Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Rocking improves sleep and memoryPerrault, Aurore ; Quairiaux, Charles ; Bayer, LaurenceM.S. Médecine sciences, 2019-08, Vol.35 (8-9), p.622-624 [Periódico revisado por pares]FranceTexto completo disponível |
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2 |
Material Type: Artigo
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Topical Corticosteroid Treatment of Dysphagia Due to Eosinophilic Esophagitis in AdultsArora, Amindra S. ; Perrault, Jean ; Smyrk, Thomas C.Mayo Clinic proceedings, 2003-07, Vol.78 (7), p.830-835 [Periódico revisado por pares]Rochester, MN: Elsevier IncTexto completo disponível |
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3 |
Material Type: Artigo
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A 10-year experience with intravenous thymoglobuline in induction of immunosuppression following heart transplantationCarrier, Michel ; White, Michel ; Perrault, Louis P ; Pelletier, Guy B ; Pellerin, Michel ; Robitaille, Danielle ; Pelletier, L.ConradThe Journal of heart and lung transplantation, 1999-12, Vol.18 (12), p.1218-1223 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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4 |
Material Type: Artigo
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Immunofluorescence revealed the presence of NHE-1 in the nuclear membranes of rat cardiomyocytes and isolated nuclei of human, rabbit, and rat aortic and liver tissuesBkaily, Ghassan ; Nader, Moni ; Avedanian, Levon ; Jacques, Danielle ; Perrault, Claudine ; Abdel-Samad, Dima ; D'Orléans-Juste, Pedro ; Gobeil, Fernand ; Hazzouri, Khaled MCanadian journal of physiology and pharmacology, 2004-08, Vol.82 (8-9), p.805-811 [Periódico revisado por pares]Ottawa, Canada: NRC Research PressTexto completo disponível |
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5 |
Material Type: Artigo
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Broadening the phenotype of the TWNK gene associated Perrault syndromeFekete, Bálint ; Pentelényi, Klára ; Rudas, Gabor ; Gál, Anikó ; Grosz, Zoltán ; Illés, Anett ; Idris, Jimoh ; Csukly, Gabor ; Domonkos, Andor ; Molnar, Maria JuditBMC medical genetics, 2019-12, Vol.20 (1), p.198-198, Article 198 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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6 |
Material Type: Artigo
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Nitric oxide inhalation in the treatment of primary graft failure following heart transplantationCarrier, Michel ; Blaise, Gilbert ; Bélisle, Sylvain ; Perrault, Louis P ; Pellerin, Michel ; Petitclerc, Robert ; Pelletier, L.ConradThe Journal of heart and lung transplantation, 1999-07, Vol.18 (7), p.664-667 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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7 |
Material Type: Artigo
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A homozygous missense variant in HSD17B4 identified in a consanguineous Chinese Han family with type II Perrault syndromeChen, Kui ; Yang, Ke ; Luo, Su-Shan ; Chen, Chen ; Wang, Ying ; Wang, Yi-Xuan ; Li, Da-Ke ; Yang, Yu-Jie ; Tang, Yi-Lin ; Liu, Feng-Tao ; Wang, Jian ; Wu, Jian-Jun ; Sun, Yi-MinBMC medical genetics, 2017-08, Vol.18 (1), p.91-91, Article 91 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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8 |
Material Type: Artigo
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Perrault Syndrome With Progressive Nervous System InvolvementKobe, Carsten ; Kracht, Lutz W ; Timmermann, Lars ; Bachmann, Juliane ; Schmidt, Matthias CClinical nuclear medicine, 2008-12, Vol.33 (12), p.922-924 [Periódico revisado por pares]United States: Lippincott Williams & Wilkins, IncTexto completo disponível |
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9 |
Material Type: Artigo
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Perrault syndrome: Report of four new cases, review and exclusion of candidate genesMarlin, Sandrine ; Lacombe, Didier ; Jonard, Laurence ; Leboulanger, Nicolas ; Bonneau, Dominique ; Goizet, Cyril ; Billette de Villemeur, Thierry ; Cabrol, Sylvie ; Houang, Muriel ; Moatti, Lucien ; Feldmann, Delphine ; Denoyelle, FrançoiseAmerican journal of medical genetics. Part A, 2008-03, Vol.146A (5), p.661-664 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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10 |
Material Type: Artigo
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Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered ProteaseJenkinson, Emma M. ; Rehman, Atteeq U. ; Walsh, Tom ; Clayton-Smith, Jill ; Lee, Kwanghyuk ; Morell, Robert J. ; Drummond, Meghan C. ; Khan, Shaheen N. ; Naeem, Muhammad Asif ; Rauf, Bushra ; Billington, Neil ; Schultz, Julie M. ; Urquhart, Jill E. ; Lee, Ming K. ; Berry, Andrew ; Hanley, Neil A. ; Mehta, Sarju ; Cilliers, Deirdre ; Clayton, Peter E. ; Kingston, Helen ; Smith, Miriam J. ; Warner, Thomas T. ; Black, Graeme C. ; Trump, Dorothy ; Davis, Julian R.E. ; Ahmad, Wasim ; Leal, Suzanne M. ; Riazuddin, Sheikh ; King, Mary-Claire ; Friedman, Thomas B. ; Newman, William G.American journal of human genetics, 2013-04, Vol.92 (4), p.605-613 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |