L.A.H. Monnens

Leigh's Encephalomyelopathy in a Patient With Cytochrome <i>c</i> Oxidase Deficiency in Muscle Tissue

J. L. Willems, L.A.H. Monnens, J. M. F. Trijbels et al. · PEDIATRICS · 1977 · 238 citations

Life Sciences, Neurology, Neuroscience +17

New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels.

S.M. Mulders, Nine V.A.M. Knoers, A.F. van Lieburg et al. · Journal of the American Society of Nephrology · 1997 · 176 citations

Life Sciences, Genetics, Physiology +16

Hereditary Mitochondrial Myopathy with Lactic Acidemia, A DeToni-Fanconi-Debr?? Syndrome, and a Defective Respiratory Chain in Voluntary Striated Muscles

J. P. G. M. Van Biervliet, L. Bruinvis, D. Ketting et al. · Pediatric Research · 1977 · 176 citations

Medicine, Genetics, Molecular Genetics +17

Clinical Presentation and Follow-Up of 30 Patients with Congenital Nephrogenic Diabetes Insipidus

A.F. van Lieburg, N. Knoers, L.A.H. Monnens · Journal of the American Society of Nephrology · 1999 · 137 citations

Medicine, Endocrinology, Nephrology +12

Hyperhomocysteinemia and other thrombotic risk factors in women with placental vasculopathy

E.F. van der Molen, Bert Verbruggen, I.R.O. Nováková et al. · BJOG An International Journal of Obstetrics & Gynaecology · 2000 · 93 citations

Medicine, Genetics, Obstetrics +14