Study by mass spectrometry of amino acid sequences in peptides containing histidine.

Por Vliegenthart, J F, Dorland, L
Publicado em 1970

Increased urinary leukotriene E(4) during febrile attacks in the hyperimmunoglobulinaemia D and periodic fever syndrome

Por Frenkel, J, Willemsen, M, Weemaes, C, Dorland, L, Mayatepek, E
Publicado em 2001

Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency

Por Helders PJM, Dorland L, Visser G, Custers J WH, Takken T, de Koning TJ
Publicado em 2005-05-01

Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency

Por Takken, T, Custers, J WH, Visser, G, Dorland, L, Helders, PJM, de Koning, TJ
Publicado em 2005

Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency.

Por Kelly, D P, Whelan, A J, Ogden, M L, Alpers, R, Zhang, Z F, Bellus, G, Gregersen, N, Dorland, L, Strauss, A W
Publicado em 1990

Expanding the clinical spectrum of 3-phosphoglycerate dehydrogenase deficiency

Por Tabatabaie, L., Klomp, L. W. J., Rubio-Gozalbo, M. E., Spaapen, L. J. M., Haagen, A. A. M., Dorland, L., de Koning, T. J.
Publicado em 2010

Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene.

Por Waterham, H R, Wijburg, F A, Hennekam, R C, Vreken, P, Poll-The, B T, Dorland, L, Duran, M, Jira, P E, Smeitink, J A, Wevers, R A, Wanders, R J
Publicado em 1998

Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy

Por Körver-Keularts, I. M. L. W., de Visser, M., Bakker, H. D., Wanders, R. J. A., Vansenne, F., Scholte, H. R., Dorland, L., Nicolaes, G. A. F., Spaapen, L. M. J., Smeets, H. J. M., Hendrickx, A. T. M., van den Bosch, B. J. C.
Publicado no JIMD Rep (2015)