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Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
June 16, 2023
[Anterior transpetrosal (Kawase) approach for petroclival meningioma with trigeminal neuralgia: case report and literature review]
R S Dzhindzhikhadze, A V Polyakov, A Yu Ermolaev, et al.
Bulletin of Experimental Biology and Medicine
|
November 1, 2006
GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children
O V Fofanova, O V Evgrafov, A V Polyakov, et al.
Genetika
|
September 29, 2015
[Clinical and Genetic Characteristics of Russian Marfan Patients]
A N Semyachkina, T A Adyan, M N Khabadze, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
May 26, 2018
[Transpalpebral craniotomy in skull base surgery]
R S Dzhindzhikhadze, O N Dreval', V A Lazarev, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
July 25, 2019
[Bilateral supraorbital keyhole approach in surgery of multiple cerebral aneurysms: a case report and literature review]
R S Dzhindzhikhadze, O N Dreval', V A Lazarev, et al.
Journal of Evolutionary Biology
|
April 22, 2011
Natural hybridization between extremely divergent chromosomal races of the common shrew (Sorex araneus, Soricidae, Soricomorpha): hybrid zone in Siberia
A V Polyakov, T A White, R M Jones, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
October 18, 2024
[Immediate and long-term results after microsurgical clipping of ruptured aneurysms in acute period of hemorrhage]
M I Derkach, R S Dzhindzhikhadze, A V Polyakov, et al.
Frontiers in Genetics
|
November 15, 2021
A Mosaic Mutation in the <i>LAMA2</i> Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy
P A Chausova, O P Ryzhkova, G E Rudenskaya, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
March 25, 2020
[Cavernous malformation of the optic nerve: clinical case and literature review]
R S Dzhindzhikhadze, O N Dreval, V A Lazarev, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 27, 2016
Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromes
T G Markova, N B Brazhkina, E A Bliznech, et al.
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of 6
Search research articles
Search
Showing results (11-20 of 56) with videos related to
Sort By:
Page
of 6
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
June 16, 2023
[Anterior transpetrosal (Kawase) approach for petroclival meningioma with trigeminal neuralgia: case report and literature review]
R S Dzhindzhikhadze, A V Polyakov, A Yu Ermolaev, et al.
Bulletin of Experimental Biology and Medicine
|
November 1, 2006
GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children
O V Fofanova, O V Evgrafov, A V Polyakov, et al.
Genetika
|
September 29, 2015
[Clinical and Genetic Characteristics of Russian Marfan Patients]
A N Semyachkina, T A Adyan, M N Khabadze, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
May 26, 2018
[Transpalpebral craniotomy in skull base surgery]
R S Dzhindzhikhadze, O N Dreval', V A Lazarev, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
July 25, 2019
[Bilateral supraorbital keyhole approach in surgery of multiple cerebral aneurysms: a case report and literature review]
R S Dzhindzhikhadze, O N Dreval', V A Lazarev, et al.
Journal of Evolutionary Biology
|
April 22, 2011
Natural hybridization between extremely divergent chromosomal races of the common shrew (Sorex araneus, Soricidae, Soricomorpha): hybrid zone in Siberia
A V Polyakov, T A White, R M Jones, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
October 18, 2024
[Immediate and long-term results after microsurgical clipping of ruptured aneurysms in acute period of hemorrhage]
M I Derkach, R S Dzhindzhikhadze, A V Polyakov, et al.
Frontiers in Genetics
|
November 15, 2021
A Mosaic Mutation in the <i>LAMA2</i> Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy
P A Chausova, O P Ryzhkova, G E Rudenskaya, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko
|
March 25, 2020
[Cavernous malformation of the optic nerve: clinical case and literature review]
R S Dzhindzhikhadze, O N Dreval, V A Lazarev, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 27, 2016
Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromes
T G Markova, N B Brazhkina, E A Bliznech, et al.
Page
of 6