Human microsomal glucose-6-phosphatase system R. C. NordlieK. A. SukalskiW. T. Johnson Biochemistry of Glucose-6-Phosphatase system and diagnosis Pages: 2 - 6
Glucose-6-phosphatase and type 1 glycogen storage disease: Some critical considerations W. J. ArionW. K. Canfield Biochemistry of Glucose-6-Phosphatase system and diagnosis Pages: 7 - 13
Identification, purification and genetic deficiencies of the glucose-6-phosphatase system transport proteins I. D. WaddellA. Burchell Biochemistry of Glucose-6-Phosphatase system and diagnosis Pages: 14 - 17
The molecular basis of the genetic deficiencies of five of the components of the glucose-6-phosphatase system: Improved diagnosis A. BurchellI. D. Waddell Biochemistry of Glucose-6-Phosphatase system and diagnosis Pages: 18 - 21
Purification of human microsomal liver glucose-6-phosphatase system by affinity chromatography and immunodetection S. KöselD. MaternY. S. Shin Biochemistry of Glucose-6-Phosphatase system and diagnosis Pages: 22 - 25
Cytosolic free Ca2+ signals in single adherent human neutrophils: Generation and functional role M. E. E. JaconiJ. M. ThelerP. D. Lew Neutrophiles and GSD type Ib Pages: 26 - 32
Defective neutrophil and monocyte functions in glycogen storage disease type Ib: A literature review R. GitzelmannN. U. Bosshard Neutrophiles and GSD type Ib Pages: 33 - 38
Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1b H. M. KorchakB. -Z. GartyL. Kilpatrick Neutrophiles and GSD type Ib Pages: 39 - 43
Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patients N. BashanR. PotashnikS. W. Moses Neutrophiles and GSD type Ib Pages: 44 - 48
Glycogen storage disease type Ib: Infectious complications and measures for prevention U. WendelH. SchrotenV. Wahn Neutrophiles and GSD type Ib Pages: 49 - 51
The long-term outcome of patients with glycogen storage disease type Ia G. P. A. Smit Treatment and complications in GSD type Ib Pages: 52 - 55
Type I glycogen storage disease: Nine years of management with cornstarch Y. -T. ChenC. H. BazzarreR. A. Coleman Treatment and complications in GSD type Ib Pages: 56 - 59
Renal complications in glycogen storage disease type I W. C. C. Reitsma-Bierens Treatment and complications in GSD type Ib Pages: 60 - 62
Glycogen storage disease I and hepatocellular tumours L. Bianchi Treatment and complications in GSD type Ib Pages: 63 - 70
Liver transplantation for type I and type IV glycogen storage disease R. SelbyT. E. StarzlR. S. Kendall Treatment and complications in GSD type Ib Pages: 71 - 76
Glucose-6-phosphate: A key compound in glycogenosis I and favism leading to hyper- or hypolipidaemia G. SchmitzH. HohageK. Ullrich Treatment and complications in GSD type Ib Pages: 77 - 84
Biochemical aspects of glycogen storage disease type I: Summary of the discussions Y. Shin Summary of the discussions Pages: 85 - 86
Clinical aspects of glycogen storage disease type I: Summary of the discussions K. UllrichG. P. A. Smit Summary of the discussions Pages: 87 - 88