Wolfram syndrome: a clinical and molecular genetic analysis

Por Eller, P., Foger, B., Gander, R., Sauper, T., Lechleitner, M., Finkenstedt, G., Patsch, J.
Publicado em 2001

Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.

Por Miesenböck, G, Hölzl, B, Föger, B, Brandstätter, E, Paulweber, B, Sandhofer, F, Patsch, J R
Publicado em 1993

ADENOVIRAL EXPRESSION OF HUMAN LCAT IN NON-HUMAN PRIMATES LEADS TO AN ANTI-ATHEROGENIC LIPOPROTEIN PHENOTYPE BY INCREASING HDL AND LOWERING LDL

Por Amar, M.J.A, Shamburek, R.D, Vaisman, B., Knapper, C, Foger, B., Hoyt, R.F., Fojo, S.S, Brewer, B.H., Remaley, T.A.
Publicado em 2009