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Nick Shaw

Showing results (41-50 of 50) with videos related to

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Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|April 30, 2008
Dual-energy X-ray aborptiometry assessment in children and adolescents with diseases that may affect the skeleton: the 2007 ISCD Pediatric Official PositionsNick Bishop, Pierre Braillon, Jon Burnham, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 2021
Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity SyndromesAfiya Andrews, Avinaash Maharaj, Emily Cottrell, et al.
Nutrients|July 2, 2021
A Three-Year Longitudinal Study Comparing Bone Mass, Density, and Geometry Measured by DXA, pQCT, and Bone Turnover Markers in Children with PKU Taking L-Amino Acid or Glycomacropeptide Protein SubstitutesAnne Daly, Wolfgang Högler, Nicola Crabtree, et al.
Human Molecular Genetics|March 2, 2010
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidismMichael R Bowl, Samantha M Mirczuk, Irina V Grigorieva, et al.
EMBO Molecular Medicine|March 14, 2023
Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stressAhmed El-Gazzar, Barbara Voraberger, Frank Rauch, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 24, 2022
Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic DysplasiaMadeline Louise Reilly, Noor Ul Ain, Mari Muurinen, et al.
Orphanet Journal of Rare Diseases|June 15, 2019
Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortiumMuhammad Kassim Javaid, Alison Boyce, Natasha Appelman-Dijkstra, et al.
Orphanet Journal of Rare Diseases|November 23, 2019
Correction to: Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortiumMuhammad Kassim Javaid, Alison Boyce, Natasha Appelman-Dijkstra, et al.
Hormone Research in Paediatrics|January 8, 2016
Global Consensus Recommendations on Prevention and Management of Nutritional RicketsCraig F Munns, Nick Shaw, Mairead Kiely, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2016
Global Consensus Recommendations on Prevention and Management of Nutritional RicketsCraig F Munns, Nick Shaw, Mairead Kiely, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|April 30, 2008
Dual-energy X-ray aborptiometry assessment in children and adolescents with diseases that may affect the skeleton: the 2007 ISCD Pediatric Official PositionsNick Bishop, Pierre Braillon, Jon Burnham, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 2021
Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity SyndromesAfiya Andrews, Avinaash Maharaj, Emily Cottrell, et al.
Nutrients|July 2, 2021
A Three-Year Longitudinal Study Comparing Bone Mass, Density, and Geometry Measured by DXA, pQCT, and Bone Turnover Markers in Children with PKU Taking L-Amino Acid or Glycomacropeptide Protein SubstitutesAnne Daly, Wolfgang Högler, Nicola Crabtree, et al.
Human Molecular Genetics|March 2, 2010
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidismMichael R Bowl, Samantha M Mirczuk, Irina V Grigorieva, et al.
EMBO Molecular Medicine|March 14, 2023
Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stressAhmed El-Gazzar, Barbara Voraberger, Frank Rauch, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 24, 2022
Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic DysplasiaMadeline Louise Reilly, Noor Ul Ain, Mari Muurinen, et al.
Orphanet Journal of Rare Diseases|June 15, 2019
Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortiumMuhammad Kassim Javaid, Alison Boyce, Natasha Appelman-Dijkstra, et al.
Orphanet Journal of Rare Diseases|November 23, 2019
Correction to: Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortiumMuhammad Kassim Javaid, Alison Boyce, Natasha Appelman-Dijkstra, et al.
Hormone Research in Paediatrics|January 8, 2016
Global Consensus Recommendations on Prevention and Management of Nutritional RicketsCraig F Munns, Nick Shaw, Mairead Kiely, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2016
Global Consensus Recommendations on Prevention and Management of Nutritional RicketsCraig F Munns, Nick Shaw, Mairead Kiely, et al.
Pageof 5