Jenna L. Bodmer

ORCID: 0000-0003-3110-6679
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About
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Research Areas
  • Congenital Diaphragmatic Hernia Studies
  • Tracheal and airway disorders
  • Bone Tumor Diagnosis and Treatments
  • Neuroblastoma Research and Treatments
  • Neonatal Respiratory Health Research
  • Gynecological conditions and treatments
  • Orthopedic Infections and Treatments
  • Esophageal and GI Pathology
  • Ureteral procedures and complications
  • Infectious Diseases and Tuberculosis
  • Soft tissue tumor case studies
  • Pulmonary Hypertension Research and Treatments
  • Tuberculosis Research and Epidemiology
  • Sarcoma Diagnosis and Treatment
  • Neurofibromatosis and Schwannoma Cases
  • Anorectal Disease Treatments and Outcomes
  • Chromatin Remodeling and Cancer
  • Congenital Heart Disease Studies
  • Airway Management and Intubation Techniques
  • Endometriosis Research and Treatment
  • Sexual Differentiation and Disorders
  • Colorectal Cancer Surgical Treatments

University of Colorado Denver
2021-2024

Children's Hospital Colorado
2021-2024

University of Colorado Hospital
2023

Abstract Neuroepithelial tumors with fusion of PLAGL1 or amplification PLAGL1/PLAGL2 have recently been described often ependymoma-like embryonal histology respectively. To further evaluate emerging entities PLAG-family genetic alterations, the histologic, molecular, clinical, and imaging features are for 8 clinical cases encountered at St. Jude ( EWSR1-PLAGL1 n = 6; 1; PLAGL2 1). A histologic feature observed on initial resection in a subset (4/6) supratentorial neuroepithelial...

10.1186/s40478-024-01809-9 article EN cc-by Acta Neuropathologica Communications 2024-09-03

Tbx4 protein, expressed in mesenchyme of the developing lung, contributes to airway branching and distal lung growth. An association between pediatric onset pulmonary arterial hypertension (PAH) genetic variations coding for T-box transcription factor 4 gene ( TBX4) has been increasingly recognized. Tbx4-related PAH a bimodal age distribution, including severe lethal newborns later PAH. We present an autopsy study 24-year-old male with heterozygous TBX4 variant, who developed at 12 years....

10.1177/10935266231199933 article EN Pediatric and Developmental Pathology 2023-10-06

10.1164/rccm.202201-0225im article EN cc-by-nc-nd American Journal of Respiratory and Critical Care Medicine 2022-09-29

Infantile myofibromatosis is a rare myofibroblastic proliferative disorder characterized by firm, skin-colored to red-purple cutaneous and subcutaneous nodules; these are the most prevalent fibrous tumors observed in infancy. A premature male infant presented at birth with multiple firm nodules measuring about 1-2cm each. Full body MRI excisional biopsy of right chest nodule confirmed diagnosis. We review case infantile discuss its highly heterogeneous presentation clinical course, as well...

10.5070/d3271156092 article EN cc-by-nc-nd Dermatology Online Journal 2022-01-18
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