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TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5
Karges, B et al. (2005)
Wissenschaftlicher Artikel
Immunological mechanisms associated with tong-term remission of human type 1 diabetes
Karges, B et al. (2006)
Wissenschaftlicher Artikel
Complete long-term recovery of beta-cell function in autoimmune type 1 diabetes after insulin treatment
Karges, B et al. (2004)
Wissenschaftlicher Artikel
Compound heterozygous and homozygous mutations of the TSH beta gene as a cause of congenital central hypothyroidism in Europe
Karges, B et al. (2004)
Wissenschaftlicher Artikel