TY  - JOUR
AU  - Huebschen, Judith M.
AU  - Mihneva, Zefira
AU  - Mentis, Andreas F.
AU  - Schneider, Francois
AU  - Aboudy, Yair
AU  - Grossman, Zehava
AU  - Rudich, Hagit
AU  - Kasymbekova, Kalia
AU  - Sarv, Inna
AU  - Nedeljković, Jasminka
AU  - Tahita, Marc C.
AU  - Tarnagda, Zekiba
AU  - Ouedraogo, Jean-Bosco
AU  - Gerasimova, A.G.
AU  - Moskaleva, T.N.
AU  - Tikhonova, Nina T.
AU  - Chitadze, Nazibrola
AU  - Forbi, J.C.
AU  - Faneye, Adedayo O.
AU  - Otegbayo, Jesse A.
AU  - Charpentier, Emilie
AU  - Muller, Claude P.
PY  - 2009
UR  - http://intor.torlakinstitut.com/handle/123456789/279
AB  - Phylogenetic analysis of 166 human parvovirus B19 sequences from 11 different countries attributed 91.57% to genotype 1, 5.42% to genotype 3b, and 3.01% to genotype 3a. Very similar viruses of genotype 1 circulated widely in Europe and Israel. Genotype 3b seems to show an increasing spread outside of Africa.
PB  - Amer Soc Microbiology, Washington
T2  - Journal of Clinical Microbiology
T1  - Phylogenetic Analysis of Human Parvovirus B19 Sequences from Eleven Different Countries Confirms the Predominance of Genotype 1 and Suggests the Spread of Genotype 3b
EP  - 3738
IS  - 11
SP  - 3735
VL  - 47
DO  - 10.1128/JCM.01201-09
ER  - 

@article{
author = "Huebschen, Judith M. and Mihneva, Zefira and Mentis, Andreas F. and Schneider, Francois and Aboudy, Yair and Grossman, Zehava and Rudich, Hagit and Kasymbekova, Kalia and Sarv, Inna and Nedeljković, Jasminka and Tahita, Marc C. and Tarnagda, Zekiba and Ouedraogo, Jean-Bosco and Gerasimova, A.G. and Moskaleva, T.N. and Tikhonova, Nina T. and Chitadze, Nazibrola and Forbi, J.C. and Faneye, Adedayo O. and Otegbayo, Jesse A. and Charpentier, Emilie and Muller, Claude P.",
year = "2009",
abstract = "Phylogenetic analysis of 166 human parvovirus B19 sequences from 11 different countries attributed 91.57% to genotype 1, 5.42% to genotype 3b, and 3.01% to genotype 3a. Very similar viruses of genotype 1 circulated widely in Europe and Israel. Genotype 3b seems to show an increasing spread outside of Africa.",
publisher = "Amer Soc Microbiology, Washington",
journal = "Journal of Clinical Microbiology",
title = "Phylogenetic Analysis of Human Parvovirus B19 Sequences from Eleven Different Countries Confirms the Predominance of Genotype 1 and Suggests the Spread of Genotype 3b",
pages = "3738-3735",
number = "11",
volume = "47",
doi = "10.1128/JCM.01201-09"
}

Huebschen, J. M., Mihneva, Z., Mentis, A. F., Schneider, F., Aboudy, Y., Grossman, Z., Rudich, H., Kasymbekova, K., Sarv, I., Nedeljković, J., Tahita, M. C., Tarnagda, Z., Ouedraogo, J., Gerasimova, A.G., Moskaleva, T.N., Tikhonova, N. T., Chitadze, N., Forbi, J.C., Faneye, A. O., Otegbayo, J. A., Charpentier, E.,& Muller, C. P.. (2009). Phylogenetic Analysis of Human Parvovirus B19 Sequences from Eleven Different Countries Confirms the Predominance of Genotype 1 and Suggests the Spread of Genotype 3b. in Journal of Clinical Microbiology
Amer Soc Microbiology, Washington., 47(11), 3735-3738.
https://doi.org/10.1128/JCM.01201-09

Huebschen JM, Mihneva Z, Mentis AF, Schneider F, Aboudy Y, Grossman Z, Rudich H, Kasymbekova K, Sarv I, Nedeljković J, Tahita MC, Tarnagda Z, Ouedraogo J, Gerasimova A, Moskaleva T, Tikhonova NT, Chitadze N, Forbi J, Faneye AO, Otegbayo JA, Charpentier E, Muller CP. Phylogenetic Analysis of Human Parvovirus B19 Sequences from Eleven Different Countries Confirms the Predominance of Genotype 1 and Suggests the Spread of Genotype 3b. in Journal of Clinical Microbiology. 2009;47(11):3735-3738.
doi:10.1128/JCM.01201-09 .

