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卷 88, 编号 12 (2016)

Hereditary afibrinogenemia: A literature review and clinical observations

Yakovleva E., Surin V., Selivanova D., Sergeeva A., Gonсharova M., Demidova E., Soboleva N., Makhinya S., Dezhenkova A., Likhacheva E., Zozulya N.

(Rus)

卷 94, 编号 4 (2022)

A rare clinical case of the patient with pulmonary hypertension associated with hereditary hemorrhagic telangiectasia. Case report

Kasparova A., Valieva Z., Martynyuk T.

(Rus)

卷 87, 编号 9 (2015)

Hereditary pheochromocytoma-associated syndromes. Part 1

Yukina M., Troshina E., Beltsevich D.

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卷 92, 编号 12 (2020)

Diagnosis and treatment of hereditary angioedema with normal C1-inhibitor level

Emelyanov A., Leshenkova E., Kameneva G.

(Rus)

卷 87, 编号 3 (2015)

Multicentric carpotarsal osteolysis in a rheumatologist’s practice

Dolgikh V., Pogodina A., Knyazeva T., Rychkova L., Lutsenko L.

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卷 91, 编号 4 (2019)

Diagnostic difficulties of primary hemochromatosis in a patient with posthemorrhagic anemia

Podzolkov V., Pokrovskaya A., Vargina T., Oganesyan K.

(Rus)

卷 86, 编号 12-2 (2014)

The problem of rare (orphan) diseases in the Russian Federation: Medical and normative legal aspects of its solution

Novikov P.

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卷 96, 编号 2 (2024)

Risk factors for irritable bowel syndrome: A review

Gaus O., Livzan M., Gavrilenko D.

(Rus)

卷 90, 编号 12 (2018)

The prognostic role of depression as a predictor of chronic somatic diseases manifestation

Neznanov N., Kibitov A., Rukavishnikov G., Mazo G.

(Rus)

卷 85, 编号 9 (2013)

Effect of eprosartan on the hemostatic system in patients with chronic kidney disease associated with hereditary thrombophilia

Kaliuzhin V., Sibireva O., Urazova O., Tkalich L., Zibnitskaia L., Kaliuzhina E., Sazonov É., Grankina V.

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卷 95, 编号 7 (2023)

Iron deficiency anemia in a patient with hereditary hemorrhagic telangiectasia. Case report

Mozdon M., Ponomarev R., Tsvetaeva N., Shabrin A., Ermachenkova E., Larichev S., Lukina E.

(Rus)

卷 90, 编号 3 (2018)

Hemochromatosis - modern condition of the problem

Voloshina N., Osipenko M., Litvinova N., Voloshin A.

(Rus)

卷 83, 编号 4 (2011)

A protective effect of Gly272Ser polymorphism of GNB3 gene in development of essential hypertension and its relations with environmental hypertension risk factors

Polonikov A., Solodilova M., Ivanov V., Shestakov A., Ushachev D., Vyalykh E., Vasil'eva O., Polyakova N., Antsupov V., Kabanina V., Kupriyanova Y., Bulgakova I., Kozhukhov M., Tevs D., Polonikov A., Solodilova M., Ivanov V., Shestakov A., Ushachev D., Vyalykh E., Vasilyeva O., Polyakova N., Antsupov V., Kabanina V., Kupriyanova Y., Bulgakova I., Kozhukhov M., Tevs D.

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卷 95, 编号 4 (2023)

A rare variant in the TTR gene (p.E112K) is associated with systemic amyloidosis and a new symptom – skin hyperemia in response to ethanol intake: family segregation analysis, literature review, and a clinical case. Case report

Chumakova O., Nasonova S., Frolova Y., Stepanova E., Mershina E., Sinitsyn V., Zateyshchikov D., Zhirov I.

(Rus)

卷 78, 编号 10 (2003)

Genetic determinants of hereditary thrombophilia in pathogenesis of venous thrombosis

Kapustin S., Blinov M., Kargin V., Filanovskaya L., Saltykova N., Belyazo O., Golovina O., Shmeleva V., Panshina A., Papayan L.

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卷 93, 编号 12 (2021)

The place of scales and questionnaires in assessing the disease’s severity and the long-term prophylaxis’s prescribing in patients with hereditary angioedema

Manto I., Latysheva E., Sorokina L., Latysheva T.

(Rus)

卷 88, 编号 4 (2016)

Molecular genetics of maturity-onset diabetes of the young

Voevoda M., Ivanova A., Shakhtshneider E., Ovsyannikova A., Mikhailova S., Astrakova K., Voevoda S., Rymar O.

(Rus)

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卷 78, 编号 4 (2003)

Prenatal diagnosis of congenital and hereditary diseases

Zarubina E., Bermisheva О., Semenova A., Troshina О.

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卷 93, 编号 7 (2021)

Li–Fraumeni syndrome in adult patients with acute lymphoblastic leukemia

Zarubina K., Parovichnikova E., Surin V., Pshenichnikova O., Gavrilina O., Isinova G., Troitskaya V., Sokolov A., Galtseva I., Kapranov N., Davydova J., Obukhova T., Nikulina E., Sudarikov A., Savchenko V.

(Rus)

卷 87, 编号 10 (2015)

Hereditary pheochromocytoma-associated syndromes. Part 2

Yukina M., Troshina E., Beltsevich D.

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