Pesquisas alternativas:
nerve system » nervous system (Expandir a Pesquisa), drive system (Expandir a Pesquisa)
genet nerve » genes serve (Expandir a Pesquisa), bent nerve (Expandir a Pesquisa), genital nerve (Expandir a Pesquisa)
cent nerve » bent nerve (Expandir a Pesquisa), recent nerve (Expandir a Pesquisa), crest nerve (Expandir a Pesquisa)
mehta nele » mehta nee (Expandir a Pesquisa), mehta adele (Expandir a Pesquisa), mehta neil (Expandir a Pesquisa)
nele cyst » nerve cyst (Expandir a Pesquisa), bile cyst (Expandir a Pesquisa), nele post (Expandir a Pesquisa)
case dis » case disc (Expandir a Pesquisa), case did (Expandir a Pesquisa), case di (Expandir a Pesquisa)
j genet » j gentet (Expandir a Pesquisa), j gene (Expandir a Pesquisa), j genes (Expandir a Pesquisa)
j mehta » a mehta (Expandir a Pesquisa), _ mehta (Expandir a Pesquisa), k mehta (Expandir a Pesquisa)
i cent » i cento (Expandir a Pesquisa), ai cent (Expandir a Pesquisa), ii cent (Expandir a Pesquisa)
nerve system » nervous system (Expandir a Pesquisa), drive system (Expandir a Pesquisa)
genet nerve » genes serve (Expandir a Pesquisa), bent nerve (Expandir a Pesquisa), genital nerve (Expandir a Pesquisa)
cent nerve » bent nerve (Expandir a Pesquisa), recent nerve (Expandir a Pesquisa), crest nerve (Expandir a Pesquisa)
mehta nele » mehta nee (Expandir a Pesquisa), mehta adele (Expandir a Pesquisa), mehta neil (Expandir a Pesquisa)
nele cyst » nerve cyst (Expandir a Pesquisa), bile cyst (Expandir a Pesquisa), nele post (Expandir a Pesquisa)
case dis » case disc (Expandir a Pesquisa), case did (Expandir a Pesquisa), case di (Expandir a Pesquisa)
j genet » j gentet (Expandir a Pesquisa), j gene (Expandir a Pesquisa), j genes (Expandir a Pesquisa)
j mehta » a mehta (Expandir a Pesquisa), _ mehta (Expandir a Pesquisa), k mehta (Expandir a Pesquisa)
i cent » i cento (Expandir a Pesquisa), ai cent (Expandir a Pesquisa), ii cent (Expandir a Pesquisa)
1
Por Shah, Javeed A., Berrington, William R., Vary, James C., Wells, Richard D., Peterson, Glenna J., Kunwar, Chhatra B., Khadge, Saraswoti, Hagge, Deanna A., Hawn, Thomas R.
Publicado no J Infect Dis (2016)
“.... TOLLIP mRNA was highly and specifically correlated with IL-1R antagonist (IL-1Ra). In a case-control gene...”Publicado no J Infect Dis (2016)
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2
Por Cezar-de-Mello, Paula F. T., Toledo-Pinto, Thiago G., Marques, Carolinne S., Arnez, Lucia E. A., Cardoso, Cynthia C., Guerreiro, Luana T. A., Antunes, Sérgio L. G., Jardim, Márcia M., Covas, Claudia de J. F., Illaramendi, Ximena, Dias-Baptista, Ida M., Rosa, Patrícia S., Durães, Sandra M. B., Pacheco, Antonio G., Ribeiro-Alves, Marcelo, Sarno, Euzenir N., Moraes, Milton O.
Publicado em 2014
“..., we enrolled 1,098 individuals and conducted a case-control analysis in order to study four miRNAs...”Publicado em 2014
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3
Por Wang, Xianling, Yang, Yanhui, Li, Xuying, Li, Cunjiang, Wang, Chaodong
Publicado no Orphanet J Rare Dis (2019)
“... (57.1%) and optic nerve damages (42.9%) than those carrying point mutations (22.2 and 11.1...”Publicado no Orphanet J Rare Dis (2019)
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4
“... demonstrated that genetic and environmental factors play a major role in the development of autism. However...”
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5
Por Young, Saroj K., Ponnighaus, Jorg M., Jain, Suman, Lucas, Sebastian, Suneetha, Sujai, Lockwood, Diana N. J., Young, Douglas B., Fine, Paul E. M.
