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Hereditary afibrinogenemia: A literature review and clinical observations
Yakovleva E.V., Surin V.L., Selivanova D.S., Sergeeva A.M., Gonсharova M.V., Demidova E.Y., Soboleva N.P., Makhinya S.A., Dezhenkova A.V., Likhacheva E.A., Zozulya N.I.
A rare clinical case of the patient with pulmonary hypertension associated with hereditary hemorrhagic telangiectasia. Case report
Kasparova A.M., Valieva Z.S., Martynyuk T.V.
Hereditary pheochromocytoma-associated syndromes. Part 1
Yukina M.Y., Troshina E.A., Beltsevich D.G.
Diagnosis and treatment of hereditary angioedema with normal C1-inhibitor level
Emelyanov A.V., Leshenkova E.V., Kameneva G.A.
Multicentric carpotarsal osteolysis in a rheumatologist’s practice
Dolgikh V.V., Pogodina A.V., Knyazeva T.S., Rychkova L.V., Lutsenko L.A.
Diagnostic difficulties of primary hemochromatosis in a patient with posthemorrhagic anemia
Podzolkov V.I., Pokrovskaya A.E., Vargina T.S., Oganesyan K.A.
The problem of rare (orphan) diseases in the Russian Federation: Medical and normative legal aspects of its solution
Novikov P.V.
Risk factors for irritable bowel syndrome: A review
Gaus O.V., Livzan M.A., Gavrilenko D.A.
The prognostic role of depression as a predictor of chronic somatic diseases manifestation
Neznanov N.G., Kibitov A.O., Rukavishnikov G.V., Mazo G.E.
Effect of eprosartan on the hemostatic system in patients with chronic kidney disease associated with hereditary thrombophilia
Kaliuzhin V.V., Sibireva O.F., Urazova O.I., Tkalich L.M., Zibnitskaia L.I., Kaliuzhina E.V., Sazonov É.A., Grankina V.I.
Iron deficiency anemia in a patient with hereditary hemorrhagic telangiectasia. Case report
Mozdon M.A., Ponomarev R.V., Tsvetaeva N.V., Shabrin A.V., Ermachenkova E.I., Larichev S.E., Lukina E.A.
Hemochromatosis - modern condition of the problem
Voloshina N.B., Osipenko M.F., Litvinova N.V., Voloshin A.N.
A protective effect of Gly272Ser polymorphism of GNB3 gene in development of essential hypertension and its relations with environmental hypertension risk factors
Polonikov A.V., Solodilova M.A., Ivanov V.P., Shestakov A.M., Ushachev D.V., Vyalykh E.K., Vasil'eva O.V., Polyakova N.V., Antsupov V.V., Kabanina V.A., Kupriyanova Y.S., Bulgakova I.V., Kozhukhov M.A., Tevs D.S., Polonikov A.V., Solodilova M.A., Ivanov V.P., Shestakov A.M., Ushachev D.V., Vyalykh E.K., Vasilyeva O.V., Polyakova N.V., Antsupov V.V., Kabanina V.A., Kupriyanova Y.S., Bulgakova I.V., Kozhukhov M.A., Tevs D.S.
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.S., Nasonova S.N., Frolova Y.V., Stepanova E.A., Mershina E.A., Sinitsyn V.E., Zateyshchikov D.A., Zhirov I.V.
Genetic determinants of hereditary thrombophilia in pathogenesis of venous thrombosis
Kapustin S.I., Blinov M.N., Kargin V.D., Filanovskaya L.I., Saltykova N.В., Belyazo O.E., Golovina O.G., Shmeleva V.M., Panshina A.M., Papayan L.P.
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.A., Latysheva E.A., Sorokina L.E., Latysheva T.V.
Molecular genetics of maturity-onset diabetes of the young
Voevoda M.I., Ivanova A.A., Shakhtshneider E.V., Ovsyannikova A.K., Mikhailova S.V., Astrakova K.S., Voevoda S.M., Rymar O.D.
Prenatal diagnosis of congenital and hereditary diseases
Zarubina E.N., Bermisheva О.A., Semenova A.L., Troshina О.N.
Li–Fraumeni syndrome in adult patients with acute lymphoblastic leukemia
Zarubina K.I., Parovichnikova E.N., Surin V.L., Pshenichnikova O.S., Gavrilina O.A., Isinova G.A., Troitskaya V.V., Sokolov A.N., Galtseva I.V., Kapranov N.M., Davydova J.O., Obukhova T.N., Nikulina E.E., Sudarikov A.B., Savchenko V.G.
Hereditary pheochromocytoma-associated syndromes. Part 2
Yukina M.Y., Troshina E.A., Beltsevich D.G.
1 - 20 of 20 Items

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