Bilaketaren emaitzak - Gropman, Andrea L

Mitochondrial Mechanisms and Neurological Disorders nork Gropman, Andrea L.

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Neuroimaging in Mitochondrial Disorders nork Gropman, Andrea L.

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Patterns of Brain Injury in Inborn Errors of Metabolism nork Gropman, Andrea L.

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Novel imaging technologies for genetic diagnoses in the inborn errors of metabolism nork Gropman, Andrea L., Anderson, Afrouz

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MR Imaging Findings in Xp21.2 Duplication Syndrome nork Whitehead, Matthew T, Helman, Guy, Gropman, Andrea L

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Multimodal imaging in urea cycle-related neurological disease – What can imaging after hyperammonemia teach us? nork Sen, Kuntal, Whitehead, Matthew T., Gropman, Andrea L.

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Select Ethical Aspects of Next-Generation Sequencing Tests for Newborn Screening and Diagnostic Evaluation of Critically Ill Newborns nork Sen, Kuntal, Harmon, Jennifer, Gropman, Andrea L.

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New frontiers in neuroimaging applications to inborn errors of metabolism nork Prust, Morgan J., Gropman, Andrea L., Hauser, Natalie

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Expanding Role of Proton Magnetic Resonance Spectroscopy: Timely Diagnosis and Treatment Initiation in Partial Ornithine Transcarbamylase Deficiency nork Sen, Kuntal, Castillo Pinto, Carlos, Gropman, Andrea L.

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MR Neuroimaging in Pediatric Inborn Errors of Metabolism nork Lai, Lillian M., Gropman, Andrea L., Whitehead, Matthew T.

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Review of Multi-Modal Imaging in Urea Cycle Disorders: The Old, the New, the Borrowed, and the Blue nork Sen, Kuntal, Anderson, Afrouz A., Whitehead, Matthew T., Gropman, Andrea L.

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Epilepsy in Muenke Syndrome: FGFR3-Related Craniosynostosis nork Agochukwu, Nneamaka B., Solomon, Benjamin D., Gropman, Andrea L., Muenke, Maximilian

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Urea cycle defects and hyperammonemia: effects on functional imaging nork Gropman, Andrea L., Prust, Morgan, Breeden, Andrew, Fricke, Stanley, VanMeter, John

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Management considerations for stroke-like episodes in MELAS with concurrent COVID-19 infection nork Sen, Kuntal, Harrar, Dana, Hahn, Andrea, Wells, Elizabeth M., Gropman, Andrea L.

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Ornithine Transcarbamylase Deficiency with Persistent Abnormality in Cerebral Glutamate Metabolism in Adults(1) nork Gropman, Andrea L., Sailasuta, Napapon, Harris, Kent C., Abulseoud, Osama, Ross, Brian D.

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Retinoschisis associated with Kearns-Sayre syndrome nork Chertkof, Julia, Hufnagel, Robert B., Blain, Delphine, Gropman, Andrea L., Brooks, Brian P.

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Response to Finsterer’s “Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome” nork Chertkof, Julia, Hufnagel, Robert B., Blain, Delphine, Gropman, Andrea L., Brooks, Brian P.

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(1)H MRS allows brain phenotype differentiation in sisters with late onset ornithine transcarbamylase deficiency (OTCD) and discordant clinical presentations nork Gropman, Andrea L, Seltzer, Rebecca R., Yudkoff, Marc, Sawyer, Alice, vanMeter, John, Fricke, Stanley T.

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Diffusion Tensor Imaging in Arginase Deficiency Reveals Damage to Corticospinal Tracts nork Oldham, Michael S., vanMeter, John W., Shattuck, Kyle F., Cederbaum, Stephen D., Gropman, Andrea L.

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Clinical NOE (13)C MRS for Neuropsychiatric Disorders of the Frontal Lobe nork Sailasuta, Napapon, Robertson, Larry W., Harris, Kent C., Gropman, Andrea L., Allen, Peter S., Ross, Brian D.

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