NEURORADIOLOGICAL, NEUROPHYSIOLOGICAL AND
MOLECULAR FINDINGS IN INFANTILE KRABBE DISEASE:
TWO CASE REPORTS
Vargiami E, Papathanasiou E, Batzios S, Kyriazi M, Dimitriou E,
Anastasiou A, Michelakakis H, Giese A-K, Zafeiriou DI,
*Corresponding Author: Dimitrios I. Zafeiriou, M.D., Ph.D., Professor in Child Neurology and Developmental
Pediatrics, 1st Department of Pediatrics, Aristotle University of Thessaloniki, Egnatia St. 106, 54622 Thessaloniki,
Greece. Tel./Fax: +30-2310-241-845. Mobile: +30-6944-330-587. E-mail: jeff@med.auth.gr
page: 85
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ACKNOWLEDGMENTS
We would like to thank Irini Mavridou (Institute
of Child Health, Athens, Greece), Lluisa Vilageliou
and David Grinberg (Department of Genetics, Faculty
of Biology, Universitat de Barcelona, IBUB, Ciberer,
Barcelona, Spain) for their help with the molecular
investigations. We are grateful to Professor Arndt
Roelfs (Neurogenetics and Metabolic Disorders Unit,
University of Rostock, Rostock, Germany) for his
critical review of the manuscript.
Declaration of Interest. The authors report no
conflicts of interest. The authors alone are responsible
for the content and writing of this article.
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