Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Inge‐Lot Klein"'
Autor:
Kim F. E. van de Loo, José A. E. Custers, Saskia Koene, Inge-Lot Klein, Mirian C. H. Janssen, Jan A. M. Smeitink, Christianne M. Verhaak
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Mitochondrial diseases (MD) are generally serious and progressive, inherited metabolic diseases. There is a high comorbidity of anxiety and depression and limitations in daily functioning. The complexity and duration of the diagno
Externí odkaz:
https://doaj.org/article/f4b30aa16e6a41bb8597d4e8ed9e6614
Autor:
Inge‐Lot Klein, Christianne M. Verhaak, Jan A. M. Smeitink, Paul de Laat, Mirian C. H. Janssen, José A. E. Custers
Publikováno v:
Journal of Inherited Metabolic Disease, 45, 6, pp. 1130-1142
Journal of Inherited Metabolic Disease, 45, 1130-1142
Journal of Inherited Metabolic Disease, 45, 1130-1142
Contains fulltext : 286871.pdf (Publisher’s version ) (Open Access) Severe fatigue is a common complaint in patients with primary mitochondrial disease. However, less is known about the course of fatigue over time. This longitudinal observational c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1f7ac32f8cefc257081658790bc2761
https://repository.ubn.ru.nl/handle/2066/286871
https://repository.ubn.ru.nl/handle/2066/286871
Autor:
E. van der Veer, Inge-Lot Klein, Jan A.M. Smeitink, José A. E. Custers, T. J. Hoogeboom, Mirian C. H. Janssen, K. F. E. van de Loo, Chris M. Verhaak
Publikováno v:
Trials, 22, 1
Trials, 22
Trials
Trials, Vol 22, Iss 1, Pp 1-11 (2021)
Trials, 22
Trials
Trials, Vol 22, Iss 1, Pp 1-11 (2021)
Background Mitochondrial disease is a rare, hereditary disease with a heterogeneous clinical presentation. However, fatigue is a common and burdensome complaint in children and adolescents with mitochondrial disease. No psychological intervention tar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e19310f2c8cb16e213216985c6c177
https://hdl.handle.net/2066/231556
https://hdl.handle.net/2066/231556
Autor:
Clara D.M. van Karnebeek, Christianne M. Verhaak, Mirian C. H. Janssen, José A.E. Custers, Elja van der Veer, Roy P. C. Kessels, Kim F. E. van de Loo, Jan A.M. Smeitink, Inge-Lot Klein
Publikováno v:
Neuroscience and Biobehavioral Reviews, 125, pp. 57-77
Neuroscience and Biobehavioral Reviews, 125, 57-77
Neuroscience and Biobehavioral Reviews, 125, 57-77
Contains fulltext : 230490.pdf (Publisher’s version ) (Open Access) Mitochondrial diseases (MDs) are rare, heterogeneous, hereditary and progressive in nature. In addition to the serious somatic symptoms, patients with MD also experience problems r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::161bbae9b44aef59f425a4e335d51608
https://pubmed.ncbi.nlm.nih.gov/33582231
https://pubmed.ncbi.nlm.nih.gov/33582231