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Gilger, Mark; Hamaker, Bruce; Nichols, Buford L; Auricchio, Salvatore; Treem, William R; Naim, Hassan Y; Heine, Martin; Zimmer, Klaus-Peter; Jones, Kyra; Eskandari, Razieh; Pinto, B Mario; Rose, David R; Lee, Byung-Hoo; Quezada-Calvillo, Roberto; Adams, Bridget; Roach, Christine M; Ma, Chang-Xing; Baker, Susan S; Slawson, Mary H; Robayo-Torres, Claudia C; ... (2012). Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency Workshop. Journal of pediatric gastroenterology and nutrition, 55 Suppl 2(0 2), S1. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1097/00005176-199507000-00001
Reinshagen, Konrad; Keller, Klaus M; Haase, Bianca; Leeb, Tosso; Naim, Hassan Y; Zimmer, Klaus P (2008). Mosaic pattern of sucrase isomaltase deficiency in two brothers. Pediatric research, 63(1), pp. 79-83. Nature Publishing Group 10.1203/PDR.0b013e31815b4bac
Sander, Petra; Alfalah, Marwan; Keiser, Markus; Korponay-Szabo, Ilma; Kovács, Judit B; Leeb, Tosso; Naim, Hassan Y (2006). Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption. Human mutation, 27(1), p. 119. Hoboken, N.J.: Wiley-Blackwell
