arrow
返回
L

Lambert P. van den Heuvel

university hospitals leuven

44H指数
135论文数
6.9K被引数
收录论文 40
发表时间
Complement Factor I Deficiency-Associated Neuroinflammatory Disease Among Old Order Amish补体因子I缺乏相关神经炎症性疾病在老秩序阿米什人群中的研究
err2025-06-30
err0
PREAI
errWhitney Reid; Laura Baas; Amy L. Stiegler; Titus J. Boggon; Portia A. Kreiger; Kathleen E. Sullivan; Edward M. Behrens; Vinay V.R. Kandula; Lambert P. van den Heuvel; Karlla W. Brigatti; Vincent J. Carson; Neil Romberg
err分享
err收藏
Protective mechanisms harnessing against injurious heme and preventing kidney damage in STEC-HUS: toward new therapies?
err2022-06-01
err1
PREAI
errWagener, Frank A. D. T. G.; van de Kar, Nicole C. A. J.; van den Heuvel, Lambert P.
err分享
err收藏
Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome
err2022-01-05
err13
errOAAI
errde Jong, Sarah; de Breuk, Anita; Bakker, Bjorn; Katti, Suresh; Hoyng, Carel B.; Nilsson, Sara C.; Blom, Anna M.; van den Heuvel, Lambert P.; den Hollander, Anneke I.; Volokhina, Elena B.
err分享
err收藏
Shiga Toxin 2a Induces NETosis via NOX-Dependent Pathway
err2021-12-01
err5
errOAAI
errFeitz, Wouter J. C.; Suntharalingham, Samuel; Khan, Meraj; Ortiz-Sandoval, Carolina G.; Palaniyar, Nades; van den Heuvel, Lambert P.; van de Kar, Nicole C. A. J.; Licht, Christoph
err分享
err收藏
Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene
err2021-09-11
err9
errOAAI
errde Jong, Sarah; de Breuk, Anita; Volokhina, Elena B.; Bakker, Bjorn; Garanto, Alejandro; Fauser, Sascha; Katti, Suresh; Hoyng, Carel B.; Lechanteur, Yara T. E.; van den Heuvel, Lambert P.; den Hollander, Anneke, I
err分享
err收藏
Implications of genetic variation in the complement system in age-related macular degeneration
err2021-09-01
err47
errOAAI
errde Jong, Sarah; Gagliardi, Giuliana; Garanto, Alejandro; de Breuk, Anita; Lechanteur, Yara T. E.; Katti, Suresh; van den Heuvel, Lambert P.; Volokhina, Elena B.; den Hollander, Anneke I.
err分享
err收藏
Effect of rare coding variants in the CFI gene on Factor I expression levels
err2020-06-08
err41
errOAAI
errde Jong, Sarah; Volokhina, Elena B.; de Breuk, Anita; Nilsson, Sara C.; de Jong, Eiko K.; van der Kar, Nicole C. A. J.; Bakker, Bjorn; Hoyng, Carel B.; van den Heuvel, Lambert P.; Blom, Anna M.; den Hollander, Anneke, I
err分享
err收藏
Biosynthetic homeostasis and resilience of the complement system in health and infectious disease
err2019-07-01
err19
errOAAI
errWillems, Esther; Alkema, Wynand; Keizer-Garritsen, Jenneke; Suppers, Anouk; van der Flier, Michiel; Philipsen, Ria H. L. A.; van den Heuvel, Lambert P.; Volokhina, Elena; van der Molen, Renate G.; Herberg, Jethro A.; Levin, Michael; Wright, Victoria J.; Ahout, Inge M. L.; Ferwerda, Gerben; Emonts, Marieke; Boeddha, Navin P.; Rivero-Calle, Irene; Martinon Torres, Federico; Wessels, Hans J. C. T.; de Groot, Ronald; van Gool, Alain J.; Gloerich, Jolein; de Jonge, Marien I.
err分享
err收藏
A Novel Choroidal Endothelial Cell Line Has a Decreased Affinity for the Age-Related Macular Degeneration-Associated Complement Factor H Variant 402H
err2018-02-01
err12
errOAAI
errLoeven, Markus A.; van Gemst, Jasper J.; Schophuizen, Carolien M. S.; Tilakaratna, Viranga; van den Heuvel, Lambert P.; Day, Anthony J.; Klevering, B. Jeroen; van der Vlag, Johan
err分享
err收藏
ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism
errBRAIN
IF11.7
err2017-05-24
err105
errOAAI
errDesai, Radha; Frazier, Ann E.; Durigon, Romina; Patel, Harshil; Jones, Aleck W.; Rosa, Ilaria Dalla; Lake, Nicole J.; Compton, Alison G.; Mountford, Hayley S.; Tucker, Elena J.; Mitchell, Alice L. R.; Jackson, Deborah; Sesay, Abdul; Di Re, Miriam; van den Heuvel, Lambert P.; Burke, Derek; Francis, David; Lunke, Sebastian; McGillivray, George; Mandelstam, Simone; Mochel, Fanny; Keren, Boris; Jardel, Claude; Turner, Anne M.; Andrews, P. Ian; Smeitink, Jan; Spelbrink, Johannes N.; Heales, Simon J.; Kohda, Masakazu; Ohtake, Akira; Murayama, Kei; Okazaki, Yasushi; Lombes, Anne; Holt, Ian J.; Thorburn, David R.; Spinazzola, Antonella
