Choosing an anesthetic technique in pregnant women with Arnold – Chiari malformation

Autor: V. D. Zukin, Ye. V. Grigimalsky, A. Y. Garga

Publikováno v: Медицина болю, Vol 3, Iss 2, Pp 75-79 (2018)

We want to present the clinical case of a female patient with the asymptomatic Chiari I type malformation, without surgical correction and with concomitant epilepsy who underwent planned C-section under epidural anesthesia. A 29-year old pregnant wom

Externí odkaz: https://doaj.org/article/e1462c0dc91344b8a0b3949a3e23d95e

Вибір методу анестезії у вагітних з аномалією Арнольда – Кіарі

Autor: Ye. V. Grigimalsky, A. Y. Garga, V. D. Zukin

Publikováno v: Медицина болю, Vol 3, Iss 2, Pp 75-79 (2018)
Medicina bolu; Том 3 № 2 (2018): Medicina bolu; 75-79
Pain medicine; Vol 3 No 2 (2018): Pain medicine; 75-79

We want to present the clinical case of a female patient with the asymptomatic Chiari I type malformation, without surgical correction and with concomitant epilepsy who underwent planned C-section under epidural anesthesia. A 29-year old pregnant wom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a52cd2aa1ba1f129c8479d98dc88c3e
https://doi.org/10.31636/pmjua.v3i2.104

Reproductive (epi)genetics

Autor: C. Lynch, N. Tee, H. Rouse, A. Gordon, L. Sati, C. Zeiss, B. Soygur, I. Bassorgun, E. Goksu, R. Demir, J. McGrath, M. L. Groendahl, L. Thuesen, A. N. Andersen, A. Loft, J. Smitz, T. Adriaenssens, J. Vikesa, R. Borup, E. Mersy, N. Kisters, M. V. E. Macville, J. J. M. Engelen, S.-E. N. N. Consortium, P. P. C. A. Menheere, J. P. Geraedts, A. B. C. Coumans, S. G. M. Frints, T. Aledani, S. Assou, S. Traver, O. Ait-ahmed, H. Dechaud, S. Hamamah, E. Mizutani, N. Suzumori, C. Sugiyama, Y. Hattori, T. Sato, H. Ando, Y. Ozaki, M. Sugiura-Ogasawara, M. Wissing, S. G. Kristensen, C. Y. Andersen, A. L. Mikkelsen, T. Hoest, A. Velthut-Meikas, J. Simm, M. Metsis, A. Salumets, S. Palini, L. Galluzzi, S. De Stefani, M. Primiterra, D. Wells, M. Magnani, C. Bulletti, P. H. Vogt, P. Frank-Herrmann, U. Bender, T. Strowitzki, B. Besikoglu, P. Heidemann, L. Wunsch, M. Bettendorf, L. Jelinkova, S. Vilimova, M. Kosarova, P. Sebek, E. Volemanova, M. Kruzelova, J. Civisova, L. Svobodova, V. Sobotka, T. Mardesic, C. van de Werken, M. A. Santos, C. Eleveld, J. S. E. Laven, E. B. Baart, L. Y. Pylyp, L. A. Spinenko, V. D. Zukin, J. Perez-Sanz, R. Matorras, J. Arluzea, J. Bilbao, N. Gonzalez-Santiago, N. Yeh, A. Koff, A. Barlas, Y. Romin, K. Manova-Todorova, C. D. l. Hoz, A. L. Mauri, A. M. Nascimento, L. D. Vagnini, C. G. Petersen, J. Ricci, F. C. Massaro, M. Cavagna, A. Pontes, J. B. A. Oliveira, R. L. R. Baruffi, J. G. Franco, E. X. Wu, S. Ma, M. Parriego, M. Sole, M. Boada, B. Coroleu, A. Veiga, G. Kakourou, M. Poulou, C. Vrettou, A. Destouni, J. Traeger-Synodinos, E. Kanavakis, A. N. Yatsenko, A. P. Georgiadis, M. M. McGuire, M. Zorrilla, K. D. Bunce, D. Peters, A. Rajkovic, M. Olszewska, M. Kurpisz, A. Z. A. Gilbertson, C. S. Ottolini, M. C. Summers, K. Sage, A. H. Handyside, A. R. Thornhill, D. K. Griffin, M. K. Chung, J. W. Kim, J. H. Lee, H. J. Jeong, M. H. Kim, M. J. Ryu, S. J. Park, H. Y. Kang, H. S. Lee, B. Zimmermann, M. Banjevic, M. Hill, P. Lacroute, M. Dodd, S. Sigurjonsson, P. Lau, D. Prosen, N. Chopra, A. Ryan, M. Hall, S. McAdoo, Z. Demko, B. Levy, M. Rabinowitz, A. Vereczeky, Z. S. Kosa, S. Savay, M. Csenki, L. Nanassy, B. Dudas, Z. S. Domotor, D. Debreceni, A. Rossi, J. R. Alegretti, J. Cuzzi, M. Bonavita, M. Tanada, P. Matunaga, P. Fettback, M. B. Rosa, V. Maia, P. Hassun, E. L. A. Motta, M. Piccolomini, C. Gomes, B. Barros, M. Nicoliello, T. Criscuolo, E. Miyadahira, D. Montjean, M. Benkhalifa, I. Berthaut, J. F. Griveau, K. Morcel, A. Bashamboo, K. McElreavey, C. Ravel, C. Rubio, L. Rodrigo, E. Mateu, A. Mercader, V. Peinado, P. Buendia, M. Milan, A. Delgado, N. Al-Asmar, L. Escrich, I. Campos-Galindo, S. Garcia-Herrero, M. E. Poo, P. Mir, C. Simon, A. Reyes-Engel, M. Cortes-Rodriguez, A. Lendinez, B. Perez-Nevot, A. R. Palomares, M. R. Galdon, A. Ruberti, M. G. Minasi, A. Biricik, A. Colasante, D. Zavaglia, E. Iammarrone, F. Fiorentino, E. Greco, N. Demir, S. Ozturk, B. Sozen, R. Morales, B. Lledo, J. A. Ortiz, J. Ten, J. Llacer, R. Bernabeu, M. Nagayoshi, A. Tanaka, I. Tanaka, H. Kusunoki, S. Watanabe, S. G. Temel, C. Beyazyurek, G. C. Ekmekci, F. Aybar, C. Cinar, S. Kahraman, S. Nordqvist, K. Karehed, H. Akerud, M. Gultomruk, P. Tulay, N. Findikli, E. Yagmur, G. Karlikaya, U. Ulug, M. Bahceci, M. F. Bargallo, M. R. Arevalo, M. M. Salat, I. V. Barbat, J. T. Lopez, M. E. Algam, A. B. Boluda, G. C. de Oya, E. N. Tolmacheva, A. A. Kashevarova, N. A. Skryabin, I. N. Lebedev, E. Semaco, A. Belo, M. Riboldi, L. Luz, N. Nobrega, R. Mazetto, J. A. Alegretti, M. Bibancos, P. Serafini, J. Neupane, M. Vandewoestyne, B. Heindryckx, T. Deroo, Y. Lu, S. Ghimire, S. Lierman, C. Qian, D. Deforce, P. De Sutter, T. Viloria, J. M. Martinez-Jabaloyas, M. Gil-Salom, A. Capalbo, N. Treff, D. Cimadomo, X. Tao, K. Ferry, F. M. Ubaldi, L. Rienzi, R. T. Scott, N. Katzorke, H. P. Vogt, A. Hehr, C. Gassner, B. Paulmann, Z. Kowalzyk, M. Klatt, S. Krauss, D. Seifert, B. Seifert, U. Hehr, M. Lobascio, M. T. Varricchio, P. Rubino, S. Bono, R. P. Cotarelo, L. Spizzichino, A. Colicchia, P. Giannini, M. Suhorutshenko, K. Rosenstein-Tamm

