Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1750-1172

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study ; volume:15 ; number:1 ; day:10 ; month:1 ; year:2020 ; pages:1-11 ; date:12.2020
Orphanet journal of rare diseases ; 15, Heft 1 (10.1.2020), 1-11, 12.2020

Creator: Wohlfart, Sigrun
Meiller, Ralph
Hammersen, Johanna
Park, Jung
Menzel-Severing, Johannes
Melichar, Volker O.
Huttner, Kenneth
Johnson, Ramsey
Porte, Florence
Schneider, Holm

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13023-019-1288-x

URN: urn:nbn:de:101:1-2020041618042840714347

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:56 AM CEST

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Associated

Wohlfart, Sigrun
Meiller, Ralph
Hammersen, Johanna
Park, Jung
Menzel-Severing, Johannes
Melichar, Volker O.
Huttner, Kenneth
Johnson, Ramsey
Porte, Florence
Schneider, Holm
SpringerLink (Online service)

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Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study

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Other Objects (12)

Lung and eye involvement in X-linked hypohidrotic ectodermal dysplasia

X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle

Early dental intervention in patients with X-linked hypohidrotic ectodermal dysplasia

X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management

Biological and structural characterizations of mutations in X-linked spondyloepiphyseal dysplasia tarda

Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia

Optical Coherence Tomography Evolution in a Case of X-Linked Juvenile Retinoschisis: 15 Years of Follow-Up

X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1

Easily misdiagnosed X-linked adrenoleukodystrophy

Co-occurrence of Spondyloepiphyseal Dysplasia and X-Linked Hypophosphatemia in a Three-Generation Chinese Family

X-linked disorders with cerebellar dysgenesis

Right ventricle speckle tracking in bronchopulmonary dysplasia: one-year follow-up

Lung and eye involvement in X-linked hypohidrotic ectodermal dysplasia

X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle

Early dental intervention in patients with X-linked hypohidrotic ectodermal dysplasia

X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management

Biological and structural characterizations of mutations in X-linked spondyloepiphyseal dysplasia tarda

Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia

Optical Coherence Tomography Evolution in a Case of X-Linked Juvenile Retinoschisis: 15 Years of Follow-Up

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Easily misdiagnosed X-linked adrenoleukodystrophy

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X-linked disorders with cerebellar dysgenesis

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X-linked disorders with cerebellar dysgenesis

Right ventricle speckle tracking in bronchopulmonary dysplasia: one-year follow-up

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