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Medicine
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January 5, 2019
The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational study
Ali Al Kaissi, Sergey Ryabykh, Olga M Pavlova, et al.
Medicine
|
December 16, 2016
Spine malformation complex in 3 diverse syndromic entities: Case reports
Ali Al Kaissi, Andreas van Egmond-Fröhlich, Sergey Ryabykh, et al.
Calcified Tissue International
|
May 18, 2021
Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus Syndrome
Ali Al Kaissi, Barbara M Misof, Franco Laccone, et al.
Medicine
|
September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports
Ali Al Kaissi, Christian Windpassinger, Farid Ben Chehida, et al.
Bone
|
October 14, 2018
Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease
Mohammad Shboul, Paul Roschger, Rudolf Ganger, et al.
Human Mutation
|
September 8, 2016
Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) Deficiency Results in a Mild Skeletal Dysplasia and Joint Laxity
Julia Vodopiutz, Shuji Mizumoto, Ekkehart Lausch, et al.
American Journal of Human Genetics
|
September 9, 2017
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays
Christian Windpassinger, Juliette Piard, Carine Bonnard, et al.
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Search research articles
Search
Showing results (101-110 of 107) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 107 results.
Medicine
|
January 5, 2019
The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational study
Ali Al Kaissi, Sergey Ryabykh, Olga M Pavlova, et al.
Medicine
|
December 16, 2016
Spine malformation complex in 3 diverse syndromic entities: Case reports
Ali Al Kaissi, Andreas van Egmond-Fröhlich, Sergey Ryabykh, et al.
Calcified Tissue International
|
May 18, 2021
Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus Syndrome
Ali Al Kaissi, Barbara M Misof, Franco Laccone, et al.
Medicine
|
September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports
Ali Al Kaissi, Christian Windpassinger, Farid Ben Chehida, et al.
Bone
|
October 14, 2018
Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease
Mohammad Shboul, Paul Roschger, Rudolf Ganger, et al.
Human Mutation
|
September 8, 2016
Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) Deficiency Results in a Mild Skeletal Dysplasia and Joint Laxity
Julia Vodopiutz, Shuji Mizumoto, Ekkehart Lausch, et al.
American Journal of Human Genetics
|
September 9, 2017
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays
Christian Windpassinger, Juliette Piard, Carine Bonnard, et al.
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of 11