Pesquisas alternativas:
absent nerve » abducent nerve (Expandir a Pesquisa), absent native (Expandir a Pesquisa), augment nerve (Expandir a Pesquisa)
cent nerve » crest nerve (Expandir a Pesquisa), central nerve (Expandir a Pesquisa), current nerve (Expandir a Pesquisa)
bent nerve » mental nerve (Expandir a Pesquisa), dental nerve (Expandir a Pesquisa), benign nerve (Expandir a Pesquisa)
nerve _ase » nerve cases (Expandir a Pesquisa), nerve based (Expandir a Pesquisa), nerve cause (Expandir a Pesquisa)
j absent » _ absent (Expandir a Pesquisa), l absent (Expandir a Pesquisa), 17 absent (Expandir a Pesquisa)
case dis » case disc (Expandir a Pesquisa), case di (Expandir a Pesquisa), case does (Expandir a Pesquisa)
nerve c » nerve cn (Expandir a Pesquisa), nerve _ (Expandir a Pesquisa), nerve a (Expandir a Pesquisa)
_ase di » base di (Expandir a Pesquisa), case di (Expandir a Pesquisa), fase di (Expandir a Pesquisa)
j cent » a cent (Expandir a Pesquisa), i cent (Expandir a Pesquisa), j center (Expandir a Pesquisa)
j bent » j benet (Expandir a Pesquisa), j bento (Expandir a Pesquisa), j bena (Expandir a Pesquisa)
c dis » c dias (Expandir a Pesquisa), c disc (Expandir a Pesquisa), c dos (Expandir a Pesquisa)
absent nerve » abducent nerve (Expandir a Pesquisa), absent native (Expandir a Pesquisa), augment nerve (Expandir a Pesquisa)
cent nerve » crest nerve (Expandir a Pesquisa), central nerve (Expandir a Pesquisa), current nerve (Expandir a Pesquisa)
bent nerve » mental nerve (Expandir a Pesquisa), dental nerve (Expandir a Pesquisa), benign nerve (Expandir a Pesquisa)
nerve _ase » nerve cases (Expandir a Pesquisa), nerve based (Expandir a Pesquisa), nerve cause (Expandir a Pesquisa)
j absent » _ absent (Expandir a Pesquisa), l absent (Expandir a Pesquisa), 17 absent (Expandir a Pesquisa)
case dis » case disc (Expandir a Pesquisa), case di (Expandir a Pesquisa), case does (Expandir a Pesquisa)
nerve c » nerve cn (Expandir a Pesquisa), nerve _ (Expandir a Pesquisa), nerve a (Expandir a Pesquisa)
_ase di » base di (Expandir a Pesquisa), case di (Expandir a Pesquisa), fase di (Expandir a Pesquisa)
j cent » a cent (Expandir a Pesquisa), i cent (Expandir a Pesquisa), j center (Expandir a Pesquisa)
j bent » j benet (Expandir a Pesquisa), j bento (Expandir a Pesquisa), j bena (Expandir a Pesquisa)
c dis » c dias (Expandir a Pesquisa), c disc (Expandir a Pesquisa), c dos (Expandir a Pesquisa)
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“... in clinical trials, several additional studies, case reports and toxicology reports have demonstrated...”
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3
“... identified. Clinical signs included absent tendon reflexes, ataxic gait, and a positive Romberg test. Nerve...”
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Bioinformatics Data Mining Approach Suggests Coexpression of AGTPBP1 with an ALS-linked Gene C9orf72
Por Kitano, Shouta, Kino, Yoshihiro, Yamamoto, Yoji, Takitani, Mika, Miyoshi, Junko, Ishida, Tsuyoshi, Saito, Yuko, Arima, Kunimasa, Satoh, Jun-ichi
Publicado no J Cent Nerv Syst Dis (2015)
“... of the chromosome 9 open reading frame 72 (C9orf72) gene represent the most common genetic abnormality for familial...”Publicado no J Cent Nerv Syst Dis (2015)
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6
Por Satoh, Jun-ichi, Yamamoto, Yoji, Kitano, Shouta, Takitani, Mika, Asahina, Naohiro, Kino, Yoshihiro
Publicado em 2014
“..., located in the noncoding region of the chromosome 9 open reading frame 72 (C9orf72) gene represent...”Publicado em 2014
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“... transporter’ and articles were screened for case reports of patients with a molecular diagnosis of a...”
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8
“... that sertindole exerts a potent antagonism at serotonin 5-HT(2A), 5-HT(2C), dopamine D(2), and α(l) adrenergic...”
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“..., combines 5HT2c antagonist and melatonin agonist action, and has shown promise in both acute treatment...”
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10
Por Turón-Viñas, Eulàlia, Pineda, Mercè, Cusí, Victòria, López-Laso, Eduardo, del Pozo, Rebeca Losada, Gutiérrez-Solana, Luis González, Moreno, David Conejo, Sierra-Córcoles, Concha, Olabarrieta-Hoyos, Naiara, Madruga-Garrido, Marcos, Aguirre-Rodríguez, Javier, González-Álvarez, Verónica, O’Callaghan, Mar, Muchart, Jordi, Armstrong-Moron, Judith
Publicado em 2014
“... cases), and eIF2B4 (1 case). In our report, the second mutation in frequency was c.318A>T; patients...”Publicado em 2014
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