1. Glycogenoseshepatiques sans deficit enzymatique reconnu se compontant cliniquement et biologiquement comme le type 1 de Cori;Badoual, J.; Lestradet, H.; Tichet, J.; Sanna, N.; Grenet, P.;Ann. Pediat,1972
2. Rodent and Human x-glucosidase;Barsy, T.de; Jacquemin, P.; Devos, P.; Hers, H.G.;Europ. J. Biochem,1972
3. An electror. microscopic and biochemical study of type II glycogenosis;Baudhuin, P.; Hers, H.G.; Loeb, H.;Lab. Invest,1964
4. Endocrinological findings in patients with glycogenosis;Bierich, J.R.; Rager, K.; Schonberg, D.;(Abstr.) Acta endocr. (Kbh.),1973
5. Type III glycogenosis: a family with an unusual tissue distribution of the enzyme lesion;Brandt, I.K.; DeLuca, Jr, V.A.;Amer. J. Med,1966