Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Rare association: sporadic lymphangioleiomyomatosis and Pi-SZ alpha-1-antitrypsin deficiency.

BMJ case reports - 1 Apr 2020

Eisner Ashley Eve, Sandhu Karanpal, Cao Kimberley

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to alpha 1-Antitrypsin
Share to alpha 1-Antitrypsin Deficiency
Share to Dyspnea
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 32241758
DOI: 10.1136/bcr-2019-233724
PMCID: PMC7167456

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

Rare association: sporadic lymphangioleiomyomatosis and Pi-SZ alpha-1-antitrypsin deficiency.PMID 32241758Read ↗

Sporadic lymphangioleiomyomatosis in a man with somatic mosaicism of TSC2 mutations, a case report.Semantic proximity Read ↗

Familial inflammatory Sneddon's syndrome-case report and review of the literature.Semantic proximity Read ↗

Apparent Sporadic Lymphangioleiomyomatosis in a Man as a Result of Extreme Mosaicism for a TSC2 Mutation.Semantic proximity Read ↗

Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis.Semantic proximity Read ↗

[Systemic vasculitis and alpha-1 antitrypsin deficiency of type PiZZ: report of a case].Semantic proximity Read ↗

Mutation analysis of the TSC1 and TSC2 genes in Japanese patients with pulmonary lymphangioleiomyomatosis.Semantic proximity Read ↗

Strong link between the alpha 1-antitrypsin PiZ allele and Wegener's granulomatosis.Semantic proximity Read ↗

Wegener's granulomatosis in a patient with severe PiZZ alpha 1-antitrypsin deficiency.Semantic proximity Read ↗

Systemic nodular panniculitis in a patient with alpha-1 antitrypsin deficiency (PiSS phenotype).Semantic proximity Read ↗

Recurrent idiopathic pericarditis: familial occurrence.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.