K E Cosgrove Selected Research

Adenosine Triphosphate (ATP)

5/2011	The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism.
7/2005	Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.
9/2000	A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.

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K E Cosgrove Research Topics

Disease

4	Hyperinsulinism (Hyperinsulinemia) 07/2005 - 03/2000
3	Congenital Hyperinsulinism 01/2019 - 03/2000
2	Hypoglycemia (Reactive Hypoglycemia) 07/2005 - 06/2000
1	Pathologic Processes 02/2014
1	Beckwith-Wiedemann Syndrome (Exomphalos Macroglossia Gigantism Syndrome) 07/2005
1	Uniparental Disomy 07/2005
1	Adenoma (Adenomas) 12/2002
1	Hyperplasia 12/2002
1	Congenital Abnormalities (Deformity) 02/2001

Drug/Important Bio-Agent (IBA)

6	KATP ChannelsIBA 01/2019 - 03/2000
3	Adenosine Triphosphate (ATP)IBA 05/2011 - 09/2000
3	Insulin (Novolin)FDA Link 02/2001 - 03/2000
2	Proteins (Proteins, Gene)FDA Link 02/2014 - 07/2005
1	Transcription Factors (Transcription Factor)IBA 02/2014
1	Potassium Channels (Potassium Channel)IBA 07/2005
1	Cyclin-Dependent Kinase Inhibitor p57IBA 12/2002

Therapy/Procedure

1	Conservative Treatment 01/2019
1	Therapeutics 01/2019
1	Pancreatectomy 07/2005