June K Marthin
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Explore the profile of June K Marthin including associated specialties, affiliations and a list of published articles.
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22
Citations
928
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Recent Articles
1.
Nygaard C, Duno M, Heilmann C, Marthin J, Nygaard S, Qvist T, et al.
Pediatr Pulmonol
. 2025 Jan;
60(1):e27485.
PMID: 39817599
No abstract available.
2.
Holgersen M, Marthin J, Raidt J, Qvist T, Johansen H, Omran H, et al.
Ann Am Thorac Soc
. 2024 Oct;
22(2):216-225.
PMID: 39447114
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterized by progressive lung disease. is a major pathogen in this disease and is known to impact lung function. Previous genotype-phenotype...
3.
Raidt J, Riepenhausen S, Pennekamp P, Olbrich H, Amirav I, Athanazio R, et al.
Eur Respir J
. 2024 Jun;
64(2).
PMID: 38871375
Background: Primary ciliary dyskinesia (PCD) represents a group of rare hereditary disorders characterised by deficient ciliary airway clearance that can be associated with laterality defects. We aimed to describe the...
4.
Marthin J, Holgersen M, Nielsen K, Mortensen J
ERJ Open Res
. 2023 Dec;
9(6).
PMID: 38076675
Background: Pulmonary radioaerosol mucociliary clearance (PRMC) is a reliable method for assessing whole lung mucociliary clearance and has been used at the Danish PCD Centre as a supplementary diagnostic test...
5.
Marthin J, Nielsen K, Mortensen J
ERJ Open Res
. 2023 Sep;
9(5).
PMID: 37701364
Background: Primary ciliary dyskinesia (PCD) is an inherited disorder in which dyskinetic cilia cause impaired mucociliary clearance of upper and lower airways. Airway ciliary movement can be indirectly tested after...
6.
Beydon N, Kouis P, Marthin J, Latzin P, Colas M, Davis S, et al.
Eur Respir J
. 2023 Feb;
61(4).
PMID: 36822632
Nasal nitric oxide (nNO) is extremely low in most people with primary ciliary dyskinesia (PCD) and its measurement is an important contributor to making the diagnosis. Existing guidelines and technical...
7.
Raidt J, Maitre B, Pennekamp P, Altenburg J, Anagnostopoulou P, Armengot M, et al.
ERJ Open Res
. 2022 Aug;
8(3).
PMID: 35983540
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by impaired mucociliary clearance leading to irreversible lung damage. In contrast to other rare lung diseases like cystic fibrosis (CF),...
8.
Nielsen K, Holgersen M, Crowley S, Marthin J
Am J Med Genet C Semin Med Genet
. 2022 Mar;
190(1):20-35.
PMID: 35352480
Primary ciliary dyskinesia (PCD) can be defined as a multiorgan ciliopathy with a dominant element of chronic airway disease affecting the nose, sinuses, middle ear, and in particular, the lower...
9.
Holgersen M, Marthin J, Johansen H, Nielsen K
Chron Respir Dis
. 2021 Dec;
18:14799731211061600.
PMID: 34854775
Primary ciliary dyskinesia (PCD) is a rare congenital disease with defective mucociliary clearance causing frequent and often persistent pulmonary infections. Achromobacter species are opportunistic pathogens renowned for the difficulty of...
10.
Marthin J, Lucas J, Boon M, Casaulta C, Crowley S, Destouches D, et al.
ERJ Open Res
. 2021 Aug;
7(3).
PMID: 34350277
Introduction: In primary ciliary dyskinesia (PCD) impaired mucociliary clearance leads to recurrent airway infections and progressive lung destruction, and concern over chronic airway infection and patient-to-patient transmission is considerable. So...