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Congenital nephrotic syndrome of the finnish type: a clinical case
Makarova T.P., Samoilova N.V., Melnikova Y.S., Galiullina G.F., Iksanova E.A.
CLINICAL CASE O THE EFFECTIVE TREATMENT OF RELAPSE OF ANAPLASTIC PLEOMORPHIC XANTHOASTROCYTOMA WITH BRAF V600E MUTATION USING TARGET DRUG VEMURAFENIB
Naskhletashvili D.R.
Idiopathic infantile hypercalcemia: a family case
Sadykova D.I., Makarova T.P., Shakirova A.R., Melnikova Y.S., Sergina P.V., Sergina A.V.
Molekulyarno-geneticheskaya geterogennost' melanomy kozhi i ee znachenie dlya razrabotki individual'nykh podkhodov k lecheniyu
Orlova K.V., Kharkevich G.Y., Demidov L.V.
The experience of using the combined targeted regimen vemurafenib+cobimetinib in the treatment of metastatic skin melanoma with a BRAF V600E mutation in a patient with HIV infection receiving antiretroviral therapy
Protsenko S.A., Anokhina E.M., Orlova R.V.
Monogennye formy sakharnogo diabeta
Zubkova N.A., Tikhonovich Y.V., Tyul'pakov A.N.
Alpelisib for the treatment of HR+HER2-metastatic breast cancer in patients with the PIK3CA mutation: results of the SOLAR-1 study
Semiglazova T.Y., Semiglazov V.V., Klimenko V.V., Brish N.A., Alekseeva Y.V., Klyuge V.A., Krutov A.A., Paltuev R.M., Kasparov B.S., Krivorotko P.V., Semiglazov V.F.
[6S]-5-METHYLTETRAHYDROFOLATE INCREASES PLASMA FOLATE MORE EFFECTIVELY THAN FOLIC ACID IN WOMEN WITH THE HOMOZYGOUS OR WILD-TYPE 677C,T POLYMORPHISM OF METHYLENETETRAHYDROFOLATE REDUCTASE *
Prints-Langekhol' R., Bremsvig S., Tobol'ski O., Smul'ders U.M., Smit D.E., Finglas P.M., P'etrtsik L., Prinz-Langenohl R., Brämswig S., Tobolski O., Smulders Y., Smith D., Finglas P., Pietrzik L.
Prognostic and predictive values of the PIK3CA gene mutation in patients with breast cancer
Semiglazova T.Y., Sorokina I.V.
Epidemiology and genetics of cystic fibrosis in Udmurt Republic
Simanova T.V., Ozhegov A.M., Simanova T.V., Ozhegov A.M.
Ways to improve efficiency of endocrino-therapy of breast cancer: new targeted cells, new therapeutic opportunities
Semiglazov V.F., Semiglazov V.V., Nikolaev K.S., Dashyan G.A., Komyakhov A.V., Paltuev R.M., Appolonova V.S., Donskikh R.V., Tseluyko A.I., Semiglazova T.Y., Zhiltsova E.K., Krivorotko P.V.
Case report: long-term response to osimertinib in metastatic non-small cell lung cancer with a rare mutation in EGFR gene exon 20
Nelyubina L.A., Reutova E.V., Laktionov K.K., Stroganova A.M.
FEATURES OF ASSOCIATED TRAITS OF 3272-16T>A MUTATION IN CYSTIC FIBROSIS IN CHILDREN: DESCRIPTION OF THREE CASES
Shadrina V.V., Krasovsky S.A., Furman E.G.
Possibilities of overcoming hormone resistance in patients with metastatic HR+ HER2- breast cancer using the drug alpelisib in various subgroups in real clinical practice
Orlova R.V., Gluzman M.I., Vakhitova A.A.
AMIOTROPHIC LATERAL SCLEROSIS IN PATIENTS WITH EXPANSION IN THE C9ORF72 GENE: DESCRIPTION OF CLINICAL CASES
Razinskaya O.D.
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