Sanda, Srinath <br/><br/>
Autosomal dominant hypoparathyroidism with severe hypomagnesemia and hypocalcemia, successfully treated with recombinant PTH and continuous subcutaneous magnesium infusion.  [electronic resource] 

 -  Journal of pediatric endocrinology & metabolism : JPEM  Apr 2008 
 - 385-91 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>0334-018X 
<br/><br/><label>Standard No.: </label>10.1515/jpem.2008.21.4.385  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Calcium--metabolism<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Hypocalcemia--drug therapy<br/>Hypoparathyroidism--complications<br/>Magnesium Deficiency--drug therapy<br/>Magnesium Sulfate--administration & dosage<br/>Parathyroid Hormone--administration & dosage<br/>Recombinant Proteins--administration & dosage