Search Results - "Kunieda, Junko"
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High prevalence of TERT aberrations in myxoid liposarcoma: TERT reactivation may play a crucial role in tumorigenesis
Published in Cancer science (01-03-2022)“…Myxoid liposarcoma (MLPS) is genetically characterized by FUS‐DDIT3 or EWSR1‐DDIT3 gene fusion and the high frequency of hotspot mutations (C228T or C250T) in…”
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Tumor B7-H3 expression in diagnostic biopsy specimens and survival in patients with metastatic prostate cancer
Published in Prostate cancer and prostatic diseases (01-09-2021)“…Background Prostate cancer spans a broad spectrum from indolent to deadly disease. In the management of prostate cancer, diagnostic biopsy specimens are…”
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A case of double‐negative prostate cancer with BRCA2 mutation and high tumor mutation burden treated sequentially with olaparib and pembrolizumab
Published in IJU case reports (01-09-2024)“…Introduction Double‐negative prostate cancer, an androgen receptor–independent prostate cancer without features of neuroendocrine tumors, is refractory to…”
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Case Report: A neonatal case of cryopyrin-associated periodic syndrome with severe funisitis and neonatal asphyxia
Published in Frontiers in pediatrics (14-05-2024)“…Cryopyrin-associated periodic syndrome (CAPS) is a genetic disorder and autoinflammatory disease characterized by chronic inflammation throughout the body. The…”
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5
Histopathological Examination of a Symptomatic Carotid Web: A Case Report
Published in NMC Case Report Journal (31-12-2024)“…Carotid webs cause ischemic stroke in young people and are associated with a high rate of stroke recurrence. Histopathological examination is crucial for…”
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6
Melorheostosis With Uniform Rib Thickening
Published in Clinical nuclear medicine (01-07-2024)“…A 16-year-old girl presented with left chest pain. Radiography and CT revealed localized abnormal calcification in the left sixth rib and sixth thoracic…”
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Enterochromaffin-like cell neuroendocrine tumor associated with parietal cell dysfunction
Published in Gastrointestinal endoscopy (01-11-2019)“…[Display omitted]…”
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A Nonsense SMAD3 Mutation in a Girl with Familial Thoracic Aortic Aneurysm and Dissection without Joint Abnormality
Published in Cardiology (2019)“…Thoracic aortic aneurysms and dissections (TAAD) are rare in children and often associated with underlying genetic disorders accompanied with other systemic…”
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9
Histopathological Examination of a Symptomatic Carotid Web: A Case Report
Published in NMC case report journal (01-01-2024)“…Carotid webs cause ischemic stroke in young people and are associated with a high rate of stroke recurrence. Histopathological examination is crucial for…”
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Report -
10
Case Report: A neonatal case of cryopyrin-associated periodic syndrome with severe funisitis and neonatal asphyxia
Published in Frontiers in pediatrics (01-01-2024)“…Cryopyrin-associated periodic syndrome (CAPS) is a genetic disorder and autoinflammatory disease characterized by chronic inflammation throughout the body. The…”
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Report