Search Results - Vanderver, Adeline

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  1. 1
    Genetic Leukoencephalopathies in Adults

    Genetic Leukoencephalopathies in Adults by Vanderver, Adeline

    Published 2016
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  2. 2
    Astrocytes, an active player in Aicardi–Goutières syndrome

    Astrocytes, an active player in Aicardi–Goutières syndrome by Sase, Sunetra, Takanohashi, Asako, Vanderver, Adeline, Almad, Akshata

    Published 2018
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  3. 3
    Isolated cranial nerve enhancement in Metachromatic Leukodystrophy

    Isolated cranial nerve enhancement in Metachromatic Leukodystrophy by Singh, Rani K., Leshner, Robert T., Kadom, Nadja, Vanderver, Adeline L.

    Published 2009
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  4. 4
    Emerging Treatments for Pediatric Leukodystrophies

    Emerging Treatments for Pediatric Leukodystrophies by Helman, Guy, Van Haren, Keith, Escolar, Maria L., Vanderver, Adeline

    Published 2015
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  5. 5
    Characterization of Transferrin Glycopeptide Structures in Human Cerebrospinal Fluid

    Characterization of Transferrin Glycopeptide Structures in Human Cerebrospinal Fluid by Brown, Kristy J., Vanderver, Adeline, Hoffman, Eric P., Schiffmann, Raphael, Hathout, Yetrib

    Published 2012
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  6. 6
    Relative incidence of inherited white matter disorders in childhood to acquired pediatric demyelinating disorders

    Relative incidence of inherited white matter disorders in childhood to acquired pediatric demyelinating disorders by Vanderver, Adeline, Hussey, Heather, Schmidt, Johanna L., Pastor, William, Hoffman, Heather J.

    Published 2012
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  7. 7
    A Point Mutation in Translation Initiation Factor 2B Leads to a Continuous Hyper Stress State in Oligodendroglial-Derived Cells

    A Point Mutation in Translation Initiation Factor 2B Leads to a Continuous Hyper Stress State in Oligodendroglial-Derived Cells by Kantor, Liraz, Pinchasi, Dalia, Mintz, Michelle, Hathout, Yetrib, Vanderver, Adeline, Elroy-Stein, Orna

    Published 2008
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  8. 8
    Focal Central White Matter Lesions in Alexander Disease

    Focal Central White Matter Lesions in Alexander Disease by Barreau, Pauline, Prust, Morgan J., Crane, Jeremy, Loewenstein, Johanna, Kadom, Nadja, Vanderver, Adeline

    Published 2011
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  9. 9
    Targeted Leukodystrophy Diagnosis Based on Charges and Yields for Testing

    Targeted Leukodystrophy Diagnosis Based on Charges and Yields for Testing by Richards, Jackson, Korgenski, E. Kent, Taft, Ryan J., Vanderver, Adeline, Bonkowsky, Joshua L.

    Published 2015
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  10. 10
    3358 Developmental Outcomes of Aicardi Goutieres Syndrome

    3358 Developmental Outcomes of Aicardi Goutieres Syndrome by Adang, Laura, Patel, Akshilkumar, Sherbini, Omar, Kramer-Golinkoff, Julia, Shults, Justine, Vanderver, Adeline

    Published 2019
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  11. 11
    Neuropathological Findings in a Case of IFIH1-Related Aicardi–Goutières Syndrome

    Neuropathological Findings in a Case of IFIH1-Related Aicardi–Goutières Syndrome by Gilani, Ahmed, Adang, Laura A, Vanderver, Adeline, Collins, Abigail, Kleinschmidt-DeMasters, BK

    Published 2019
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  12. 12
    Time Series Proteome Profiling

    Time Series Proteome Profiling by Formolo, Catherine A., Mintz, Michelle, Takanohashi, Asako, Brown, Kristy J., Vanderver, Adeline, Halligan, Brian, Hathout, Yetrib

    Published 2011
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  13. 13
    Acquisition of Developmental Milestones in Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy

    Acquisition of Developmental Milestones in Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy by Gavazzi, Francesco, Charsar, Brittany A., Williams, Catherine, Shults, Justine, Alves, Cesar A., Adang, Laura, Vanderver, Adeline

    Published 2021
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  14. 14
    Novel biallelic variants in NRROS associated with a lethal microgliopathy, brain calcifications and neurodegeneration

    Novel biallelic variants in NRROS associated with a lethal microgliopathy, brain calcifications and neurodegeneration by Macintosh, Julia, Derksen, Alexa, Poulin, Chantal, Braverman, Nancy, Vanderver, Adeline, Thiffault, Isabelle, Albrecht, Steffen, Bernard, Geneviève

    Published 2022
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  15. 15
    Family History of Autoimmune Disease in Patients with Aicardi-Goutières Syndrome

    Family History of Autoimmune Disease in Patients with Aicardi-Goutières Syndrome by Schmidt, Johanna L., Olivieri, Ivana, Vento, Jodie M., Fazzi, Elisa, Gordish-Dressman, Heather, Orcesi, Simona, Vanderver, Adeline

    Published 2012
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  16. 16
    Adult-Onset Vanishing White Matter Disease Due to a Novel EIF2B3 Mutation

    Adult-Onset Vanishing White Matter Disease Due to a Novel EIF2B3 Mutation by La Piana, Roberta, Vanderver, Adeline, van der Knaap, Marjo, Roux, Louise, Tampieri, Donatella, Brais, Bernard, Bernard, Geneviève

    Published 2012
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  17. 17
    Functionally pathogenic EARS2 variants in vitro may not manifest a phenotype in vivo

    Functionally pathogenic EARS2 variants in vitro may not manifest a phenotype in vivo by McNeill, Nathan, Nasca, Alessia, Reyes, Aurelio, Lemoine, Benjamin, Cantarel, Brandi, Vanderver, Adeline, Schiffmann, Raphael, Ghezzi, Daniele

    Published 2017
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  18. 18
    More Than Hypomyelination in Pol-III Disorder

    More Than Hypomyelination in Pol-III Disorder by Vanderver, Adeline, Tonduti, Davide, Bernard, Genevieve, Lai, Jinping, Rossi, Christopher, Carosso, Giovanni, Quezado, Martha, Wong, Kondi, Schiffmann, Raphael

    Published 2013
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  19. 19
    Dystonia in RNA Polymerase III‐Related Leukodystrophy

    Dystonia in RNA Polymerase III‐Related Leukodystrophy by Al Yazidi, Ghalia, Tran, Luan T., Guerrero, Kether, Vanderver, Adeline, Schiffmann, Raphael, Wolf, Nicole I., Chouinard, Sylvain, Bernard, Geneviève

    Published 2019
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  20. 20
    MRI Features of 4 Female Patients with Pyruvate Dehydrogenase E1 alpha Deficiency

    MRI Features of 4 Female Patients with Pyruvate Dehydrogenase E1 alpha Deficiency by Mew, Nicholas Ah, Loewenstein, Johanna B., Kadom, Nadja, Lichter-Konecki, Uta, Gropman, Andrea L., Martin, Jodie M., Vanderver, Adeline

    Published 2011
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