Cargando…

Pathogenetic mechanism of lipoid proteinosis caused by mutation of the extracellular matrix protein 1 gene

Detalles Bibliográficos
Autores principales:	Gao, Dong, Ma, Xianying, Lian, Peiwen, Zhou, Surong, Chen, Jian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2019
Materias:	Retraction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423551/ https://www.ncbi.nlm.nih.gov/pubmed/30720111 http://dx.doi.org/10.3892/mmr.2019.9925

Ejemplares similares

Extracellular Matrix Protein 1 Gene Mutation in Turkish Patients with Lipoid Proteinosis
por: Dertlioğlu, Selma Bakar, et al.
Publicado: (2019)

Novel Mutations in Extracellular Matrix Protein 1 Gene in a Chinese Patient with Lipoid Proteinosis
por: Bai, Xiao, et al.
Publicado: (2016)

Lipoid proteinosis
por: Rao, Roopa Shamsundar, et al.
Publicado: (2009)

Lipoid Proteinosis
por: Mittal, Hitesh C, et al.
Publicado: (2016)

Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosis
por: Izadi, Farzad, et al.
Publicado: (2016)

Acitretin Treatment for Lipoid Proteinosis
por: Gündüz, Özgür, et al.
Publicado: (2012)

Identification of a Novel Mutation of Extracellular Matrix Protein 1 Gene in a Chinese Family with Lipoid Proteinosis
por: Xu, Mengjun, et al.
Publicado: (2023)

Lipoid proteinosis: A rare entity
por: Mukherjee, Bipasha, et al.
Publicado: (2015)

Lipoid Proteinosis Masquerading as Seborrheic Dermatitis
por: Tripathi, Alka, et al.
Publicado: (2021)

Lipoid proteinosis: Review of Indian cases
por: Shah, Jigna S, et al.
Publicado: (2022)

Clinical and Molecular Study of the Extracellular Matrix Protein 1 Gene in a Spanish Family with Lipoid Proteinosis
por: Mondejar, Rufino, et al.
Publicado: (2014)

Esophageal Aperistalsis in a Patient with Lipoid Proteinosis
por: Afshar, Behrooz, et al.
Publicado: (2018)

Lipoid Proteinosis: Curious Case of Two Siblings!
por: Agarwal, Pooja, et al.
Publicado: (2020)

Association Between Lipoid Proteinosis and Coeliac Disease
por: Bendaoud, Layla, et al.
Publicado: (2023)

Lipoid Proteinosis: A Rare Case Revisited
por: Achar, Arun, et al.
Publicado: (2023)

A novel nonsense mutation in exon 9 in the extracellular matrix protein 1 gene associated with lipoid proteinosis: A case report
por: Ghazawi, Feras M, et al.
Publicado: (2019)

N-Glycosylation of extracellular matrix protein 1 (ECM1) regulates its secretion, which is unrelated to lipoid proteinosis
por: Uematsu, Shiho, et al.
Publicado: (2014)

Severe Short Stature: an unusual finding in lipoid proteinosis
por: Poyrazoğlu, Şükran, et al.
Publicado: (2008)

Lipoid proteinosis: Histopathological characterization of early papulovesicular lesions
por: Gutte, Rameshwar, et al.
Publicado: (2012)

Lipoid proteinosis in a six-year-old child
por: Nayak, Surajit, et al.
Publicado: (2012)

Lipoid proteinosis: A review with two case reports
por: Kabre, Vishal, et al.
Publicado: (2015)

Lipoid proteinosis (Urbach-Wiethe disease) in two siblings
por: Thaddanee, Rekha, et al.
Publicado: (2014)

Lipoid Proteinosis: A Rare Encounter in Dental Office
por: Deshpande, Prasannasrinivas, et al.
Publicado: (2015)

Lipoid proteinosis: Unfamiliar skin findings delay diagnosis
por: Larkin, Sydney, et al.
Publicado: (2018)

An Unusual Case of Erythropoietic Protoporphyria Mimicking Lipoid Proteinosis
por: Kaur, Sarabjit, et al.
Publicado: (2019)

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis
por: Salih, Mustafa A, et al.
Publicado: (2011)

Ocular manifestations in lipoid proteinosis: A rare clinical entity
por: Kamath, Sumana J, et al.
Publicado: (2015)

Urbach–Weithe disease (lipoid proteinosis): A classical presentation
por: Sangwan, Ankita, et al.
Publicado: (2016)

Intra-Familial Variability of Lipoid Proteinosis: An Indian Case Series
por: Lohia, Kriti, et al.
Publicado: (2021)

Ultrastructural aspects of the skin in lipoid proteinosis (Urbach-Wiethe disease)()()
por: de Almeida, Hiram Larangeira, et al.
Publicado: (2021)

Radiologic presentation of lipoid proteinosis with symmetrical medial temporal lobe calcifications
por: Chandrasekaran, Subhashree, et al.
Publicado: (2016)

Lipoid Proteinosis with Esotropia: Report of a Rare Case and Dermoscopic Findings
por: Tabassum, Hera, et al.
Publicado: (2020)

Lipoid Proteinosis presenting as beaded papules of the eyelid: report of three cases
por: Wei, Zhenyu, et al.
Publicado: (2021)

Lipoid Proteinosis in two Iranian Sisters: A Case Report and Review of Literature
por: Malekzad, F, et al.
Publicado: (2011)

Late presentation of laryngeal lipoid proteinosis: a case report and review of the literature
por: Alrusayyis, Danah F, et al.
Publicado: (2022)

Lipoid proteinosis: a first report of mutation Val10Gly in the signal peptide of the ECM1 gene
por: Ludew, Dominik, et al.
Publicado: (2018)

Assessment of dynamic thiol-disulfide homeostasis in patients with lipoid proteinosis (Urbach-Wiethe syndrome)
por: Taskin, Seyhan, et al.
Publicado: (2022)

Molecular analysis of lipoid proteinosis: identification of a novel nonsense mutation in the ECM1 gene in a Pakistani family
por: Nasir, Muhammad, et al.
Publicado: (2011)

Lipoid Proteinosis (Urbach-Wiethe Disease): A Rare Genodermatosis with Characteristic Dermatological and Neuroimaging Findings
por: Chatterjee, Aparajita, et al.
Publicado: (2021)

Oral Manifestations and Dental Management Considerations of Lipoid Proteinosis: A Case Report and Review of Literature
por: Jahanimoghadam, Fatemeh, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_h21m7o3vq1mffr861064t9ee58