Get Help in Rhode Island
Assistant Professor
Division of Hematology/Oncology, Department of Pediatrics
University of Utah School of Medicine
Utah Center for Bleeding and Clotting Disorders
Primary Children's Hospital
100 N. Mario Capecchi Drive
Salt Lake City, UT 84113
https://healthcare.utah.edu/fad/mddetail.php?physicianID=u0714430&name=...
Dr. Meznarich received her medical degree from the University of Washington School of Medicine in Seattle, Washington. She then completed her residency in Pediatrics and fellowship in Pediatric Hematology and Oncology at the University of Utah/Primary Children’s Hospital in Salt Lake City, Utah.
She joined the faculty of the University of Utah in 2016, where she is currently an Assistant Professor of Pediatrics in the Division of Pediatric Hematology and Oncology. Her clinical and research interests are in benign hematology, hemophilia and other bleeding disorders, thrombosis and clotting disorders, and sickle cell disease.
No conflicts of interest (05/11/2022).
Niss O, Lorsbach RB, Berger M, Chonat S, McLemore M, Buchbinder D, McCavit T, Shaffer LG, Simpson J, Schwartz JH, Meznarich
J, Emberesh M, Seu KG, Zhang W, Kalfa TA.
Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America
(CDAR).
Blood Cells Mol Dis.
2021;87:102534.
PubMed abstract
Bahr TM, Knudsen MC, Lozano-Chinga M, Agarwal AM, Meznarich JA, Ohls RK, Christensen RD.
Infantile Pyknocytosis: End-Tidal CO, %Micro-R Measurements, Next-Generation Sequencing, and Transfusion Avoidance with Darbepoetin.
Biomed Hub.
2020;5(3):227-234.
PubMed abstract / Full Text
Seu KG, Trump LR, Emberesh S, Lorsbach RB, Johnson C, Meznarich J, Underhill HR, Chou ST, Sakthivel H, Nassar NN, Seu KJ,
Blanc L, Zhang W, Lutzko CM, Kalfa TA.
VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects.
Am J Hum Genet.
2020;107(6):1149-1156.
PubMed abstract / Full Text
Bahr TM, Lozano-Chinga M, Agarwal AM, Meznarich JA, Gerday E, Smoot JL, Taylor A, Christensen RD.
Dizygotic twins with prolonged jaundice and microcytic, hypochromic, hemolytic anemia with pyropoikilocytosis.
Blood Cells Mol Dis.
2020;85:102462.
PubMed abstract
Meznarich JA, Draper L, Christensen RD, Yaish HM, Luem ND, Pysher TJ, Jung G, Nemeth E, Ganz T, Ward DM.
Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations.
Blood Cells Mol Dis.
2018;71:63-66.
PubMed abstract / Full Text