Three years of growth hormone treatment in young adults with Prader-Willi syndrome: Sustained positive effects on body composition

Layla Damen; Stephany Donze; RJ Kuppens; Nienke Bakker; Laura de Graaff; JAM van der Velden; Anita Hokken - Koelega

doi:10.1186/s13023-020-01440-6

Three years of growth hormone treatment in young adults with Prader-Willi syndrome: Sustained positive effects on body composition

Layla Damen, Stephany Donze, RJ Kuppens, Nienke Bakker, Laura de Graaff, JAM van der Velden, Anita Hokken - Koelega

Research output: Contribution to journal › Article › Academic › peer-review

20 Citations (Scopus)

39 Downloads (Pure)

Original language	English
Article number	163
Journal	Orphanet Journal of Rare Diseases
Volume	15
Issue number	1
DOIs	https://doi.org/10.1186/s13023-020-01440-6
Publication status	Published - 2020

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EMC MM-01-54-01

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10.1186/s13023-020-01440-6

Repub_128212_O-A.pdfFinal published version, 898 KB

http://hdl.handle.net/1765/128212

Cite this

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title = "Three years of growth hormone treatment in young adults with Prader-Willi syndrome: Sustained positive effects on body composition",

author = "Layla Damen and Stephany Donze and RJ Kuppens and Nienke Bakker and \{de Graaff\}, Laura and \{van der Velden\}, JAM and \{Hokken - Koelega\}, Anita",

year = "2020",

doi = "10.1186/s13023-020-01440-6",

language = "English",

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journal = "Orphanet Journal of Rare Diseases",

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AU - Damen, Layla

AU - Donze, Stephany

AU - Kuppens, RJ

AU - Bakker, Nienke

AU - de Graaff, Laura

AU - van der Velden, JAM

AU - Hokken - Koelega, Anita

PY - 2020

Y1 - 2020

U2 - 10.1186/s13023-020-01440-6

DO - 10.1186/s13023-020-01440-6

M3 - Article

C2 - 32580778

SN - 1750-1172

VL - 15

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

IS - 1

M1 - 163

ER -