Thomas S DeNapoli - JoVE Visualize

Showing results (1-10 of 5) with videos related to

Pageof 1

Sort By:

Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 18, 2015

Coexistent Chorangioma and Hepatic Adenoma in One Twin Placenta: A Case Report and Review of the LiteratureThomas S DeNapoli

JBJS Case Connector|February 15, 2021

Necrotizing Fasciitis of the Right Lower Extremity from Ruptured Appendicitis: Case ReportShawn Funk, Kelley Warren, Thomas S DeNapoli, et al.

Journal of Pediatric Hematology/Oncology|October 7, 2003

Anemia and hepatosplenomegaly as presenting features in a child with rickets and secondary myelofibrosisBarbara A Gruner, Thomas S DeNapoli, Said Elshihabi, et al.

Human Mutation|August 8, 2018

LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPVPrzemyslaw Szafranski, Ewelina Kośmider, Qian Liu, et al.

Human Genetics|April 14, 2016

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veinsPrzemyslaw Szafranski, Tomasz Gambin, Avinash V Dharmadhikari, et al.

Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:

Pageof 1

Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 18, 2015

Coexistent Chorangioma and Hepatic Adenoma in One Twin Placenta: A Case Report and Review of the LiteratureThomas S DeNapoli

JBJS Case Connector|February 15, 2021

Necrotizing Fasciitis of the Right Lower Extremity from Ruptured Appendicitis: Case ReportShawn Funk, Kelley Warren, Thomas S DeNapoli, et al.

Journal of Pediatric Hematology/Oncology|October 7, 2003

Anemia and hepatosplenomegaly as presenting features in a child with rickets and secondary myelofibrosisBarbara A Gruner, Thomas S DeNapoli, Said Elshihabi, et al.

Human Mutation|August 8, 2018

LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPVPrzemyslaw Szafranski, Ewelina Kośmider, Qian Liu, et al.

Human Genetics|April 14, 2016

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veinsPrzemyslaw Szafranski, Tomasz Gambin, Avinash V Dharmadhikari, et al.

Pageof 1