Pulmonale Lymphangioleiomyomatose (LAM)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pathology and Forensic Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00292-020-00901-w.pdf
Reference17 articles.
1. Costabel U, Guzman J (2002) Pulmonale Lymphangioleiomyomatose. Pneumologie 56(5):309–315
2. Ferrans VJ, Yu ZX, Nelson WK et al (2000) Lymphangioleiomyomatosis (LAM): a review of clinical and morphological features. J Nippon Med Sch 67(5):311–329
3. Guo M, Yu JJ, Perl AK et al (2020) Single cell transcriptomic analysis identifies a unique pulmonary lymphangioleiomyomatosis cell. Am J Respir Crit Care Med. https://doi.org/10.1164/rccm.201912-2445OC
4. Gupta N, Finlay GA, Kotloff RM et al (2017) ATS assembly on clinical problems. Lymphangioleiomyomatosis diagnosis and management: high-resolution chest computed tomography, transbronchial lung biopsy, and pleural disease management. An official American thoracic society/Japanese respiratory society clinical practice guideline. Am J Respir Crit Care Med 196(10):1337–1348
5. Gupta N, Henske EP (2018) Pulmonary manifestations in tuberous sclerosis complex. Am J Med Genet C Semin Med Genet 178(3):326–337
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1. Physiotherapy in lymphangioleiomyomatosis: a systematic review;Annals of Medicine;2022-10-10
2. A pulmonary lymphangioleiomyomatosis with multi-site angiomyolipoma: a case report;Translational Cancer Research;2022-07
3. Multidisciplinary team approach to diagnosing lymphangioleiomyomatosis;BMJ Case Reports;2021-08
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