G. F. Hoffmann

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis

Michèl A.A.P. Willemsen, Marcel M. Verbeek, Erik‐Jan Kamsteeg et al. · Brain · 2010 · 234 citations · Full text

Medicine, Neurology, Neuroscience +14

Clinical Course, Early Diagnosis, Treatment, and Prevention of Disease in Glutaryl-CoA Dehydrogenase Deficiency

G. F. Hoffmann, S. Athanassopoulos, A Burlina et al. · Neuropediatrics · 1996 · 227 citations

Life Sciences, Neurology, Nutrition +15

High prevalence of vitamin D deficiency in young children in a highly sunny humid country: a global health problem.

Abdülbari Bener, M Al-Ali, G. F. Hoffmann · PubMed · 2009 · 123 citations

Medicine, Child Health, Pediatrics +12

Leukoencephalopathy with ataxia, hypodontia, and hypomyelination

Nicole I. Wolf, Inga Harting, Eugen Boltshauser et al. · Neurology · 2005 · 80 citations

Medicine, Neurology, Neuroscience +15

Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations

Martina Witsch‐Baumgartner, Elżbieta Ciara, Jürgen Löffler et al. · European Journal of Human Genetics · 2001 · 71 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7