Lipoid Proteinosis: A Rare Cause of Hoarseness
Author:
Publisher
Elsevier BV
Subject
LPN and LVN,Speech and Hearing,Otorhinolaryngology
Reference32 articles.
1. Otolaryngological manifestations and genetic characteristics of lipoid proteinosis;Xu;Ann Otol Rhinol Laryngol,2010
2. Lipoid proteinosis in an inbred Namaqualand community;Gordon;Lancet,1969
3. Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation;Hamada;J Invest Dermatol,2003
4. Differentiation-dependent alternative splicing and expression of the extracellular matrix protein 1 gene in human keratinocytes;Smits;J Invest Dermatol,2000
5. Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1);Hamada;Hum Mol Genet,2002
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1. Laryngeal features in Lipoid proteinosis: a systematic review and meta-analysis of individual participant data;European Archives of Oto-Rhino-Laryngology;2024-05-07
2. A Sporadic Family of Lipoid Proteinosis with Novel ECM1 Gene Mutations;Clinical, Cosmetic and Investigational Dermatology;2024-04
3. Advances in treatment for lipoid proteinosis (Urbach–Wiethe disease): a case report and systematic review;Clinical and Experimental Dermatology;2024-02-03
4. Multiple oral submucosal nodules in a young adult;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2023-10
5. Assessment of dynamic thiol-disulfide homeostasis in patients with lipoid proteinosis (Urbach-Wiethe syndrome);Revista da Associação Médica Brasileira;2022-09
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