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

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

Research output: Contribution to journalReview ArticleScientificpeer-review

Original languageEnglish
Article number58
JournalOrphanet journal of rare diseases
Volume14
Number of pages25
ISSN1750-1172
DOIs
Publication statusPublished - 26 Feb 2019
MoE publication typeA2 Review article in a scientific journal

Fields of Science

  • X-linked hypophosphatemia (XLH)
  • fibroblast growth factor 23 (FGF23)
  • phosphate regulating endopeptidase homolog
  • X-linked (PHEX)
  • hypophosphatemia
  • vitamin D deficiency
  • rickets
  • osteomalacia
  • bone dysplasia
  • ectopic calcification
  • muscle weakness
  • dental abscess
  • hearing impairment
  • FIBROBLAST-GROWTH-FACTOR
  • ALKALINE-PHOSPHATASE GENE
  • VITAMIN-D
  • MOUSE MODEL
  • HYP-MOUSE
  • COTRANSPORTER GENE
  • TRANSGENIC MICE
  • PHEX MUTATION
  • MURINE MODEL
  • HEARING-LOSS
  • 3111 Biomedicine
  • 1184 Genetics, developmental biology, physiology

Cite this

Beck-Nielsen, S. S., Mughal, Z., Haffner, D., Nilsson, O., Levtchenko, E., Ariceta, G., ... Mäkitie, O. (2019). FGF23 and its role in X-linked hypophosphatemia-related morbidity. Orphanet journal of rare diseases, 14, [58]. https://doi.org/10.1186/s13023-019-1014-8
Beck-Nielsen, Signe Sparre ; Mughal, Zulf ; Haffner, Dieter ; Nilsson, Ola ; Levtchenko, Elena ; Ariceta, Gema ; Collantes, Carmen de Lucas ; Schnabel, Dirk ; Jandhyala, Ravi ; Mäkitie, Outi. / FGF23 and its role in X-linked hypophosphatemia-related morbidity. In: Orphanet journal of rare diseases. 2019 ; Vol. 14.
@article{407373aabc004481954aa5e29b069dc6,
title = "FGF23 and its role in X-linked hypophosphatemia-related morbidity",
keywords = "X-linked hypophosphatemia (XLH), fibroblast growth factor 23 (FGF23), phosphate regulating endopeptidase homolog, X-linked (PHEX), hypophosphatemia, vitamin D deficiency, rickets, osteomalacia, bone dysplasia, ectopic calcification, muscle weakness, dental abscess, hearing impairment, FIBROBLAST-GROWTH-FACTOR, ALKALINE-PHOSPHATASE GENE, VITAMIN-D, MOUSE MODEL, HYP-MOUSE, COTRANSPORTER GENE, TRANSGENIC MICE, PHEX MUTATION, MURINE MODEL, HEARING-LOSS, 3111 Biomedicine, 1184 Genetics, developmental biology, physiology",
author = "Beck-Nielsen, {Signe Sparre} and Zulf Mughal and Dieter Haffner and Ola Nilsson and Elena Levtchenko and Gema Ariceta and Collantes, {Carmen de Lucas} and Dirk Schnabel and Ravi Jandhyala and Outi M{\"a}kitie",
year = "2019",
month = "2",
day = "26",
doi = "10.1186/s13023-019-1014-8",
language = "English",
volume = "14",
journal = "Orphanet journal of rare diseases",
issn = "1750-1172",
publisher = "BMC",

}

Beck-Nielsen, SS, Mughal, Z, Haffner, D, Nilsson, O, Levtchenko, E, Ariceta, G, Collantes, CDL, Schnabel, D, Jandhyala, R & Mäkitie, O 2019, 'FGF23 and its role in X-linked hypophosphatemia-related morbidity' Orphanet journal of rare diseases, vol. 14, 58. https://doi.org/10.1186/s13023-019-1014-8

FGF23 and its role in X-linked hypophosphatemia-related morbidity. / Beck-Nielsen, Signe Sparre; Mughal, Zulf; Haffner, Dieter; Nilsson, Ola; Levtchenko, Elena; Ariceta, Gema; Collantes, Carmen de Lucas; Schnabel, Dirk; Jandhyala, Ravi; Mäkitie, Outi.

In: Orphanet journal of rare diseases, Vol. 14, 58, 26.02.2019.

Research output: Contribution to journalReview ArticleScientificpeer-review

TY - JOUR

T1 - FGF23 and its role in X-linked hypophosphatemia-related morbidity

AU - Beck-Nielsen, Signe Sparre

AU - Mughal, Zulf

AU - Haffner, Dieter

AU - Nilsson, Ola

AU - Levtchenko, Elena

AU - Ariceta, Gema

AU - Collantes, Carmen de Lucas

AU - Schnabel, Dirk

AU - Jandhyala, Ravi

AU - Mäkitie, Outi

PY - 2019/2/26

Y1 - 2019/2/26

KW - X-linked hypophosphatemia (XLH)

KW - fibroblast growth factor 23 (FGF23)

KW - phosphate regulating endopeptidase homolog

KW - X-linked (PHEX)

KW - hypophosphatemia

KW - vitamin D deficiency

KW - rickets

KW - osteomalacia

KW - bone dysplasia

KW - ectopic calcification

KW - muscle weakness

KW - dental abscess

KW - hearing impairment

KW - FIBROBLAST-GROWTH-FACTOR

KW - ALKALINE-PHOSPHATASE GENE

KW - VITAMIN-D

KW - MOUSE MODEL

KW - HYP-MOUSE

KW - COTRANSPORTER GENE

KW - TRANSGENIC MICE

KW - PHEX MUTATION

KW - MURINE MODEL

KW - HEARING-LOSS

KW - 3111 Biomedicine

KW - 1184 Genetics, developmental biology, physiology

U2 - 10.1186/s13023-019-1014-8

DO - 10.1186/s13023-019-1014-8

M3 - Review Article

VL - 14

JO - Orphanet journal of rare diseases

JF - Orphanet journal of rare diseases

SN - 1750-1172

M1 - 58

ER -

Beck-Nielsen SS, Mughal Z, Haffner D, Nilsson O, Levtchenko E, Ariceta G et al. FGF23 and its role in X-linked hypophosphatemia-related morbidity. Orphanet journal of rare diseases. 2019 Feb 26;14. 58. https://doi.org/10.1186/s13023-019-1014-8