Rustam Salimkhanov
Overview
Explore the profile of Rustam Salimkhanov including associated specialties, affiliations and a list of published articles.
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Articles
3
Citations
4
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Recent Articles
1.
Bondarenko E, Kalinin D, Urusova L, Pastukhova D, Salimkhanov R, Mokrysheva N
Front Med (Lausanne)
. 2025 Feb;
11:1458586.
PMID: 39917266
Intrahepatic cholangiocarcinoma is a highly malignant tumor with a poor prognosis. Radical surgical resection remains the "gold standard" for improving patient outcomes; however, only a minority of patients qualify for...
2.
Kim E, Lavreniuk A, Spasskaya O, Eremkina A, Salimkhanov R, Urusova L, et al.
Front Oncol
. 2025 Jan;
14:1441083.
PMID: 39886673
Parathyroid carcinoma (PC) is one of the rarest malignant neoplasms of the human endocrine system, with a prevalence of approximately 0.005% of all oncological diseases. Despite its indolent course, PC...
3.
Utkina M, Shcherbakova A, Deviatiiarov R, Ryabova A, Loguinova M, Trofimov V, et al.
Front Cell Dev Biol
. 2025 Jan;
12():1469955.
PMID: 39839668
Current dissociation methods for solid tissues in scRNA-seq studies do not guarantee intact single-cell isolation, especially for sensitive and complex human endocrine tissues. Most studies rely on enzymatic dissociation of...
4.
Kim E, Kalinchenko N, Eremkina A, Urusova L, Salimkhanov R, Mokrysheva N
Ther Adv Med Oncol
. 2024 Aug;
16:17588359241265222.
PMID: 39099848
Parathyroid carcinoma (PC) is extremely rare in children and adolescent. PC is more often sporadic, but also it could be associated with germline mutations. The clinical features of primary hyperparathyroidism...
5.
Salimkhanov R, Bondarenko E, Eremkina A, Bibik E, Kim E, Begova K, et al.
Front Endocrinol (Lausanne)
. 2024 Jan;
14:1292993.
PMID: 38250739
Sagliker syndrome (SS) is an extremely rare disorder that manifests in patients with advanced chronic kidney disease (CKD) undergoing programmed hemodialysis as a renal replacement therapy. Treatment of secondary hyperparathyroidism...
6.
Gorbacheva A, Pogoda T, Bogdanov V, Zakharova V, Salimkhanov R, Eremkina A, et al.
Genes (Basel)
. 2023 Feb;
14(2).
PMID: 36833251
Pseudohypoparathyroidism (PHP) is a heterogeneous orphan disease characterized by multihormonal resistance and several phenotypic features. In some cases, PHP is caused by a mutation in the that encodes the alpha...