Osteodystrophy due to congenital deficiency of phosphatase.
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Biochemical Phenomena↗
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Results for “PHOSPHATASES/deficiency”
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Hypophosphatasia.
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Phosphoric Monoester Hydrolases↗
[Two cases of hypophasphatasia; first Italian case report].
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Language↗
Genetic, clinical, biochemical, and pathological features of hypophosphatasia; based on the study of a family.
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Hypophosphatasia↗
[Hypophatasia & its osseous manifestations].
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Bone Diseases↗
[Atypical rickets in congenital alkaline phosphatase deficiency].
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Alkaline Phosphatase↗
Hypophosphatasia.
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Phosphoric Monoester Hydrolases↗
[Glycogen polycoria of the liver in two brothers due to glucose phosphatase insufficiency].
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Child↗
[Hepatic glycogenoses. Correlations between the clinical and biochemical characteristics and the type of enzymatic deficiency: glucose-6-phosphatase, amylo-1-6-glucosidase, phosphorylase].
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Glucose-6-Phosphatase↗
[Hypophosphatasia. New osteopathic syndrome].
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Bone Diseases↗
[Hepatic glycogenosis caused by glucose-6-phosphatase associated with a thrombopathy].
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Glucose-6-Phosphatase↗
[The problems of ''enzymophaties'' in pediatrics, as shown by the symptomatology of hypophosphatasia].
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Bone Diseases↗
Hypophosphatasia with congenital dimples.
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Hypophosphatasia↗
Syndrome caused by congenital absence of glucose-6-phosphatase in 2 adults, brother and sister
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Glucose-6-Phosphatase↗
[Phosphatase deficiency in a 4-year-old boy with female sex chromatin].
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Biological Phenomena↗