X linked hypophosphataemia: treatment, height gain, and nephrocalcinosis.

Author:

Reusz G S,Hoyer P F,Lucas M,Krohn H P,Ehrich J H,Brodehl J

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference24 articles.

1. Growth disturbances in hereditary hypophosphataemia;Harrison, H.E.; Harrison, H.C.; Lifshitz, F.; Johnson, A.D.;Am J Dis Child,1966

2. Clinical experience with 41 typical familial hypophosphatemic patients and 2 atypical nonfamilial cases;Stickler, G.B.; Beabout, J.W.; Riggs, B.L.

3. Familial forms of vitamin D-resistant rickets revisited. X-linked hypophosphatemia and autosomal recessive vitamin D dependency;Fraser, D.; Scriver, C.R.;AmJ Clin Nutr,1976

4. Hereditary hypophosphatemic rickets with hypercalciuria;Tieder, M.; Modai, D.; Samuel, R.;N EnglJr Med,1985

5. Tubularer Phosphattransport bei Vitamin-D-resistenter Rachitis;Krohn, H.P.; Brandis, M.; Brodehl, J.; Offner, G.;Monatsschr Kinderheilkd,1974

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