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E Flanagan

Showing results (451-460 of 583) with videos related to

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Acta Neuropathologica Communications|January 3, 2023
Differential vulnerability of the dentate gyrus to tauopathies in dementiasAllegra Kawles, Grace Minogue, Antonia Zouridakis, et al.
Journal of the Endocrine Society|April 2, 2026
Comprehensive genetic rescreening improves diagnostic yield in congenital hyperinsulinismJonna M E Männistö, Jayne A L Houghton, Jasmin J Bennett, et al.
Journal of the American Academy of Dermatology|May 8, 2022
A prospective pilot study of narrowband UV-B treatment of lichen planopilarisJames T Pathoulas, Kelly E Flanagan, Mack Y Su, et al.
European Journal of Endocrinology|April 2, 2014
Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutationsHuseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, et al.
Frontiers in Endocrinology|September 27, 2021
Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K<sub>ATP</sub>-Channel Neonatal Diabetes Mellitus in Vietnam National Children's HospitalCan Thi Bich Ngoc, Tran Minh Dien, Elisa De Franco, et al.
European Journal of Endocrinology|March 11, 2015
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutationsHuseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous familiesOscar Rubio-Cabezas, Ann-Marie Patch, Jayne A L Minton, et al.
EMBO Molecular Medicine|January 6, 2010
Adjacent mutations in the gating loop of Kir6.2 produce neonatal diabetes and hyperinsulinismKenju Shimomura, Sarah E Flanagan, Brittany Zadek, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 31, 2015
Efficacy and safety of sirolimus in a neonate with persistent hypoglycaemia following near-total pancreatectomy for hyperinsulinaemic hypoglycaemiaMary B Abraham, Vinutha B Shetty, Glynis Price, et al.
The Journal of Experimental Medicine|July 29, 2021
Hypoxia-inducible factors individually facilitate inflammatory myeloid metabolism and inefficient cardiac repairMatthew DeBerge, Connor Lantz, Shirley Dehn, et al.
Pageof 59

Showing results (451-460 of 583) with videos related to

Sort By:
Pageof 59
Acta Neuropathologica Communications|January 3, 2023
Differential vulnerability of the dentate gyrus to tauopathies in dementiasAllegra Kawles, Grace Minogue, Antonia Zouridakis, et al.
Journal of the Endocrine Society|April 2, 2026
Comprehensive genetic rescreening improves diagnostic yield in congenital hyperinsulinismJonna M E Männistö, Jayne A L Houghton, Jasmin J Bennett, et al.
Journal of the American Academy of Dermatology|May 8, 2022
A prospective pilot study of narrowband UV-B treatment of lichen planopilarisJames T Pathoulas, Kelly E Flanagan, Mack Y Su, et al.
European Journal of Endocrinology|April 2, 2014
Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutationsHuseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, et al.
Frontiers in Endocrinology|September 27, 2021
Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K<sub>ATP</sub>-Channel Neonatal Diabetes Mellitus in Vietnam National Children's HospitalCan Thi Bich Ngoc, Tran Minh Dien, Elisa De Franco, et al.
European Journal of Endocrinology|March 11, 2015
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutationsHuseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous familiesOscar Rubio-Cabezas, Ann-Marie Patch, Jayne A L Minton, et al.
EMBO Molecular Medicine|January 6, 2010
Adjacent mutations in the gating loop of Kir6.2 produce neonatal diabetes and hyperinsulinismKenju Shimomura, Sarah E Flanagan, Brittany Zadek, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 31, 2015
Efficacy and safety of sirolimus in a neonate with persistent hypoglycaemia following near-total pancreatectomy for hyperinsulinaemic hypoglycaemiaMary B Abraham, Vinutha B Shetty, Glynis Price, et al.
The Journal of Experimental Medicine|July 29, 2021
Hypoxia-inducible factors individually facilitate inflammatory myeloid metabolism and inefficient cardiac repairMatthew DeBerge, Connor Lantz, Shirley Dehn, et al.
Pageof 59