FGF23 and its role in X-linked hypophosphatemia-related morbidity

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1750-1172

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: FGF23 and its role in X-linked hypophosphatemia-related morbidity ; volume:14 ; number:1 ; day:26 ; month:2 ; year:2019 ; pages:1-25 ; date:12.2019
Orphanet journal of rare diseases ; 14, Heft 1 (26.2.2019), 1-25, 12.2019

Creator: Beck-Nielsen, Signe Sparre
Mughal, Zulf
Haffner, Dieter
Nilsson, Ola
Levtchenko, Elena
Ariceta, Gema
Lucas Collantes, Carmen de
Schnabel, Dirk
Jandhyala, Ravi
Mäkitie, Outi

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13023-019-1014-8

URN: urn:nbn:de:101:1-2019032422142254168857

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

Last update: 14.08.2025, 10:53 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Beck-Nielsen, Signe Sparre
Mughal, Zulf
Haffner, Dieter
Nilsson, Ola
Levtchenko, Elena
Ariceta, Gema
Lucas Collantes, Carmen de
Schnabel, Dirk
Jandhyala, Ravi
Mäkitie, Outi
SpringerLink (Online service)

Other Objects (12)

FGF23 and cell stress in SaOS-2 cells : A model reflecting X-linked hypophosphatemia dynamics

Easily misdiagnosed X-linked adrenoleukodystrophy

Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets

X-linked disorders with cerebellar dysgenesis

X-linked intellectual disability related to a novel variant of KLHL15

Health-related quality of life of X-linked hypophosphatemia in Spain

Hochschulschrift

Cardiac phenotype and Fgf23/Fgfr4 signaling in animal models with genetic disruption of klotho and phospate-regulating endopeptidase homolog X-linked, [Band]

Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

X-linked SCID with a rare mutation

Health-related quality of life of children with X-linked hypophosphatemia in Germany

X-linked Hyper-IgM Syndrome with Bronchiectasis

FGF23 and cell stress in SaOS-2 cells : A model reflecting X-linked hypophosphatemia dynamics

Easily misdiagnosed X-linked adrenoleukodystrophy

Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets

X-linked disorders with cerebellar dysgenesis

X-linked intellectual disability related to a novel variant of KLHL15

Health-related quality of life of X-linked hypophosphatemia in Spain

Hochschulschrift

Cardiac phenotype and Fgf23/Fgfr4 signaling in animal models with genetic disruption of klotho and phospate-regulating endopeptidase homolog X-linked, [Band]

Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

X-linked SCID with a rare mutation

Health-related quality of life of children with X-linked hypophosphatemia in Germany

X-linked Hyper-IgM Syndrome with Bronchiectasis

FGF23 and cell stress in SaOS-2 cells : A model reflecting X-linked hypophosphatemia dynamics

Easily misdiagnosed X-linked adrenoleukodystrophy

Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets

X-linked disorders with cerebellar dysgenesis

X-linked intellectual disability related to a novel variant of KLHL15

Health-related quality of life of X-linked hypophosphatemia in Spain

Hochschulschrift

Cardiac phenotype and Fgf23/Fgfr4 signaling in animal models with genetic disruption of klotho and phospate-regulating endopeptidase homolog X-linked, [Band]

Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

X-linked SCID with a rare mutation

Health-related quality of life of children with X-linked hypophosphatemia in Germany

X-linked Hyper-IgM Syndrome with Bronchiectasis

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

FGF23 and its role in X-linked hypophosphatemia-related morbidity

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

FGF23 and cell stress in SaOS-2 cells : A model reflecting X-linked hypophosphatemia dynamics

Easily misdiagnosed X-linked adrenoleukodystrophy

Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets

X-linked disorders with cerebellar dysgenesis

X-linked intellectual disability related to a novel variant of KLHL15

Health-related quality of life of X-linked hypophosphatemia in Spain

Cardiac phenotype and Fgf23/Fgfr4 signaling in animal models with genetic disruption of klotho and phospate-regulating endopeptidase homolog X-linked, [Band]

Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

X-linked SCID with a rare mutation

Health-related quality of life of children with X-linked hypophosphatemia in Germany

X-linked Hyper-IgM Syndrome with Bronchiectasis

FGF23 and cell stress in SaOS-2 cells : A model reflecting X-linked hypophosphatemia dynamics

Easily misdiagnosed X-linked adrenoleukodystrophy

Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets

X-linked disorders with cerebellar dysgenesis

X-linked intellectual disability related to a novel variant of KLHL15

Health-related quality of life of X-linked hypophosphatemia in Spain

Cardiac phenotype and Fgf23/Fgfr4 signaling in animal models with genetic disruption of klotho and phospate-regulating endopeptidase homolog X-linked, [Band]

Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

X-linked SCID with a rare mutation

Health-related quality of life of children with X-linked hypophosphatemia in Germany

X-linked Hyper-IgM Syndrome with Bronchiectasis

FGF23 and cell stress in SaOS-2 cells : A model reflecting X-linked hypophosphatemia dynamics

Easily misdiagnosed X-linked adrenoleukodystrophy

Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets

X-linked disorders with cerebellar dysgenesis

X-linked intellectual disability related to a novel variant of KLHL15

Health-related quality of life of X-linked hypophosphatemia in Spain

Cardiac phenotype and Fgf23/Fgfr4 signaling in animal models with genetic disruption of klotho and phospate-regulating endopeptidase homolog X-linked, [Band]

Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

X-linked SCID with a rare mutation

Health-related quality of life of children with X-linked hypophosphatemia in Germany

X-linked Hyper-IgM Syndrome with Bronchiectasis

Related objects

Reset password