Zobrazeno 1 - 10
of 74
pro vyhledávání: '"I. Jonckheere"'
Publikováno v:
Biogeosciences, Vol 7, Iss 1, Pp 199-215 (2010)
In this study, we quantified the predictive accuracy loss involved with omitting photosynthetic capacity variation for a Scots pine (Pinus sylvestris L.) stand in Flanders, Belgium. Over the course of one phenological year, we measured the maximum ca
Externí odkaz:
https://doaj.org/article/43eb8213215e4d17af88599382c487a1
Autor:
Dulce Quelhas, Sandra D.K. Kingma, An I. Jonckheere, Claudia S. Smeets-Peels, Daniel Costa Gomes, José Duro, Anabela Oliveira, Gert Matthijs, Laura K.M. Steinbusch, Jaak Jaeken, Isabel Rivera, Estela Rubio-Gozalbo
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 38, Iss , Pp 101057- (2024)
The authors report the natural history of three patients with late-diagnosed Classic Galactosemia (CG) (at 16, 19 and 28 years). This was due to a combination of factors: absence of neonatal screening, absence of some typical acute neonatal symptoms,
Externí odkaz:
https://doaj.org/article/6931300d149b424894c7347156a86442
Autor:
T. C. Mangodt, K. Vanden Driessche, K. K. Norga, N. Moes, M. De Bruyne, F. Haerynck, V. Bordon, A. C. Jansen, A. I. Jonckheere
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background LPS-responsive beige-like anchor protein (LRBA) deficiency is a primary immunodeficiency disease (PID) characterized by a regulatory T cell defect resulting in immune dysregulation and autoimmunity. We present two siblings born to
Externí odkaz:
https://doaj.org/article/11417f224627461098abc6129ad14cdc
Autor:
Anne-Sophie Weyns, Annelies A.J. Verlaet, Maxim Van Herreweghe, Annelies Breynaert, Erik Fransen, Ingrid De Meester, Emilie Logie, Wim Vanden Berghe, Helene Verhelst, Dirk Van West, Ingrid Van Ingelghem, An I. Jonckheere, Diane Beysen, Sandra Kenis, Els Moens, Aalt P.J. van Roest, Huub F.J. Savelkoul, Tess De Bruyne, Luc Pieters, Berten Ceulemans, Nina Hermans
Publikováno v:
Journal of Functional Foods, Vol 97, Iss , Pp 105247- (2022)
Objectives: To evaluate the effect of French Maritime Pine Bark Extract (PBE; Pycnogenol®) on immune, oxidative stress and neurochemical biomarkers in paediatric Attention-Deficit Hyperactivity Disorder (ADHD) as compared to methylphenidate (MPH) an
Externí odkaz:
https://doaj.org/article/05af4a40e8b14b9b860799696b1893fd
Autor:
Anne-Sophie Weyns, Annelies A.J. Verlaet, Annelies Breynaert, Tania Naessens, Erik Fransen, Helene Verhelst, Dirk Van West, Ingrid Van Ingelghem, An I. Jonckheere, Diane Beysen, Sandra Kenis, Els Moens, Aalt P.J. van Roest, Huub F.J. Savelkoul, Tess De Bruyne, Luc Pieters, Berten Ceulemans, Nina Hermans
Publikováno v:
Journal of Functional Foods, Vol 97, Iss , Pp 105246- (2022)
Objectives: Determine the effect of French Maritime Pine Bark Extract (PBE; Pycnogenol®) on Attention-Deficit Hyperactivity Disorder (ADHD) behaviour and co-morbid physical/psychiatric symptoms, compared to placebo and the medicine MPH, and to asses
Externí odkaz:
https://doaj.org/article/f0948939a4bd4a3e90ca5fb76c49b8e1
Publikováno v:
JIMD Reports, Vol 59, Iss 1, Pp 90-103 (2021)
Abstract Monosialotetrahexosylganglioside (GMI) gangliosidosis and Morquio type B (MorB) are two lysosomal storage disorders (LSDs) caused by the same enzyme deficiency, β‐galactosidase (βgal). GMI gangliosidosis, associated with GMI ganglioside
Externí odkaz:
https://doaj.org/article/6c127b94a3e94d2eb2d0d33fd1bb903d
Autor:
An I. Jonckheere, Sandra D. K. Kingma
Publikováno v:
Journal of inherited metabolic disease
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder characterized by α-L-iduronidase deficiency. Patients present with a broad spectrum of disease severity ranging from the most severe phenotype (Hurler) with devastating neurocognit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80cb4d2eb2eb801156cf0d726c2abba8
https://doi.org/10.1002/jimd.12431
https://doi.org/10.1002/jimd.12431
Publikováno v:
JIMD Reports, Vol 59, Iss 1, Pp 90-103 (2021)
JIMD Reports
JIMD Reports
Monosialotetrahexosylganglioside (GMI) gangliosidosis and Morquio type B (MorB) are two lysosomal storage disorders (LSDs) caused by the same enzyme deficiency, β‐galactosidase (βgal). GMI gangliosidosis, associated with GMI ganglioside accumulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b38882778877a5299e25367f2cd2044
https://doaj.org/article/6c127b94a3e94d2eb2d0d33fd1bb903d
https://doaj.org/article/6c127b94a3e94d2eb2d0d33fd1bb903d
Akademický článek
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Autor:
Martin Lammens, Merei Huigsloot, Richard J. Rodenburg, Radek Szklarczyk, Ute Spiekerkoetter, Lambert P. van den Heuvel, Martijn A. Huynen, Werner J.H. Koopman, Jürgen-Christoph von Kleist-Retzow, Marleen Forkink, Jack A.M. Fransen, Jitske Jansen, An I. Jonckheere, Jan A.M. Smeitink
Publikováno v:
Mitochondrion, 11, 6, pp. 954-63
Mitochondrion, 11, 954-63
ResearcherID
Mitochondrion, 11, 954-63
ResearcherID
Contains fulltext : 97316.pdf (Publisher’s version ) (Closed access) We report a fragmented mitochondrial network and swollen and irregularly shaped mitochondria with partial to complete loss of the cristae in fibroblasts of a patient with a novel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::972fd7a78c5871d452ab572f18693111
https://hdl.handle.net/2066/97316
https://hdl.handle.net/2066/97316