Search Results - "Saratsis, Amanda M"

Refine Results
  1. 1
  2. 2
  3. 3

    Standardization of the liquid biopsy for pediatric diffuse midline glioma using ddPCR by Li, Daphne, Bonner, Erin R., Wierzbicki, Kyle, Panditharatna, Eshini, Huang, Tina, Lulla, Rishi, Mueller, Sabine, Koschmann, Carl, Nazarian, Javad, Saratsis, Amanda M.

    Published in Scientific reports (03-03-2021)
    “…Diffuse midline glioma (DMG) is a highly morbid pediatric brain tumor. Up to 80% of DMGs harbor mutations in histone H3-encoding genes, associated with poor…”
    Get full text
    Journal Article
  4. 4

    Detection of Histone H3 mutations in cerebrospinal fluid-derived tumor DNA from children with diffuse midline glioma by Huang, Tina Y, Piunti, Andrea, Lulla, Rishi R, Qi, Jin, Horbinski, Craig M, Tomita, Tadanori, James, C David, Shilatifard, Ali, Saratsis, Amanda M

    Published in Acta neuropathologica communications (17-04-2017)
    “…Diffuse midline gliomas (including diffuse intrinsic pontine glioma, DIPG) are highly morbid glial neoplasms of the thalamus or brainstem that typically arise…”
    Get full text
    Journal Article
  5. 5
  6. 6

    Insights into pediatric diffuse intrinsic pontine glioma through proteomic analysis of cerebrospinal fluid by Saratsis, Amanda M, Yadavilli, Sridevi, Magge, Suresh, Rood, Brian R, Perez, Jennifer, Hill, D Ashley, Hwang, Eugene, Kilburn, Lindsay, Packer, Roger J, Nazarian, Javad

    Published in Neuro-oncology (Charlottesville, Va.) (01-05-2012)
    “…Diffuse intrinsic pontine glioma (DIPG) is a leading cause of brain tumor-related death in children. DIPG is not surgically resectable, resulting in a paucity…”
    Get full text
    Journal Article
  7. 7

    Effects of H3.3G34V mutation on genomic H3K36 and H3K27 methylation patterns in isogenic pediatric glioma cells by Huang, Tina Yi-Ting, Piunti, Andrea, Qi, Jin, Morgan, Marc, Bartom, Elizabeth, Shilatifard, Ali, Saratsis, Amanda M

    Published in Acta neuropathologica communications (07-12-2020)
    “…Histone H3.3 mutation (H3F3A) occurs in 50% of cortical pediatric high-grade gliomas. This mutation replaces glycine 34 with arginine or valine (G34R/V),…”
    Get full text
    Journal Article
  8. 8

    Choroidal artery embolization in the management of cerebrospinal fluid overproduction: case report and review of the literature by Li, Daphne, Shokuhfar, Tahaamin, Pantalone, Julia, Rothstein, Brian, Alden, Tord D, Shaibani, Ali, Saratsis, Amanda M

    Published in Journal of neurosurgery. Pediatrics (01-06-2019)
    “…Diffuse villous hyperplasia of the choroid plexus (DVHCP) is a rare cause of communicating hydrocephalus. DVHCP may be diagnosed radiographically and through…”
    Get full text
    Journal Article
  9. 9

    Ventricular Cerebrospinal Fluid Sampling in Pediatric Diffuse Midline Glioma Patients: Institutional Experience and Review of the Literature by Li, Daphne, Stellpflug, Wendy, Romanski, Kathy, Kilgallon, Maureen, Speck, Stacy, Saratsis, Amanda M.

    Published in Frontiers in pediatrics (27-10-2020)
    “…Purpose: Increasing evidence suggests that circulating biomarkers may serve diagnostic and longitudinal monitoring purposes in pediatric neuro-oncology. Mutant…”
    Get full text
    Journal Article
  10. 10

    H3K27M mutant glioma: Disease definition and biological underpinnings by Saratsis, Amanda M, Knowles, Truman, Petrovic, Antonela, Nazarian, Javad

    Published in Neuro-oncology (Charlottesville, Va.) (03-05-2024)
    “…High-grade glioma (HGG) is the most common cause of cancer death in children and the most common primary central nervous system tumor in adults. While…”
    Get full text
    Journal Article
  11. 11

    H3 K27M-altered glioma and diffuse intrinsic pontine glioma: Semi-systematic review of treatment landscape and future directions by van den Bent, Martin, Saratsis, Amanda M, Geurts, Marjolein, Franceschi, Enrico

    Published in Neuro-oncology (Charlottesville, Va.) (03-05-2024)
    “…H3 K27M-mutant diffuse glioma is a recently identified brain tumor associated with poor prognosis. As of 2016, it is classified by the World Health…”
    Get full text
    Journal Article
  12. 12

    Detection of histone H3 K27M mutation and post-translational modifications in pediatric diffuse midline glioma via tissue immunohistochemistry informs diagnosis and clinical outcomes by Huang, Tina, Garcia, Roxanna, Qi, Jin, Lulla, Rishi, Horbinski, Craig, Behdad, Amir, Wadhwani, Nitin, Shilatifard, Ali, James, Charles, Saratsis, Amanda M

    Published in Oncotarget (14-12-2018)
    “…Pediatric diffuse midline glioma is a highly morbid glial neoplasm that may arise in the thalamus or brainstem (also known as diffuse intrinsic pontine glioma…”
    Get full text
    Journal Article
  13. 13
  14. 14

    Gorham Stout disease of the temporal bone with cerebrospinal fluid leak by Aouad, Pascale, Young, Nancy M., Saratsis, Amanda M., Reynolds, Meredith A., Ryan, Maura E.

    Published in Child's nervous system (01-02-2022)
    “…Gorham Stout disease (GSD) is a rare disease characterized by the proliferation of endothelial lined vessels and replacement of bone by fibrous tissue. The…”
    Get full text
    Journal Article
  15. 15

    LIN28B and Let-7 in Diffuse Midline Glioma: A Review by Knowles, Truman, Huang, Tina, Qi, Jin, An, Shejuan, Burket, Noah, Cooper, Scott, Nazarian, Javad, Saratsis, Amanda M

    Published in Cancers (19-06-2023)
    “…Diffuse midline glioma (DMG) is the most lethal of all childhood cancers. DMGs are driven by histone-tail-mutation-mediated epigenetic dysregulation and…”
    Get full text
    Journal Article
  16. 16
  17. 17
  18. 18
  19. 19

    Safety of Ventricular Reservoir Sampling in Pediatric Posthemorrhagic Hydrocephalus Patients: Institutional Experience and Review of the Literature by Li, Daphne, Romanski, Kathy, Kilgallon, Maureen, Speck, Stacy, Bowman, Robin, DiPatri, Arthur, Alden, Tord, Tomita, Tadanori, Lam, Sandi, Saratsis, Amanda M.

    Published in The Journal of neuroscience nursing (01-02-2021)
    “…INTRODUCTION: Posthemorrhagic hydrocephalus (PHH) is a common disease process encountered in neonates. Management often includes cerebrospinal fluid (CSF)…”
    Get full text
    Journal Article
  20. 20