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Journal of Inherited Metabolic Disease|May 26, 2004
Carnitine-acylcarnitine translocase deficiency: identification of a novel molecular defect in a Bedouin patientD Galron, O S Birk, A Kazanovitz, et al.European Journal of Pediatrics|January 1, 1993
Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patientsN Bashan, R Potashnik, A Peist, et al.The Journal of Biological Chemistry|February 20, 1999
Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1bH Hiraiwa, C J Pan, B Lin, et al.Toxicon : Official Journal of the International Society on Toxinology|January 1, 1985
Criteria map audit of scorpion envenomation in the Negev, IsraelY Hershkovich, Y Elitsur, C Z Margolis, et al.Pediatrics|January 1, 1983
Dexamethasone and salbutamol in the treatment of acute wheezing in infantsA Tal, C Bavilski, D Yohai, et al.European Journal of Pediatrics|April 1, 1984
Necrotizing enterocolitis beyond the neonatal periodR Dagan, O Ben-Yacov, A J Mares, et al.Pediatric Research|April 1, 1981
Glycogenosis due to liver and muscle phosphorylase kinase deficiencyN Bashan, T C Iancu, A Lerner, et al.The American Journal of Clinical Nutrition|November 1, 1983
Growth and nutritional status of Bedouin infants in the Negev Desert, Israel: evidence for marked stunting in the presence of only mild malnutritionR Dagan, S Sofer, W J Klish, et al.Neurology|April 1, 1986
Adult muscle phosphorylase "b" kinase deficiencyJ M Abarbanel, N Bashan, R Potashnik, et al.Neurology|February 1, 1987
Myophosphorylase deficiency: the course of an unusual congenital myopathyJ M Abarbanel, R Potashnik, S Frisher, et al.Pageof 4