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Azizun Nessa

Showing results (1-10 of 9) with videos related to

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Frontiers in Endocrinology|April 12, 2016
Hyperinsulinemic Hypoglycemia - The Molecular MechanismsAzizun Nessa, Sofia A Rahman, Khalid Hussain
Journal of Molecular Endocrinology|March 4, 2015
Molecular mechanisms of congenital hyperinsulinismSofia A Rahman, Azizun Nessa, Khalid Hussain
International Journal of Pediatric Endocrinology|January 14, 2015
Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapyVed Bhushan Arya, Qadeer Aziz, Azizun Nessa, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemiaAzizun Nessa, Anitha Kumaran, Richard Kirk, et al.
Human Molecular Genetics|June 21, 2015
Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8Azizun Nessa, Qadeer H Aziz, Alison M Thomas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2017
Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?Klara Rozenkova, Azizun Nessa, Barbora Obermannova, et al.
Hormone Research in Paediatrics|April 28, 2012
Severe resistance to weight gain, lack of stored triglycerides in adipose tissue, hypoglycaemia, and increased energy expenditure: a novel disorder of energy homeostasisRaja Padidela, Kate Bennett, Azizun Nessa, et al.
European Journal of Endocrinology|September 10, 2014
Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutationsVed Bhushan Arya, Maria Guemes, Azizun Nessa, et al.
The Journal of Clinical Endocrinology and Metabolism|October 3, 2015
High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital HyperinsulinismKlara Rozenkova, Jana Malikova, Azizun Nessa, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Frontiers in Endocrinology|April 12, 2016
Hyperinsulinemic Hypoglycemia - The Molecular MechanismsAzizun Nessa, Sofia A Rahman, Khalid Hussain
Journal of Molecular Endocrinology|March 4, 2015
Molecular mechanisms of congenital hyperinsulinismSofia A Rahman, Azizun Nessa, Khalid Hussain
International Journal of Pediatric Endocrinology|January 14, 2015
Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapyVed Bhushan Arya, Qadeer Aziz, Azizun Nessa, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemiaAzizun Nessa, Anitha Kumaran, Richard Kirk, et al.
Human Molecular Genetics|June 21, 2015
Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8Azizun Nessa, Qadeer H Aziz, Alison M Thomas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2017
Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?Klara Rozenkova, Azizun Nessa, Barbora Obermannova, et al.
Hormone Research in Paediatrics|April 28, 2012
Severe resistance to weight gain, lack of stored triglycerides in adipose tissue, hypoglycaemia, and increased energy expenditure: a novel disorder of energy homeostasisRaja Padidela, Kate Bennett, Azizun Nessa, et al.
European Journal of Endocrinology|September 10, 2014
Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutationsVed Bhushan Arya, Maria Guemes, Azizun Nessa, et al.
The Journal of Clinical Endocrinology and Metabolism|October 3, 2015
High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital HyperinsulinismKlara Rozenkova, Jana Malikova, Azizun Nessa, et al.
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