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Laurie Demmer

Showing results (1-10 of 20) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|July 24, 2007
Growth hormone therapy in progeriaAb Sadeghi-Nejad, Laurie Demmer
Anesthesia and Analgesia|September 16, 2010
Genetics for the pediatric anesthesiologist: a primer on congenital malformations, pharmacogenetics, and proteomicsJeffrey L Galinkin, Laurie Demmer, Myron Yaster
American Journal of Medical Genetics. Part A|April 25, 2012
Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infantRebecca Hoban, Amy E Roberts, Laurie Demmer, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2019
An unusual case of nephrotic syndrome in a microcephalic infant: AnswersElizabeth Baker, Donald Weaver, Susan Massengill, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2019
An unusual case of nephrotic syndrome in a microcephalic infant: QuestionsElizabeth Baker, Donald Weaver, Susan Massengill, et al.
Journal of Pediatric Genetics|May 9, 2024
Matthew-Wood Syndrome in Monochorionic, Diamnionic TwinsIrina Geiculescu, Matthew A Saxonhouse, Laurie Demmer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2012
The development and implementation of an in-service exam for medical genetics residency programsNathaniel H Robin, V Reid Sutton, John Caldwell, et al.
AJP Reports|November 9, 2016
Development, Implementation, and Assessment of a Genetics Curriculum Across InstitutionsSarah Dotters-Katz, Ginger Hocutt, C Michael Osborne, et al.
American Journal of Medical Genetics. Part A|March 10, 2016
Autosomal recessive MFN2-related Charcot-Marie-Tooth disease with diaphragmatic weakness: Case report and literature reviewChristopher A Tan, Marina Rabideau, Amy Blevins, et al.
Epilepsia Open|December 10, 2023
Early genetic testing in pediatric epilepsy: Diagnostic and cost implicationsShanna M Swartwood, Ana Morales, Kathryn E Hatchell, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 24, 2007
Growth hormone therapy in progeriaAb Sadeghi-Nejad, Laurie Demmer
Anesthesia and Analgesia|September 16, 2010
Genetics for the pediatric anesthesiologist: a primer on congenital malformations, pharmacogenetics, and proteomicsJeffrey L Galinkin, Laurie Demmer, Myron Yaster
American Journal of Medical Genetics. Part A|April 25, 2012
Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infantRebecca Hoban, Amy E Roberts, Laurie Demmer, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2019
An unusual case of nephrotic syndrome in a microcephalic infant: AnswersElizabeth Baker, Donald Weaver, Susan Massengill, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2019
An unusual case of nephrotic syndrome in a microcephalic infant: QuestionsElizabeth Baker, Donald Weaver, Susan Massengill, et al.
Journal of Pediatric Genetics|May 9, 2024
Matthew-Wood Syndrome in Monochorionic, Diamnionic TwinsIrina Geiculescu, Matthew A Saxonhouse, Laurie Demmer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2012
The development and implementation of an in-service exam for medical genetics residency programsNathaniel H Robin, V Reid Sutton, John Caldwell, et al.
AJP Reports|November 9, 2016
Development, Implementation, and Assessment of a Genetics Curriculum Across InstitutionsSarah Dotters-Katz, Ginger Hocutt, C Michael Osborne, et al.
American Journal of Medical Genetics. Part A|March 10, 2016
Autosomal recessive MFN2-related Charcot-Marie-Tooth disease with diaphragmatic weakness: Case report and literature reviewChristopher A Tan, Marina Rabideau, Amy Blevins, et al.
Epilepsia Open|December 10, 2023
Early genetic testing in pediatric epilepsy: Diagnostic and cost implicationsShanna M Swartwood, Ana Morales, Kathryn E Hatchell, et al.
Pageof 2