Publikováno v: Human Reproduction. 28:i291-i311

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69a22b8992e702541326b39c2a0ebeba
https://doi.org/10.1093/humrep/det220

[Meiotic segregation of chromosomes 13 and 14 of heterozygous Robertsonian translocation der(13;14) (q10; q10) carriers]

Autor: L Ia, Pilip, L A, Spinenko, V D, Zukin, N M, Bil'ko

Publikováno v: TSitologiia i genetika. 48(3)

Meiotic segregation of chromosomes 13 and 14 was assessed by fluorescence in situ hybridization on sperm of five heterozygous carriers of the most frequent Robertsonian translocation der(13;14). Alternate segregation mode was predominant (mean 78.2 +

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e931419c4eaa0af46bae03522dc2e393
https://pubmed.ncbi.nlm.nih.gov/25016829

[A case of deletion of the short arm of the chromosome 21 (21p-) (christchurch chromosome) discovered prenatally:clinical and cytogenetic data]

Autor: L V, Tavokina, S G, Vorsanova, V D, Zukin, N I, Sopko, V M, Zinchenko, V V, Veselovskiĭ, A M, Bychkova, T V, Nikitchina, Iu B, Iurov

Publikováno v: TSitologiia i genetika. 38(1)

Results of cytogenetic research of placental villi and amniotic fluid cells culture of the 22-weeks-old fetus with multiple congenital malformations (MCM) are presented. The absence of the short arm in one of the homologue of the chromosome 21 was re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b2acc4ba38902aeae3cc4698d603d52c
https://pubmed.ncbi.nlm.nih.gov/15098444