Pesquisas alternativas:
segment nerve » segmental nerve (Expandir a Pesquisa), augment nerve (Expandir a Pesquisa), segmental nerves (Expandir a Pesquisa)
crest drive » crest derived (Expandir a Pesquisa), forest drive (Expandir a Pesquisa), test drive (Expandir a Pesquisa)
genes nerve » genes serve (Expandir a Pesquisa), genes server (Expandir a Pesquisa), genes serves (Expandir a Pesquisa)
system dis » system dias (Expandir a Pesquisa), system dcs (Expandir a Pesquisa), system di (Expandir a Pesquisa)
1 segment » a1 segment (Expandir a Pesquisa), m1 segment (Expandir a Pesquisa), 17 segment (Expandir a Pesquisa)
case dis » case disc (Expandir a Pesquisa), case di (Expandir a Pesquisa), case does (Expandir a Pesquisa)
i crest » i crestr (Expandir a Pesquisa), _ crest (Expandir a Pesquisa), a crest (Expandir a Pesquisa)
j genes » j gene (Expandir a Pesquisa), j genesca (Expandir a Pesquisa), vdj genes (Expandir a Pesquisa)
nerve a » nerve _ (Expandir a Pesquisa)
a diets » a dietas (Expandir a Pesquisa), a diet's (Expandir a Pesquisa), a dinets (Expandir a Pesquisa)
segment nerve » segmental nerve (Expandir a Pesquisa), augment nerve (Expandir a Pesquisa), segmental nerves (Expandir a Pesquisa)
crest drive » crest derived (Expandir a Pesquisa), forest drive (Expandir a Pesquisa), test drive (Expandir a Pesquisa)
genes nerve » genes serve (Expandir a Pesquisa), genes server (Expandir a Pesquisa), genes serves (Expandir a Pesquisa)
system dis » system dias (Expandir a Pesquisa), system dcs (Expandir a Pesquisa), system di (Expandir a Pesquisa)
1 segment » a1 segment (Expandir a Pesquisa), m1 segment (Expandir a Pesquisa), 17 segment (Expandir a Pesquisa)
case dis » case disc (Expandir a Pesquisa), case di (Expandir a Pesquisa), case does (Expandir a Pesquisa)
i crest » i crestr (Expandir a Pesquisa), _ crest (Expandir a Pesquisa), a crest (Expandir a Pesquisa)
j genes » j gene (Expandir a Pesquisa), j genesca (Expandir a Pesquisa), vdj genes (Expandir a Pesquisa)
nerve a » nerve _ (Expandir a Pesquisa)
a diets » a dietas (Expandir a Pesquisa), a diet's (Expandir a Pesquisa), a dinets (Expandir a Pesquisa)
1
Por Kahn, Benjamin M., Corman, Tanya S., Lovelace, Korah, Hong, Mingi, Krauss, Robert S., Epstein, Douglas J.
Publicado no Dis Model Mech (2017)
“...Septo-optic dysplasia (SOD) is a congenital disorder characterized by optic nerve, pituitary...”Publicado no Dis Model Mech (2017)
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2
Assuntos:
“...Case Report...”
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3
Por Weissenböck, Herbert, Bakonyi, Tamás, Sekulin, Karin, Ehrensperger, Felix, Doneley, Robert J.T., Dürrwald, Ralf, Hoop, Richard, Erdélyi, Károly, Gál, János, Kolodziejek, Jolanta, Nowotny, Norbert
Publicado em 2009
“... nerve system of the gastrointestinal tract provides strong evidence for a causative role of ABVs...”Publicado em 2009
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4
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)
“...%, including one patient with a FLNC mutation and two with mutations in the DES gene. In four index patients...”Publicado no Orphanet J Rare Dis (2014)
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5
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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6
Assuntos:
“...Case Report...”
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7
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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8
9
Por Shenoy, Anant M., Markowitz, Jennifer A., Bonnemann, Carsten G., Krishnamoorthy, Kalpathy, Bossler, Aaron D., Tseng, Brian S.
Publicado em 2010
“... in the alpha-dystroglycan complex. Of the 6 known related genes, testing of the POMGnT1 gene showed three...”Publicado em 2010
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10
“... transporters RFVT1 and RFVT3. A third riboflavin transporter (RFVT2) is expressed in the brain. In 2010...”
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11
Por Gonzalez-Rivas, Diego, Yang, Yang, Lei, Jiang, Hernandez, Luis, Jiang, Gening
Publicado no J Thorac Dis (2016)
“... the intercostal nerve damage created by the transthoracic incision has led to the creation of a novel procedure...”Publicado no J Thorac Dis (2016)
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12
Por Lenaers, Guy, Hamel, Christian, Delettre, Cécile, Amati-Bonneau, Patrizia, Procaccio, Vincent, Bonneau, Dominique, Reynier, Pascal, Milea, Dan
Publicado em 2012
“... and their axons. Molecular diagnosis is provided by the identification of a mutation in the OPA1 gene (75% of DOA...”Publicado em 2012
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13
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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14
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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15
“... in pathologically confirmed cases of PD. METHODS: Post-mortem skin biopsy samples from 11 individuals with PD, and 5...”
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16
Por Liaw, Hsiang-Ru, Lee, Hsiu-Fen, Chi, Ching-Shiang, Tsai, Chi-Ren
Publicado no Orphanet J Rare Dis (2015)
“... reviewed. The genetic features of such patients reported in Asian countries during a period of 20 years...”Publicado no Orphanet J Rare Dis (2015)
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17
“... young adults, predominantly males. Prevalence is estimated at 0.5–1.0/1,000. CH has a circannual...”
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18
“...Type I autosomal dominant cerebellar ataxia (ADCA) is a type of spinocerebellar ataxia (SCA...”
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19
“... examination revealed segmental atrophy and gliosis of the optic nerves bearing a resemblance to chronic...”
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20
Por Amelia Hana, Sarmin Sarmin, Claude Mona Airin, Christin Marganingsih Santosa, Pudji Astuti
Publicado em 2019-05-01
Assuntos:
“...fat diet...”Publicado em 2019-05-01
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