Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Report
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Phase I Cultural Resources Survey and Archeological Inventory of the 4.94 HA (12.21 AC) Keystone Lock and Dam Project Parcel, St. Martin Parish, LouisianaKrause, Kari ; George, David R ; Coyle, Katy ; Snead, Meredith ; Athens, William P2001Texto completo disponível |
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2 |
Material Type: Artigo
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Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1Richards, Allan J ; McNinch, Annie ; Martin, Howard ; Oakhill, Kim ; Rai, Harjeet ; Waller, Sarah ; Treacy, Becky ; Whittaker, Joanne ; Meredith, Sarah ; Poulson, Arabella ; Snead, Martin PHuman mutation, 2010-06, Vol.31 (6), p.E1461-E1471 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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3 |
Material Type: Artigo
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FEASIBILITY OF REAL-TIME COMBINED PATIENT AND PROVIDER TEACHING TO IMPROVE GUIDELINE-DIRECTED THERAPY IN COPD EXACERBATIONSonnick, Mark ; Viavant, Maya ; Bean, Lorenzo ; Wu, Xian ; Snead, Jessica ; Spinelli, Maria ; Krishnan, Jamuna ; Turetz, MeredithChest, 2020-10, Vol.158 (4), p.A1777-A1777 [Periódico revisado por pares]Elsevier IncTexto completo disponível |
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4 |
Material Type: Artigo
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Clinical characterisation and molecular analysis of Wagner syndromeMeredith, Sarah P ; Richards, Allan J ; Flanagan, Declan W ; Scott, John D ; Poulson, Arabella V ; Snead, Martin PBritish journal of ophthalmology, 2007-05, Vol.91 (5), p.655-659 [Periódico revisado por pares]BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group LtdTexto completo disponível |
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5 |
Material Type: Artigo
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Significant ocular findings are a feature of heritable bone dysplasias resulting from defects in type II collagenMeredith, Sarah P ; Richards, Allan J ; Bearcroft, Philip ; Pouson, Arabella V ; Snead, Martin PBritish journal of ophthalmology, 2007-09, Vol.91 (9), p.1148-1151 [Periódico revisado por pares]BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group LtdTexto completo disponível |
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6 |
Material Type: Artigo
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A Novel Mutation of COL2A1 Resulting in Dominantly Inherited Rhegmatogenous Retinal DetachmentRichards, Allan J ; Meredith, Sarah ; Poulson, Arabella ; Bearcroft, Philip ; Crossland, Graeme ; Baguley, David M ; Scott, John D ; Snead, Martin PInvestigative ophthalmology & visual science, 2005-02, Vol.46 (2), p.663-668 [Periódico revisado por pares]Rockville, MD: ARVOTexto completo disponível |
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7 |
Material Type: Artigo
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Missense and silent mutations in COL2A1 result in Stickler syndrome but via different molecular mechanismsRichards, Allan J. ; Laidlaw, Maureen ; Meredith, Sarah P. ; Shankar, Pallavi ; Poulson, Arabella V. ; Scott, John D. ; Snead, Martin P.Human mutation, 2007-06, Vol.28 (6), p.639-639 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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8 |
Material Type: Artigo
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Feasibility of a Novel Real-Time Provider Teaching Intervention in Acute Exacerbation of Chronic Obstructive Pulmonary DiseaseSonnick, Mark A ; Viavant, Maya ; Turetz, Meredith L ; Bean, Lorenzo D ; Jannat-Khah, Deanna ; Krishnan, Jamuna K ; Snead, Jessica ; Spinelli, Maria ; Wu, Xian ; Lee, Jennifer IATS scholar, 2022-03, Vol.3 (1), p.87-98 [Periódico revisado por pares]United States: American Thoracic SocietyTexto completo disponível |
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9 |
Material Type: Artigo
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Vitreous phenotype: A key diagnostic sign in Stickler syndrome types 1 and 2 complicated by double heterozygosityAng, Alan ; Ung, Tsiang ; Puvanachandra, Narman ; Wilson, Louise ; Howard, Frances ; Ryalls, Michael ; Richards, Allan ; Meredith, Sarah ; Laidlaw, Maureen ; Poulson, Arabella ; Scott, John ; Snead, MartinAmerican journal of medical genetics. Part A, 2007-03, Vol.143A (6), p.604-607 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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10 |
Material Type: Capítulo de Livro
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Hereditary VitreoretinopathiesNixon, Thomas ; Meredith, Sarah ; Snead, MartinReference Module in Neuroscience and Biobehavioral Psychology, 2017Elsevier IncTexto completo disponível |