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Literature DB >> 14876389

[Chronic disorders of calcium and phosphate metabolism in children].

G FANCONI.

Abstract

Entities: Chemical Species

Keywords: CALCIUM/metabolism; PHOSPHATES/metabolism

Mesh：

Substances：

Year: 1951 PMID： 14876389

Source DB: PubMed Journal: Schweiz Med Wochenschr ISSN： 0036-7672

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Cited

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10 in total

1. Severe infantile hypercalcaemia with special reference to the facies.

Authors: M C JOSEPH; D PARROTT
Journal: Arch Dis Child Date: 1958-10 Impact factor: 3.791

2. Severe type of infantile hypercalcaemia.

Authors: B E SCHLESINGER; N R BUTLER; J A BLACK
Journal: Br Med J Date: 1956-01-21

3. Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.

Authors: Karl P Schlingmann; Justyna Ruminska; Martin Kaufmann; Ismail Dursun; Monica Patti; Birgitta Kranz; Ewa Pronicka; Elzbieta Ciara; Teoman Akcay; Derya Bulus; Elisabeth A M Cornelissen; Aneta Gawlik; Przemysław Sikora; Ludwig Patzer; Matthias Galiano; Veselin Boyadzhiev; Miroslav Dumic; Asaf Vivante; Robert Kleta; Benjamin Dekel; Elena Levtchenko; René J Bindels; Stephan Rust; Ian C Forster; Nati Hernando; Glenville Jones; Carsten A Wagner; Martin Konrad
Journal: J Am Soc Nephrol Date: 2015-06-05 Impact factor: 10.121

4. Bone sclerosis in infancy.

Authors: J M MacCarthy
Journal: Postgrad Med J Date: 1968-12 Impact factor: 2.401

Review 5. Interactions of vitamin D and the proximal tubule.

Authors: Russell W Chesney
Journal: Pediatr Nephrol Date: 2015-01-25 Impact factor: 3.714

6. First description of frequent occurrence of supernumerary lumbar ribs and transitional vertebrae in children with Williams-Beuren syndrome.

Authors: Annette Schmitz; Elke Reutershahn; Peter Seiffert; Marco Das
Journal: Pediatr Radiol Date: 2022-08-31

[Chronic disorders of calcium and phosphate metabolism in children].

1. Severe infantile hypercalcaemia with special reference to the facies.

2. Severe type of infantile hypercalcaemia.

3. Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.

4. Bone sclerosis in infancy.

Review 5. Interactions of vitamin D and the proximal tubule.

6. First description of frequent occurrence of supernumerary lumbar ribs and transitional vertebrae in children with Williams-Beuren syndrome.

7. Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene.

8. Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake.

9. Prevalence of scoliosis in Williams-Beuren syndrome patients treated at a regional reference center.

10. Juvenile onset IIH and CYP24A1 mutations.