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M T Collins

Showing results (141-150 of 147) with videos related to

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JAMA|March 22, 1995
Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer diseaseG W Small, J C Mazziotta, M T Collins, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.
Journal of Dental Research|April 5, 2014
Rare bone diseases and their dental, oral, and craniofacial manifestationsB L Foster, M S Ramnitz, R I Gafni, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 26, 2000
Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of boneP Bianco, M Riminucci, A Majolagbe, et al.
Archives of Osteoporosis|March 1, 2017
Improving patient outcomes in fibrous dysplasia/McCune-Albright syndrome: an international multidisciplinary workshop to inform an international partnershipA M Boyce, A Turner, L Watts, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 8, 2016
Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatmentD Ovejero, Y H Lim, A M Boyce, et al.
Journal of Dental Research|December 16, 2017
Hypercementosis Associated with ENPP1 Mutations and GACIV Thumbigere-Math, A Alqadi, N I Chalmers, et al.
Pageof 15

Showing results (141-150 of 147) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 147 results.
JAMA|March 22, 1995
Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer diseaseG W Small, J C Mazziotta, M T Collins, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.
Journal of Dental Research|April 5, 2014
Rare bone diseases and their dental, oral, and craniofacial manifestationsB L Foster, M S Ramnitz, R I Gafni, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 26, 2000
Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of boneP Bianco, M Riminucci, A Majolagbe, et al.
Archives of Osteoporosis|March 1, 2017
Improving patient outcomes in fibrous dysplasia/McCune-Albright syndrome: an international multidisciplinary workshop to inform an international partnershipA M Boyce, A Turner, L Watts, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 8, 2016
Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatmentD Ovejero, Y H Lim, A M Boyce, et al.
Journal of Dental Research|December 16, 2017
Hypercementosis Associated with ENPP1 Mutations and GACIV Thumbigere-Math, A Alqadi, N I Chalmers, et al.
Pageof 15