Taylor-Miller, Tashunka <br/><br/>
Congenital hyperinsulinism due to compound heterozygous mutations in ABCC8 responsive to diazoxide therapy.  [electronic resource] 

 -  Journal of pediatric endocrinology & metabolism : JPEM  May 2020 
 - 671-674 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>2191-0251 
<br/><br/><label>Standard No.: </label>10.1515/jpem-2019-0457  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Congenital Hyperinsulinism--drug therapy<br/>Diazoxide--therapeutic use<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Sulfonylurea Receptors--genetics<br/>Treatment Outcome<br/>Vasodilator Agents--therapeutic use