Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Janese, Trimaldi"'
Publikováno v:
Diagnostic Cytopathology. 44:685-687
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d441295f180a7e342c6bbc9d0cbae371
https://doi.org/10.1002/dc.23511
https://doi.org/10.1002/dc.23511
Autor:
Janese Trimaldi, Ling Zhang, Steven J. Agosti, Loveleen Kang, Alan F. List, Estrella M. Carballido, Bijal D. Shah, Jeremy W. Bowers, Zhong J. Zhang, Salvador Bruno, Terrence Grady, Lynn C. Moscinski, Arturo Anguiano
Publikováno v:
Acta Haematologica. 130:127-134
Myeloid and lymphoid neoplasms with fibroblastic growth factor receptor-1 (FGFR1) abnormalities originate from mutated pluripotent stem cells and have a heterogeneous clinical presentation. There are 12 identified partner genes commonly involved in F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc2eb1f365972377800642ee5d6ef5d6
https://doi.org/10.1159/000347030
https://doi.org/10.1159/000347030
Publikováno v:
Diagnostic cytopathology. 44(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eda814456c3f098989c94f4f5eb20d40
https://pubmed.ncbi.nlm.nih.gov/27278852
https://pubmed.ncbi.nlm.nih.gov/27278852
Autor:
Janese Trimaldi, Rodney E. Shackelford, Maisoun Abdelbaqi, Wade J. Sexton, Philippe E. Spiess, Shang-Tian Chuang
Publikováno v:
Molecular Pathology and Diagnostics of Cancer ISBN: 9789400771918
Prostate cancer (PCa) is the most common malignancy among men and is the second leading cause of cancer-related deaths in the United States and Europe. The molecular alterations underlying PCa have recently been shown to be quite complex, involving m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f54f710b6a1e37837d95994e2a47712
https://doi.org/10.1007/978-94-007-7192-5_9
https://doi.org/10.1007/978-94-007-7192-5_9
Autor:
Janese, Trimaldi, Estrella M, Carballido, Jeremy W, Bowers, Arturo L, Anguiano, Zhong J, Zhang, Bijal D, Shah, Salvador, Bruno, Alan F, List, Lynn C, Moscinski, Terrence, Grady, Steven J, Agosti, Loveleen, Kang, Ling, Zhang
Publikováno v:
Acta haematologica. 130(3)
Myeloid and lymphoid neoplasms with fibroblastic growth factor receptor-1 (FGFR1) abnormalities originate from mutated pluripotent stem cells and have a heterogeneous clinical presentation. There are 12 identified partner genes commonly involved in F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b983bdc03e5ca85d90c33b82a6b83809
https://pubmed.ncbi.nlm.nih.gov/23594707
https://pubmed.ncbi.nlm.nih.gov/23594707
Publikováno v:
Journal of the American Society of Cytopathology. 4:S11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdffdbcf91164ca74f21da6facddf8c6
https://doi.org/10.1016/j.jasc.2015.09.026
https://doi.org/10.1016/j.jasc.2015.09.026
Publikováno v:
Journal of the American Society of Cytopathology. 4:S37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b453285285e8fe4268be549544889c6
https://doi.org/10.1016/j.jasc.2015.09.086
https://doi.org/10.1016/j.jasc.2015.09.086
Publikováno v:
American Journal of Clinical Pathology. 140:A184-A184
Adenocarcinoma arising from esophageal submucosal gland duct (ESGD) is a rare entity. We found several reports of esophageal adenomas originating from these glands, but there is only one case report in the literature describing …
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a683deba21f037bc3e3d6d038ab8506b
https://doi.org/10.1093/ajcp/140.suppl1.184
https://doi.org/10.1093/ajcp/140.suppl1.184
Publikováno v:
International Journal of Case Reports and Images. 4:1
Introduction: Granular cell tumors of the central nervous system are rare tumors. To date, eight cases arising from cranial nerves have been reported. Granular cell tumors have also been found arising from the neurohypophysis and its stalk. Due to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d8a8e04b844f1388d087cd14b6ffcef
https://doi.org/10.5348/ijcri-2013-01-247-cs-1
https://doi.org/10.5348/ijcri-2013-01-247-cs-1