C. Schandl

发表

A Case Example of Asphyxia Due to Occupational Exposure to Airborne Chemicals and Review of Workplace Fatalities

Meredith H. Frame, C. Schandl, 2015, Journal of forensic sciences.

Mitotic Chromosomal Bcl-2: I. Stable Expression Throughout the Cell Cycle and Association with Isolated Chromosomes

M. Willingham, G. G. Re, C. Schandl, 1999, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Fat embolism in pediatric patients: an autopsy evaluation of incidence and etiology.

S. Fakhry, Stuart M. Leon, E. Eriksson, 2015, Journal of critical care.

Verapamil Toxicity: An Unusual Case Report and Review of the Literature

R. Harley, C. Schandl, Nicholas I Batalis, 2007, American Journal of Forensic Medicine and Pathology.

Use of an Automated Nested Multiplex Respiratory Pathogen PCR Panel Postmortem in the Pediatric Forensic Setting†

F. Nolte, C. Schandl, T. Baker, 2017, Journal of forensic sciences.

Investigation of Pregnancy-Related Deaths

C. Schandl, 2014 .

The Elder Autopsy

C. Schandl, 2020 .

Major DNA Fragmentation Is a Late Event in Apoptosis

Cynthia A. Schandl, M. Willingham, Mark C. Willingham, 1997, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Acute Deaths in Nonpregnant Adults Due to Invasive Streptococcal Infections

M. Caplan, C. Schandl, Nicholas I Batalis, 2007, The American journal of forensic medicine and pathology.

The Importance of Microscopic Examination of the Lungs in Decedents with Sustained Central Intravascular Catheters: A Nine‐Case Series

C. Schandl, Nicholas I Batalis, L. Tormos, 2015, Journal of forensic sciences.

Sudden Cardiac Death in a Young Man with Migraine‐associated Arrhythmia

C. Schandl, J. Meehan, Darren J Monroe, 2015, Journal of forensic sciences.

Amyloidosis and Unexpected Death: A Review of Seven Cases

C. Schandl, S. E. Presnell, 2016, Academic forensic pathology.

Molecular profiling of vitreous fluid by massively parallel sequencing: a case series.

C. Schandl, J. Hirschhorn, Kathyrn G Lindsey, 2020, Journal of the American Society of Cytopathology.

First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination

D. Wolff, C. Schandl, S. Patwardhan, 2018, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

A 27-Year Retrospective Study of Pediatric Suicide Cases Referred to the Medical University of South Carolina (1988-2014)

C. Schandl, Balvir Singh, L. Tormos, 2016, Academic forensic pathology.

Chromothripsis in Two Patients With Renal Cell Carcinoma: A Case Series.

Jonathan C. Gullett, D. Wolff, C. Schandl, 2017, Clinical genitourinary cancer.

Apparent coexistence of ETV6::RUNX1 and KMT2A::MLLT3 fusions due to a nonproductive KMT2A rearrangement in B-ALL

J. Smadbeck, P. Blackburn, Y. Akkari, 2022, Leukemia & lymphoma.

Benign Fibromyxoid Lesion of the Breast: A Distinct Entity From Benign Spindle Cell Tumors of the Mammary Stroma?

F. Darvishian, A. Rapkiewicz, C. Schandl, 2018, International journal of surgical pathology.

Mitotic Chromosomal Bcl-2: II. Localization to Interphase Nuclei

M. Willingham, G. G. Re, C. Schandl, 1999, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Maternal Epidural Steroids to Prevent Neonatal Exposure to Hyperthermia and Inflammation

R. Newman, L. Hebbar, C. Schandl, 2018, American Journal of Perinatology.

Urothelial carcinoma of donor origin in a kidney transplant patient

H. Drabkin, D. Wolff, C. Schandl, 2016, Journal of Immunotherapy for Cancer.

Clinical utility of chromosomal microarray in establishing clonality and high risk features in patients with Richter transformation

B. Hess, N. Wagner-Johnston, D. Wolff, 2019, Cancer genetics.

Glycogen Storage Disease Type IV Diagnosed at Fetal Autopsy

C. Schandl, Daniel C. Butler, A. Phillips, 2019, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Novel high-risk acute myeloid leukemia subgroup with ERG amplification and Biallelic loss of TP53.

Dongjun Chung, B. Hess, D. Wolff, 2023, Cancer genetics.

Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia

J. Smadbeck, P. Blackburn, G. Vasmatzis, 2020, Genes, chromosomes & cancer.

Fatal Neurotoxic Response to Neuroleptic Medications: Case Report and Review of the Literature

R. Harley, C. Schandl, K. A. Collins, 2007, The American journal of forensic medicine and pathology.

Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophilia.

B. Pitel, N. Hoppman, D. Wolff, 2020, Cancer genetics.