Potential biomarkers of metastasizing paragangliomas and pheochromocytomas
A Snezhkina, V Pavlov, A Dmitriev, N Melnikova… - Life, 2021 - mdpi.com
Paragangliomas and pheochromocytomas (PPGLs) are rare neuroendocrine tumors
originating from paraganglionic tissue in many sites of the body. Most PPGLs are …
originating from paraganglionic tissue in many sites of the body. Most PPGLs are …
Somatic mutation profiling in head and neck paragangliomas
M Savvateeva, A Kudryavtseva… - The Journal of …, 2022 - academic.oup.com
Context Head and neck paragangliomas (HNPGLs) are rare neoplasms with a high degree
of heritability. Paragangliomas present as polygenic diseases caused by combined …
of heritability. Paragangliomas present as polygenic diseases caused by combined …
Immunohistochemistry and Mutation Analysis of SDHx Genes in Carotid Paragangliomas
AV Snezhkina, DV Kalinin, VS Pavlov… - International Journal of …, 2020 - mdpi.com
Carotid paragangliomas (CPGLs) are rare neuroendocrine tumors often associated with
mutations in SDHx genes. The immunohistochemistry of succinate dehydrogenase (SDH) …
mutations in SDHx genes. The immunohistochemistry of succinate dehydrogenase (SDH) …
The SDHD:p.H102R Variant Is Frequent in Russian Patients with Head and Neck Paragangliomas and Associated with Loss of 11p15.5 Region and …
A Snezhkina, M Fedorova, A Kobelyatskaya… - International Journal of …, 2022 - mdpi.com
Head and neck paragangliomas (HNPGLs) are rare neuroendocrine neoplasms derived
from the parasympathetic paraganglia of the head and neck. At least 30% of HNPGLs are …
from the parasympathetic paraganglia of the head and neck. At least 30% of HNPGLs are …
Medical genomics at the systems biology and bioinformatics (SBB-2019) school
https://doi. org/10.1186/s12920-020-00786-x 46% of all pathogenic T> C variants, while A>
G editors may precisely target 6900 mutations (34% of all pathogenic G> A variants). Thus …
G editors may precisely target 6900 mutations (34% of all pathogenic G> A variants). Thus …
[PDF][PDF] Multiple Primary Paragangliomas in a Pediatric Patient With von Hippel Lindau: A Diagnostic Dilemma
K Magnan, Q Wang, J Meade - JCEM Case Reports, 2024 - academic.oup.com
Pheochromocytoma and paragangliomas (PPGLs) are rare chromaffin cell tumors arising
from neural crest tissue. The majority of these tumors are nonmetastatic, with complete cure …
from neural crest tissue. The majority of these tumors are nonmetastatic, with complete cure …
Клинический случай интратиреоидной параганглиомы.
ЕВ БОНДАРЕНКО, ДГ БЕЛЬЦЕВИЧ… - Profilakticheskaya …, 2022 - elibrary.ru
Параганглиомы щитовидной железы представлены в мировой литературе
единичными случаями. Мы приводим описание редкого клинического наблюдения …
единичными случаями. Мы приводим описание редкого клинического наблюдения …