Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

about

Surgical management of digital ischemia caused by constriction band formation in a patient with ichthyosis vulgaris.Familiar palmoplantar keratoderma, flaccid blisters, and widespread scaling

P2860

Q48499134-94CB5607-56D3-448F-B8D0-936B4B5657BA Q58700716-9E718308-AAE5-4C95-95D1-2448F7F096BC

P2860

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

Item

http://www.wikidata.org/entity/Q48055869

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

@en

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

@nl

type

Item

label

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

@en

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

@nl

prefLabel

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

@en

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

@nl

P1476

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

@en

P2093

Judith Fischer

http://www.w3.org/2001/XMLSchema#string

P275

Creative Commons Attribution-NonCommercial

P2860

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia

Lipoxygenases mediate the effect of essential fatty acid in skin barrier formation: a proposed role in releasing omega-hydroxyceramide for construction of the corneocyte lipid envelope

PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans

In search for function of two human orphan SDR enzymes: hydroxysteroid dehydrogenase like 2 (HSDL2) and short-chain dehydrogenase/reductase-orphan (SDR-O)

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

Biochemical, structural, and transglutaminase substrate properties of human loricrin, the major epidermal cornified cell envelope protein

The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis

Recent advances in understanding ichthyosis pathogenesis

Nonsyndromic types of ichthyoses - an update

P2888

s40257-017-0313-x

P304

51-66

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

review article

P356

10.1007/S40257-017-0313-X

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Hans Törmä

Anders Vahlquist

P5008

ScienceSource

P577

2017-08-16T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

2018-02-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28815464

http://www.w3.org/2001/XMLSchema#string

P921

cytoskeletal proteins

macromolecular substances

P932

5797567

http://www.w3.org/2001/XMLSchema#string

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

about

P2860

P2860

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.

description

name

type

label

prefLabel

P1433

P1476

P2093

P275

P2860

P2888

P304

P31

P356

P433

P478

P50

P5008

P577

P698

P921

P932

P356

P1433

P1476

P2093

P275

P2860

P2888

P304

P31

P356

P433

P478

P50

P5008

P577

P698

P921

P932