Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Anand C Loya"'
Case Report: Giant Paraganglioma of the Skull Base With Two Somatic Mutations in SDHB and PTEN Genes
Autor:
Ailsa Maria Main, Götz Benndorf, Ulla Feldt-Rasmussen, Kåre Fugleholm, Thomas Kistorp, Anand C. Loya, Lars Poulsgaard, Åse Krogh Rasmussen, Maria Rossing, Christine Sølling, Marianne Christina Klose
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Head and neck paragangliomas (HNPGLs) are neuroendocrine tumors. They arise from the parasympathetic ganglia and can be either sporadic or due to hereditary syndromes (up to 40%). Most HNPGLs do not produce significant amounts of catecholamines. We r
Externí odkaz:
https://doaj.org/article/898bddc8304f4c71ae12ade34f9ed2e3
Autor:
Diana Andrejeva, Jan-Michael Kugler, Hung Thanh Nguyen, Anders Malmendal, Mette Lind Holm, Birgitte Groenkaer Toft, Anand C. Loya, Stephen M. Cohen
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-15 (2018)
Abstract Background Changes in cellular metabolism are now recognized as potential drivers of cancer development, rather than as secondary consequences of disease. Here, we explore the mechanism by which metabolic changes dependent on aldehyde dehydr
Externí odkaz:
https://doaj.org/article/a6495beced824a7bb0848faca5a95386
Autor:
Urszula Maria Ciochon, Grethe Schmidt, Ruben Juhl Jensen, Anand C. Loya, Lars Birger Lönn, Nitesh Shekhrajka
Publikováno v:
Diagnostics, Vol 11, Iss 1, p 62 (2021)
Solitary fibrous tumors (SFTs) are mesenchymal, fibroblastic tumors with mostly favorable, but still unpredictable prognosis. Their rarity and occurrence at a variety of locations coupled with variable histological appearance make the diagnosis a cha
Externí odkaz:
https://doaj.org/article/fd61a35756394a499c4c5c459653a73e
Publikováno v:
International Journal of Surgical Pathology. 29:850-855
Basal cell carcinomas of prostate (BCCP) are very rare. Most arise in the transition zone and thus are associated with lower urinary tract symptoms and rarely associated with elevated prostate-specific antigen (PSA). These features make diagnosis/ear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bcd56342158dbf677a71e86db811446
https://doi.org/10.1177/10668969211017321
https://doi.org/10.1177/10668969211017321
Autor:
Anand C. Loya, Niels Junker, Marie Christine Wulff Westergaard, Inge Marie Svane, Dorrit Hovgaard, Michael Mørk Petersen, Anders Krarup-Hansen, Morten Nielsen
Publikováno v:
Cancer Immunology, Immunotherapy. 69:2179-2191
Tumor-specific tumor-infiltrating lymphocytes (TILs) can be in vitro expanded and have the ability to induce complete and durable tumor regression in some patients with melanoma following adoptive cell therapy (ACT). In this preclinical study, we inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eeb9aee8880cb08ecaedbfbb4dfaf588
https://doi.org/10.1007/s00262-020-02568-x
https://doi.org/10.1007/s00262-020-02568-x
Autor:
Andrew E. Rosenberg, Lei Zhang, Katharina Perell, Ziyu Xie, Anand C. Loya, Cristina R. Antonescu
Publikováno v:
Genes Chromosomes Cancer
Undifferentiated sarcomas remain difficult to classify. Despite the remarkable advances in sarcoma classification made by the increased application of RNA sequencing in clinical practice, the unexpected result of a novel gene fusion raises further qu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::586cdfbd5a6e5e11ac70322836df7873
https://pubmed.ncbi.nlm.nih.gov/33987888
https://pubmed.ncbi.nlm.nih.gov/33987888
Publikováno v:
Tehrani, S G, Kaltoft, N S, Melchior, L C & Loya, A C 2021, ' Extra-axial chordoma of the thumb : Report of a rare case with clinicopathologic and molecular analysis ', Pathology, Research and Practice, vol. 225, 153564 . https://doi.org/10.1016/j.prp.2021.153564
Chordoma is a very rare malignant tumor, with a phenotype that recapitulates notochord, and is chiefly located in the axial skeleton with only few cases reported in the extra-axial skeleton and soft tissues. The diagnosis can be challenging for both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b785446d210e1532def00671cbfa424
https://pubmed.ncbi.nlm.nih.gov/34340129
https://pubmed.ncbi.nlm.nih.gov/34340129
Autor:
Anand C. Loya, Urszula Maria Ciochon, Ruben Juhl Jensen, Grethe Schmidt, Nitesh Shekhrajka, Lars Lönn
Publikováno v:
Diagnostics, Vol 11, Iss 62, p 62 (2021)
Ciochon, U M, Shekhrajka, N, Schmidt, G, Jensen, R J, Loya, A C & Lönn, L B 2021, ' Preoperative embolization of a solitary fibrous tumor originating from external auditory meatus : A case report with literature review ', Diagnostics, vol. 11, no. 1, 62 . https://doi.org/10.3390/DIAGNOSTICS11010062
Diagnostics
Ciochon, U M, Shekhrajka, N, Schmidt, G, Jensen, R J, Loya, A C & Lönn, L B 2021, ' Preoperative embolization of a solitary fibrous tumor originating from external auditory meatus : A case report with literature review ', Diagnostics, vol. 11, no. 1, 62 . https://doi.org/10.3390/DIAGNOSTICS11010062
Diagnostics
Solitary fibrous tumors (SFTs) are mesenchymal, fibroblastic tumors with mostly favorable, but still unpredictable prognosis. Their rarity and occurrence at a variety of locations coupled with variable histological appearance make the diagnosis a cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0786f316ded766ab762ddc537144591
https://www.mdpi.com/2075-4418/11/1/62
https://www.mdpi.com/2075-4418/11/1/62
Autor:
Helle Pappot, Anand C Loya, Bára Oladóttir á Dunga, Line Hammer Dohn, Maria Elisabeth Lendorf
Publikováno v:
Scandinavian Journal of Urology. 52:87-93
The aim of the present study was to emphasize the critical importance of the clinician's awareness of signet-ring cell carcinoma (SRCC) of the urinary bladder, a rare and aggressive disease entity.A review of the current literature was conducted and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65f456c6102b7741897365141d031686
https://doi.org/10.1080/21681805.2017.1418020
https://doi.org/10.1080/21681805.2017.1418020
Autor:
Anders Juul, Hanne Frederiksen, Martin Blomberg Jensen, Ewa Rajpert-De Meyts, Anne Jørgensen, Niels E. Skakkebæk, Birgitte Grønkær Toft, Li Juel Mortensen, John E. Nielsen, Ann-Margrethe Rønholt, Anand C Loya, Peter Christiansen
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 102:4411-4416
Context Testotoxicosis is an autosomal-dominant, male-limited disorder. Activating mutations in the luteinizing hormone receptor gene (LHCGR) cause high autonomous testosterone secretion, resulting in early-onset peripheral precocious puberty. Little
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baaf2716a66af2f0d82f2d5bd78e67ee
https://doi.org/10.1210/jc.2017-01761
https://doi.org/10.1210/jc.2017-01761