PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23275527-6	2013	In mutation-positive diazoxide-responsive probands, 42% were GLUD1, 41% were dominant KATP mutations, and 16% were in rare genes (HADH, UCP2, HNF4A, and HNF1A).	Diazoxide	21-30	hydroxyacyl-CoA dehydrogenase	Homo sapiens	130-134	
21252247-0	2011	Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees.	Diazoxide	78-87	hydroxyacyl-CoA dehydrogenase	Homo sapiens	42-46	
21252247-1	2011	CONTEXT AND OBJECTIVE: Recessive mutations in the hydroxyacyl-CoA dehydrogenase (HADH) gene encoding the enzyme 3-hydroxyacyl-CoA dehydrogenase are a rare cause of diazoxide-responsive hyperinsulinemic hypoglycemia (HH) with just five probands reported to date.	Diazoxide	164-173	hydroxyacyl-CoA dehydrogenase	Homo sapiens	50-79	
21252247-1	2011	CONTEXT AND OBJECTIVE: Recessive mutations in the hydroxyacyl-CoA dehydrogenase (HADH) gene encoding the enzyme 3-hydroxyacyl-CoA dehydrogenase are a rare cause of diazoxide-responsive hyperinsulinemic hypoglycemia (HH) with just five probands reported to date.	Diazoxide	164-173	hydroxyacyl-CoA dehydrogenase	Homo sapiens	81-85	
21252247-1	2011	CONTEXT AND OBJECTIVE: Recessive mutations in the hydroxyacyl-CoA dehydrogenase (HADH) gene encoding the enzyme 3-hydroxyacyl-CoA dehydrogenase are a rare cause of diazoxide-responsive hyperinsulinemic hypoglycemia (HH) with just five probands reported to date.	Diazoxide	164-173	hydroxyacyl-CoA dehydrogenase	Homo sapiens	114-143	
21252247-10	2011	CONCLUSION: HADH mutations are a relatively common cause of diazoxide-responsive HH with a frequency similar to that of GLUD1 and HNF4A mutations.	Diazoxide	60-69	hydroxyacyl-CoA dehydrogenase	Homo sapiens	12-16	
21252247-11	2011	We recommend that HADH sequence analysis is considered in all patients with diazoxide-responsive HH when recessive inheritance is suspected.	Diazoxide	76-85	hydroxyacyl-CoA dehydrogenase	Homo sapiens	18-22	
20931292-1	2010	Mutations in the HADH and HNF4A genes are rare causes of diazoxide responsive congenital hyperinsulinism (CHI).	Diazoxide	57-66	hydroxyacyl-CoA dehydrogenase	Homo sapiens	17-21	
27771675-7	2016	MESSAGE: HADH mutations are rare causes of hypoglycemia and can be mitigated with diazoxide and appropriate dietary therapy if identified early.	Diazoxide	82-91	hydroxyacyl-CoA dehydrogenase	Homo sapiens	9-13	
25915078-8	2015	HADH mutations can present in later infancy or childhood with severe HH that is usually diazoxide responsive.	Diazoxide	88-97	hydroxyacyl-CoA dehydrogenase	Homo sapiens	0-4