(Q44969464)

7 December 2017

title

Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy (English)

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7 December 2017

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4

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5

Treena Cranston

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7 December 2017

Simon Waller

1

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7 December 2017

Tom Kurzawinski

2

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7 December 2017

Lewis Spitz

3

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7 December 2017

Simon Pearce

6

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7 December 2017

Tim Cheetham

7

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7 December 2017

William G van't Hoff

8

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7 December 2017

publication date

1 October 2004

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European Journal of Pediatrics

7 December 2017

published in

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7 December 2017

volume

163

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7 December 2017

issue

10

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7 December 2017

page(s)

589-594

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Bone turnover in children and adolescents with McCune-Albright syndrome treated with pamidronate for bone fibrous dysplasia

7 December 2017

cites work

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12 December 2020

Neonatal severe hyperparathyroidism, secondary hyperparathyroidism, and familial hypocalciuric hypercalcemia: multiple different phenotypes associated with an inactivating Alu insertion mutation of the calcium-sensing receptor gene

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12 December 2020

Severe immobilization-induced hypercalcemia in a child after liver transplantation successfully treated with pamidronate

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12 December 2020

Regulation of murine fetal-placental calcium metabolism by the calcium-sensing receptor

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12 December 2020

Normal urinary calcium/creatinine ratios in African-American and Caucasian children

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12 December 2020

Casting new light on the clinical spectrum of neonatal severe hyperparathyroidism

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12 December 2020

The role of bisphosphonates in diseases of childhood

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12 December 2020

Expanding role of bisphosphonate therapy in children

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12 December 2020

Use of bisphosphonates in hypercalcemia associated with childhood cancer

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12 December 2020

Long-term effects of bisphosphonates on the growing skeleton. Studies of young patients with severe osteoporosis

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12 December 2020

Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia

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12 December 2020

An adult patient with severe hypercalcaemia and hypocalciuria due to a novel homozygous inactivating mutation of calcium-sensing receptor

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12 December 2020

Functional characterization of calcium-sensing receptor mutations expressed in human embryonic kidney cells

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12 December 2020

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype

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12 December 2020

The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone

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12 December 2020

Bisphosphonates: from the laboratory to the clinic and back again

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12 December 2020

Physiology and pathophysiology of the extracellular calcium-sensing receptor

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12 December 2020

Use of bisphosphonates in children and adolescents

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12 December 2020

Do bisphosphonates make children's bones better or brittle?

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12 December 2020

An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds

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12 December 2020

Familial hypocalciuric hypercalcemia associated with mutation in the human Ca(2+)-sensing receptor gene

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12 December 2020

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism

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12 December 2020

Cyclic administration of pamidronate in children with severe osteogenesis imperfecta

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12 December 2020

10.1007/S00431-004-1491-0

Identifiers

DOI

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7 December 2017

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