Gene polymorphism in Netherton and common atopic disease.

Gene polymorphism in Netherton and common atopic disease.

Atopic dermatitis (AD) and asthma are characterized by IgE-mediated atopic (allergic) responses to common proteins (allergens), many of which are proteinases. Loci influencing atopy have been localized to a number of chromosomal regions, including the chromosome 5q31 cytokine cluster. Netherton dise...

Descripció completa

Dades bibliogràfiques
Autors principals:	Walley, A, Chavanas, S, Moffatt, M, Esnouf, R, Ubhi, B, Lawrence, R, Wong, K, Abecasis, G, Jones, E, Harper, J, Hovnanian, A, Cookson, W
Format:	Journal article
Idioma:	English
Publicat:	2001

Ítems similars

Biological treatments for pediatric Netherton syndrome
per: Matteo Pontone, et al.
Publicat: (2022-12-01)

Research advances of Netherton syndrome
per: Xiaoxuan CHEN, et al.
Publicat: (2022-04-01)

Comèl–Netherton's syndrome in siblings
per: Asha Gowrappala Shanmukhappa, et al.
Publicat: (2016-01-01)

Severe Hypernatremia as Presentation of Netherton Syndrome
per: A. Di Nora, et al.
Publicat: (2023-12-01)

A case of Netherton's syndrome with cerebral infarction
per: E Calikoğlu, et al.
Publicat: (2001-07-01)

Trichoscopy in Unveiling the Triad of Netherton Syndrome
per: H Bangaru, et al.
Publicat: (2025-01-01)

Netherton syndrome: A rare genodermatosis
per: Vivek Kumar Dey
Publicat: (2011-01-01)

Successful use of secukinumab in Netherton syndrome
per: Sarah K. Blanchard, MD, et al.
Publicat: (2020-06-01)

Comèl-Netherton syndrome – case report
per: Izabela Błażewicz, et al.
Publicat: (2014-11-01)

Netherton syndrome—A therapeutic challenge in childhood
per: Polina Kostova, et al.
Publicat: (2024-04-01)

Síndrome de Netherton com 20 anos de acompanhamento Netherton's Syndrome with a 20-year follow-up
per: Rodrigo Pereira Duquia, et al.
Publicat: (2006-12-01)

Síndrome de Netherton: relato de caso
per: Sabrina Hernandes Conceição, et al.
Publicat: (2023-03-01)

Skin Microbiota and Clinical Associations in Netherton Syndrome
per: Veera Sillanpää, et al.
Publicat: (2021-06-01)

Positional cloning of susceptibility genes for atopic dermatitis in the epidermal differentiation complex
per: Morar, N, et al.
Publicat: (2007)

Results of Combined Pathogenetic Therapy in Netherton Syndrome: Clinical Case
per: Nikolay N. Murashkin, et al.
Publicat: (2023-11-01)

Is c.1431-12G>A A common European mutation of SPINK5? report of a patient with Netherton Syndrome
per: Śmigiel R, et al.
Publicat: (2016-12-01)

Netherton's syndrome and neonatal hypernatremia. A case report
per: H Ergin, et al.
Publicat: (1997-07-01)

Síndrome de netherton: reporte de un caso
per: Daisy M. Blanco, et al.
Publicat: (2024-10-01)

Vulvovaginal involvement in Netherton syndrome: A case report
per: Cassandra Bertrand, MD, et al.
Publicat: (2024-03-01)

Netherton Syndrome: A Case Report With Literature Review
per: Fereshteh Salari, et al.
Publicat: (2019-10-01)

Immune cell phenotype and functional defects in Netherton syndrome
per: Elina Eränkö, et al.
Publicat: (2018-11-01)

Primary cutaneous CD30+T-cell lymphoproliferative disorder following cardiac transplantation in a 15-year-old boy with Netherton's syndrome
per: Katugampola, R, et al.
Publicat: (2004)

Primary cutaneous CD30+ T-cell lymphoproliferative disorder following cardiac transplantation in a 15-year-old boy with Netherton's syndrome.
per: Katugampola, R, et al.
Publicat: (2005)

Comparative analyses of Netherton syndrome patients and Spink5 conditional knock-out mice uncover disease-relevant pathways
per: Evgeniya Petrova, et al.
Publicat: (2024-02-01)

The role of SPINK5 mutation distribution in phenotypes of Netherton syndrome
per: Min Xu, et al.
Publicat: (2025-01-01)

An 8-Year-Old Child with Delayed Diagnosis of Netherton Syndrome
per: Alexander K. C. Leung, et al.
Publicat: (2018-01-01)

Dupilumab Improves Pruritus in Netherton Syndrome: A Case Study
per: Yutaka Inaba, et al.
Publicat: (2022-02-01)

Netherton Syndrome, a Rare Genetic Disorder—Case Report
per: Yahya Almalki, et al.
Publicat: (2023-02-01)

Fine mapping of susceptibility genes for atopic dermatitis in the epidermal differentiation complex on chromosome 1q21
per: Morar, N, et al.
Publicat: (2007)

A novel mutation in SPINK5 gene underlies a case of atypical Netherton syndrome
per: Yu Wang, et al.
Publicat: (2022-09-01)

A heterozygous missense mutation of CARD14 gene in a case of Netherton-Like syndrome
per: Surya Ravindran, et al.
Publicat: (2021-01-01)

Outcomes of Systemic Treatment in Children and Adults With Netherton Syndrome: A Systematic Review
per: Anouk E. M. Nouwen, et al.
Publicat: (2022-03-01)

Common apolipoprotein E polymorphisms and risk of clinical malaria in the Gambia.
per: Aucan, C, et al.
Publicat: (2004)

Case report: Interleukin-17 targeted biological therapy in netherton syndrome
per: Rahul Mahajan, et al.
Publicat: (2023-11-01)

Netherton syndrome in one Chinese adult with a novel mutation in the SPINK5 gene and immunohistochemical studies of LEKTI
per: Zhang Xi-Bao, et al.
Publicat: (2012-01-01)

Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Keratinocytes to Recapitulate Genodermatoses: Modeling of Netherton Syndrome
per: Victoria Gálvez, et al.
Publicat: (2020-09-01)

Netherton Syndrome in a Neonate with Possible Growth Hormone Deficiency and Transient Hyperaldosteronism
per: Chatziioannidis Ilias, et al.
Publicat: (2015-01-01)

A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome
per: Fatma Derya Bulut, et al.
Publicat: (2018-03-01)

Gene Polymorphisms of 22 Cytokines in Macedonian Children with Atopic Dermatitis
per: Katarina Stavric, et al.
Publicat: (2012-03-01)

表现为先天性红皮病的Netherton综合征2例报道
Publicat: (2014-01-01)