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Therapeutic Innovation & Regulatory Science
|
August 17, 2023
Strategy for Generating Blinded Evidence for Single-Arm Trials with External Controls Using Expert Review of Home Video
Xinruo Zhang, Katherine Brind'Amour, Kelly E King, et al.
International Journal of Molecular Sciences
|
September 9, 2022
A Mouse Model of Glycogen Storage Disease Type IX-Beta: A Role for <i>Phkb</i> in Glycogenolysis
Charles J Arends, Lane H Wilson, Ana Estrella, et al.
Hormone Research in Paediatrics
|
March 21, 2024
Idiopathic Pathological Ketotic Hypoglycemia: Finding the Needle in a Haystack
Joseph I Wolfsdorf, Terry G J Derks, Danielle Drachmann, et al.
Advances in Nutrition (Bethesda, Md.)
|
October 31, 2019
Dietary Management of the Glycogen Storage Diseases: Evolution of Treatment and Ongoing Controversies
Katalin M Ross, Iris A Ferrecchia, Kathryn R Dahlberg, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
July 8, 2009
A detailed characterization of the adult mouse model of glycogen storage disease Ia
Susan V Salganik, David A Weinstein, Thomas D Shupe, et al.
Pediatric Blood & Cancer
|
October 13, 2005
Urinary hepcidin in congenital chronic anemias
Susan L Kearney, Elizabeta Nemeth, Ellis J Neufeld, et al.
Blood
|
October 24, 2002
Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease
David A Weinstein, Cindy N Roy, Mark D Fleming, et al.
International Wound Journal
|
October 15, 2013
Topical application of recombinant platelet-derived growth factor increases the rate of healing and the level of proteins that regulate this response
Santosh Gowda, David A Weinstein, Timothy D Blalock, et al.
Molecular Genetics and Metabolism
|
July 31, 2019
Complex patterns of inheritance, including synergistic heterozygosity, in inborn errors of metabolism: Implications for precision medicine driven diagnosis and treatment
Jerry Vockley, Steven F Dobrowolski, Georgianne L Arnold, et al.
The Journal of Pediatrics
|
December 23, 2008
Vascular dysfunction in glycogen storage disease type I
Angelina V Bernier, Catherine E Correia, Michael J Haller, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 91) with videos related to
Sort By:
Page
of 10
Therapeutic Innovation & Regulatory Science
|
August 17, 2023
Strategy for Generating Blinded Evidence for Single-Arm Trials with External Controls Using Expert Review of Home Video
Xinruo Zhang, Katherine Brind'Amour, Kelly E King, et al.
International Journal of Molecular Sciences
|
September 9, 2022
A Mouse Model of Glycogen Storage Disease Type IX-Beta: A Role for <i>Phkb</i> in Glycogenolysis
Charles J Arends, Lane H Wilson, Ana Estrella, et al.
Hormone Research in Paediatrics
|
March 21, 2024
Idiopathic Pathological Ketotic Hypoglycemia: Finding the Needle in a Haystack
Joseph I Wolfsdorf, Terry G J Derks, Danielle Drachmann, et al.
Advances in Nutrition (Bethesda, Md.)
|
October 31, 2019
Dietary Management of the Glycogen Storage Diseases: Evolution of Treatment and Ongoing Controversies
Katalin M Ross, Iris A Ferrecchia, Kathryn R Dahlberg, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
July 8, 2009
A detailed characterization of the adult mouse model of glycogen storage disease Ia
Susan V Salganik, David A Weinstein, Thomas D Shupe, et al.
Pediatric Blood & Cancer
|
October 13, 2005
Urinary hepcidin in congenital chronic anemias
Susan L Kearney, Elizabeta Nemeth, Ellis J Neufeld, et al.
Blood
|
October 24, 2002
Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease
David A Weinstein, Cindy N Roy, Mark D Fleming, et al.
International Wound Journal
|
October 15, 2013
Topical application of recombinant platelet-derived growth factor increases the rate of healing and the level of proteins that regulate this response
Santosh Gowda, David A Weinstein, Timothy D Blalock, et al.
Molecular Genetics and Metabolism
|
July 31, 2019
Complex patterns of inheritance, including synergistic heterozygosity, in inborn errors of metabolism: Implications for precision medicine driven diagnosis and treatment
Jerry Vockley, Steven F Dobrowolski, Georgianne L Arnold, et al.
The Journal of Pediatrics
|
December 23, 2008
Vascular dysfunction in glycogen storage disease type I
Angelina V Bernier, Catherine E Correia, Michael J Haller, et al.
Page
of 10