Huebschen, Judith M., Mihneva, Zefira, Mentis, Andreas F., Schneider, Francois, Aboudy, Yair, Grossman, Zehava, Rudich, Hagit, Kasymbekova, Kalia, Sarv, Inna, Nedeljković, Jasminka, Tahita, Marc C., Tarnagda, Zekiba, Ouedraogo, Jean-Bosco, Gerasimova, A.G., Moskaleva, T.N., Tikhonova, Nina T., Chitadze, Nazibrola, Forbi, J.C., Faneye, Adedayo O., Otegbayo, Jesse A., Charpentier, Emilie, Muller, Claude P., "Phylogenetic Analysis of Human Parvovirus B19 Sequences from Eleven Different Countries Confirms the Predominance of Genotype 1 and Suggests the Spread of Genotype 3b" in Journal of Clinical Microbiology, 47, no. 11 (2009):3735-3738,
https://doi.org/10.1128/JCM.01201-09 . .

TY  - JOUR
AU  - Kremer, Jacques R.
AU  - Brown, Kevin E.
AU  - Jin, Li
AU  - Santibanez, Sabine
AU  - Shulga, Sergey V.
AU  - Aboudy, Yair
AU  - Demchyshyna, Irina V.
AU  - Đemileva, Sultana
AU  - Echevarria, Juan E.
AU  - Featherstone, David F.
AU  - Hukić, Mirsada
AU  - Johansen, Kari
AU  - Litwinska, Bogumila
AU  - Lopareva, Elena
AU  - Lupulescu, Emilia
AU  - Mentis, Andreas F.
AU  - Mihneva, Zefira
AU  - Mosquera, Maria M.
AU  - Muscat, Mark
AU  - Naumova, M.A.
AU  - Nedeljković, Jasminka
AU  - Nekrasova, Ljubov S.
AU  - Magurano, Fabio
AU  - Fortuna, Claudia
AU  - De Andrade, Helena Rebelo
AU  - Richard, Jean-Luc
AU  - Robo, Alma
AU  - Rota, Paul A.
AU  - Samoilovich, Elena O.
AU  - Sarv, Inna
AU  - Semeiko, Galina V.
AU  - Shugayev, Nazim
AU  - Utegenova, Elmira S.
AU  - van Binnendijk, Rob
AU  - Vinner, Lasse
AU  - Waku-Kouomou, Diane
AU  - Wild, Fabian T.
AU  - Brown, David W.G.
AU  - Mankertz, Annette
AU  - Muller, Claude P.
AU  - MuldersJJ, Mick N.
PY  - 2008
UR  - http://intor.torlakinstitut.com/handle/123456789/249
AB  - During 2005-2006, nine measles virus (MV) genotypes were identified throughout the World Health Organization European Region. All major epidemics were associated with genotypes D4, D6, and B3. Other genotypes (B2, D5, D8, D9, G2, and H1) were only found in limited numbers of cases after importation from other continents. The genetic diversity of endemic D6 strains was low; genotypes C2 and D7, circulating in Europe until recent years, were no longer identified. The transmission chains of several indigenous MV strains may thus have been interrupted by enhanced vaccination. However, multiple importations from Africa and Asia and virus introduction into highly mobile and unvaccinated communities caused a massive spread of D4 and B3 strains throughout much of the region. Thus, despite the reduction of endemic MV circulation, importation of MV from other continents caused prolonged circulation and large outbreaks after their introduction into unvaccinated and highly mobile communities.
PB  - Centers  Disease Control & Prevention, Atlanta
T2  - Emerging Infectious Diseases
T1  - High genetic diversity of measles virus, World Health Organization European region, 2005-2006
EP  - 114
IS  - 1
SP  - 107
VL  - 14
DO  - 10.3201/eid1401.070778
ER  - 

