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Israel Journal of Medical Sciences|November 1, 1984
Infant feeding practices among Bedouins in transition from seminomadic to settlement conditions in the Negev area of IsraelR Dagan, S Sofer, W J Klish, et al.Hormone Research|January 1, 1982
Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyA Rösler, E Leiberman, J Sack, et al.Acta Paediatrica Scandinavica|March 1, 1986
Neuromuscular involvement in glycogen storage disease type IIIS W Moses, N Gadoth, N Bashan, et al.American Journal of Human Genetics|June 13, 1998
Mutations in the liver glycogen phosphorylase gene (PYGL) underlying glycogenosis type VIB Burwinkel, H D Bakker, E Herschkovitz, et al.Israel Journal of Medical Sciences|March 1, 1977
Salt conservation in familial dysautonomia (Riley-Day syndrome)H Landau, J Friedman, A Rösler, et al.Journal of Inherited Metabolic Disease|January 1, 1994
Postnatal regression of glucose transport in a patient with glycogen storage disease type 1bJ Levy, M T Abu-Ras, T Berenstein, et al.Journal of Inherited Metabolic Disease|January 1, 1990
The long-term outcome of patients with glycogen storage diseasesG P Smit, J Fernandes, J V Leonard, et al.European Journal of Pediatrics|April 1, 1988
Glycogen storage disease: recommendations for treatmentJ Fernandes, J V Leonard, S W Moses, et al.American Journal of Medical Genetics|October 23, 1997
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studiesR Parvari, K J Lei, N Bashan, et al.American Journal of Human Genetics|April 16, 1998
The gene for glycogen-storage disease type 1b maps to chromosome 11q23B Annabi, H Hiraiwa, B C Mansfield, et al.Pageof 4