Search research articles
Contact Us
Filters
Showing results (11-20 of 12) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 12 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 9, 2020
Congenital hyperinsulinism due to compound heterozygous mutations in ABCC8 responsive to diazoxide therapy
Tashunka Taylor-Miller, Jayne Houghton, Paul Munyard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 30, 2009
A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly
Siddharth Shah, Yadlapalli Kumar, Brendan McLean, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 12) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 12 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 9, 2020
Congenital hyperinsulinism due to compound heterozygous mutations in ABCC8 responsive to diazoxide therapy
Tashunka Taylor-Miller, Jayne Houghton, Paul Munyard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 30, 2009
A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly
Siddharth Shah, Yadlapalli Kumar, Brendan McLean, et al.
Page
of 2