err分享
err收藏
Mutations in COA6 cause Cytochrome c Oxidase Deficiency and Neonatal Hypertrophic CardiomyopathyCOA6突变导致细胞色素c氧化酶缺乏和新生儿肥厚型心肌病
err2014-11-18
err76
PREAI
errBaertling, Fabian; van den Brand, Mariel A. M.; Hertecant, Jozef L.; Al-Shamsi, Aisha; van den Heuvel, Lambert P.; Distelmaier, Felix; Mayatepek, Ertan; Smeitink, Jan A.; Nijtmans, Leo G. J.; Rodenburg, Richard J. T.
err分享
err收藏
SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors
err2014-04-30
err75
errOAAI
errRenkema, G. Herma; Wortmann, Saskia B.; Smeets, Roel J.; Venselaar, Hanka; Antoine, Marion; Visser, Gepke; Ben-Omran, Tawfeg; van den Heuvel, Lambert P.; Timmers, Henri J. L. M.; Smeitink, Jan A.; Rodenburg, Richard J. T.
err分享
err收藏
Compound heterozygous mutations in the C6 gene of a child with recurrent infections
err2014-04-01
err12
PREAI
errWestra, Dineke; Kurvers, Roel A. J.; van den Heuvel, Lambert P.; Wuerzner, Reinhard; Hoppenreijs, Esther P. A. H.; van der Flier, Michiel; van de Kar, Nicole C. A. J.; Warris, Adilia
err分享
err收藏
A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy
errBRAIN
IF11.7
err2013-04-18
err84
errOAAI
errJonckheere, An I.; Renkema, G. Herma; Bras, Maaike; van den Heuvel, Lambert P.; Hoischen, Alexander; Gilissen, Christian; Nabuurs, Sander B.; Huynen, Martijn A.; de Vries, Maaike C.; Smeitink, Jan A. M.; Rodenburg, Richard J. T.
err分享
err收藏
A novel mutation in COQ2 leading to fatal infantile multisystem disease
err2013-03-01
err48
PREAI
errJakobs, Bernadette S.; van den Heuvel, Lambert P.; Smeets, Roel J. P.; de Vries, Maaike C.; Hien, Steffen; Schaible, Thomas; Smeitink, Jan A. M.; Wevers, Ron A.; Wortmann, Saskia B.; Rodenburg, Richard J. T.
err分享
err收藏
Molecular base of biochemical complex I deficiency
err2012-09-01
err35
PREAI
errHoefs, Saskia J. G.; Rodenburg, Richard J.; Smeitink, Jan A. M.; van den Heuvel, Lambert P.
err分享
err收藏
A comprehensive full factorial LC-MS/MS proteomics benchmark data set
err2012-08-06
err11
errOAAI
errWessels, Hans J. C. T.; Bloemberg, Tom G.; van Dael, Maurice; Wehrens, Ron; Buydens, Lutgarde M. C.; van den Heuvel, Lambert P.; Gloerich, Jolein
err分享
err收藏
Impaired ubiquitin-proteasome-mediated PGC-1α protein turnover and induced mitochondrial biogenesis secondary to complex-I deficiency
err2012-05-16
err8
PREAI
errFarhoud, Murtada H.; Nijtmans, Leo G.; Wanders, Ronald J. A.; Wessels, Hans J. C. T.; Lasonder, Edwin; Janssen, Antoon J. M.; Rodenburg, Richard R. J.; van den Heuvel, Lambert P.; Smeitink, Jan A. M.
err分享
err收藏
Iterative orthology prediction uncovers new mitochondrial proteins and identifies C12orf62 as the human ortholog of COX14, a protein involved in the assembly of cytochrome c oxidase
err2012-02-22
err95
errOAAI
errSzklarczyk, Radek; Wanschers, Bas F. J.; Cuypers, Thomas D.; Esseling, John J.; Riemersma, Moniek; van den Brand, Mariel A. M.; Gloerich, Jolein; Lasonder, Edwin; van den Heuvel, Lambert P.; Nijtmans, Leo G.; Huynen, Martijn A.
err分享
err收藏
Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology
err2011-11-01
err39
PREAI
errJonckheere, An I.; Huigsloot, Merei; Lammens, Martin; Jansen, Jitske; van den Heuvel, Lambert P.; Spiekerkoetter, Ute; von Kleist-Retzow, Juergen-Christoph; Forkink, Marleen; Koopman, Werner J. H.; Szklarczyk, Radek; Huynen, Martijn A.; Fransen, Jack A.; Smeitink, Jan A. M.; Rodenburg, Richard J. T.
err分享
err收藏