Výsledky vyhledávání - "Gregory E. Halligan"

Unusual Genetic Aberrations Including a Deletion of KLF6 Tumor Suppressor Gene Revealed by Integrated Cytogenetic Approaches in a Pediatric Ewing Sarcoma

Autor: Jean-Pierre de Chadarévian, Gregory E. Halligan, Hope H. Punnet, Jinglan Liu, Judy Mae Pascasio, Jason C. White

Publikováno v: Journal of Pediatric Hematology/Oncology. 37:e51-e54

Ewing sarcoma is the third most common sarcoma in children and young adults. Its characteristic chromosomal rearrangement results in a chimerical EWSR1-ETS transcription factor. Secondary genetic alterations are very common. Membranous expression of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56956b1adf699e50d2d2a758f04ac354
https://doi.org/10.1097/mph.0000000000000081

Zobrazit plný text záznamu

Malignant glioma with primitive neuroectodermal tumor-like component (MG-PNET): novel microarray findings in a pediatric patient

Autor: Matthew Keisling, Gregory E. Halligan, Jinglan Liu, Judy Mae Pascasio, Christos D. Katsetos, Ayman Samkari

Publikováno v: Clinical neuropathology. 35(6)

Central nervous system (CNS) tumors exhibiting dual features of malignant glioma (MG) and primitive neuroectodermal tumor (PNET) are rare and diagnostically challenging. Previous studies have shown that MG-PNET carry MYCN or MYC gene amplifications w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa3632497a7447eb001b81d41eb40d49
https://pubmed.ncbi.nlm.nih.gov/27781423

Zobrazit plný text záznamu

Autor: Karmaine A. Millington, Jean Pierre De Chadarévian, Gregory E. Halligan, Judy Mae Pascasio

Publikováno v: Modern Pathology. 25:289-294

Anthracycline, used in oncological chemotherapy, has one well-known side effect: cardiotoxicity. Another is abnormal intestinal motility such as constipation and ileus, the pathogenesis of which, to our knowledge, has not been morphologically investi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429034d507698c4050d9714071f955b8
https://doi.org/10.1038/modpathol.2011.115

Zobrazit plný text záznamu

FOXO1–FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma

Autor: Jinglan Liu, John E. Hauptman, Matthew Keisling, Jean-Pierre de Chadarévian, Miguel A. Guzman, Gregory E. Halligan, Dilipkumar M Patel, Hope H. Punnett, Steve J Hou, Donna M Pezanowski, Peter Papenhausen, Judy Mae Pascasio

Publikováno v: Modern Pathology. 24:1327-1335

Rhabdomyosarcoma is the most common pediatric soft tissue malignancy. Two major subtypes, alveolar rhabdomyosarcoma and embryonal rhabdomyosarcoma, constitute 20 and 60% of all cases, respectively. Approximately 80% of alveolar rhabdomyosarcoma carry

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e68afdc6fb486c05995b178c6f1e8e7b
https://doi.org/10.1038/modpathol.2011.98

Zobrazit plný text záznamu

Cerebellar Gliomatosis in a Toddler

Autor: Eric N. Faerber, Agustin Legido, Jennifer J.D. Morrissette, Christos D. Katsetos, Joseph H. Piatt, Gregory E. Halligan, Jean-Pierre de Chadarévian, Jahan Ara, Mitzie Grant

Publikováno v: Journal of Child Neurology. 27:511-520

Gliomatosis confined to the cerebellum is most unusual. We report such a case in a 20-month-old male who presented with unsteadiness. Magnetic resonance imaging revealed a diffuse area of abnormal signal intensity within both cerebellar hemispheres,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c918641a290198afcf9f222c3f9762ef
https://doi.org/10.1177/0883073811419315

Zobrazit plný text záznamu

Glioneuronal Phenotype in a Diencephalic Pilomyxoid Astrocytoma

Autor: Louise Bertrand, Goutham Reddy, Gregory E. Halligan, Christos D. Katsetos, Judy Mae Pascasio, Jean-Pierre de Chadarévian, Eric N. Faerber

Publikováno v: Pediatric and Developmental Pathology. 9:480-487

We report the presence of divergent populations of cells in a hypothalamic/chiasmatic pilomyxoid astrocytoma of an 11-month-old male, exhibiting differential immunohistochemical localizations for glial fibrillary acidic protein (GFAP) and synaptophys

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57f9c441cb71f903368e89985de79ecf
https://doi.org/10.2350/06-03-0054.1

Zobrazit plný text záznamu

Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia

Autor: J.P. de Chadarévian, Jennifer J.D. Morrissette, Hope H. Punnett, Felicula Guerrero, Ann Shoemaker McKenzie, Gregory E. Halligan

Publikováno v: Cancer Genetics and Cytogenetics. 169:58-61

We describe the rare finding of a 33-month-old child neonatally diagnosed with Down syndrome, who presented with pre-B acute lymphoblastic leukemia (ALL) with a pretreatment bone marrow karyotype in which a low hypodiploid cell line (38 chromosomes)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bf2f5fa48c19bf186c4ce2ae5ab49d8
https://doi.org/10.1016/j.cancergencyto.2006.02.007

Zobrazit plný text záznamu

Clonal trisomy 4 cells detected in the ossifying renal tumor of infancy: study of 3 cases

Autor: Gregory E. Halligan, Jean-Pierre de Chadarévian, Miguel A. Guzman, Donna M Pezanowski, Dilipkumar M Patel, Bruce R. Pawel, Jinglan Liu, Jonathan A Roth

Publikováno v: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 26(2)

The ossifying renal tumor of infancy is a rare neoplasm diagnosed in the first 2 years of life, predominantly in boys. The neoplasm is primarily characterized by the presence of a large ossifying component. Its most common mode of presentation is hem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb9d53589581c65420fc0af079def9ee
https://pubmed.ncbi.nlm.nih.gov/22976287

Zobrazit plný text záznamu

Hyperdiploidy with trisomy 9 and deletion of the CDKN2A locus in T-cell acute lymphoblastic leukemia

Autor: Gregory E. Halligan, Ann Shoemaker McKenzie, Kelley R. Healey, S. Lauren Gray, Jean-Pierre de Chadarévian, Jennifer J.D. Morrissette

Publikováno v: Cancer genetics and cytogenetics. 190(2)

We describe the rare finding of a T-cell acute lymphoblastic leukemia (T-ALL) and a pretreatment bone marrow karyotype mosaic for four distinct cell lines in a 4-year-old boy. G-banding analysis of metaphase cells identified a hyperdiploid cell line

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7db94ab64c8e867ed8ab2aa779898cf
https://pubmed.ncbi.nlm.nih.gov/19380031

Zobrazit plný text záznamu

Pediatric granular cell tumor of the tracheobronchial tree

Autor: Marta Rozans, Christopher Newton, Shaheen J. Timmapuri, Christine Finck, Jean-Pierre de Chadarévian, Jane Lyons, Matthew L. Moront, Gregory E. Halligan

Publikováno v: Journal of pediatric surgery. 43(3)

Granular cell tumors are lesions of neural crest origin with a predilection for the skin and soft tissue. Granular cell tumors of the tracheobronchial tree are exceedingly rare in the pediatric population, with only 5 reported cases. All 5 of these l

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::960163c67208707588d30c2676bc1044
https://pubmed.ncbi.nlm.nih.gov/18358305

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání