Search Results - "Ermarth, Anna K"

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  1. 1

    Clinical diagnostic predictive score for Meckel diverticulum by Jaramillo, Catalina, Jensen, M. Kyle, McClain, Amber, Stoddard, Gregory, Barnhart, Douglas, Ermarth, Anna K.

    Published in Journal of pediatric surgery (01-09-2021)
    “…Background/Purpose: Meckel diverticulum (MD) is present in 2% of the population. Many practitioner feel the diagnosis relies upon technetium-99 m pertechnetate…”
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    Journal Article
  2. 2

    Neonatal cholestasis and hepatosplenomegaly caused by congenital dyserythropoietic anemia type 1: A case report by Jaramillo, Catalina, Ermarth, Anna K, Putnam, Angelica R, Deneau, Mark

    Published in World journal of hepatology (27-05-2019)
    “…Congenital dyserythropoietic anemia type 1 (CDA1) is an autosomal recessive disorder of ineffective erythropoiesis, resulting in increased iron storage. CDA1…”
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    Journal Article
  3. 3

    Flexible Sigmoidoscopy Utility in the Diagnosis of Pediatric Gastrointestinal Disorders by Jaramillo, Catalina, Ermarth, Anna K, Collier, John S, Pohl, John F, Patel, Raza A

    Published in Curēus (Palo Alto, CA) (04-05-2023)
    “… Although flexible sigmoidoscopy (FS) is utilized in children for the diagnosis of pediatric gastrointestinal conditions, such as inflammatory bowel disease…”
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    Journal Article
  4. 4

    Congenital Chylous Ascites and Ehlers-Danlos Syndrome Type VI by Ermarth, Anna K, Pohl, John, Esty, Brittany, Sempler, Jessica K, Carey, John C, O'Gorman, Molly A

    Published in ACG case reports journal (21-12-2016)
    “…We report the first observation of a patient with contgenital chylous ascites (CCA) and Ehlers-Danlos syndrome type VI due to primary lymphatic defect with…”
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    Journal Article
  5. 5

    Neonatal cholestasis and hepatosplenomegaly caused by congenital dyserythropoietic anemia type 1: A case report by Jaramillo, Catalina, Ermarth, Anna K, Putnam, Angelica R, Deneau, Mark

    Published in World journal of hepatology (27-05-2019)
    “…BACKGROUNDCongenital dyserythropoietic anemia type 1 (CDA1) is an autosomal recessive disorder of ineffective erythropoiesis, resulting in increased iron…”
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  6. 6