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khalid Hussain
khalid Hussain
Sidra Medicine
Verifisert e-postadresse på sidra.org
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Recommendations from the pediatric endocrine society for evaluation and management of persistent hypoglycemia in neonates, infants, and children
PS Thornton, CA Stanley, DD De Leon, D Harris, MW Haymond, ...
The Journal of pediatrics 167 (2), 238-245, 2015
5792015
Insulin Mutation Screening in 1,044 Patients With Diabetes: Mutations in the INS Gene Are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes …
EL Edghill, SE Flanagan, AM Patch, C Boustred, A Parrish, B Shields, ...
Diabetes 57 (4), 1034-1042, 2008
4712008
Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency
RS Jackson, JWM Creemers, IS Farooqi, ML Raffin-Sanson, A Varro, ...
The Journal of clinical investigation 112 (10), 1550-1560, 2003
4092003
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
F Brioude, JM Kalish, A Mussa, AC Foster, J Bliek, GB Ferrero, ...
Nat Rev Endocrinol 14 (4), 229-249, 2018
3742018
Practical management of hyperinsulinism in infancy
A Aynsley-Green, K Hussain, J Hall, JM Saudubray, C Nihoul-Fekete, ...
Archives of Disease in Childhood-Fetal and Neonatal Edition 82 (2), F98-F107, 2000
3672000
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
M Bitner-Glindzicz, KJ Lindley, P Rutland, D Blaydon, VV Smith, PJ Milla, ...
Nature genetics 26 (1), 56-60, 2000
3642000
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion
PT Clayton, S Eaton, A Aynsley-Green, M Edginton, K Hussain, ...
The Journal of clinical investigation 108 (3), 457-465, 2001
3632001
Noninvasive Diagnosis of Focal Hyperinsulinism of Infancy With [18F]-DOPA Positron Emission Tomography
T Otonkoski, K Näntö-Salonen, M Seppänen, R Veijola, H Huopio, ...
Diabetes 55 (1), 13-18, 2006
3152006
Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis
MN Weedon, I Cebola, AM Patch, SE Flanagan, E De Franco, R Caswell, ...
Nature genetics 46 (1), 61-64, 2014
3042014
What is a normal blood glucose?
M Güemes, SA Rahman, K Hussain
Archives of disease in childhood 101 (6), 569-574, 2016
2752016
Re-evaluating “transitional neonatal hypoglycemia”: mechanism and implications for management
CA Stanley, PJ Rozance, PS Thornton, DD De Leon, D Harris, ...
The Journal of pediatrics 166 (6), 1520-1525. e1, 2015
2682015
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism
RR Kapoor, SE Flanagan, VB Arya, JP Shield, S Ellard, K Hussain
European journal of endocrinology 168 (4), 557-564, 2013
2462013
The genetic basis of congenital hyperinsulinism
C James, RR Kapoor, D Ismail, K Hussain
Journal of medical genetics 46 (5), 289-299, 2009
2272009
Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis
I Garin, EL Edghill, I Akerman, O Rubio-Cabezas, I Rica, JM Locke, ...
Proceedings of the National Academy of Sciences 107 (7), 3105-3110, 2010
2182010
An activating mutation of AKT2 and human hypoglycemia
K Hussain, B Challis, N Rocha, F Payne, M Minic, A Thompson, A Daly, ...
Science 334 (6055), 474-474, 2011
1932011
Hyperinsulinaemic hypoglycaemia
RR Kapoor, SE Flanagan, C James, J Shield, S Ellard, K Hussain
Archives of Disease in Childhood 94 (6), 450-457, 2009
1822009
Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management
S Senniappan, B Shanti, C James, K Hussain
Journal of inherited metabolic disease 35, 589-601, 2012
1752012
Diagnosis and management of hyperinsulinaemic hypoglycaemia of infancy
K Hussain
Hormone Research in Paediatrics 69 (1), 2-13, 2007
1672007
Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families
O Rubio-Cabezas, AM Patch, JAL Minton, SE Flanagan, EL Edghill, ...
The Journal of Clinical Endocrinology & Metabolism 94 (11), 4162-4170, 2009
1642009
Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations
RR Kapoor, J Locke, K Colclough, J Wales, JJ Conn, AT Hattersley, ...
Diabetes 57 (6), 1659-1663, 2008
1642008
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