Publicaties in de kijker

The spectrum of epilepsy caused by POLG mutations
Janssen Wouter   Quaegebeur Annelies   Van Goethem Gert   Löfgren Ann   Smets Katrien   Vandenberghe Rik   Van Paesschen Wim  
Acta neurologica Belgica - ISSN 0300-9009-116:1 (2016) p. 17-25
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Biopsy in a patient with PMP22 exon 2 mutation recapitulates pathology of Trembler-J mouse
Madrid Ricardo E.   Löfgren Ann   Baets Jonathan   Timmerman Vincent  
Neuromuscular disorders - ISSN 0960-8966-23:4 (2013) p. 345-348
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A novel **POL** gene mutation in 4 children with alpers-like hepatocerebral syndromes
Kurt Bulent   Jaeken Jaak   Van Hove Johan   Löfgren Ann   Van Goethem Gert   et al.  
Archives of neurology - ISSN 0003-9942-67:2 (2010) p. 239-244
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Novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia and multisystem failure
Bohlega S.   Van Goethem Gert   al Semari A.   Löfgren Ann   al Hamed M.   Van Broeckhoven Christine   Kambouris M.  
Neuromuscular disorders - ISSN 0960-8966-19:12 (2009) p. 845-848
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Charcot-Marie-Tooth disease: a clinico-genetic confrontation
Barisic N.   Claeys Kristl G.   Sirotković-Skerlev M.   Löfgren Ann   Nelis Eva   De Jonghe Peter   Timmerman Vincent  
Annals of human genetics - ISSN 0003-4800-72:3 (2008) p. 416-441
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