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Authors: Xueyan Yu; Ramón A Espinoza-Lewis; Cheng Sun; Lisong Lin; Fenglei He; Wei Xiong; Jing Yang; Alun Wang; Yiping Chen
Journal: Cell Tissue Res Date: 2010-11-16 Impact factor: 5.249

2. Ichthyosis molecular fingerprinting shows profound T_H17 skewing and a unique barrier genomic signature.

Authors: Kunal Malik; Helen He; Thy Nhat Huynh; Gary Tran; Kelly Mueller; Kristina Doytcheva; Yael Renert-Yuval; Tali Czarnowicki; Shai Magidi; Margaret Chou; Yeriel D Estrada; Huei-Chi Wen; Xiangyu Peng; Hui Xu; Xiuzhong Zheng; James G Krueger; Amy S Paller; Emma Guttman-Yassky
Journal: J Allergy Clin Immunol Date: 2018-05-24 Impact factor: 10.793

3. [The ichthyoses. Pathophysiological models of epidermal differentiation].

Authors: D Hohl; M Huber
Journal: Hautarzt Date: 2013-01 Impact factor: 0.751

4. Pre-Descemet corneal dystrophy and X-linked ichthyosis associated with deletion of Xp22.31 containing the STS gene.

Authors: Crystal Hung; Reed I Ayabe; Cynthia Wang; Ricardo F Frausto; Anthony J Aldave
Journal: Cornea Date: 2013-09 Impact factor: 2.651

5. A family with X-linked ichthyosis and hypogonadism.

Authors: M G Pike; M Hammerton; J Edge; D J Atherton; D B Grant
Journal: Eur J Pediatr Date: 1989-02 Impact factor: 3.183

6. Absence of testicular steroid sulphatase activity in a boy with recessive X-linked ichthyosis and testicular maldescent.

Authors: G Lykkesfeldt; J Müller; N E Skakkebaek; E Bruun; A E Lykkesfeldt
Journal: Eur J Pediatr Date: 1985-09 Impact factor: 3.183

10. Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.

Authors: S J Brown; C L Relton; H Liao; Y Zhao; A Sandilands; W H I McLean; H J Cordell; N J Reynolds
Journal: Br J Dermatol Date: 2009-06-11 Impact factor: 9.302

Clinical features of autosomal dominant and sex-linked ichthyosis in an English population.

Review 1. [ON THE CLASSIFICATION OF THE ICHTHYOSIS GROUP].

2. [Attempted classification of congenital keratoses].

3. Ichthyosis involving the eye.

1. Overexpression of constitutively active BMP-receptor-IB in mouse skin causes an ichthyosis-vulgaris-like disease.

2. Ichthyosis molecular fingerprinting shows profound T_H17 skewing and a unique barrier genomic signature.

3. [The ichthyoses. Pathophysiological models of epidermal differentiation].

4. Pre-Descemet corneal dystrophy and X-linked ichthyosis associated with deletion of Xp22.31 containing the STS gene.

5. A family with X-linked ichthyosis and hypogonadism.

6. Absence of testicular steroid sulphatase activity in a boy with recessive X-linked ichthyosis and testicular maldescent.

7. X-linked icthyosis. A sulphatase deficiency.

8. Linkage analysis suggests a locus of ichthyosis vulgaris on 1q22.

9. Placental steroid deficiency: association with arylsulfatase A deficiency.

10. Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.