W Voss

A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene

Ana Ferreiro, Nicole Monnier, Norma B. Romero et al. · Annals of Neurology · 2002 · 200 citations

Genetics, Genetic Epidemiology, Pathology +24

Outcome of extremely low birth weight survivors at school age: the influence of perinatal parameters on neurodevelopment

A Neubauer, W Voss, E Kattner · European Journal of Pediatrics · 2007 · 149 citations

Prenatal Development, Brain Development, School Age +13

Erythropoietin improves neurodevelopmental outcome of extremely preterm infants

A Neubauer, W Voss, M Wachtendorf et al. · Annals of Neurology · 2010 · 116 citations

Long‐term cognitive outcomes of extremely low‐birth‐weight infants: the influence of the maternal educational background

W Voss, Tanja Jungmann, M Wachtendorf et al. · Acta Paediatrica · 2012 · 98 citations · Full text

Neurodevelopmental outcome in extremely low birth weight infants: what is the minimum age for reliable developmental prognosis?

W Voss, A Neubauer, M Wachtendorf et al. · Acta Paediatrica · 2007 · 72 citations