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  • Tag › nephrocalcinosis

     Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN19 mutations

    Редактор | 2026, Clinical case, Practical medicine part 24 №3. 2026 | 3 июня, 2026

    N.M. ZAIKOVA1, S.L. MOROZOV1, 2, M.P. SAFONOVA2  1Pirogov Russian National Research Medical University, Moscow 2Veltischev Research and Clinical Institute for Pediatrics and Pediatric Surgery of the Pirogov Russian National Research Medical University, Moscow Contact details: Morozov S.L. — PhD (Medicine), Leading Researcher of the Department of Hereditary and Acquired Kidney Diseases named after Prof. M.S. Ignatova, […]

    Tag: 2026, CLDN16, CLDN19, hypercalcemia, hypomagnesemia, M.P. SAFONOVA, N.M. ZAIKOVA, nephrocalcinosis, Practical medicine part 24 №3. 2026, S.L. MOROZOV
    Комментарии к записи  Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN19 mutations отключены

    Nephrocalcinosis with hereditary diseases and syndromes in children

    Редактор | 2019, Original articles, Practical medicine part 17 №5. 2019 | 2 декабря, 2019

    T.V. MIKHAILOVA1, S.V. MALTSEV1, T.V. PUDOVIK2 1Kazan State Medical Academy – Branch Campus of RMACPE MH Russia, Kazan 2Children’s Municipal Hospital № 2, Kazan Contact details: Mikhailova T.V. – Ph. D. (medicine), Associate Professor of the Department of Pediatrics and Neonatology Address: 36 Butlerov St., Kazan, Russian Federation, 420012, tel.: +7-917-860-04-47, e-mail: tatiana.mih@mail.ru The work […]

    Tag: 2019, distal renal tubular acidosis, hypercalciuria, nephrocalcinosis, Practical medicine part 17 №5. 2019, renal dysfunction, S.V. MALTSEV, T.V. MIKHAILOVA, T.V. PUDOVIK, Williams syndrome
    Комментарии к записи Nephrocalcinosis with hereditary diseases and syndromes in children отключены

    Genetic and clinical aspects of nephrolithiasis and nephrocalcinosis in children with hypercalciuria 

    Редакция | 2014, Original articles, Practical medicine 09 (14) Pediatrics | 1 декабря, 2014

    S.V. MALTSEV1, T.V. MIKHAILOVA1, O.A. KRAVTSOVA2 1Kazan State Medical Academy, 36 Butlerov St., Kazan, Russian Federation, 420012 2Kazan (Volga region) Federal University, Kremlevskaya St., Kazan, Russian Federation, 420008 Maltsev S.V. — D. Med. Sc., Professor, Head of the Department of Pediatrics with a course in Polyclinic Pediatrics, tel. (843) 236-20-84, e-mail: maltc@mail.ru Mikhailova T.V. — Cand. Med. […]

    Tag: analysis of the polymorphism аssociations of TRPV6, and SLC26A6 genes, CLDN16, hypercalciuria, nephrocalcinosis, nephrolithiasis, O.A. KRAVTSOVA, Practical medicine 09 (14) Pediatrics, S.V. MALTSEV, T.V. MIKHAILOVA
    Комментарии к записи Genetic and clinical aspects of nephrolithiasis and nephrocalcinosis in children with hypercalciuria  отключены
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