Endocrine manifestations and management of Prader-Willi syndrome

Por Emerick, Jill E, Vogt, Karen S
Publicado em 2013

Growth Hormone Therapy in Adults with Prader-Willi Syndrome

Por Vogt, Karen S., Emerick, Jill E.
Publicado no Diseases (2015)

Successful Transition From Insulin to Sulfonylurea Therapy in a Patient With Monogenic Neonatal Diabetes Owing to a KCNJ11 P333L Mutation

Por Philla, Katherine Q., Bauer, Andrew J., Vogt, Karen S., Greeley, Siri Atma W.
Publicado em 2013

Successful Transition From Insulin to Sulfonylurea Therapy in a Patient With Monogenic Neonatal Diabetes Owing to a KCNJ11 P333L Mutation. Diabetes Care 2013;36:e201

Por Philla, Katherine Q., Bauer, Andrew J., Vogt, Karen S., Greeley, Siri Atma W.
Publicado no Diabetes Care (2014)

QRICH1 Mutations cause a Chondrodysplasia with Developmental Delay

Por Lui, Julian C., Hee Jee, Youn, Lee, Audrey, Yue, Shanna, Wagner, Jacob, Donnelly, Deirdre E., Vogt, Karen S., Baron, Jeffrey
Publicado no Clin Genet (2018)