Search Results - Andrea Gropman

Andrea Gropman

Andrea L. Gropman (née Saperstein) is an American pediatric neurologist specializing in neurodevelopmental disabilities and neurogenetics. She is a professor of pediatrics and neurology at the George Washington University School of Medicine & Health Sciences. Gropman is chief of neurogenetics and neurodevelopmental pediatrics and an attending neurologist at Children's National Hospital. Provided by Wikipedia
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  1. 1
    Neuroimaging in Mitochondrial Disorders

    Neuroimaging in Mitochondrial Disorders by Andrea Gropman

    Published 2012
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  2. 2
    Brain imaging in urea cycle disorders

    Brain imaging in urea cycle disorders by Andrea Gropman

    Published 2010
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  3. 3
    Neurological implications of urea cycle disorders

    Neurological implications of urea cycle disorders by Andrea Gropman, Marshall Summar, James V. Leonard

    Published 2007
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  4. 4
    Improving long term outcomes in urea cycle disorders‐report from the Urea Cycle Disorders Consortium

    Improving long term outcomes in urea cycle disorders‐report from the Urea Cycle Disorders Consortium by Susan E. Waisbren, Andrea Gropman, Mark L. Batshaw

    Published 2016
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  5. 5
    Treatment of Mitochondrial Disorders

    Treatment of Mitochondrial Disorders by Sreenivas Avula, Sumit Parikh, Scott Demarest, Jonathan E. Kurz, Andrea Gropman

    Published 2014
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  6. 6
    Evidence Report: Genetic and metabolic testing on children with global developmental delay [RETIRED]

    Evidence Report: Genetic and metabolic testing on children with global developmental delay [RETIRED] by David Michelson, Michael Shevell, Elliott H. Sherr, John B. Moeschler, Andrea Gropman, Stephen Ashwal

    Published 2011
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  7. 7
    Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome

    Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome by Ryan W.Y. Lee, Sandra K. Conley, Andrea Gropman, Forbes D. Porter, Eva H. Baker

    Published 2013
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  8. 8
    Neurodevelopment of Children Under 3 Years of Age With Smith-Magenis Syndrome

    Neurodevelopment of Children Under 3 Years of Age With Smith-Magenis Syndrome by Pamela L. Wolters, Andrea Gropman, Staci Martin, Michaele R. Smith, Hanna Hildenbrand, Carmen C. Brewer, Ann C. M. Smith

    Published 2009
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  9. 9
    MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia

    MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia by Eva H. Baker, Jennifer L. Sloan, Natalie Hauser, Andrea Gropman, Dan Adams, Camilo Toro, Irini Manoli, Charles P. Venditti

    Published 2014
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  10. 10
    Nckβ Interacts with Tyrosine-Phosphorylated Disabled 1 and Redistributes in Reelin-Stimulated Neurons

    Nckβ Interacts with Tyrosine-Phosphorylated Disabled 1 and Redistributes in Reelin-Stimulated Neurons by Albéna Pramatarova, Pawel G. Ochalski, Ke‐lian Chen, Andrea Gropman, Sage R. Myers, Kyung‐Tai Min, Brian W. Howell

    Published 2003
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  11. 11
    Early prediction of phenotypic severity in Citrullinemia Type 1

    Early prediction of phenotypic severity in Citrullinemia Type 1 by Matthias Zielonka, Stefan Kölker, Florian Gleich, Nicolas Stützenberger, Sandesh C.S. Nagamani, Andrea Gropman, Georg F. Hoffmann, Sven F. Garbade, Roland Posset

    Published 2019
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  12. 12
    Neurocognitive Phenotype of Isolated Methylmalonic Acidemia

    Neurocognitive Phenotype of Isolated Methylmalonic Acidemia by Colin J. O’Shea, Jennifer L. Sloan, Edythe Wiggs, Maryland Pao, Andrea Gropman, Eva H. Baker, Irini Manoli, Charles P. Venditti, Joseph Snow

    Published 2012
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  13. 13
    Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

    Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population by Carole Samango‐Sprouse, Eser Kırkızlar, Megan P. Hall, Patrick Lawson, Zachary Demko, Susan Mahler Zneimer, Kirsten J. Curnow, Susan J. Gross, Andrea Gropman

    Published 2016
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  14. 14
    A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome

    A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome by Christopher A. Wassif, Lisa E. Kratz, Susan Sparks, Courtney Wheeler, Simona Bianconi, Andrea Gropman, Karim A. Calis, Richard I. Kelley, Elaine Tierney, Forbes D. Porter

    Published 2016
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  15. 15
    Compound heterozygosity for mutations in <i>PAX6</i> in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia

    Compound heterozygosity for mutations in <i>PAX6</i> in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia by Benjamin D. Solomon, Daniel Pineda‐Alvarez, Joan Z. Balog, Donald W. Hadley, Andrea Gropman, R. Nandagopal, Joan C. Han, Jin S. Hahn, Delphine Blain, Brian P. Brooks, Maximilian Muenke

    Published 2009
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  16. 16
    The Phenotype of a Germline Mutation in PIGA: The Gene Somatically Mutated in Paroxysmal Nocturnal Hemoglobinuria

    The Phenotype of a Germline Mutation in PIGA: The Gene Somatically Mutated in Paroxysmal Nocturnal Hemoglobinuria by Jennifer J. Johnston, Andrea Gropman, Julie C. Sapp, Jamie K. Teer, Jodie M. Martin, Cyndi F. Liu, Xuan Yuan, Zhaohui Ye, Linzhao Cheng, Robert A. Brodsky, Leslie G. Biesecker

    Published 2012
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  17. 17
    Linear clinical progression, independent of age of onset, in Niemann–Pick disease, type C

    Linear clinical progression, independent of age of onset, in Niemann–Pick disease, type C by Nicole M. Yanjanin, Jorge I. Vélez, Andrea Gropman, Kelly King, Simona Bianconi, Sandra K. Conley, Carmen C. Brewer, Beth Solomon, William J. Pavan, Mauricio Arcos‐Burgos, Marc C. Patterson, Forbes D. Porter

    Published 2009
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  18. 18
    Global Regulatory and Public Health Initiatives to Advance Pediatric Drug Development for Rare Diseases

    Global Regulatory and Public Health Initiatives to Advance Pediatric Drug Development for Rare Diseases by Carla Epps, Ralph Bax, Alysha Croker, Dionna Green, Andrea Gropman, Ágnes Klein, Hannah Landry, Anne Pariser, Marc B. Rosenman, Michiyo Sakiyama, Junko Sato, Kuntal Sen, Monique Stone, Fumi Takeuchi, Jonathan M. Davis

    Published 2022
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  19. 19
    Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study

    Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study by Sondra W. Levin, Eva H. Baker, Wadih M. Zein, Zhongjian Zhang, Zenaide Quezado, Ning Miao, Andrea Gropman, Kurt Griffin, Simona Bianconi, Goutam Chandra, Omar Khan, Rafael C. Caruso, Aiyi Liu, Anil B. Mukherjee

    Published 2014
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  20. 20
    Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

    Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37 by Zubair M. Ahmed, Robert J. Morell, Saima Riazuddin, Andrea Gropman, Shahzad Shaukat, Mussaber M. Ahmad, Saidi Mohiddin, Lameh Fananapazir, Rafael C. Caruso, Tayyab Husnain, Shaheen N. Khan, Sheikh Riazuddin, Andrew J. Griffith, Thomas B. Friedman, Edward R. Wilcox

    Published 2003
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