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Neonatal Diabetes Mellitus in the Structure of IPEX Syndrome
Turkunova M.E., Ditkovskaya L.V., Suspitsin E.N., Tyrtova L.V., Jelenina L.A., Guseva M.N.
Hypothesis about the protective role of ccr5delta32 mutations in juvenile idiopathic arthritis: fiction or reality?
Fedorova E.V., Egorov A.S., Ammosova T., Avrusin S.L., Santimov A.V., Kostik M.M., Dubko M.F., Kalashnikova O.V., Masalova V.V., Likhacheva T.S., Snegireva L.S., Grom A.A., Nekhai S., Chasnyk V.G.
Phenotype of cystic kidney disease in children with orphan diseases and hereditary syndromes due to genetic or chromosomal pathology (description of 9 clinical cases)
Andreeva E.F., Savenkova N.D.
Congenital organic hyperinsulinism associated with a variant in the ABCC8 gene. Description of a family case
Ivanov D.O., Ditkovskaya L.V., Turkunova M.E., Suspitsin E.N.
Neonatal diabetes mellitus and polycystic ovaries in a child with severe insulin resistance caused by a variant in the INSR gene. Description of the clinical case
Ivanov D.O., Taits A.N., Ditkovskaya L.V., Matveeva N.N., Krasnogorskaya O.L., Pozdnyakov A.V., Myznikova I.V., Malysheva A.A., Kuzminykh S.V., Orlova A.D., Veretennikova A.A.
In memoriam of Evgeny Iosifovich Schwartz
Gorbunova V.N.
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