Search research articles
Contact Us
Filters
Showing results (51-60 of 79) with videos related to
Page
of 8
Sort By:
Acta Orthopaedica Belgica
|
October 18, 2007
Postradiation soft tissue sarcoma of the shoulder: a case report
Philippe Debeer, Bart Van de Meulebroucke, Jos Stuyck, et al.
Human Molecular Genetics
|
December 9, 2008
A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype
Sebastian Fantini, Giulia Vaccari, Nathalie Brison, et al.
Biomechanics and Modeling in Mechanobiology
|
June 17, 2025
Covariation between rotator cuff muscle quality and shoulder morphometric bony features in B-glenoids: a statistical modeling approach
Nazanin Daneshvarhashjin, Philippe Debeer, Harold Matthews, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 10, 2005
A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features
Hilde Van Esch, Anil K Agarwal, Philippe Debeer, et al.
Surgical and Radiologic Anatomy : SRA
|
June 10, 2011
A 3D-CT scan study of the humeral and glenoid planes in 150 normal shoulders
Lieven De Wilde, Saartje Defoort, Tom R G M Verstraeten, et al.
Journal of Shoulder and Elbow Surgery
|
February 17, 2019
Treatment of severe glenoid deficiencies in reverse shoulder arthroplasty: the Glenius Glenoid Reconstruction System experience
Philippe Debeer, Bart Berghs, Nicole Pouliart, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
July 4, 2012
In regard to: "In vivo strain analysis of the intact supraspinatus tendon by ultrasound speckles tracking imaging" (Journal of Orthopaedic Research, Vol. 29, No. 12, pp. 1931-1937, May 2011)
Pieter Slagmolen, Lennart Scheys, Jan D'Hooge, et al.
European Journal of Medical Genetics
|
February 25, 2006
Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion
Katherine Horsnell, Manir Ali, Saghira Malik, et al.
American Journal of Medical Genetics. Part A
|
March 1, 2005
Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutation
Philippe Debeer, Christel Huysmans, Wim J M Van de Ven, et al.
Human Molecular Genetics
|
March 1, 2012
An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning
Nathalie Brison, Philippe Debeer, Sebastian Fantini, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 79) with videos related to
Sort By:
Page
of 8
Acta Orthopaedica Belgica
|
October 18, 2007
Postradiation soft tissue sarcoma of the shoulder: a case report
Philippe Debeer, Bart Van de Meulebroucke, Jos Stuyck, et al.
Human Molecular Genetics
|
December 9, 2008
A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype
Sebastian Fantini, Giulia Vaccari, Nathalie Brison, et al.
Biomechanics and Modeling in Mechanobiology
|
June 17, 2025
Covariation between rotator cuff muscle quality and shoulder morphometric bony features in B-glenoids: a statistical modeling approach
Nazanin Daneshvarhashjin, Philippe Debeer, Harold Matthews, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 10, 2005
A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features
Hilde Van Esch, Anil K Agarwal, Philippe Debeer, et al.
Surgical and Radiologic Anatomy : SRA
|
June 10, 2011
A 3D-CT scan study of the humeral and glenoid planes in 150 normal shoulders
Lieven De Wilde, Saartje Defoort, Tom R G M Verstraeten, et al.
Journal of Shoulder and Elbow Surgery
|
February 17, 2019
Treatment of severe glenoid deficiencies in reverse shoulder arthroplasty: the Glenius Glenoid Reconstruction System experience
Philippe Debeer, Bart Berghs, Nicole Pouliart, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
July 4, 2012
In regard to: "In vivo strain analysis of the intact supraspinatus tendon by ultrasound speckles tracking imaging" (Journal of Orthopaedic Research, Vol. 29, No. 12, pp. 1931-1937, May 2011)
Pieter Slagmolen, Lennart Scheys, Jan D'Hooge, et al.
European Journal of Medical Genetics
|
February 25, 2006
Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion
Katherine Horsnell, Manir Ali, Saghira Malik, et al.
American Journal of Medical Genetics. Part A
|
March 1, 2005
Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutation
Philippe Debeer, Christel Huysmans, Wim J M Van de Ven, et al.
Human Molecular Genetics
|
March 1, 2012
An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning
Nathalie Brison, Philippe Debeer, Sebastian Fantini, et al.
Page
of 8