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American Journal of Medical Genetics. Part A
|
February 12, 2009
Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2
Eissa Faqeih, Peter Roughley, Francis H Glorieux, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 27, 2016
Diaphyseal Femur Fractures in Osteogenesis Imperfecta: Characteristics and Relationship With Bisphosphonate Treatment
Pamela Trejo, François Fassier, Francis H Glorieux, et al.
Bone
|
January 16, 2007
Long-bone changes after pamidronate discontinuation in children and adolescents with osteogenesis imperfecta
Frank Rauch, Sylvie Cornibert, Moira Cheung, et al.
European Journal of Human Genetics : EJHG
|
January 21, 2010
Genotype-phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I
Frank Rauch, Liljana Lalic, Peter Roughley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 26, 2009
Relationship between genotype and skeletal phenotype in children and adolescents with osteogenesis imperfecta
Frank Rauch, Liljana Lalic, Peter Roughley, et al.
Pediatrics
|
May 3, 2003
Height and weight development during four years of therapy with cyclical intravenous pamidronate in children and adolescents with osteogenesis imperfecta types I, III, and IV
Leonid Zeitlin, Frank Rauch, Horacio Plotkin, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 29, 2012
Abnormalities in muscle density and muscle function in hypophosphatemic rickets
Louis-Nicolas Veilleux, Moira Cheung, Mouna Ben Amor, et al.
Clinical Nurse Specialist CNS
|
April 7, 2020
Exploring the Perceived Self-management Needs of Young Adults With Osteogenesis Imperfecta
Alisha Michalovic, Charlotte Anderson, Kelly Thorstad, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2025
Tall Stature and Scoliosis Associated With a Novel Homozygous Loss-of-Function Missense Variant in NPR3
Pierre Moffatt, Chantal Janelle, Valancy Miranda, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2010
Wormian bones in osteogenesis imperfecta: Correlation to clinical findings and genotype
Oliver Semler, Moira S Cheung, Francis H Glorieux, et al.
Page
of 31
Search research articles
Search
Showing results (61-70 of 307) with videos related to
Sort By:
Page
of 31
American Journal of Medical Genetics. Part A
|
February 12, 2009
Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2
Eissa Faqeih, Peter Roughley, Francis H Glorieux, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 27, 2016
Diaphyseal Femur Fractures in Osteogenesis Imperfecta: Characteristics and Relationship With Bisphosphonate Treatment
Pamela Trejo, François Fassier, Francis H Glorieux, et al.
Bone
|
January 16, 2007
Long-bone changes after pamidronate discontinuation in children and adolescents with osteogenesis imperfecta
Frank Rauch, Sylvie Cornibert, Moira Cheung, et al.
European Journal of Human Genetics : EJHG
|
January 21, 2010
Genotype-phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I
Frank Rauch, Liljana Lalic, Peter Roughley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 26, 2009
Relationship between genotype and skeletal phenotype in children and adolescents with osteogenesis imperfecta
Frank Rauch, Liljana Lalic, Peter Roughley, et al.
Pediatrics
|
May 3, 2003
Height and weight development during four years of therapy with cyclical intravenous pamidronate in children and adolescents with osteogenesis imperfecta types I, III, and IV
Leonid Zeitlin, Frank Rauch, Horacio Plotkin, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 29, 2012
Abnormalities in muscle density and muscle function in hypophosphatemic rickets
Louis-Nicolas Veilleux, Moira Cheung, Mouna Ben Amor, et al.
Clinical Nurse Specialist CNS
|
April 7, 2020
Exploring the Perceived Self-management Needs of Young Adults With Osteogenesis Imperfecta
Alisha Michalovic, Charlotte Anderson, Kelly Thorstad, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2025
Tall Stature and Scoliosis Associated With a Novel Homozygous Loss-of-Function Missense Variant in NPR3
Pierre Moffatt, Chantal Janelle, Valancy Miranda, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2010
Wormian bones in osteogenesis imperfecta: Correlation to clinical findings and genotype
Oliver Semler, Moira S Cheung, Francis H Glorieux, et al.
Page
of 31