H. H. Schmidt

Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease

A. Członkowska, T. Litwin, G. Gromadzka, 2005, Clinical genetics.

p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease

A. Członkowska, M. Rodo, H. H. Schmidt, 2006, Movement disorders : official journal of the Movement Disorder Society.

Relation of cholesterol-year score to severity of calcific atherosclerosis and tissue deposition in homozygous familial hypercholesterolemia.

E. Makariou, H. H. Schmidt, K. Dugi, 1996, The American journal of cardiology.

Delayed low density lipoprotein (LDL) catabolism despite a functional intact LDL-apolipoprotein B particle and LDL-receptor in a subject with clinical homozygous familial hypercholesterolemia.

H. Brewer, R. Shamburek, H. H. Schmidt, 1998, The Journal of clinical endocrinology and metabolism.

Erdheim-Chester disease: low low-density lipoprotein levels due to rapid catabolism.

B. Brewer, R. Gregg, R. Shamburek, 1997, Metabolism: clinical and experimental.