Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Elke Schubert"'
Autor:
Elke Schubert-Hjalmarsson, Anders Fasth, Kelly Ickmans, Eva-Lott Mårdbrink, Ann-Charlott Söderpalm, Mari Lundberg
Publikováno v:
Pilot and Feasibility Studies, Vol 9, Iss 1, Pp 1-10 (2023)
Abstract Background Pain is a major symptom in adolescents with hypermobility spectrum disorder or hypermobile Ehlers-Danlos syndrome. Although the underlying mechanism causing generalized pain in children with hypermobility spectrum disorder or hype
Externí odkaz:
https://doaj.org/article/749020901d794c398217c6cff2add2b3
Autor:
Nóra Kerekes, Sara Lundqvist, Elke Schubert Hjalmarsson, Åsa Torinsson Naluai, Anne-Katrin Kantzer, Rajna Knez
Publikováno v:
PLoS ONE, Vol 17, Iss 9, p e0273653 (2022)
New research shows that the prevalence of neurodevelopmental disorders, such as attention-deficit/hyperactivity disorder (ADHD), is increased in children and adolescents as well as in adults with chronic pain, compared to those without chronic pain.
Externí odkaz:
https://doaj.org/article/028cfe7e469f415bbfa01f9009c3e02b
Autor:
Gé-Ann Kuiper, Eveline J. Langereis, Sandra Breyer, Marco Carbone, René M. Castelein, Deborah M. Eastwood, Christophe Garin, Nathalie Guffon, Peter M. van Hasselt, Pauline Hensman, Simon A. Jones, Vladimir Kenis, Moyo Kruyt, Johanna H. van der Lee, William G. Mackenzie, Paul J. Orchard, Neil Oxborrow, Rossella Parini, Amy Robinson, Elke Schubert Hjalmarsson, Klane K. White, Frits A. Wijburg
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-16 (2019)
Abstract Background In all patients with mucopolysaccharidosis type I (MPS I), skeletal disease (dysostosis multiplex) is a prominent, debilitating, condition related complication that may impact strongly on activities of daily living. Unfortunately,
Externí odkaz:
https://doaj.org/article/3516abfc646b46ba92eb0ac2089ec009
Autor:
Elke Schubert
Publikováno v:
Hebammen Wissen. 3:42-44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c74a898679d759f89b915744af77f183
https://doi.org/10.1007/s43877-022-0710-0
https://doi.org/10.1007/s43877-022-0710-0
Akademický článek
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Autor:
Elke Schubert Hjalmarsson, Anders Fasth, Kelly Ickmans, Eva-Lott Mårdbrink, Ann-Charlott Söderpalm, Mari Lundberg
Background: Pain is a major symptom in adolescents with Hypermobility Spectrum Disorder or Hypermobile Ehlers-Danlos Syndrome. Although the underlying mechanism causing generalized pain in children with Hypermobility Spectrum Disorder or Hypermobile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26f570d32b1d0953470ae8b10af8e6c5
https://doi.org/10.21203/rs.3.rs-1549755/v1
https://doi.org/10.21203/rs.3.rs-1549755/v1
Autor:
GĂŠ-Ann Kuiper, Langereis, Eveline, Breyer, Sandra, Carbone, Marco, RenĂŠ Castelein, Eastwood, Deborah, Garin, Christophe, Guffon, Nathalie, Hasselt, Peter, Hensman, Pauline, Jones, Simon, Kenis, Vladimir, Moyo Kruyt, Lee, Johanna, Mackenzie, William, Orchard, Paul, Oxborrow, Neil, Parini, Rossella, Robinson, Amy, Hjalmarsson, Elke Schubert, Klane White, Wijburg, Frits
Written round 1. (DOC 625 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30d93d7627027742d43880a86669e649
Autor:
Rossella Parini, Moyo C. Kruyt, Neil Oxborrow, Amy Robinson, Eveline J. Langereis, Deborah M. Eastwood, Simon Jones, Gé-Ann Kuiper, Johanna H. van der Lee, William G. Mackenzie, Sandra Breyer, Frits A. Wijburg, Klane K. White, Peter M. van Hasselt, René M. Castelein, Elke Schubert Hjalmarsson, Christophe Garin, Vladimir Kenis, Marco Carbone, Nathalie Guffon, Paul J. Orchard, Pauline Hensman
Publikováno v:
Orphanet journal of rare diseases, 14(1). BioMed Central
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 14(1). BioMed Central
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-16 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 14(1). BioMed Central
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-16 (2019)
Background In all patients with mucopolysaccharidosis type I (MPS I), skeletal disease (dysostosis multiplex) is a prominent, debilitating, condition related complication that may impact strongly on activities of daily living. Unfortunately, it is no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::430aba4cabd0cdd7a8fe01538e9ff4db
https://pure.amc.nl/en/publications/treatment-of-thoracolumbar-kyphosis-in-patients-with-mucopolysaccharidosis-type-i-results-of-an-international-consensus-procedure(60904828-f42b-49eb-9bee-e83ca4d1eb70).html
https://pure.amc.nl/en/publications/treatment-of-thoracolumbar-kyphosis-in-patients-with-mucopolysaccharidosis-type-i-results-of-an-international-consensus-procedure(60904828-f42b-49eb-9bee-e83ca4d1eb70).html
Autor:
GĂŠ-Ann Kuiper, Langereis, Eveline, Breyer, Sandra, Carbone, Marco, RenĂŠ Castelein, Eastwood, Deborah, Garin, Christophe, Guffon, Nathalie, Hasselt, Peter, Hensman, Pauline, Jones, Simon, Kenis, Vladimir, Moyo Kruyt, Lee, Johanna, Mackenzie, William, Orchard, Paul, Oxborrow, Neil, Parini, Rossella, Robinson, Amy, Hjalmarsson, Elke Schubert, Klane White, Wijburg, Frits
Draft statements to be discussed at the face-to-face meeting. (DOC 67 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ed8a837f1f2c835d6426af37d00aaa2