Pesquisas alternativas:
cestero » estero (Expandir a Pesquisa), cestaro (Expandir a Pesquisa), cesteria (Expandir a Pesquisa)
nerve » serve (Expandir a Pesquisa)
reserve » reserved (Expandir a Pesquisa)
cestero » estero (Expandir a Pesquisa), cestaro (Expandir a Pesquisa), cesteria (Expandir a Pesquisa)
nerve » serve (Expandir a Pesquisa)
reserve » reserved (Expandir a Pesquisa)
1
“... pharmacological advances such as tyrosine kinase inhibitors have determined c-kit (i.e., CD117) as the most...”
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2
“... botulinum. Botulism in Canada is predominately due to C botulinum type E and affects mainly the First...”
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3
Por Rodella, Umberto, Negro, Samuele, Scorzeto, Michele, Bergamin, Elisanna, Jalink, Kees, Montecucco, Cesare, Yuki, Nobuhiro, Rigoni, Michela
Publicado no Dis Model Mech (2017)
“... of Miller Fisher syndrome, we recently reported that a monoclonal anti-polysialoganglioside GQ1b antibody...”Publicado no Dis Model Mech (2017)
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4
“... number of recent empiric studies have emerged from Japan. The majority of such cases of hikikomori...”
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5
Por Ghabili, Kamyar, Golzari, Samad E J, Salehpour, Firooz, Imani, Taghi, Bazzazi, Amir Mohammad, Ghaffari, Alireza, Khanli, Hadi Mohammad, Tizro, Parastou, Taghizade, Shabnam, Shakouri, Seyed Kazem
Publicado em 2013
“... in the recent twin earthquakes, northwest Iran was limited and caused less nerve injuries compared...”Publicado em 2013
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6
“...Recent advances in the understanding of circadian rhythms have led to an interest in the treatment...”
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7
“.... This promise has been recently supported by a Phase-I human trial in which a replication-defective herpes...”
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8
Por Huang, X, Sun, J, Rong, W, Zhao, T, Li, D-h, Ding, X, Wu, L-y, Wu, K, Schachner, M, Xiao, Z-C, Zhu, L-l, Fan, M
Publicado em 2013
“... development and for the maintenance of neural circuits in adults. Recent studies revealed that CHL1 has...”Publicado em 2013
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9
“...Glaucoma is one of the leading causes of irreversible blindness that is characterized...”
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10
Por McMillan, Hugh J., Telegrafi, Aida, Singleton, Amanda, Cho, Megan T., Lelli, Daniel, Lynn, Francis C., Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E., Koolen, David A., Haaxma, Charlotte A., Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J., Henderson, Lindsay B., McLaughlin, Heather, Molday, Laurie L., Molday, Robert S., Yoon, Grace
Publicado no Orphanet J Rare Dis (2018)
“...BACKGROUND: ATP8A2 mutations have recently been described in several patients with severe, early...”Publicado no Orphanet J Rare Dis (2018)
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