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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Khalid Hussain

Clinical and Molecular Genetics Unit

The Developmental Endocrinology Research Group

Institute of Child Health

Hospital for Children NHS Trust

UK

[email]@ich.ucl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Clinical and Molecular Genetics Unit, The Developmental Endocrinology Research Group, Institute of Child Health, Hospital for Children NHS Trust, UK. 2010
  • Department of Paediatric Endocrinology and Diabetes, Great Ormond Street Hospital for Children, London, UK. 2009
  • London Centre for Paediatric Endocrinology and Metabolism, Great Ormond Street Hospital for Children NHS Trust, Institute of Child Health, University College London, UK. 2003 - 2009
  • The Institute of Child Health, Unit of Biochemistry, Endocrinology and Metabolism, University College London, UK. 2005
  • Neonatal Intensive Care Unit, Basildon General Hospital, Essex, UK. 2000

References

  1. Mutations in pancreatic ß-cell Glucokinase as a cause of hyperinsulinaemic hypoglycaemia and neonatal diabetes mellitus. Hussain, K. Rev. Endocr. Metab. Disord (2010) [Pubmed]
  2. Diabetes mellitus, exocrine pancreatic deficiency, hypertrichosis, hyperpigmentation, and chronic inflammation: confirmation of a syndrome. Hussain, K., Padidela, R., Kapoor, R.R., James, C., Banerjee, K., Harper, J., Wilson, L.C., Hennekam, R.C. Pediatr. Diabetes (2009) [Pubmed]
  3. Diagnosis and management of hyperinsulinaemic hypoglycaemia of infancy. Hussain, K. Horm. Res. (2008) [Pubmed]
  4. Insights in congenital hyperinsulinism. Hussain, K. Endocr. Dev (2007) [Pubmed]
  5. Hyperinsulinaemic hypoglycaemia: biochemical basis and the importance of maintaining normoglycaemia during management. Hussain, K., Blankenstein, O., De Lonlay, P., Christesen, H.T. Arch. Dis. Child. (2007) [Pubmed]
  6. The diagnosis of ectopic focal hyperinsulinism of infancy with [18F]-dopa positron emission tomography. Hussain, K., Seppänen, M., Näntö-Salonen, K., Adzick, N.S., Stanley, C.A., Thornton, P., Minn, H. J. Clin. Endocrinol. Metab. (2006) [Pubmed]
  7. Ketotic hypoglycaemia in children with diazoxide responsive hyperinsulinism of infancy. Hussain, K. Eur. J. Pediatr. (2005) [Pubmed]
  8. Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels. Hussain, K., Cosgrove, K.E., Shepherd, R.M., Luharia, A., Smith, V.V., Kassem, S., Gregory, J.W., Sivaprasadarao, A., Christesen, H.T., Jacobsen, B.B., Brusgaard, K., Glaser, B., Maher, E.A., Lindley, K.J., Hindmarsh, P., Dattani, M., Dunne, M.J. J. Clin. Endocrinol. Metab. (2005) [Pubmed]
  9. Congenital hyperinsulinism. Hussain, K. Seminars. Fetal. &. Neonatal. Medicine (2005) [Pubmed]
  10. From congenital hyperinsulinism to diabetes mellitus: the role of pancreatic beta-cell KATP channels. Hussain, K., Cosgrove, K.E. Pediatr. Diabetes (2005) [Pubmed]
  11. Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinism. Hussain, K., Bryan, J., Christesen, H.T., Brusgaard, K., Aguilar-Bryan, L. Diabetes (2005) [Pubmed]
  12. Hyperinsulinaemic hypoglycaemia in preterm neonates. Hussain, K., Aynsley-Green, A. Arch. Dis. Child. Fetal Neonatal Ed. (2004) [Pubmed]
  13. Hypoketotic hypofattyacidaemic hypoinsulinaemic hypoglycaemia in a child with hemihypertrophy? A new syndrome. Hussain, K., Bodamer, O.A., Cameron, F.J., Camacho-Hubner, C., Soos, M.A., Jones, J., Krywawych, S., O'Rahilly, S., Aynsley-Green, A. Horm. Res. (2004) [Pubmed]
  14. Severe transient neonatal hyperinsulinism associated with hyperlactataemia in non-asphyxiated infants. Hussain, K., Thornton, P.S., Otonkoski, T., Aynsley-Green, A. J. Pediatr. Endocrinol. Metab. (2004) [Pubmed]
  15. Hyperinsulinaemic hypoglycaemia in infancy and childhood--resolving the enigma. Hussain, K., Aynsley-Green, A. J. Pediatr. Endocrinol. Metab. (2004) [Pubmed]
  16. Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p. Hussain, K., Bitner-Glindzicz, M., Blaydon, D., Lindley, K.J., Thompson, D.A., Kriss, T., Rajput, K., Ramadan, D.G., Al-Mazidi, Z., Cosgrove, K.E., Dunne, M.J., Aynsley-Green, A. J. Pediatr. Endocrinol. Metab. (2004) [Pubmed]
  17. Medications used in the treatment of hypoglycemia due to congenital hyperinsulinism of infancy (HI). Hussain, K., Aynsley-Green, A., Stanley, C.A. Pediatr. Endocrinol. Rev (2004) [Pubmed]
  18. Hyperinsulinism in infancy: understanding the pathophysiology. Hussain, K., Aynsley-Green, A. Int. J. Biochem. Cell Biol. (2003) [Pubmed]
  19. Neonates with symptomatic hyperinsulinemic hypoglycemia generate inappropriately low serum cortisol counterregulatory hormonal responses. Hussain, K., Hindmarsh, P., Aynsley-Green, A. J. Clin. Endocrinol. Metab. (2003) [Pubmed]
  20. The inaccuracy of venous and capillary blood glucose measurement using reagent strips in the newborn period and the effect of haematocrit. Hussain, K., Sharief, N. Early Hum. Dev. (2000) [Pubmed]
 
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