Kurt Ullrich

A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

Per Guldberg, Françoise Rey, Johannes Zschocke et al. · The American Journal of Human Genetics · 1998 · 352 citations · Full text

Metabolic Syndrome, Mendelian Disorder, Biochemistry +11

Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I)

Jan Peter Rake, Gepke Visser, Philippe Labrune et al. · European Journal of Pediatrics · 2002 · 320 citations

Clinical Course, Inherited Metabolic Disease, Diabetes +3

Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European study on glycogen storage disease type I (ESGSD I)

Jan Peter Rake, Gepke Visser, Philippe Labrune et al. · European Journal of Pediatrics · 2002 · 294 citations

Clinical Course, Inherited Metabolic Disease, Diabetes +3

Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type Ib: Results of the European Study on Glycogen Storage Disease Type I

Gepke Visser, J. P. Rake, John Fernandes et al. · The Journal of Pediatrics · 2000 · 253 citations

Gastroenterology, Pathology, Clinical Gastroenterology +6

Guidelines for management of glycogen storage disease type I—European study on glycogen storage disease type I (ESGSD I)

Jan Peter Rake, Gepke Visser, Philippe Labrune et al. · European Journal of Pediatrics · 2002 · 196 citations

Global Health, Inherited Metabolic Disease, Clinical Epidemiology +4