M. Kreiter

A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.

K. White, M. Econs, M. Mohammadi, 2007, Journal of musculoskeletal & neuronal interactions.

Familial tumoral calcinosis is characterized by ectopic calcifications and hyperphosphatemia due to inactivating mutations in FGF 23 or UDP-N-acetyl-α-D-galactosamine : polypeptide

K. White, M. Econs, M. Mohammadi, 2007 .

A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.

K. White, M. Econs, M. Mohammadi, 2007, The Journal of clinical investigation.

Preserving adult height potential in girls with idiopathic true precocious puberty.

G. W. Moll, L. Levitsky, L. Cuttler, 1990, The Journal of pediatrics.

Height prognosis of children with true precocious puberty and growth hormone deficiency: effect of combination therapy with gonadotropin releasing hormone agonist and growth hormone.

J. Cara, R. Rosenfield, M. Kreiter, 1992, The Journal of pediatrics.

3C (cranio-cerebello-cardiac) syndrome: a recently delineated and easily recognizable congenital malformation syndrome.

J. Hoo, A. Perszyk, M. Kreiter, 1994, American journal of medical genetics.

Maturation of gonadotropin and sex steroid responses to gonadotropin-releasing hormone agonist in males.

L. Levitsky, D. Ehrmann, L. Cuttler, 1993, The Journal of clinical endocrinology and metabolism.