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Author/Creator Vanlander, Arnaud V.

2. Forearm Deoxyhemoglobin and Deoxymyoglobin (Deoxy[Hb + Mb]) Measured by Near-Infrared Spectroscopy (NIRS) Using a Handgrip Test in Mitochondrial Myopathy. Issue 3 (March 2015)

Authors:
Celie, Bert M.; Boone, Jan; Smet, Joél E.; Vanlander, Arnaud V.; De Bleecker, Jan L.; Van Coster, Rudy N.; Bourgois, Jan G.
Journal:
Applied spectroscopy
Issue:
Volume 69:Issue 3(2015)
Page Start:
342
Record Type:
Journal Article
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3. Mutation of the iron‐sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy. Issue 6 (14th May 2015)

Authors:
Debray, François‐Guillaume; Stümpfig, Claudia; Vanlander, Arnaud V.; Dideberg, Vinciane; Josse, Claire; Caberg, Jean‐Hubert; Boemer, François; Bours, Vincent; Stevens, René; Seneca, Sara; Smet, Joél; Lill, Roland; van Coster, Rudy
Journal:
Journal of inherited metabolic disease
Issue:
Volume 38:Issue 6(2015)
Page Start:
1147
Record Type:
Journal Article
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4. Severe congenital neutropenia with neurological impairment due to a homozygous VPS45 p.E238K mutation: A case report suggesting a genotype–phenotype correlation. (11th September 2015)

Authors:
Meerschaut, Ilse; Bordon, Victoria; Dhooge, Catharina; Delbeke, Patricia; Vanlander, Arnaud V.; Simon, Amos; Klein, Christoph; Kooy, R. Frank; Somech, Raz; Callewaert, Bert
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 12(2015:Dec.)
Page Start:
3214
Record Type:
Journal Article
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5. TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism. Issue 5 (24th July 2019)

Authors:
Jennions, Elizabeth; Hedberg‐Oldfors, Carola; Berglund, Anna‐Karin; Kollberg, Gittan; Törnhage, Carl‐Johan; Eklund, Erik A.; Oldfors, Anders; Verloo, Patrick; Vanlander, Arnaud V.; De Meirleir, Linda; Seneca, Sara; Sterky, Fredrik H.; Darin, Niklas
Journal:
Journal of inherited metabolic disease
Issue:
Volume 42:Issue 5(2019)
Page Start:
898
Record Type:
Journal Article
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6. Two Siblings with Homozygous Pathogenic Splice‐Site Variant in Mitochondrial Asparaginyl–tRNA Synthetase (NARS2). Issue 2 (February 2015)

Authors:
Vanlander, Arnaud V.; Menten, Björn; Smet, Joél; De Meirleir, Linda; Sante, Tom; De Paepe, Boel; Seneca, Sara; Pearce, Sarah F.; Powell, Christopher A.; Vergult, Sarah; Michotte, Alex; De Latter, Elien; Vantomme, Lies; Minczuk, Michal; Van Coster, Rudy
Journal:
Human mutation
Issue:
Volume 36:Issue 2(2015:Feb.)
Page Start:
222
Record Type:
Journal Article
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