E. M. Bleeker‐Wagemakers

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

Roelof‐Jan Oostra, P. A. Bolhuis, Frits A. Wijburg et al. · Journal of Medical Genetics · 1994 · 120 citations · Full text

Ocular Disease, Genetics, Visual Outcome +18

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy

Pieter A. Bolhuis, E. M. Bleeker‐Wagemakers, Nico J. Ponne et al. · Biochemical and Biophysical Research Communications · 1990 · 80 citations

Biology, Neurodegenerative Diseases, Mendelian Disorder +12

Orbital cyst in addition to congenital cerebral and focal dermal malformations: a new entity

J.W. Delleman, J. W. E. Oorthuys, E. M. Bleeker‐Wagemakers et al. · Clinical Genetics · 1984 · 44 citations

Developmental Anomaly, Focal Dermal Malformations, Pediatric Brain Tumors +7

Additional eye findings in a girl with the velo‐cardio‐facial syndrome

Frits A. Beemer, J. J. E. M. De Nef, J.W. Delleman et al. · American Journal of Medical Genetics · 1986 · 42 citations

Ophthalmology, Additional Eye Findings, Pediatric Ophthalmology +3

The Mitochondrial DNA Mutation ND6*14,484C Associated with Leber Hereditary Optic Neuropathy, Leads to Deficiency of Complex I of the Respiratory Chain

Roelof‐Jan Oostra, M.J.M. Vangalen, P. A. Bolhuis et al. · Biochemical and Biophysical Research Communications · 1995 · 38 citations

Neurodegenerative Diseases, Respiratory Chain, Mendelian Disorder +10