0000000000644285

AUTHOR

Are Martin Holm

showing 2 related works from this author

ISHLT consensus document on lung transplantation in patients with connective tissue disease: Part I: Epidemiology, assessment of extrapulmonary condi…

2021

Patients with connective tissue disease (CTD) and advanced lung disease are often considered suboptimal candidates for lung transplantation (LTx) due to their underlying medical complexity and potential surgical risk. There is substantial variability across LTx centers regarding the evaluation and listing of these patients. The International Society for Heart and Lung Transplantation-supported consensus document on lung transplantation in patients with CTD standardization aims to clarify definitions of each disease state included under the term CTD, to describe the extrapulmonary manifestations of each disease requiring consideration before transplantation, and to outline the absolute contr…

Pulmonary and Respiratory Medicinemedicine.medical_specialtyConsensusmedicine.medical_treatmentDiseaseGlobal HealthEpidemiologyHumansMedicineLung transplantationConnective Tissue DiseasesIntensive care medicineSelection (genetic algorithm)TransplantationLungbusiness.industryContraindicationsPatient Selectionmedicine.diseaseConnective tissue diseaseTransplantationmedicine.anatomical_structureSurgeryCTDMorbidityCardiology and Cardiovascular MedicinebusinessLung TransplantationThe Journal of Heart and Lung Transplantation
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Eight novel variants in the SLC34A2 gene in pulmonary alveolar microlithiasis

2020

BackgroundPulmonary alveolar microlithiasis (PAM) is caused by genetic variants in the SLC34A2 gene, which encodes the sodium-dependent phosphate transport protein 2B (NaPi-2b). PAM is characterised by deposition of calcium phosphate concretions (microliths) in the alveoli leading to pulmonary dysfunction. The variant spectrum of SLC34A2 has not been well investigated and it is not yet known whether a genotype–phenotype correlation exists.MethodsWe collected DNA from 14 patients with PAM and four relatives, and analysed the coding regions of SLC34A2 by direct DNA sequencing. To determine the phenotype characteristics, clinical data were collected and a severity score was created for each va…

0301 basic medicinePulmonary and Respiratory MedicineGeneticsbusiness.industrymedicine.diseasePhenotypeAsymptomaticDNA sequencing03 medical and health sciences030104 developmental biology0302 clinical medicine030228 respiratory systemPulmonary alveolar microlithiasismedicineCoding regionMissense mutationAllelemedicine.symptombusinessGene
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