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Rudolf Ganger

Showing results (101-110 of 107) with videos related to

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Medicine|January 5, 2019
The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational studyAli Al Kaissi, Sergey Ryabykh, Olga M Pavlova, et al.
Medicine|December 16, 2016
Spine malformation complex in 3 diverse syndromic entities: Case reportsAli 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 SyndromeAli Al Kaissi, Barbara M Misof, Franco Laccone, et al.
Medicine|September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reportsAli 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 diseaseMohammad 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 LaxityJulia 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 DelaysChristian Windpassinger, Juliette Piard, Carine Bonnard, et al.
Pageof 11

Showing results (101-110 of 107) with videos related to

Sort By:
Pageof 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 studyAli Al Kaissi, Sergey Ryabykh, Olga M Pavlova, et al.
Medicine|December 16, 2016
Spine malformation complex in 3 diverse syndromic entities: Case reportsAli 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 SyndromeAli Al Kaissi, Barbara M Misof, Franco Laccone, et al.
Medicine|September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reportsAli 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 diseaseMohammad 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 LaxityJulia 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 DelaysChristian Windpassinger, Juliette Piard, Carine Bonnard, et al.
Pageof 11