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Bone
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November 28, 2017
Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5)
Ghada A Otaify, Michael P Whyte, Gary S Gottesman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 9, 2022
Effect of Burosumab Compared With Conventional Therapy on Younger vs Older Children With X-linked Hypophosphatemia
Leanne M Ward, Francis H Glorieux, Michael P Whyte, et al.
Bone
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April 25, 2017
Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS
Michael P Whyte, Malachi Griffith, Lee Trani, et al.
American Journal of Human Genetics
|
December 31, 2005
Epimerase-deficiency galactosemia is not a binary condition
Kimberly K Openo, Jenny M Schulz, Claudia A Vargas, et al.
JBMR Plus
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May 1, 2024
Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period
Leanne M Ward, Wolfgang Högler, Francis H Glorieux, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 21, 2023
Burosumab vs Phosphate/Active Vitamin D in Pediatric X-Linked Hypophosphatemia: A Subgroup Analysis by Dose Level
Erik A Imel, Francis H Glorieux, Michael P Whyte, et al.
Calcified Tissue International
|
January 23, 2021
Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia
Raja Padidela, Michael P Whyte, Francis H Glorieux, et al.
Lancet (London, England)
|
May 21, 2019
Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial
Erik A Imel, Francis H Glorieux, Michael P Whyte, et al.
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of 17
Search research articles
Search
Showing results (161-170 of 168) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 168 results.
Bone
|
November 28, 2017
Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5)
Ghada A Otaify, Michael P Whyte, Gary S Gottesman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 9, 2022
Effect of Burosumab Compared With Conventional Therapy on Younger vs Older Children With X-linked Hypophosphatemia
Leanne M Ward, Francis H Glorieux, Michael P Whyte, et al.
Bone
|
April 25, 2017
Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS
Michael P Whyte, Malachi Griffith, Lee Trani, et al.
American Journal of Human Genetics
|
December 31, 2005
Epimerase-deficiency galactosemia is not a binary condition
Kimberly K Openo, Jenny M Schulz, Claudia A Vargas, et al.
JBMR Plus
|
May 1, 2024
Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period
Leanne M Ward, Wolfgang Högler, Francis H Glorieux, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 21, 2023
Burosumab vs Phosphate/Active Vitamin D in Pediatric X-Linked Hypophosphatemia: A Subgroup Analysis by Dose Level
Erik A Imel, Francis H Glorieux, Michael P Whyte, et al.
Calcified Tissue International
|
January 23, 2021
Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia
Raja Padidela, Michael P Whyte, Francis H Glorieux, et al.
Lancet (London, England)
|
May 21, 2019
Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial
Erik A Imel, Francis H Glorieux, Michael P Whyte, et al.
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of 17