Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Suely Marie"'
Autor:
Gustavo Alencastro Veiga Cruzeiro, Karina Bezerra Salomão, Carlos Alberto Oliveira de Biagi Jr, Martin Baumgartner, Dominik Sturm, Régia Caroline Peixoto Lira, Taciani de Almeida Magalhães, Mirella Baroni Milan, Vanessa da Silva Silveira, Fabiano Pinto Saggioro, Ricardo Santos de Oliveira, Paulo Henrique dos Santos Klinger, Ana Luiza Seidinger, José Andrés Yunes, Rosane Gomes de Paula Queiroz, Sueli Mieko Oba-Shinjo, Carlos Alberto Scrideli, Suely Marie Kazue Nagahashi, Luiz Gonzaga Tone, Elvis Terci Valera
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-10 (2019)
Abstract Next-generation sequencing platforms are routinely used for molecular assignment due to their high impact for risk stratification and prognosis in medulloblastomas. Yet, low and middle-income countries still lack an accurate cost-effective p
Externí odkaz:
https://doaj.org/article/ac6cfc7ec6ce483ebbb41923ea82f3dc
Autor:
Dipika Mohan, Kleiton Borges, Isabella Finco, Christopher LaPensee, Juilee Rege, Donald Little, Tobias Else, Madson Almeida, Ana Claudia Latronico, Berenice Mendonca, Richard Auchus, William Rainey, Suely Marie, Thomas Giordano, Sriram Venneti, Maria Candida Fragoso, David Breault, Antonio Lerario, Gary Hammer
Publikováno v:
Journal of the Endocrine Society. 6:A136-A136
Adrenocortical carcinoma (ACC) is a rare, aggressive, and poorly understood cancer of the adrenal cortex. Abnormal epigenetic patterning is a major predictor of dismal disease outcomes. Patients with genome-wide CpG island hypermethylation (CIMP-high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06232ef3330e4819c469c417acbeef67
https://doi.org/10.1210/jendso/bvac150.277
https://doi.org/10.1210/jendso/bvac150.277
Autor:
Silvana Angelina D'Orio Nishioka, Martino Martinelli Filho, Suely Marie, Mayana Zatz, Roberto Costa
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 84, Iss 4, Pp 330-336 (2005)
OBJETIVO: Estudar a prevalência e a evolução natural dos eventos arrítmicos e distúrbios da condução, correlacionar o defeito genético com achados cardiovasculares, avaliar a mortalidade cardíaca, freqüência e fatores preditivos de morte s
Externí odkaz:
https://doaj.org/article/3998ea665941464d93ae193a84b3f823
Autor:
Ricardo Santos de Oliveira, Elvis Terci Valera, Luiz Gonzaga Tone, Carlos Alberto Oliveira de Biagi, Rosane Gomes de Paula Queiroz, Régia Caroline Peixoto Lira, Carlos Alberto Scrideli, Martin Baumgartner, Paulo Henrique dos Santos Klinger, Suely Marie Kazue Nagahashi, Taciani de Almeida Magalhães, Ana Luiza Seidinger, Mirella Baroni Milan, Fabiano Pinto Saggioro, Sueli Mieko Oba-Shinjo, José Andrés Yunes, Dominik Sturm, Karina Bezerra Salomão, Gustavo Alencastro Veiga Cruzeiro, Vanessa da Silva Silveira
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-10 (2019)
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-10 (2019)
Next-generation sequencing platforms are routinely used for molecular assignment due to their high impact for risk stratification and prognosis in medulloblastomas. Yet, low and middle-income countries still lack an accurate cost-effective platform t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af891644884e1a4b3e714ddf18bdad9a
https://doi.org/10.5167/uzh-182360
https://doi.org/10.5167/uzh-182360
Akademický článek
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Autor:
Suely Marie
Evaluation of cerebrospinal fluid is of essential importance in the diagnosis of central nervous system infections, with a major role in the diagnosis of meningitis and encephalitis. In bacterial and viral meningitis, CSF evaluation is usually straig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da6327834f9f4a22a6fadee020f1f21b
https://doi.org/10.1093/med/9780199937837.003.0145
https://doi.org/10.1093/med/9780199937837.003.0145
Autor:
Caroline Sewry, Lucy R. Wedderburn, Frances Hall, Sisa Grubnic, Susan C. Charman, Brenda Banwell, Alexandra M. Higton, Tilly Ratnaike, Eleni Sidiropoulou, Anthony A. Amato, Robert Busch, Felix Chua, Thomas S. Jacques, Ingrid E. Lundberg, Nicola Maguire, Carlo Minetti, Clive Kelly, Loukas Settas, Nicholas Hughes, Nada Hassan, Hemlata Varsani, Nazar Alsanjari, Janice L. Holton, Matthew Rogers, Vasiliki Tsavdaridou, Philippa A. Watson, Andrea M. Corse, Nagui Gendi, Inger Nenesmo, Susan Pugmire, Elisabeth J. Rushing, Patrick D W Kiely, Timothy Ho, M Field, Kevin E. Bove, Zoe McKinstry, Katrina McNulty, Clarissa Pilkington, Elizabeth J. Edwards, Brian Fang, Vadivelu Saravanan, Eleanor Murray, David A. Isenberg, Ana Campar, Andreas V. Hadjinicolaou, Ioannides Vlahos, Theodoros Dimitroulas, Martin Edward Perry, Suely Marie, Carolyn Lavelle, Alison Emslie-Smith, David Paton, Mark Lloyd
Publikováno v:
Rheumatology. 49:i115-i119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::939d0203a989e4d25c2d6821d65628e1
https://doi.org/10.1093/rheumatology/keq727
https://doi.org/10.1093/rheumatology/keq727
Publikováno v:
DIGITUM. Depósito Digital Institucional de la Universidad de Murcia
instname
ResearcherID
instname
ResearcherID
Pediatric normal brachial biceps (14 specimens) and quadriceps muscles (14 specimens) were studied by immunohistochemistry to quantify fiber-type, diameter and distribution, capillary density, presence of inflammatory cells (CD3, CD20, CD68) and expr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::383a1e37bee8a33292d80810195cebcd
http://hdl.handle.net/10201/57134
http://hdl.handle.net/10201/57134
Publikováno v:
Arquivos de Neuro-Psiquiatria, Volume: 63, Issue: 3b, Pages: 791-800, Published: SEP 2005
Arquivos de Neuro-Psiquiatria v.63 n.3b 2005
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
ResearcherID
Arquivos de Neuro-Psiquiatria v.63 n.3b 2005
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
ResearcherID
The congenital muscular dystrophies (CMD) are heterogeneous muscular diseases with early and dystrophic pattern on muscle biopsy. Many different subtypes have been genetically identified and most phenotypes not yet identified belong to the merosin-po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::25403ba8f7f73df99ce335127e75f8d7
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2005000500014&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2005000500014&lng=en&tlng=en
Autor:
Silvana Angelina D'Orio, Nishioka, Martino, Martinelli Filho, Suely, Marie, Mayana, Zatz, Roberto, Costa
Publikováno v:
Arquivos brasileiros de cardiologia. 84(4)
To study the prevalence and natural evolution of arrhythmic events and conduction disturbances in myotonic dystrophy; to correlate the genetic defect with cardiovascular findings; to assess cardiac mortality, frequency, and predictive factors of sudd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc370d9ef55f2b8d294d18ec68765d24
https://pubmed.ncbi.nlm.nih.gov/15880208
https://pubmed.ncbi.nlm.nih.gov/15880208