Professor, Pathology, Baylor College of Medicine
Pathology
Dr. Adekunle M. Adesina, MD
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Adekunle M. Adesina is an expert in the field of Pathology. Adekunle M. Adesina, MD is a published MD. He has 86 publications published. The most current publication "Antigen-induced protective and nonprotective cell-mediated immune components against Cryptococcus neoformans."
Publications
- Preservation of KIT genotype in a novel pair of patient-derived orthotopic xenograft mouse models of metastatic pediatric CNS germinoma.
- Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.
- Is CMV a target in pediatric glioblastoma? Expression of CMV proteins, pp65 and IE1-72 and CMV nucleic acids in a cohort of pediatric glioblastoma patients.
- Repeated Isoflurane Exposure and Neuroapoptosis in the Mid-gestation Fetal Sheep Brain.
- Therapeutic implications of CD1d expression and tumor-infiltrating macrophages in pediatric medulloblastomas.
- A phase I trial of veliparib (ABT-888) and temozolomide in children with recurrent CNS tumors: a Pediatric Brain Tumor Consortium report†.
- Multilevel thoracic hemangioma with spinal cord compression in a pediatric patient: case report and review of the literature.
- Adult pilocytic astrocytomas: clinical features and molecular analysis.
- A patient tumor-derived orthotopic xenograft mouse model replicating the group 3 supratentorial primitive neuroectodermal tumor in children.
- Genome-wide analysis of DNA copy number alterations and loss of heterozygosity in intracranial germ cell tumors.
- Mutations in VRK1 Associated With Complex Motor and Sensory Axonal Neuropathy Plus Microcephaly.
- Novel cardiovascular findings in association with a POMT2 mutation: three siblings with α-dystroglycanopathy.
- Intravenous injection of oncolytic picornavirus SVV-001 prolongs animal survival in a panel of primary tumor-based orthotopic xenograft mouse models of pediatric glioma.
- Intensity-modulated radiotherapy (IMRT) in pediatric low-grade glioma.
- Long-term outcome of centrally located low-grade glioma in children.
- Improvement of pathology in sub-Saharan Africa.
- Glutathione S-transferase P1 single nucleotide polymorphism predicts permanent ototoxicity in children with medulloblastoma.
- Implications of Tumor Location on Subtypes of Medulloblastoma.
- Nigeria: "ground zero" for the high prevalence neglected tropical diseases.
- Glioblastoma multiforme of the conus medullaris in a 28-year-old female: A case report and review of the literature.
- Cerebral pleomorphic xanthoastrocytoma associated with NF1: an updated review with a rare atypical case from Africa.
- Recurrent PIK3CA mutations in rosette-forming glioneuronal tumor.
- Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation.
- Low-grade myofibroblastic sarcoma of the sacrum.
- Atypical teratoid/rhabdoid tumor of the pineal region in an adult.
- Cerebral aspergillosis caused by Aspergillus granulosus.
- Gene expression profiling reveals signatures characterizing histologic subtypes of hepatoblastoma and global deregulation in cell growth and survival pathways.
- Histologic subtypes of hepatoblastoma are characterized by differential canonical Wnt and Notch pathway activation in DLK+ precursors.
- Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl.
- A 2-month-old girl with an enlarging lesion of the nasal root. Nasal glioma.
- Low-level copy gain versus amplification of myc oncogenes in medulloblastoma: utility in predicting prognosis and survival. Laboratory investigation.
- Direct orthotopic transplantation of fresh surgical specimen preserves CD133+ tumor cells in clinically relevant mouse models of medulloblastoma and glioma.
- Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations.
- Anaplastic ganglioglioma arising from a Lhermitte-Duclos-like lesion. Case report.
- The Azzopardi phenomenon.
- FOXG1 is overexpressed in hepatoblastoma.
- Cytomorphologic characteristics, differential diagnosis and utility during intraoperative consultation for medulloblastoma.
- Phase II study of oxaliplatin in children with recurrent or refractory medulloblastoma, supratentorial primitive neuroectodermal tumors, and atypical teratoid rhabdoid...
- Chordoid glioma of the third ventricle: Report of a case with cytologic features and utility during intraoperative consultation.
- Intraoperative consultation in the diagnosis of pediatric brain tumors.
- Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children.
- Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
- Increased expression of alpha-1-antitrypsin, glutathione S-transferase pi and vascular endothelial growth factor in human pancreatic adenocarcinoma.
- Giant invasive spinal schwannoma in children: a case report and review of the literature.
