ReviewRadiologie (Heidelberg, Germany)2025
[Childhood interstitial lung disease].
Review in Radiologie (Heidelberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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.
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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.
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Authors and funding
2 authors.
Funding
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Abstract
clinical issueChildren's interstitial lung disease (chILD) encompasses a large group of rare and heterogeneous pulmonary disorders associated with diagnostic challenges for all disciplines. Due to the substantial morbidity and mortality, a timely and accurate diagnosis is required for optimal patient care. STANDARD RADIOLOGICAL
methodsRadiology plays a crucial role in the diagnosis of chILD; computed tomography (CT) represents the current gold standard imaging modality. PRACTICAL RECOMMENDATIONS: To make an accurate diagnosis, a systematic approach in a multidisciplinary team is essential. CT confirms the presence of chILD and enables exclusion of more frequent disorders. In conjunction with patient history and clinical presentation, knowledge of imaging patterns in chILD may lead to a specific diagnosis; otherwise unspecific changes can narrow differential diagnosis, guide further diagnostics, and prevent more invasive procedures.
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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.