Hanna Huopio

Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1

Hanna Huopio, Frank Reimann, Rebecca Ashfield et al. · Journal of Clinical Investigation · 2000 · 275 citations · Full text

Noninvasive Diagnosis of Focal Hyperinsulinism of Infancy With [18F]-DOPA Positron Emission Tomography

Timo Otonkoski, Kirsti Näntö‐Salonen, Marko Seppänen et al. · Diabetes · 2006 · 262 citations · Full text

Positron Emission Tomography, Focal Hyperinsulinism, Health Sciences +14

Severe Persistent Hyperinsulinemic Hypoglycemia due to a De Novo Glucokinase Mutation

Antonio L. Cuesta‐Muñoz, Hanna Huopio, Timo Otonkoski et al. · Diabetes · 2004 · 192 citations · Full text

A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1

Hanna Huopio, Timo Otonkoski, Ilkka Vauhkonen et al. · The Lancet · 2003 · 182 citations

Genetic Determinant, Autosomal Dominant Diabetes, Genetic Disorder +10

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

Timo Otonkoski, Carina Ämmälä, Hanna Huopio et al. · Diabetes · 1999 · 154 citations

Sulfonylurea Receptor, Insulin Signaling, Persistent Hyperinsulinemic Hypoglycemia +15