- Postoperative Rhizopus scleritis in a diabetic man.
- Dementia: the University of Oklahoma autopsy experience.
- Conjunctival sporotrichosis in the absence of antecedent trauma.
- In vivo administration of TNF-alpha prevents EMC-M virus induced viral encephalitis.
- Indirect role of T cells in development of polioencephalitis and encephalomyelitis induced by encephalomyocarditis virus.
- The high mitotic count detected by phospho-histone H3 immunostain does not alter the benign behavior of angiocentric glioma.
- Thrombin, a mediator of neurotoxicity and memory impairment.
- A clinically relevant orthotopic xenograft model of ependymoma that maintains the genomic signature of the primary tumor and preserves cancer stem cells in vivo.
- A single intravenous injection of oncolytic picornavirus SVV-001 eliminates medulloblastomas in primary tumor-based orthotopic xenograft mouse models.
- Medullomyoblastoma: case report.
- Genome-wide allelic imbalance analysis of pediatric gliomas by single nucleotide polymorphic allele array.
- Unicameral bone cyst of a cervical vertebral body and lateral mass with associated pathological fracture in a child. Case report and review of the literature.
- Benign autosomal dominant syndrome of neuronal Charcot-Marie-Tooth disease, ptosis, parkinsonism, and dementia.
- Central nervous system pathology in fatal swine-origin influenza A H1N1 virus infection in patients with and without neurological symptoms: an autopsy study of 15 cases.
- Valproic Acid prolongs survival time of severe combined immunodeficient mice bearing intracerebellar orthotopic medulloblastoma xenografts.
- Solid variant of aneurysmal bone cyst of the thoracic spine: a case report.
- Genomics identifies medulloblastoma subgroups that are enriched for specific genetic alterations.
- Expression analysis of juvenile pilocytic astrocytomas by oligonucleotide microarray reveals two potential subgroups.
- Antigen-induced protective and nonprotective cell-mediated immune components against Cryptococcus neoformans.
- Malignant rhabdoid tumor of the spine in an infant: case report and review of the literature.
- Differential expression of survivin splice isoforms in medulloblastomas.
- Differential role for protein kinase C-mediated signaling in the proliferation of medulloblastoma cell lines.
- p53 gene mutation and mdm2 gene amplification are uncommon in medulloblastoma.
- Focal neuropathy preceding chronic inflammatory demyelinating polyradiculoneuropathy by several years.
- Bronchiolar inflammation and fibrosis associated with smoking. A morphologic cross-sectional population analysis.
- Inclusion body myositis with cricopharyngeus muscle involvement and severe dysphagia.
- Expression of p27kip1 and p53 in medulloblastoma: relationship with cell proliferation and survival.
- Neuromuscular dysfunction in the jejunum and colon of human leukocyte antigen B27 transgenic rats.
- Molecular heterogeneity in medulloblastoma with implications for differing tumor biology.
- Differential regulation of immune responses by highly and weakly virulent Cryptococcus neoformans isolates.
- MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation.
- Fatal Epstein-Barr virus meningitis: an autopsy report.
- Increased blood-brain barrier permeability with thymidine phosphorylase deficiency.
- Medulloblastoma outcome is adversely associated with overexpression of EEF1D, RPL30, and RPS20 on the long arm of chromosome 8.
- Expression of oligodendroglial differentiation markers in pilocytic astrocytomas identifies two clinical subsets and shows a significant correlation with proliferation...
- Overexpressed TP73 induces apoptosis in medulloblastoma.
- FOXG1 dysregulation is a frequent event in medulloblastoma.
- Melanotic paraganglioma arising in the temporal horn following Langerhans cell histiocytosis.
- Primary disseminated intradural malignant peripheral nerve sheath tumor of the spine in a child: case report and review of the literature.
- Solitary subependymal giant cell astrocytoma incidentally found at autopsy in an elderly woman without tuberous sclerosis complex.
- The good news about cancer in developing countries--pathology answers the call.
Schools
McGill University Faculty of Medicine
University of Ibadan College of Medicine
University College Hospital
Med Center Hospital Vt
Fox Chase Cancer Center
Ludwig Institute Canc Rsch
Med Center Hospital Vt University Vt
Montreal Neuro Institute
Doctors Specialties
- Molecular Genetic Pathology
- Neuropathology
- Pathology
Accepted Insurances
Education
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University of Vermont - Fletcher Allen Health Care -
University of Ibadan
Hospital
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Texas Children's Hospital
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