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V A Peterkova

Showing results (21-30 of 43) with videos related to

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Casopis Lekaru Ceskych|November 24, 1999
[Long-term treatment with desmopressin in children with primary nocturnal enuresis. An international multicenter study]M Snajderová, V Lehotská, N Kocnarová, et al.
Genetika|July 16, 2008
[Association of the chromosomal region 2q35 with type 1 diabetes mellitus in the Russian patients from Moscow]A Chernysheva, N M Tsitlidze, K V Savost'ianov, et al.
Endocrine Journal|July 8, 1999
A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasiaO V Fofanova, N Takamura, E Kinoshita, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|January 15, 2009
[The use of achievements in human molecular immunogenetics in the management of type 1 diabetes mellitus]I I Dedov, R M Khaitov, L P Alekseev, et al.
Problemy Endokrinologii|November 7, 2024
[Main epidemiological indicators of type 1 diabetes mellitus in children in the Russian Federation for 2014-2023]D N Laptev, O B Bezlepkina, E L Sheshko, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|May 4, 2012
[Immunogenetics of type 1 diabetes mellitus--from fundamental ideas to medical practice]L P Alekseev, I I Dedov, R M Khaitov, et al.
American Journal of Medical Genetics|June 19, 1998
Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiencyO V Fofanova, N Takamura, E Kinoshita, et al.
Problemy Endokrinologii|July 29, 2024
[Adrenal insufficiency as part of X-linked adrenoleukodystrophy]S R Enikeeva, I S Chugunov, M A Kareva, et al.
Molekuliarnaia Biologiia|July 1, 2010
[Association of the polymorphisms of the ERBB3 and SH2B3 genes with type 1 diabetes]A G Nikitin, E Iu Lavrikova, Iu A Seregin, et al.
Molekuliarnaia Biologiia|January 22, 2010
[Association of the C1858T polymorphism of the PTPN22 gene with type 1 diabetes]E Iu Lavrikova, A G Nikitin, Iu A Seregin, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Casopis Lekaru Ceskych|November 24, 1999
[Long-term treatment with desmopressin in children with primary nocturnal enuresis. An international multicenter study]M Snajderová, V Lehotská, N Kocnarová, et al.
Genetika|July 16, 2008
[Association of the chromosomal region 2q35 with type 1 diabetes mellitus in the Russian patients from Moscow]A Chernysheva, N M Tsitlidze, K V Savost'ianov, et al.
Endocrine Journal|July 8, 1999
A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasiaO V Fofanova, N Takamura, E Kinoshita, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|January 15, 2009
[The use of achievements in human molecular immunogenetics in the management of type 1 diabetes mellitus]I I Dedov, R M Khaitov, L P Alekseev, et al.
Problemy Endokrinologii|November 7, 2024
[Main epidemiological indicators of type 1 diabetes mellitus in children in the Russian Federation for 2014-2023]D N Laptev, O B Bezlepkina, E L Sheshko, et al.
Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|May 4, 2012
[Immunogenetics of type 1 diabetes mellitus--from fundamental ideas to medical practice]L P Alekseev, I I Dedov, R M Khaitov, et al.
American Journal of Medical Genetics|June 19, 1998
Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiencyO V Fofanova, N Takamura, E Kinoshita, et al.
Problemy Endokrinologii|July 29, 2024
[Adrenal insufficiency as part of X-linked adrenoleukodystrophy]S R Enikeeva, I S Chugunov, M A Kareva, et al.
Molekuliarnaia Biologiia|July 1, 2010
[Association of the polymorphisms of the ERBB3 and SH2B3 genes with type 1 diabetes]A G Nikitin, E Iu Lavrikova, Iu A Seregin, et al.
Molekuliarnaia Biologiia|January 22, 2010
[Association of the C1858T polymorphism of the PTPN22 gene with type 1 diabetes]E Iu Lavrikova, A G Nikitin, Iu A Seregin, et al.
Pageof 5