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2. Brain catecholamine depletion and motor impairment in a Th knock-in mouse with type B tyrosine hydroxylase deficiency. (14th August 2015)

3. Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures. Issue 4 (April 2018)

5. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study. Issue 7 (July 2020)

6. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study. Issue 7 (July 2020)

8. Fas (CD95) expression in myeloid cells promotes obesity‐induced muscle insulin resistance. Issue 1 (6th November 2013)

9. Genotype–phenotype spectrum in isolated and syndromic nanophthalmos. Issue 4 (30th September 2020)

10. Gonadectomy in conditions affecting sex development: a registry-based cohort study. Issue 6 (4th May 2021)