Peter J. Milla

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

Maria Bitner‐Glindzicz, Keith Lindley, Paul Rutland et al. · Nature Genetics · 2000 · 324 citations

Infantile Hyperinsulinism, Mendelian Disorder, Genetic Disorder +9

Manganese toxicity in children receiving long-term parenteral nutrition

J. M. Fell, N Meadows, Karim Khan et al. · The Lancet · 1996 · 310 citations

Nutrition, Infant Nutrition, Clinical Nutrition +9

Confocal Endomicroscopy Shows Food-Associated Changes in the Intestinal Mucosa of Patients With Irritable Bowel Syndrome

Annette Fritscher‐Ravens, Detlef Schuppan, Mark Ellrichmann et al. · Gastroenterology · 2014 · 309 citations · Full text

Nutrition, Food Intolerance, Functional Gastrointestinal Disorder +8

Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

Robert S. Jackson, John W.M. Creemers, I. Sadaf Farooqi et al. · Journal of Clinical Investigation · 2003 · 304 citations

Metabolic Disorder, Genetics, Immunology +18

Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

Robert S. Jackson, John W.M. Creemers, I. Sadaf Farooqi et al. · Journal of Clinical Investigation · 2003 · 296 citations · Full text