Zobrazeno 1 - 10
of 2 004
pro vyhledávání: '"CARCINOMA SYNDROME"'
Autor:
Joanna Mietlińska-Sauter, Elena Varotto, Elżbieta Żądzińska, Wiesław Lorkiewicz, Francesco Maria Galassi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract The anomaly known as a bifid rib is difficult to quantify in bioarchaeological collections not only because of its rarity in the population itself (less than 1.5%), but also because of vulnerability to postmortem damage of this part of the s
Externí odkaz:
https://doaj.org/article/6286898f7cd646ca803d32f169a99e8a
Publikováno v:
BMC Women's Health, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background To demonstrate and analyze the 18F-FDG positron emission tomography/computed tomography (PET/CT) findings in this rare nevoid basal cell carcinoma syndrome (NBCCS). Case presentation A 71-year-old woman with the left invasive brea
Externí odkaz:
https://doaj.org/article/f5274bf5c9104098b2e42477773434e3
Publikováno v:
Oral Oncology Reports, Vol 10, Iss , Pp 100494- (2024)
Nevoid basal cell carcinoma syndrome (NBCCS) is a typical autosomal dominant disorder distinguished by malformations in development and an increased susceptibility to cancer. Keratocystic Odontogenic Tumors (KOTs) are highly malignant lesions of the
Externí odkaz:
https://doaj.org/article/b6ddfc94e4af4826b95a97a9218013e6
Autor:
Raquel Wescott, Wolfram Samlowski
Publikováno v:
Current Oncology, Vol 30, Iss 10, Pp 9156-9167 (2023)
Nevoid basal-cell carcinoma syndrome (Gorlin syndrome) is characterized by numerous cutaneous basal cell carcinomas mediated by mutations in the hedgehog pathway. Vismodegib or sonidegib represent promising treatment options. We identified 10 Gorlin
Externí odkaz:
https://doaj.org/article/ffc8d9b2bd3f458f98baa7f3cd625719
Publikováno v:
Archives of Plastic Surgery, Vol 50, Iss 04, Pp 384-388 (2023)
Gorlin–Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is an autosomal dominant disease characterized by multisystemic developmental defects caused by pathogenic variants such as patched-1 (PTCH1) gene variants and/or SUFU gene
Externí odkaz:
https://doaj.org/article/650f58e358d740609b15c1efa1ca1b75
Autor:
Xiaoqing Lang, Ting Wang, Shuping Guo, Yao Dang, Yingjie Zhang, Hongye Liu, Hongxia He, Li Li, Huajie Yuan, Ting He, Qiong Wang, Shiyu Qin, Runping Cheng, Xingquan Yan, Hongzhou Cui
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
A patient presenting with several basal cell carcinomas, pigmented nevi, and developmental defects was diagnosed with nevoid basal cell carcinoma syndrome. Gene panel sequencing and Sanger sequencing were used to identify a novel heterozygous framesh
Externí odkaz:
https://doaj.org/article/fa215df5f07d4631bc07a787c5b2695e
Publikováno v:
Journal of Oral Biology and Craniofacial Research, Vol 13, Iss 3, Pp 436-441 (2023)
Introduction: Odontogenic keratocysts (OKC) has a high potential for recurrence. Resection is currently the only fool-proof method to ensure that recurrence does not occur; however, it drastically affects the patient's function and aesthetics. Applic
Externí odkaz:
https://doaj.org/article/6d1cd776f7cc443c960ddfd6cd3c2a3a
Publikováno v:
JEADV Clinical Practice, Vol 2, Iss 2, Pp 389-391 (2023)
Externí odkaz:
https://doaj.org/article/45db8e1e83cd4f5d9a7c412bd3ca2d96
Autor:
Zhaojuan Qin, Ai Zheng
Publikováno v:
Asian Journal of Surgery, Vol 46, Iss 12, Pp 5603-5604 (2023)
Externí odkaz:
https://doaj.org/article/b8298f54b9ff4bdda160215e3449376f
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