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Author/Creator Gottesman, Gary S

1. Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial. Issue 10189 (15th June 2019)

Authors:
Imel, Erik A; Glorieux, Francis H; Whyte, Michael P; Munns, Craig F; Ward, Leanne M; Nilsson, Ola; Simmons, Jill H; Padidela, Raja; Namba, Noriyuki; Cheong, Hae Il; Pitukcheewanont, Pisit; Sochett, Etienne; Högler, Wolfgang; Muroya, Koji; Tanaka, Hiroyuki; Gottesman, Gary S; Biggin, Andrew; Perwa...
Journal:
Lancet
Issue:
Volume 393:Issue 10189(2019)
Page Start:
2416
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. PHEX 3′‐UTR c.*231A>G Near The Polyadenylation Signal is a Relatively Common, Mild, American Mutation That Masquerades as Sporadic or X‐Linked Recessive Hypophosphatemic Rickets. (January 2015)

Authors:
Mumm, Steven; Huskey, Margaret; Cajic, Adela; Wollberg, Valerie; Zhang, Fan; Madson, Katherine L; Wenkert, Deborah; McAlister, William H; Gottesman, Gary S; Whyte, Michael P
Journal:
Journal of bone and mineral research
Issue:
Volume 30:Number 1(2015:Jan.)
Page Start:
137
Record Type:
Journal Article
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4. Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy1. (15th January 2013)

Authors:
Otero, Jesse E; Gottesman, Gary S; McAlister, William H; Mumm, Steven; Madson, Katherine L; Kiffer‐Moreira, Tina; Sheen, Campbell; Millán, José Luis; Ericson, Karen L; Whyte, Michael P
Journal:
Journal of bone and mineral research
Issue:
Volume 28:Number 2(2013:Feb.)
Page Start:
419
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy1. (15th January 2013)

Authors:
Otero, Jesse E; Gottesman, Gary S; McAlister, William H; Mumm, Steven; Madson, Katherine L; Kiffer‐Moreira, Tina; Sheen, Campbell; Millán, José Luis; Ericson, Karen L; Whyte, Michael P
Journal:
Journal of bone and mineral research
Issue:
Volume 28:Number 2(2013:Feb.)
Page Start:
419
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1, 25‐Dihydroxyvitamin D‐Mediated Hypercalcemia and Generalized Osteosclerosis. (30th July 2018)

Authors:
Whyte, Michael P; Lim, Emilina; McAlister, William H; Gottesman, Gary S; Trinh, Lien; Veis, Deborah J; Bijanki, Vinieth N; Boden, Matthew G; Nenninger, Angela; Mumm, Steven; Buchbinder, David
Journal:
Journal of bone and mineral research
Issue:
Volume 33:Number 11(2018)
Page Start:
2071
Record Type:
Journal Article
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7. X‐Linked Hypophosphatemia Caused by the Prevailing North American PHEX Variant c.*231A>G; Exon 13–15 Duplication Is Often Misdiagnosed as Ankylosing Spondylitis and Manifests in Both Men and Women. (2nd November 2022)

Authors:
Dahir, Kathryn McCrystal; Black, Margo; Gottesman, Gary S; Imel, Erik A; Mumm, Steven; Nichols, Cindy M; Whyte, Michael P
Journal:
JBMR plus
Issue:
Volume 6:Number 12(2022)
Page Start:
n/a
Record Type:
Journal Article
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8. X‐Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3′‐UTR Mutation c.*231A>G (A Retrospective Case–Control Study). (10th March 2020)

Authors:
Smith, Pamela S; Gottesman, Gary S; Zhang, Fan; Cook, Fiona; Ramirez, Beatriz; Wenkert, Deborah; Wollberg, Valerie; Huskey, Margaret; Mumm, Steven; Whyte, Michael P
Journal:
Journal of bone and mineral research
Issue:
Volume 35:Number 5(2020)
Page Start:
920
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