Hilal; Gurses, Hulya Nilgun; Zeren, Melih; Ucgun, Hikmet; Cakir, Erkan.

Afiliação

Denizoglu Kulli H; Department of Cardiopulmonary Physiotherapy and Rehabilitation, Division of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bezmialem Vakif University, Istanbul, Turkey.
Gurses HN; Department of Cardiopulmonary Physiotherapy and Rehabilitation, Division of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bezmialem Vakif University, Istanbul, Turkey.
Zeren M; Division of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Izmir Bakircay University, Izmir, Turkey.
Ucgun H; Department of Cardiopulmonary Physiotherapy and Rehabilitation, Division of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bezmialem Vakif University, Istanbul, Turkey.
Cakir E; Division of Pediatric Pulmonology, Faculty of Medicine, Bezmialem University, Istanbul, Turkey.

Pediatr Pulmonol ; 55(11): 3067-3073, 2020 11.

Article em En | MEDLINE | ID: mdl-32877003

Assuntos

Transtornos da Motilidade Ciliar/fisiopatologia; Fibrose Cística/fisiopatologia; Adolescente; Criança; Feminino; Humanos; Pulmão/fisiopatologia; Masculino; Força Muscular/fisiologia; Músculo Esquelético/fisiopatologia; Testes de Função Respiratória

Palavras-chave

cystic fibrosis; functional capacity; lung function; muscle strength; primary ciliary dyskinesia; respiratory muscle strength

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Motilidade Ciliar / Fibrose Cística Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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