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1
A Novel Mutation of COL2A1 Resulting in Dominantly Inherited Rhegmatogenous Retinal Detachment
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Artigo
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A Novel Mutation of COL2A1 Resulting in Dominantly Inherited Rhegmatogenous Retinal Detachment

Richards, Allan J ; Meredith, Sarah ; Poulson, Arabella ; Bearcroft, Philip ; Crossland, Graeme ; Baguley, David M ; Scott, John D ; Snead, Martin P

Investigative ophthalmology & visual science, 2005-02, Vol.46 (2), p.663-668 [Periódico revisado por pares]

Rockville, MD: ARVO

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2
Clinical characterisation and molecular analysis of Wagner syndrome
Material Type:
Artigo
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Clinical characterisation and molecular analysis of Wagner syndrome

Meredith, Sarah P ; Richards, Allan J ; Flanagan, Declan W ; Scott, John D ; Poulson, Arabella V ; Snead, Martin P

British 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 Ltd

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3
Feasibility of a Novel Real-Time Provider Teaching Intervention in Acute Exacerbation of Chronic Obstructive Pulmonary Disease
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Artigo
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Feasibility of a Novel Real-Time Provider Teaching Intervention in Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Sonnick, Mark A ; Viavant, Maya ; Turetz, Meredith L ; Bean, Lorenzo D ; Jannat-Khah, Deanna ; Krishnan, Jamuna K ; Snead, Jessica ; Spinelli, Maria ; Wu, Xian ; Lee, Jennifer I

ATS scholar, 2022-03, Vol.3 (1), p.87-98 [Periódico revisado por pares]

United States: American Thoracic Society

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4
FEASIBILITY OF REAL-TIME COMBINED PATIENT AND PROVIDER TEACHING TO IMPROVE GUIDELINE-DIRECTED THERAPY IN COPD EXACERBATION
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Artigo
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FEASIBILITY OF REAL-TIME COMBINED PATIENT AND PROVIDER TEACHING TO IMPROVE GUIDELINE-DIRECTED THERAPY IN COPD EXACERBATION

Sonnick, Mark ; Viavant, Maya ; Bean, Lorenzo ; Wu, Xian ; Snead, Jessica ; Spinelli, Maria ; Krishnan, Jamuna ; Turetz, Meredith

Chest, 2020-10, Vol.158 (4), p.A1777-A1777 [Periódico revisado por pares]

Elsevier Inc

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5
Hereditary Vitreoretinopathies
Material Type:
Capítulo de Livro
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Hereditary Vitreoretinopathies

Nixon, Thomas ; Meredith, Sarah ; Snead, Martin

Reference Module in Neuroscience and Biobehavioral Psychology, 2017

Elsevier Inc

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6
Hereditary Vitreoretinopathies
Material Type:
Capítulo de Livro
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Hereditary Vitreoretinopathies

Meredith, S. ; Snead, M.

Encyclopedia of the Eye, 2010, Vol.2, p.233-243

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7
Missense and silent mutations in COL2A1 result in Stickler syndrome but via different molecular mechanisms
Material Type:
Artigo
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Missense and silent mutations in COL2A1 result in Stickler syndrome but via different molecular mechanisms

Richards, 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 Company

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8
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, Louisiana
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, Louisiana

Krause, Kari ; George, David R ; Coyle, Katy ; Snead, Meredith ; Athens, William P

2001

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9
Significant ocular findings are a feature of heritable bone dysplasias resulting from defects in type II collagen
Material Type:
Artigo
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Significant ocular findings are a feature of heritable bone dysplasias resulting from defects in type II collagen

Meredith, Sarah P ; Richards, Allan J ; Bearcroft, Philip ; Pouson, Arabella V ; Snead, Martin P

British 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 Ltd

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10
Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1
Material Type:
Artigo
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Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1

Richards, Allan J ; McNinch, Annie ; Martin, Howard ; Oakhill, Kim ; Rai, Harjeet ; Waller, Sarah ; Treacy, Becky ; Whittaker, Joanne ; Meredith, Sarah ; Poulson, Arabella ; Snead, Martin P

Human mutation, 2010-06, Vol.31 (6), p.E1461-E1471 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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