Theresa Penger

Adrenarche and pubarche in girls with turner syndrome during growth-promoting therapy with human growth hormone

M. Rauh, P. Oppelt, H. Dörr, 2019, BMC Endocrine Disorders.

Lipid profiles in Children and Adolescents with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency (CAH)

M. Rauh, H. Doerr, J. Woelfle, 2020 .

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency

P. Oppelt, H. Dörr, Theresa Penger, 2018, BMC Pregnancy and Childbirth.

Birth Sizes of Neonates with Congenital Adrenal Hyperplasia Secondary to 21-Hydroxylase Deficiency

H. Dörr, Theresa Penger, M. Marx, 2018, Journal of Clinical Research in Pediatric Endocrinology.

Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency

H. Dörr, Theresa Penger, M. Marx, 2019, Journal of clinical research in pediatric endocrinology.

Adrenal crisis in a 14-year-old boy 12 years after hematopoietic stem cell transplantation

H. Dörr, M. Metzler, Theresa Penger, 2018, Endocrinology, diabetes & metabolism case reports.

Short-term adverse effects of testosterone used for priming in prepubertal boys before growth hormone stimulation test

H. Dörr, Theresa Penger, M. Marx, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

BDV-syndrome: An emerging syndrome with profound obesity and neurodevelopmental delay resembling Prader-Willi syndrome.

A. Ekici, A. Reis, M. Krumbiegel, 2021, The Journal of clinical endocrinology and metabolism.