Research output per year
Research output per year
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Dive into the research topics where Erik Gerlo is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Homozygosity for aquaporin 7G264V in three unrelated children with hyperglyceroluria and a mild platelet secretion defect.
Goubau, C., Martens, G. & Gerlo, E., 2012, In: Genet. Med.. 15, p. 55-63 9 p.Research output: Contribution to journal › Article › peer-review
33 Citations (Scopus) -
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disorders.
Meulemans, A., Gerlo, E., Seneca, S., Lissens, W., Smet, J., Vancoster, R. & De Meirleir, L., 2007, In: Acta Neurol Belg. 107, September, p. 78-83 6 p.Research output: Contribution to journal › Article › peer-review
18 Citations (Scopus) -
Preliminary performance evaluation of blood gas analyzers
Couck, P., Ghys, T., Van Gastel, E., Van Coillie, M., Gorus, F. & Gerlo, E., 2006, In: Clinical Chemistry and Laboratory Medicine. 44, 8, p. 1030-1034 5 p.Research output: Contribution to journal › Article › peer-review
8 Citations (Scopus) -
Aminoacylase I deficiency: a novel inborn error of metabolism.
Van Coster, R., Gerlo, E., Giardina, T. G., Engelke, U., Smet, J., De Praeter, C. M., Meersschaut, V. A., De Meirleir, L., Seneca, S., Devreese, B., Leroy, B., Herga, S., Pierrier, J. P., Wevers, R. A. & Lissens, W., Dec 2005, In: Biochem Biophys Res Commun. 338, December, p. 1322-1326 5 p.Research output: Contribution to journal › Article › peer-review
54 Citations (Scopus) -
Clinical and diagnostic characteristics of complex III deficiency due to mutations in BCS1L
De Meirleir, L., Seneca, S., Gerlo, E., Lissens, W., Damis, E., Garcia Silva, M., Hernandez, E., Hoorens, A., Sepulchre, B. & Van Coster, R., Aug 2003, In: Am J Med Genet A. 121, August, p. 126-131 6 p.Research output: Contribution to journal › Article › peer-review