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Irini Manoli

Showing results (41-50 of 72) with videos related to

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Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|October 18, 2023
Inability to move one's face dampens facial expression perceptionShruti Japee, Jessica Jordan, Judith Licht, et al.
BMC Neurology|January 31, 2007
Intravenous immune globulin in hereditary inclusion body myopathy: a pilot studySusan Sparks, Goran Rakocevic, Galen Joe, et al.
The Journal of Clinical Investigation|June 6, 2007
Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamineBelinda Galeano, Riko Klootwijk, Irini Manoli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 29, 2019
Chronic kidney disease in propionic acidemiaOleg A Shchelochkov, Irini Manoli, Jennifer L Sloan, et al.
Muscle & Nerve|January 3, 2021
Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studiesTanya Lehky, Reversa Joseph, Camilo Toro, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Chediak-Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1Irini Manoli, Gretchen Golas, Wendy Westbroek, et al.
Brain Communications|April 25, 2020
Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometryNeda Sadeghi, Elizabeth Hutchinson, Carol Van Ryzin, et al.
Molecular Genetics and Metabolism|January 9, 2025
Breath biopsy in inborn errors of metabolism: A proof-of-principle study in propionic acidemiaOleg A Shchelochkov, Huw Davies, Robert P Mohney, et al.
The American Journal of Pathology|February 11, 2012
The Gne M712T mouse as a model for human glomerulopathySravan Kakani, Tal Yardeni, Justin Poling, et al.
Journal of Inherited Metabolic Disease|May 27, 2023
Biomarkers to predict disease progression and therapeutic response in isolated methylmalonic acidemiaIrini Manoli, Abigael Gebremariam, Samantha McCoy, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|October 18, 2023
Inability to move one's face dampens facial expression perceptionShruti Japee, Jessica Jordan, Judith Licht, et al.
BMC Neurology|January 31, 2007
Intravenous immune globulin in hereditary inclusion body myopathy: a pilot studySusan Sparks, Goran Rakocevic, Galen Joe, et al.
The Journal of Clinical Investigation|June 6, 2007
Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamineBelinda Galeano, Riko Klootwijk, Irini Manoli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 29, 2019
Chronic kidney disease in propionic acidemiaOleg A Shchelochkov, Irini Manoli, Jennifer L Sloan, et al.
Muscle & Nerve|January 3, 2021
Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studiesTanya Lehky, Reversa Joseph, Camilo Toro, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Chediak-Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1Irini Manoli, Gretchen Golas, Wendy Westbroek, et al.
Brain Communications|April 25, 2020
Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometryNeda Sadeghi, Elizabeth Hutchinson, Carol Van Ryzin, et al.
Molecular Genetics and Metabolism|January 9, 2025
Breath biopsy in inborn errors of metabolism: A proof-of-principle study in propionic acidemiaOleg A Shchelochkov, Huw Davies, Robert P Mohney, et al.
The American Journal of Pathology|February 11, 2012
The Gne M712T mouse as a model for human glomerulopathySravan Kakani, Tal Yardeni, Justin Poling, et al.
Journal of Inherited Metabolic Disease|May 27, 2023
Biomarkers to predict disease progression and therapeutic response in isolated methylmalonic acidemiaIrini Manoli, Abigael Gebremariam, Samantha McCoy, et al.
Pageof 8