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Works (14)

Utility of personalized medicine in cardiology practice

Voprosy praktičeskoj pediatrii
2023 | Journal article
Contributors: E.V. Dolgova; N.A. Bodunova; A.I. Khavkin; M.M. Litvinova
Source: check_circle
Crossref

Genetic factors contributing to a severe course of pneumonia: a systematic review

Bulletin of Siberian Medicine
2023-01-22 | Journal article
Contributors: M. A. Karnaushkina; P. S. Sviridov; V. I. Korchagin; S. A. Salamaikina; I. S. Vasilyeva; M. M. Litvinova; M. V. Vatsik-Gorodetskaya
Source: check_circle
Crossref

TLRs Gene Polymorphisms Associated with Pneumonia before and during COVID-19 Pandemic

Diagnostics
2022-12-30 | Journal article
Contributors: Svetlana Salamaikina; Maria Karnaushkina; Vitaly Korchagin; Maria Litvinova; Konstantin Mironov; Vasily Akimkin
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Crossref
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Preferred source (of 2)‎

Medullary nephrocalcinosis in children with Williams syndrome: diagnosis, treatment, and prevention of complications

Voprosy detskoj dietologii
2021 | Journal article
Contributors: T.V. Filippova; M.M. Litvinova; S.Z. Nuralieva; A.I. Khavkin; M.V. Shumikhina
Source: check_circle
Crossref

TNFRSF13B gene mutation in adult patient with common variable immunodeficiency. Case report

Terapevticheskii arkhiv
2021-12-15 | Journal article
Contributors: Philipp S. Sviridov; Natalia A. Bodunova; Anastasiia M. Danishevich; Mariia M. Litvinova
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Crossref

Genetic and clinical features of shwachman–diamond syndrome in Russian population: Prospective study,Генетические и клинико-лабораторные особенности синдрома Швахмана–Даймонда в России: проспективное исследование

Voprosy Sovremennoi Pediatrii - Current Pediatrics
2019 | Journal article
EID:

2-s2.0-85081076666

Part of ISBN:

16825535 16825527

Contributors: Ipatova, M.G.; Deordieva, E.A.; Shvets, O.A.; Mukhinа, A.A.; Moiseevа, A.A.; Rodina, Y.A.; Shumilov, P.V.; Pavlova, A.V.; Raikina, E.V.; Asanov, A.Y. et al.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

Genetic aspects of primary hyperoxaluria: Diagnostics and treatment

Urologiia
2019 | Journal article
EID:

2-s2.0-85076296712

Part of ISBN:

24149020 17282985

Contributors: Filippova, T.V.; Svetlichnaya, D.V.; Rudenko, V.I.; Alyaev, Y.G.; Shumikhina, M.V.; Azova, M.M.; Subbotina, T.I.; Gadzhieva, Z.K.; Asanov, A.Y.; Litvinova, M.M.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

Genetic aspects of primary hyperoxaluria: Epidemiology, ethiology, pathogenesis, and clinical signs of the disorder

Urologiia
2019 | Journal article
EID:

2-s2.0-85078711344

Part of ISBN:

24149020 17282985

Contributors: Filippova, T.V.; Svetlichnaya, D.V.; Rudenko, V.I.; Alyaev, Y.G.; Tadevosyan, E.G.; Azova, M.M.; Subbotina, T.I.; Gadzhieva, Z.K.; Asanov, A.Y.; Khamidullin, K.R. et al.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

Lynch syndrome associated with a MLH1 gene mutation: Preventive and personalized monitoring based on the results of molecular testing

Voprosy Prakticheskoi Pediatrii
2019 | Journal article
EID:

2-s2.0-85082430580

Part of ISBN:

18177646

Contributors: Litvinova, M.M.; Lisitsa, T.S.; Bodunova, N.A.; Nasedkina, T.V.; Akhmedzyanova, D.A.; Movsesian, G.V.; Alikhanov, R.B.; Khatkov, I.E.; Asanov, A.Y.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

Genetic factors for monogenic forms of calcium urolithiasis

Urologiia (Moscow, Russia : 1999)
2018 | Journal article
EID:

2-s2.0-85061592656

Part of ISBN:

17282985

Contributors: Filippova, T.V.; Litvinova, M.M.; Rudenko, V.I.; Gadzhieva, Z.K.; Rapoport, L.M.; Kazilov, Y.B.; Asanov, A.Y.; Subbotina, T.I.; Khafizov, K.F.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

Genetic factors of the development of chronic pancreatitis

Voprosy Prakticheskoi Pediatrii
2018 | Journal article
EID:

2-s2.0-85053426326

Part of ISBN:

18177646

Contributors: Litvinova, М.М.; Khafizov, K.F.; Shipulin, G.A.; Аyginin, А.А.; Vinokurova, L.V.; Nikolskaya, K.А.; Dubtsova, E.А.; Bordin, D.S.; Asanov, A.Y.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

A pediatric perspective on hemochromatosis: Not just "an old man's disease"

LaboratoriumsMedizin
2006 | Journal article
EID:

2-s2.0-33644983740

Part of ISBN:

03423026 14390477

Contributors: Lockitch, G.; Litvinova, M.M.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

A novel ferroportin mutation in a Canadian family with autosomal dominant hemochromatosis

Blood Cells, Molecules, and Diseases
2005 | Journal article
EID:

2-s2.0-27744583501

Part of ISBN:

10799796

Contributors: Morris, T.J.; Litvinova, M.M.; Ralston, D.; Mattman, A.; Holmes, D.; Lockitch, G.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier

Unique genetic profile of hereditary hemochromatosis in Russians: High frequency of C282Y mutation in population, but not in patients

Blood Cells, Molecules, and Diseases
2005 | Journal article
EID:

2-s2.0-24644443139

Part of ISBN:

10799796

Contributors: Potekhina, E.S.; Lavrov, A.V.; Samokhodskaya, L.M.; Efimenko, A.Y.; Balatskiy, A.V.; Baev, A.A.; Litvinova, M.M.; Nikitina, L.A.; Shipulin, G.A.; Bochkov, N.P. et al.
Source: Self-asserted source
Maria Litvinova via Scopus - Elsevier