M. B. Mets

Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Bech-Hansen Nt, Ben F. Koop, M. B. Mets et al. · Nature Genetics · 1998 · 518 citations

Life Sciences, Genetics, Molecular Genetics +14

Early and Longitudinal Evaluations of Treated Infants and Children and Untreated Historical Patients with Congenital Toxoplasmosis: The Chicago Collaborative Treatment Trial

James McAuley, K. M. Boyer, Dushyant V. Patel et al. · Clinical Infectious Diseases · 1994 · 401 citations

Medicine, Neurology, Pediatrics +8

Outcome of Treatment for Congenital Toxoplasmosis, 1981-2004: The National Collaborative Chicago-Based, Congenital Toxoplasmosis Study

Rima McLeod, K. M. Boyer, Theodore Karrison et al. · Clinical Infectious Diseases · 2006 · 352 citations

Medicine, Child Health, Pediatrics +7

Neurologic and Developmental Outcome in Treated Congenital Toxoplasmosis

Nancy Roizen, Charles N. Swisher, Joyce Hopkins et al. · PEDIATRICS · 1995 · 156 citations

Medicine, Neurology, Pediatrics +13

Congenital Toxoplasmosis Transmitted from an Immunologically Competent Mother Infected Before Conception

Nicolas Vogel, Mary Jo Kirisits, E. Michael et al. · Clinical Infectious Diseases · 1996 · 130 citations · Full text

Veterinary Medicine, Immunology, Infectious Diseases +17