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Philip Bearcroft

Showing results (1-10 of 7) with videos related to

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Seminars in Musculoskeletal Radiology|May 21, 2010
Compartment syndromesScott McDonald, Philip Bearcroft
AJR. American Journal of Roentgenology|April 28, 2005
16-MDCT in the detection of occult wrist fractures: a comparison with skeletal scintigraphyAshley M Groves, Heok Cheow, Kottekkattu Balan, et al.
The British Journal of Ophthalmology|March 10, 2007
Significant ocular findings are a feature of heritable bone dysplasias resulting from defects in type II collagenSarah P Meredith, Allan J Richards, Philip Bearcroft, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
A novel mutation of COL2A1 resulting in dominantly inherited rhegmatogenous retinal detachmentAllan J Richards, Sarah Meredith, Arabella Poulson, et al.
Medicine|January 5, 2011
Osseous manifestations of adult Gaucher disease in the era of enzyme replacement therapyPatrick B Deegan, Elena Pavlova, Jane Tindall, et al.
Human Mutation|June 6, 2006
High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1Allan J Richards, Maureen Laidlaw, Joanne Whittaker, et al.
Archives of Disease in Childhood|March 7, 2023
Legg-Calve-Perthes' disease: an opportunity to prevent blindness?Aijing Wang, Thomas Nixon, Howard Martin, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Seminars in Musculoskeletal Radiology|May 21, 2010
Compartment syndromesScott McDonald, Philip Bearcroft
AJR. American Journal of Roentgenology|April 28, 2005
16-MDCT in the detection of occult wrist fractures: a comparison with skeletal scintigraphyAshley M Groves, Heok Cheow, Kottekkattu Balan, et al.
The British Journal of Ophthalmology|March 10, 2007
Significant ocular findings are a feature of heritable bone dysplasias resulting from defects in type II collagenSarah P Meredith, Allan J Richards, Philip Bearcroft, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
A novel mutation of COL2A1 resulting in dominantly inherited rhegmatogenous retinal detachmentAllan J Richards, Sarah Meredith, Arabella Poulson, et al.
Medicine|January 5, 2011
Osseous manifestations of adult Gaucher disease in the era of enzyme replacement therapyPatrick B Deegan, Elena Pavlova, Jane Tindall, et al.
Human Mutation|June 6, 2006
High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1Allan J Richards, Maureen Laidlaw, Joanne Whittaker, et al.
Archives of Disease in Childhood|March 7, 2023
Legg-Calve-Perthes' disease: an opportunity to prevent blindness?Aijing Wang, Thomas Nixon, Howard Martin, et al.
Pageof 1