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European Journal of Endocrinology
|
March 23, 2011
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism
So Eun Park, Sarah E Flanagan, Khalid Hussain, et al.
Diabetes Care
|
March 6, 2007
Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick days
Ethel Codner, Sarah E Flanagan, Francisca Ugarte, et al.
Diabetes
|
October 19, 2007
An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinism
Khalid Hussain, Sarah E Flanagan, Virpi V Smith, et al.
European Journal of Endocrinology
|
January 25, 2013
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism
Ritika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 18, 2014
Long-term follow-up of children with congenital hyperinsulinism on octreotide therapy
Huseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, et al.
Clinical Endocrinology
|
June 4, 2016
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey
Belma Haliloglu, Gerald Hysenaj, Zeynep Atay, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
December 9, 2017
Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia
Belma Haliloğlu, Heybet Tüzün, Sarah E. Flanagan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 29, 2018
p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid Cancer
Chey Loveday, Katherine Josephs, Daniel Chubb, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2009
An in-frame deletion in Kir6.2 (KCNJ11) causing neonatal diabetes reveals a site of interaction between Kir6.2 and SUR1
Tim J Craig, Kenju Shimomura, Reinhard W Holl, et al.
Diabetes
|
June 25, 2010
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities
Oscar Rubio-Cabezas, Jayne A L Minton, Iren Kantor, et al.
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of 44
Search research articles
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Showing results (111-120 of 439) with videos related to
Sort By:
Page
of 44
European Journal of Endocrinology
|
March 23, 2011
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism
So Eun Park, Sarah E Flanagan, Khalid Hussain, et al.
Diabetes Care
|
March 6, 2007
Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick days
Ethel Codner, Sarah E Flanagan, Francisca Ugarte, et al.
Diabetes
|
October 19, 2007
An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinism
Khalid Hussain, Sarah E Flanagan, Virpi V Smith, et al.
European Journal of Endocrinology
|
January 25, 2013
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism
Ritika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 18, 2014
Long-term follow-up of children with congenital hyperinsulinism on octreotide therapy
Huseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, et al.
Clinical Endocrinology
|
June 4, 2016
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey
Belma Haliloglu, Gerald Hysenaj, Zeynep Atay, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
December 9, 2017
Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia
Belma Haliloğlu, Heybet Tüzün, Sarah E. Flanagan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 29, 2018
p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid Cancer
Chey Loveday, Katherine Josephs, Daniel Chubb, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2009
An in-frame deletion in Kir6.2 (KCNJ11) causing neonatal diabetes reveals a site of interaction between Kir6.2 and SUR1
Tim J Craig, Kenju Shimomura, Reinhard W Holl, et al.
Diabetes
|
June 25, 2010
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities
Oscar Rubio-Cabezas, Jayne A L Minton, Iren Kantor, et al.
Page
of 44