基因突变相关肺泡蛋白沉积症（CCR2和GATA2缺乏）的CT表现。

IF 4.9 2区医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING

Diagnostic and Interventional Imaging Pub Date : 2025-05-07 DOI:10.1016/j.diii.2025.04.007

Gael Dournes, Hugues Bégueret, Xavier Demant, Jean Delmas, Michael Fayon, Nathalie Aladjidi

引用次数: 0

摘要

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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CT features of genetic mutation-related pulmonary alveolar proteinosis (CCR2 and GATA2 deficiency.

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来源期刊

Diagnostic and Interventional Imaging Medicine-Radiology, Nuclear Medicine and Imaging

CiteScore

8.50

自引率

29.10%

发文量

126

审稿时长

11 days

期刊介绍： Diagnostic and Interventional Imaging accepts publications originating from any part of the world based only on their scientific merit. The Journal focuses on illustrated articles with great iconographic topics and aims at aiding sharpening clinical decision-making skills as well as following high research topics. All articles are published in English. Diagnostic and Interventional Imaging publishes editorials, technical notes, letters, original and review articles on abdominal, breast, cancer, cardiac, emergency, forensic medicine, head and neck, musculoskeletal, gastrointestinal, genitourinary, interventional, obstetric, pediatric, thoracic and vascular imaging, neuroradiology, nuclear medicine, as well as contrast material, computer developments, health policies and practice, and medical physics relevant to imaging.