Search research articles
Contact Us
Filters
Showing results (1-10 of 5) with videos related to
Page
of 1
Sort By:
Early Human Development
|
September 28, 2014
Translating research into political advocacy to improve infant and child health
Albert Aynsley-Green Kt
Pediatric Endocrinology Reviews : PER
|
February 4, 2006
Medications used in the treatment of hypoglycemia due to congenital hyperinsulinism of infancy (HI)
Khalid Hussain, Albert Aynsley-Green, Charles A Stanley
Physiological Reviews
|
January 13, 2004
Hyperinsulinism in infancy: from basic science to clinical disease
Mark J Dunne, Karen E Cosgrove, Ruth M Shepherd, et al.
Hormone Research
|
February 26, 2004
Genetics and pathophysiology of hyperinsulinism in infancy
Karen E Cosgrove, Ruth M Shepherd, Eva M Fernandez, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 14, 2005
Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p
Khalid Hussain, Maria Bitner-Glindzicz, Diana Blaydon, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Early Human Development
|
September 28, 2014
Translating research into political advocacy to improve infant and child health
Albert Aynsley-Green Kt
Pediatric Endocrinology Reviews : PER
|
February 4, 2006
Medications used in the treatment of hypoglycemia due to congenital hyperinsulinism of infancy (HI)
Khalid Hussain, Albert Aynsley-Green, Charles A Stanley
Physiological Reviews
|
January 13, 2004
Hyperinsulinism in infancy: from basic science to clinical disease
Mark J Dunne, Karen E Cosgrove, Ruth M Shepherd, et al.
Hormone Research
|
February 26, 2004
Genetics and pathophysiology of hyperinsulinism in infancy
Karen E Cosgrove, Ruth M Shepherd, Eva M Fernandez, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 14, 2005
Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p
Khalid Hussain, Maria Bitner-Glindzicz, Diana Blaydon, et al.
Page
of 1