Publicado em 2008
“... of leprosy in northern Malawi, and from members of multi-case households in Hyderabad, India. In the Malawi...”Publicado em 2008
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6
Por Semmler, Anna-Lena, Sacconi, Sabrina, Bach, J Elisa, Liebe, Claus, Bürmann, Jan, Kley, Rudolf A, Ferbert, Andreas, Anderheiden, Roland, Van den Bergh, Peter, Martin, Jean-Jacques, De Jonghe, Peter, Neuen-Jacob, Eva, Müller, Oliver, Deschauer, Marcus, Bergmann, Markus, Schröder, J Michael, Vorgerd, Matthias, Schulz, Jörg B, Weis, Joachim, Kress, Wolfram, Claeys, Kristl G
Publicado no Orphanet J Rare Dis (2014)
“... be considered even in cases with a mild phenotype or an adult onset. We identified a genetic defect in one...”Publicado no Orphanet J Rare Dis (2014)
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7
Por Liaw, Hsiang-Ru, Lee, Hsiu-Fen, Chi, Ching-Shiang, Tsai, Chi-Ren
Publicado no Orphanet J Rare Dis (2015)
“...BACKGROUND: This study was conducted to describe the clinical and genetic features of patients...”Publicado no Orphanet J Rare Dis (2015)
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8
Por Knoester, Marjolein, Helfferich, Jelte, Poelman, Randy, Van Leer-Buter, Coretta, Brouwer, Oebele F., Niesters, Hubert G. M.
Publicado no Pediatr Infect Dis J (2019)
“... and the family of Picornaviridae. Genetically, it is closely related to rhinovirus that replicates...”Publicado no Pediatr Infect Dis J (2019)
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9
Assuntos:
“...Case Report...”
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10
Por Shenoy, Anant M., Markowitz, Jennifer A., Bonnemann, Carsten G., Krishnamoorthy, Kalpathy, Bossler, Aaron D., Tseng, Brian S.
Publicado em 2010
“..., and genetic studies are all consistent with the diagnosis of Muscle-Eye-Brain (MEB) disease. MEB is one...”Publicado em 2010
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11
Por Wilby, Martin J, Best, Ashley, Wood, Eifiona, Burnside, Girvan, Bedson, Emma, Short, Hannah, Wheatley, Dianne, Hill-McManus, Daniel, Sharma, Manohar, Clark, Simon, Bostock, Jennifer, Hay, Sally, Baranidharan, Ganesan, Price, Cathy, Mannion, Richard, Hutchinson, Peter J, Hughes, Dyfrig A, Marson, Anthony, Williamson, Paula R
Publicado no Health Technol Assess (2021)
“... to either (1) microdiscectomy or (2) transforaminal epidural steroid injection. DESIGN: A pragmatic...”Publicado no Health Technol Assess (2021)
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12
“... with mutations in DOK7 and GFPT1, and less frequently with mutations in COLQ, ALG2, ALG14 and DPAGT. Genetic...”
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13
“..., at least in part, the cyclic aspects of CH. The disease is familial in about 10% of cases. Genetic factors...”
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14
Por Bischoff, Allison N., Reiersen, Angela M., Buttlaire, Anna, Al-lozi, Amal, Doty, Tasha, Marshall, Bess A., Hershey, Tamara
Publicado no Orphanet J Rare Dis (2015)
“... nerve atrophy, vision loss, hearing impairment, motor abnormalities, and neurodegeneration, but has been...”Publicado no Orphanet J Rare Dis (2015)
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15
Por Lenaers, Guy, Hamel, Christian, Delettre, Cécile, Amati-Bonneau, Patrizia, Procaccio, Vincent, Bonneau, Dominique, Reynier, Pascal, Milea, Dan
Publicado em 2012
“... due to a founder effect, to 1/30000 in the rest of the world. CLINICAL DESCRIPTION: DOA patients...”Publicado em 2012
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16
Por Piotrowska-Nowak, Agnieszka, Krawczyński, Maciej R., Kosior-Jarecka, Ewa, Ambroziak, Anna M., Korwin, Magdalena, Ołdak, Monika, Tońska, Katarzyna, Bartnik, Ewa
Publicado no Metab Brain Dis (2020)
“... single tissue, optic nerve, resulting in vision loss. In the majority of cases it is caused by one...”Publicado no Metab Brain Dis (2020)
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17
Por Moramarco, Antonietta, Himmelblau, Ehud, Miraglia, Emanuele, Mallone, Fabiana, Roberti, Vincenzo, Franzone, Federica, Iacovino, Chiara, Giustini, Sandra, Lambiase, Alessandro
Publicado no Orphanet J Rare Dis (2019)
“... expressivity. It is caused in 85% of the cases with a known etiology by pathogenic variants in the PTCH1 gene...”Publicado no Orphanet J Rare Dis (2019)
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18
Por Auer-Grumbach, Michaela
Publicado em 2008
“... and gastrooesophageal reflux have been observed in rare cases. HSN I is a genetically heterogenous condition with three...”Publicado em 2008
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19
“... be further divided based on the proposed pathogenetic mechanism into 3 subclasses: subclass 1 includes type I...”
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20
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
“... patients were diagnosed according to genetics: we found mutations in the genes eIF2B5 (13 cases), eIF2B3 (2...”Publicado em 2014
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