@article{
author = "Kremer, Jacques R. and Brown, Kevin E. and Jin, Li and Santibanez, Sabine and Shulga, Sergey V. and Aboudy, Yair and Demchyshyna, Irina V. and Đemileva, Sultana and Echevarria, Juan E. and Featherstone, David F. and Hukić, Mirsada and Johansen, Kari and Litwinska, Bogumila and Lopareva, Elena and Lupulescu, Emilia and Mentis, Andreas F. and Mihneva, Zefira and Mosquera, Maria M. and Muscat, Mark and Naumova, M.A. and Nedeljković, Jasminka and Nekrasova, Ljubov S. and Magurano, Fabio and Fortuna, Claudia and De Andrade, Helena Rebelo and Richard, Jean-Luc and Robo, Alma and Rota, Paul A. and Samoilovich, Elena O. and Sarv, Inna and Semeiko, Galina V. and Shugayev, Nazim and Utegenova, Elmira S. and van Binnendijk, Rob and Vinner, Lasse and Waku-Kouomou, Diane and Wild, Fabian T. and Brown, David W.G. and Mankertz, Annette and Muller, Claude P. and MuldersJJ, Mick N.",
year = "2008",
abstract = "During 2005-2006, nine measles virus (MV) genotypes were identified throughout the World Health Organization European Region. All major epidemics were associated with genotypes D4, D6, and B3. Other genotypes (B2, D5, D8, D9, G2, and H1) were only found in limited numbers of cases after importation from other continents. The genetic diversity of endemic D6 strains was low; genotypes C2 and D7, circulating in Europe until recent years, were no longer identified. The transmission chains of several indigenous MV strains may thus have been interrupted by enhanced vaccination. However, multiple importations from Africa and Asia and virus introduction into highly mobile and unvaccinated communities caused a massive spread of D4 and B3 strains throughout much of the region. Thus, despite the reduction of endemic MV circulation, importation of MV from other continents caused prolonged circulation and large outbreaks after their introduction into unvaccinated and highly mobile communities.",
publisher = "Centers  Disease Control & Prevention, Atlanta",
journal = "Emerging Infectious Diseases",
title = "High genetic diversity of measles virus, World Health Organization European region, 2005-2006",
pages = "114-107",
number = "1",
volume = "14",
doi = "10.3201/eid1401.070778"
}

Kremer, J. R., Brown, K. E., Jin, L., Santibanez, S., Shulga, S. V., Aboudy, Y., Demchyshyna, I. V., Đemileva, S., Echevarria, J. E., Featherstone, D. F., Hukić, M., Johansen, K., Litwinska, B., Lopareva, E., Lupulescu, E., Mentis, A. F., Mihneva, Z., Mosquera, M. M., Muscat, M., Naumova, M.A., Nedeljković, J., Nekrasova, L. S., Magurano, F., Fortuna, C., De Andrade, H. R., Richard, J., Robo, A., Rota, P. A., Samoilovich, E. O., Sarv, I., Semeiko, G. V., Shugayev, N., Utegenova, E. S., van Binnendijk, R., Vinner, L., Waku-Kouomou, D., Wild, F. T., Brown, D. W.G., Mankertz, A., Muller, C. P.,& MuldersJJ, M. N.. (2008). High genetic diversity of measles virus, World Health Organization European region, 2005-2006. in Emerging Infectious Diseases
Centers  Disease Control & Prevention, Atlanta., 14(1), 107-114.
https://doi.org/10.3201/eid1401.070778

Kremer JR, Brown KE, Jin L, Santibanez S, Shulga SV, Aboudy Y, Demchyshyna IV, Đemileva S, Echevarria JE, Featherstone DF, Hukić M, Johansen K, Litwinska B, Lopareva E, Lupulescu E, Mentis AF, Mihneva Z, Mosquera MM, Muscat M, Naumova M, Nedeljković J, Nekrasova LS, Magurano F, Fortuna C, De Andrade HR, Richard J, Robo A, Rota PA, Samoilovich EO, Sarv I, Semeiko GV, Shugayev N, Utegenova ES, van Binnendijk R, Vinner L, Waku-Kouomou D, Wild FT, Brown DW, Mankertz A, Muller CP, MuldersJJ MN. High genetic diversity of measles virus, World Health Organization European region, 2005-2006. in Emerging Infectious Diseases. 2008;14(1):107-114.
doi:10.3201/eid1401.070778 .

Kremer, Jacques R., Brown, Kevin E., Jin, Li, Santibanez, Sabine, Shulga, Sergey V., Aboudy, Yair, Demchyshyna, Irina V., Đemileva, Sultana, Echevarria, Juan E., Featherstone, David F., Hukić, Mirsada, Johansen, Kari, Litwinska, Bogumila, Lopareva, Elena, Lupulescu, Emilia, Mentis, Andreas F., Mihneva, Zefira, Mosquera, Maria M., Muscat, Mark, Naumova, M.A., Nedeljković, Jasminka, Nekrasova, Ljubov S., Magurano, Fabio, Fortuna, Claudia, De Andrade, Helena Rebelo, Richard, Jean-Luc, Robo, Alma, Rota, Paul A., Samoilovich, Elena O., Sarv, Inna, Semeiko, Galina V., Shugayev, Nazim, Utegenova, Elmira S., van Binnendijk, Rob, Vinner, Lasse, Waku-Kouomou, Diane, Wild, Fabian T., Brown, David W.G., Mankertz, Annette, Muller, Claude P., MuldersJJ, Mick N., "High genetic diversity of measles virus, World Health Organization European region, 2005-2006" in Emerging Infectious Diseases, 14, no. 1 (2008):107-114,
https://doi.org/10.3201/eid1401.070778 . .