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Genetic causes of neonatal and infantile hypercalcaemia
Caroline M Gorvin
Metabolism and Systems Research
Centre for Endocrinology, Diabetes and Metabolism
Research output
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Contribution to journal
›
Review article
›
peer-review
241
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Dive into the research topics of 'Genetic causes of neonatal and infantile hypercalcaemia'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Infantile Hypercalcemia
100%
Hypercalcemia
60%
Parathyroid Hormone
43%
Serum
24%
calcium phosphate
23%
Jansen type metaphyseal chondrodysplasia
21%
Hypocalciuric hypercalcemia, familial, type 1
18%
Hypophosphatasia
17%
Creatinine
17%
Parathyroid Diseases
16%
Newborn Infant
16%
Williams Syndrome
15%
Calcium
14%
Inborn Errors Metabolism
13%
Polyuria
13%
Mothers
13%
Failure to Thrive
13%
Lethargy
13%
Muscle Hypotonia
13%
Hyperparathyroidism
12%
Hypocalcemia
12%
Subcutaneous Fat
12%
Constipation
11%
Vitamin D
10%
Albumins
9%
Seizures
8%
Child
4%
Therapeutics
1%