ReviewClinics in chest medicine2016
Pulmonary Alveolar Microlithiasis.
Review in Clinics in chest medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
25 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.
- New insights in the genetic variant spectrum of SLC34A2 in pulmonary alveolar microlithiasis; a systematic review.Orphanet journal of rare diseases · 2023Pooled it
- A compound heterozygous combination of SLC34A2 variants in pulmonary alveolar microlithiasis: A case report and literature review.The Journal of international medical research · 2026Review
- Article
- Pulmonary alveolar microlithiasis: A case report and brief review of literature.Caspian journal of internal medicine · 2025Article
- Article
- Pulmonary alveolar microlithiasis: a rare case report from Syria.Annals of medicine and surgery (2012) · 2023Article
- Two novel gene mutations identified in a child with pulmonary alveolar microlithiasis complicated with bronchitis obliterans: A case report and literature review.Clinical case reports · 2023Article
- Diagnostic Images of Pulmonary Alveolar Microlithiasis: A Rare, Autosomal Recessive Disorder.European journal of case reports in internal medicine · 2022Article
- Pulmonary Alveolar Microlithiasis and Rheumatoid Arthritis: A Case Report and Review of the Literature.Case reports in rheumatology · 2021Article
- Pulmonary Alveolar Microlithiasis: A Unique Case of Familial PAM Complicated by Transplant Rejection.Case reports in pathology · 2021Article
- Tricuspid valve calcification in familial pulmonary alveolar microlithiasis: A case report.Annals of medicine and surgery (2012) · 2020Article
- Pulmonary alveolar microlithiasis: no longer in the stone age.ERJ open research · 2020Review
- Pulmonary Alveolar Microlithiasis.Seminars in respiratory and critical care medicine · 2020Review
- Pulmonary Alveolar Microlithiasis: A Case Report.Oman medical journal · 2020Article
- Pulmonary Alveolar Microlithiasis: a Case Report in King Hussein Medical Center (KHMC), Amman, Jordan.Medical archives (Sarajevo, Bosnia and Herzegovina) · 2020Article
- Pulmonary alveolar microlithiasis: A report of two unique cases.Respiratory medicine case reports · 2020Article
- Images of the month 1: Cough before the storm: A case of pulmonary alveolar microlithiasis.Clinical medicine (London, England) · 2020Article
- Pulmonary alveolar microlithiasis and interstitial pneumonitis: a case report of the west of Iran.BioMedicine · 2019Article
- Single-lung transplantation for pulmonary alveolar microlithiasis: A case report.World journal of clinical cases · 2019Article
- Pulmonary Hypertension and Polycythemia Secondary to Pulmonary Alveolar Microlithiasis Treated with Sequential Bilateral Lung Transplant: A Case Study and Literature Review.The American journal of case reports · 2019Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 2 institutions in 2 countries.
Funding
Abstract
Pulmonary alveolar microlithiasis (PAM) is a genetic lung disorder that is characterized by the accumulation of calcium phosphate deposits in the alveolar spaces of the lung. Mutations in the type II sodium phosphate cotransporter, NPT2b, have been reported in patients with PAM. PAM progresses gradually, often producing incremental dyspnea on exertion, desaturation in young adulthood, and respiratory insufficiency by late middle age. Treatment remains supportive, including supplemental oxygen therapy. For patients with end-stage disease, lung transplantation is available as a last resort. The recent development of a laboratory animal model has revealed several promising treatment approaches for future trials.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.