Mutations in the Liver Glycogen Phosphorylase Gene ( PYGL) Underlying Glycogenosis Type VI (Hers Disease) von Burwinkel, Barbara, Bakker, Henk D., Herschkovitz, Eliezer, Moses, Shimon W., Shin, Yoon S., Kilimann, Manfred W.

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The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23 von Annabi, Borhane, Mansfield, Brian C., Hiraiwa, Hisayuki, Lei, Ke-Jian, Ubagai, Tsuneyuki, Polymeropoulos, Mihael H., Moses, Shimon W., Parvari, Ruti, Hershkovitz, Eli, Mandel, Hanna, Fryman, Moshe, Chou, Janice Yang

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Carnitine‐acylcarnitine translocase deficiency: Identification of a novel molecular defect in a Bedouin patient von Galron, D., Birk, O. S., Kazanovitz, A., Moses, S. W., Hershkovitz, E.

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Glycogen storage disease type 1a in three siblings with the G270V mutation von Parvari, R., Isam, J., Moses, S. W.

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Two new mutations in the 3′ coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patient von Parvari, R., Shen, J., Hershkovitz, E., Chen, Y. T., Moses, S. W.

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Inactivation of the Glucose 6-Phosphate Transporter Causes Glycogen Storage Disease Type 1b von Hiraiwa, H, Pan, C J, Lin, B, Moses, S W, Chou, J Y

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Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the β subunit gene (PHKB) von BURWINKEL, B, MOSES, S. W, KILIMANN, M. W

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The long‐term outcome of patients with glycogen storage diseases von Smit, G. P. A., Fernandes, J., Leonard, J. V., Matthews, E. E., Moses, S. W., Odievre, M., Ullrich, K.

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Impaired carbohydrate metabolism of polymorphonuclear leukocytes in glycogen storage disease Ib von BASHAN, N, HAGAI, Y, POTASHNIK, R, MOSES, S. W

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Dexamethasone and salbutamol in the treatment of acute wheezing in infants von Tal, A, Bavilski, C, Yohai, D, Bearman, J E, Gorodischer, R, Moses, S W

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Muscle glycogenosis von Moses, S. W.

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Neurophysiologic studies in congenital insensitivity to pain with anhidrosis von Shorer, Zamir, Moses, Shimon W, Hershkovitz, Eliahu, Pinsk, Vered, Levy, Jacov

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Postnatal regression of glucose transport in a patient with glycogen storage disease type 1b von Levy, J., Abu‐Ras, M. T., Berenstein, T., Potashnik, R., Meisner, I., Moses, S. W., Bashan, N.

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Glycogen storage disease: recommendations for treatment von FERNANDES, J, LEONARD, J. V, MOSES, S. W, ODIEVRE, M, DI ROCCO, M, SCHAUB, J, SMIT, G. P. A, ULLRICH, K, DURAND, P

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The dietary treatment of children with type I glycogen storage disease with slow release carbohydrate von SMIT, G. P. A, BERGER, R, POTASNICK, R, MOSES, S. W, FERNANDES, J

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Impaired glucose transport in polymorphonuclear leukocytes in glycogen storage disease Ib von Bashan, N., Potashnik, R., Hagay, Y., Moses, S. W.

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Uptake and transport of hexoses into polymorphonuclear leukocytes of patients with glycogen storage disease type 1b von Bashan, N., Potashnik, R., Peleg, N., Moran, A., Moses, S. W.

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Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IX von Bashan, N., Potashnik, R., Ehrlich, T., Moses, S. W.

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An algorithmic approach to diagnosis of hypoglycemia von Phillip, M., Bashan, N., Smith, C.P.A., Moses, S.W.

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3‐Hydroxy‐3‐methylglutaryl‐coenzyme A lyase deficiency von Moses, S. W., Aviram, M., Geiger, R., Berger, R., Smit, P. C.

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