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Nicholas J Shaw

Showing results (11-20 of 22) with videos related to

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Archives of Disease in Childhood|August 24, 2012
Successful public health action to reduce the incidence of symptomatic vitamin D deficiencyRobert John Moy, Eleanor McGee, Geoff D Debelle, et al.
The Journal of Pediatrics|February 21, 2016
A Diagnostic Algorithm for Children with Low Alkaline Phosphatase Activities: Lessons Learned from Laboratory Screening for HypophosphatasiaVrinda Saraff, Vidya K Narayanan, Alexander J Lawson, et al.
European Journal of Endocrinology|March 10, 2021
Clinical characteristics and treatment requirements of children with autosomal recessive pseudohypoaldosteronismMeena Bandhakavi, Amy Wanaguru, Loveline Ayuk, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 18, 2015
Reply: Response to: Rapid Skeletal Turnover in a Radiographic Mimic of Osteopetrosis Might Be Secondary to Systemic MastocytosisMichael P Whyte, Katherine L Madson, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 16, 2015
Response to: A rapid skeletal turnover in radiographic mimic of osteopetrosis might be secondary to systemic mastocytosisMichael P Whyte, Katherine L Madson, William H McAlister, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 12, 2013
Clinical characteristics and management of cranial diabetes insipidus in infantsAmbika Karthikeyan, Noina Abid, Prem C B Sundaram, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 13, 2014
Rapid skeletal turnover in a radiographic mimic of osteopetrosisMichael P Whyte, Katherine L Madson, Steven Mumm, et al.
Human Molecular Genetics|August 10, 2012
Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosisPhilippe M Campeau, James T Lu, Gautam Sule, et al.
The Journal of Clinical Investigation|February 21, 2018
CYP3A4 mutation causes vitamin D-dependent rickets type 3Jeffrey D Roizen, Dong Li, Lauren O'Lear, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 5, 2016
Amalgamated Reference Data for Size-Adjusted Bone Densitometry Measurements in 3598 Children and Young Adults-the ALPHABET StudyNicola J Crabtree, Nicholas J Shaw, Nicholas J Bishop, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Archives of Disease in Childhood|August 24, 2012
Successful public health action to reduce the incidence of symptomatic vitamin D deficiencyRobert John Moy, Eleanor McGee, Geoff D Debelle, et al.
The Journal of Pediatrics|February 21, 2016
A Diagnostic Algorithm for Children with Low Alkaline Phosphatase Activities: Lessons Learned from Laboratory Screening for HypophosphatasiaVrinda Saraff, Vidya K Narayanan, Alexander J Lawson, et al.
European Journal of Endocrinology|March 10, 2021
Clinical characteristics and treatment requirements of children with autosomal recessive pseudohypoaldosteronismMeena Bandhakavi, Amy Wanaguru, Loveline Ayuk, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 18, 2015
Reply: Response to: Rapid Skeletal Turnover in a Radiographic Mimic of Osteopetrosis Might Be Secondary to Systemic MastocytosisMichael P Whyte, Katherine L Madson, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 16, 2015
Response to: A rapid skeletal turnover in radiographic mimic of osteopetrosis might be secondary to systemic mastocytosisMichael P Whyte, Katherine L Madson, William H McAlister, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 12, 2013
Clinical characteristics and management of cranial diabetes insipidus in infantsAmbika Karthikeyan, Noina Abid, Prem C B Sundaram, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 13, 2014
Rapid skeletal turnover in a radiographic mimic of osteopetrosisMichael P Whyte, Katherine L Madson, Steven Mumm, et al.
Human Molecular Genetics|August 10, 2012
Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosisPhilippe M Campeau, James T Lu, Gautam Sule, et al.
The Journal of Clinical Investigation|February 21, 2018
CYP3A4 mutation causes vitamin D-dependent rickets type 3Jeffrey D Roizen, Dong Li, Lauren O'Lear, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 5, 2016
Amalgamated Reference Data for Size-Adjusted Bone Densitometry Measurements in 3598 Children and Young Adults-the ALPHABET StudyNicola J Crabtree, Nicholas J Shaw, Nicholas J Bishop, et al.
Pageof 3