academic hospital pathology

Pathology

Doctor Kevin E. Bove, MD practices Pathology. He attended University Hospital - University of Cincinnati College of Medicine. Kevin Bove is also a published doctor. He has 38 publication published. The most recent publication is: Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.

Publications

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• Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.
• Multifocal hepatic neoplasia in 3 children with APC gene mutation.
• Genetic Defects In Bile Acid Conjugation Cause Fat-Soluble Vitamin Deficiency.
• Rectal biopsy in children with Down syndrome and chronic constipation: Hirschsprung disease vs. non-Hirschsprung disease.
• Juvenile dermatomyositis: correlation of MRI at presentation with clinical outcome.
• A welcome surprise: nodular fasciitis presenting as soft tissue sarcoma.
• Morphologic findings in progressive familial intrahepatic cholestasis 2 (PFIC2): correlation with genetic and immunohistochemical studies.
• Leukocyte adhesion deficiency type 1 presenting with recurrent pyoderma gangrenosum and flaccid scarring.
• A fetus with hypertrophic cardiomyopathy, restrictive, and single-ventricle physiology, and a beta-myosin heavy chain mutation.
• Porcine allograft mandible revitalization using autologous adipose-derived stem cells, bone morphogenetic protein-2, and periosteum.
• Ductal plate malformation-like arrays in early explants after a Kasai procedure are independent of splenic malformation complex (heterotaxy).
• Concurrent course of transient neonatal diabetes with cholestasis and paucity of interlobular bile ducts: a case report.
• Phenotypic and microscopic description of a new case of Ermine phenotype.
• Megalencephalic leukoencephalopathy with subcortical cysts: a third confirmed case with literature review.
• Variability of acetylcholinesterase hyperinnervation patterns in distal rectal suction biopsy specimens in Hirschsprung disease.
• Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.
• Inborn errors of bile acid metabolism.
• DNA sequence of the translocation breakpoints in undifferentiated embryonal sarcoma arising in mesenchymal hamartoma of the liver harboring the t(11;19)(q11;q13.4) tra...
• Combined omphalomesenteric and urachal remnants in an 18-month-old girl.
• Proliferative activity of human thyroid cells in various age groups and its correlation with the risk of thyroid cancer after radiation exposure.
• Fulminant neonatal liver failure in siblings: probable congenital hemophagocytic lymphohistiocytosis.
• Non-lethal congenital hypotonia due to glycogen storage disease type IV.
• Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods.
• Association between lack of angiogenic response in muscle tissue and high expression of angiostatic ELR-negative CXC chemokines in patients with juvenile dermatomyosit...
• Rotavirus deaths: rare or unrecognized?
• Muscle coenzyme Q: a potential test for mitochondrial activity and redox status.
• Hepatocyte glycogen accumulation in patients undergoing dietary management of urea cycle defects mimics storage disease.
• MRI appearance of accessory breast tissue: a diagnostic consideration for an axillary mass in a peripubertal or pubertal girl.
• Bile acid synthetic defects and liver disease: a comprehensive review.
• MALT Lymphoma in Children: Case Report and Review of the Literature.
• GLUT1 endothelial reactivity distinguishes hepatic infantile hemangioma from congenital hepatic vascular malformation with associated capillary proliferation.
• The challenge of using autopsy information for quality improvement.
• Expanding the limits of the Fryns syndrome.
• Giant botryoid fibroepithelial polyp of bladder with myofibroblastic stroma and cystitis cystica et glandularis.
• Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy.
• Early failure of the Shelhigh pulmonary valve conduit in infants.
• Combination of diaphragmatic eventration and microphthalmia/anophthalmia is probably nonrandom.

Schools

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• State University of New York At Buffalo

• Cincinnati Genl Hospital

Doctors Specialties

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• Pediatric Pathology
• Pathology

Accepted Insurances

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Education

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• University Hospital - University of Cincinnati College of Medicine
• University at Buffalo, School of Medicine and Biomedical Sciences

Hospital

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• Cincinnati Children's Hospital Medical Center

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