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Общее количество найденных документов : 76
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1.
| A potential role for muscle in glucose homeostasis: In vivo kinetic studies in glycogen storage disease type 1a and fructose-1,6-bisphosphatase deficiency // J. Inherit. Metab. Disease, 2010. Vol. 33, N 1.-С.25-31
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| Advanced glycation end products and the absence of premature atherosclerosis in glycogen storage disease Ia // J. Inherit. Metab. Disease, 2007. Vol. 30, N 6.-С.916-923
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| Yoshida Anti-Lafora body monoclonal antibody
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| Benvenuti Luiz A. Atrial natriuretic peptide, ventricular myocyte hypertrophy, and hemodynamic overload // Circulation, 1997. Vol. 96, N 8.-С.2733-2734
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| Wolfsdorf J.I. Biochemical evidence for the requirement of continuous glucose therapy in young adults with type 1 glycogen storage disease // J. Inherit. Metab. Disease, 1994. Vol. 17, N 2.-С.234-241
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| Wolfsdorf J.I. Biochemical evidence for the requirement of continuous glucose therapy in young adults with type 1 glycogen storage disease // J. Inherit. Metab. Disease, 1994. Vol. 17, N 2.-С.234-241
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| Blood lipids and endothelial function in glycogen storage disease type III // J. Inherit. Metab. Disease, 1999. Vol. 22, N 8.-С.891-898
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| Blood lipids and endothelial function in glycogen storage disease type III // J. Inherit. Metab. Disease, 1999. Vol. 22, N 8.-С.891-898
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| Bone mineral density in children, adolescents and adults with glycogen storage disease type Ia: A cross-sectional and longitudinal study // J. Inherit. Metab. Disease, 2003. Vol. 26, N 4.-С.371-384
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| Bone mineral density in children, adolescents and adults with glycogen storage disease type Ia: A cross-sectional and longitudinal study // J. Inherit. Metab. Disease, 2003. Vol. 26, N 4.-С.371-384
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| Bone mineral density in children, adolescents and adults with glycogen storage disease type Ia: A cross-sectional and longitudinal study // J. Inherit. Metab. Disease, 2003. Vol. 26, N 4.-С.371-384
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| Chorionic villus ultrastructure in type II glycogen storage disease (pompe's disease) // N. Engl. J. Med., 1991. Vol. 324, N 5.-С.342-343
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| Michon Cognitive profile of patients with glycogen storage disease type III // J. Inherit. Metab. Disease, 2015. Vol. 38, N 3.-С.573-580
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| Complex carbohydrates in the dietary management of patients with glycogenosis caused by glucose-6-phosphatase deficiency // Amer. J. Clin. Nutr., 1988. Vol. 48, N 1.-С.95-97
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| Buhrdel P. Diatische Behandlung von Kindern mit Glykogenose Typ I // Ernahrungsforschung, 1989. Vol. 34, N 6.-С.182-184, 177
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| Die glykogenose type II (Morbus Pompe) // Schweiz. Arch. Neurol. und Psychiat., 2010. Vol. 161, N 2.-С.55-59
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| Die glykogenose type II (Morbus Pompe) // Schweiz. Arch. Neurol. und Psychiat., 2010. Vol. 161, N 2.-С.55-59
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| Pela I. Effect of ramipril in a patient with glycogen storage disease type I and nephrotic-range proteinuria. Case report // J. Inherit. Metab. Disease, 2001. Vol. 24, N 6.-С.681-682
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| Pela I. Effect of ramipril in a patient with glycogen storage disease type I and nephrotic-range proteinuria. Case report // J. Inherit. Metab. Disease, 2001. Vol. 24, N 6.-С.681-682
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| Efficacy of multidisciplinary approach in the treatment of two cases of nonclassical infantile glycogenosis type II // J. Inherit. Metab. Disease, 2003. Vol. 26, N 7.-С.675-681
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