Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hasanain Hamid Shukur"'
Autor:
Hasanain Hamid Shukur, Yolanda B. de Rijke, Elisabeth F. C. van Rossum, Laith Hussain-Alkhateeb, Charlotte Höybye
Publikováno v:
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Prader-Willi syndrome (PWS) is a multisymptomatic, rare, genetic, neurodevelopmental disorder in adults mainly characterized by hyperphagia, cognitive dysfunction, behavioral problems and risk of morbid obesity. Although endocrine
Externí odkaz:
https://doaj.org/article/5080015b797c4e3eb9376aa89777cf85
Effects of Growth Hormone Treatment on Sleep-Related Parameters in Adults With Prader-Willi Syndrome
Autor:
Stense Farholt, Anders Palmstrøm Jørgensen, Hasanain Hamid Shukur, Laith Hussain-Alkhateeb, Ole Nørregaard, Charlotte Höybye
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Shukur, H H, Hussain-Alkhateeb, L, Farholt, S, Nørregaard, O, Jørgensen, A P & Hoybye, C 2021, ' Effects of Growth Hormone Treatment on Sleep-Related Parameters in Adults with Prader-Willi Syndrome ', Journal of Clinical Endocrinology and Metabolism, vol. 106, no. 9, pp. E3634-E3643 . https://doi.org/10.1210/clinem/dgab300
Shukur, H H, Hussain-Alkhateeb, L, Farholt, S, Nørregaard, O, Jørgensen, A P & Hoybye, C 2021, ' Effects of Growth Hormone Treatment on Sleep-Related Parameters in Adults with Prader-Willi Syndrome ', Journal of Clinical Endocrinology and Metabolism, vol. 106, no. 9, pp. E3634-E3643 . https://doi.org/10.1210/clinem/dgab300
Context Prader-Willi syndrome (PWS) is a rare, genetic, multisymptom, neurodevelopmental disease due to lack of the expression of the paternal genes in the q11 to q13 region of chromosome 15. The main characteristics of PWS are muscular hypotonia, hy
Autor:
Laith Hussain-Alkhateeb, Hasanain Hamid Shukur, Elisabeth F.C. van Rossum, Charlotte Höybye, Yolanda B. de Rijke
Publikováno v:
BMC Endocrine Disorders
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-7 (2020)
BMC Endocrine Disorders, 20(1):166. BioMed Central Ltd.
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-7 (2020)
BMC Endocrine Disorders, 20(1):166. BioMed Central Ltd.
Background Prader-Willi syndrome (PWS) is a multisymptomatic, rare, genetic, neurodevelopmental disorder in adults mainly characterized by hyperphagia, cognitive dysfunction, behavioral problems and risk of morbid obesity. Although endocrine insuffic
Autor:
Charlotte Höybye, Yolanda B de Rijke, Hasanain Hamid Shukur, Laith Hussain-Alkhateeb, Elisabeth F.C. van Rossum
Background: Prader-Willi syndrome (PWS) is a multisymptomatic, rare, genetic, neurodevelopmental disorder in adults mainly characterized by hyperphagia, cognitive dysfunction, behavioral problems and risk of morbid obesity. Although endocrine insuffi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00bae0df4eaeb0fbfd5cee531c042bac
https://doi.org/10.21203/rs.3.rs-31626/v1
https://doi.org/10.21203/rs.3.rs-31626/v1
Autor:
Yolanda B de Rijke, Olle Kämpe, Elisabeth F.C. van Rossum, Hasanain Hamid Shukur, Charlotte Höybye
Publikováno v:
Endocrine Abstracts.