Results 101 to 110 of about 16,014 (252)

Recurrent Pneumonia in Children: A Reasoned Diagnostic Approach and a Single Centre Experience [PDF]

open access: yes, 2017
Recurrent pneumonia (RP), i.e., at least two episodes of pneumonia in one year or three episodes ever with intercritical radiographic clearing of densities, occurs in 7.7%-9% of children with community-acquired pneumonia.
Corcione, Adele   +2 more
core   +2 more sources

Cytomegalovirus pneumonia in an immunocompetent host with primary ciliary dyskinesia: A case report

open access: diamond, 2021
Vasiliki Georgakopoulou   +8 more
openalex   +2 more sources

Genotypes and associations with symptoms in primary ciliary dyskinesia [PDF]

open access: gold, 2023
Eva S.L. Pedersen   +7 more
openalex   +1 more source

Primary ciliary dyskinesia: mechanisms and management

open access: yesThe Application of Clinical Genetics, 2017
Nadirah Damseh,1 Nada Quercia,1,2 Nisreen Rumman,3 Sharon D Dell,4 Raymond H Kim5 1Division of Clinical and Metabolic Genetics, 2Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada; 3Pediatric Department, Makassed Hospital ...
Damseh N   +4 more
doaj  

Radial Spoke Proteins of \u3cem\u3eChlamydomonas\u3c/em\u3e Flagella [PDF]

open access: yes, 2006
The radial spoke is a ubiquitous component of `9+2\u27 cilia and flagella, and plays an essential role in the control of dynein arm activity by relaying signals from the central pair of microtubules to the arms. The Chlamydomonas reinhardtii radial spoke
Agrin, Nathan S.   +11 more
core   +1 more source

Measuring the burden of treatment for chronic disease: implications of a scoping review of the literature [PDF]

open access: yes, 2017
Background: Although there has been growing research on the burden of treatment, the current state of evidence on measuring this concept is unknown.
Mair, Frances S.   +3 more
core   +3 more sources

Primary Ciliary Dyskinesia: A Clinical Review

open access: yesCells
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous, motile ciliopathy, characterized by neonatal respiratory distress, recurrent upper and lower respiratory tract infections, subfertility, and laterality defects.
Katherine A. Despotes   +3 more
doaj   +1 more source

EARLY DIAGNOSIS AND TREATMENT IN PATIENT WITH A PRIMARY CILIARY DYSKINESIA (KARTAGENER SYNDROME): CASE REPORT

open access: yesАрхивъ внутренней медицины, 2018
Primary ciliar dyskinesia is а rare orphan disease known for its multiple and variable symptoms caused by the marked genetic heterogenity beyond. As per the abundant symptoms in pediatric patients, a frequent inflammatory diseases of both upper and lower
I. V. Rybakova   +4 more
doaj   +1 more source

Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study [PDF]

open access: yes, 2017
BACKGROUND: Primary ciliary dyskinesia (PCD) and cystic fibrosis (CF) are increasingly compared. There are no chest magnetic resonance imaging (MRI) comparative studies of PCD and CF. We assessed clinical, functional, microbiological and MRI findings in
Carnovale, Vincenzo   +9 more
core   +1 more source

Definition of sinonasal and otological exacerbation in patients with primary ciliary dyskinesia: an expert consensus

open access: yesERJ Open Research
Background Recurrent infections of the nose, sinuses and ears are common problems for people with primary ciliary dyskinesia. While pulmonary exacerbations in primary ciliary dyskinesia are defined, there is no definition for ear-nose-throat ...
Myrofora Goutaki   +24 more
doaj   +1 more source

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