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Case Reports in Endocrinology
|
February 12, 2024
Case Presentation: Functional Assessment of a <i>CASR</i> Variant Identified in a Patient with Hypercalcaemia Confirms Familial Hypocalciuric Hypercalcaemia in the Patient and a Sister Previously Misdiagnosed with Primary Hyperparathyroidism
Bryan K Ward, Kirsten A Loffell, John P Walsh, et al.
Bone
|
May 12, 2009
Further genetic evidence suggesting a role for the RhoGTPase-RhoGEF pathway in osteoporosis
Ben H Mullin, Richard L Prince, Cyril Mamotte, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
November 3, 2009
A comparative study between corresponding structural geometric variables using 2 commonly implemented hip structural analysis algorithms applied to dual-energy X-ray absorptiometry images
Benjamin C C Khoo, Scott G Wilson, Graeme K Worth, et al.
Fertility and Sterility
|
February 6, 2008
Polymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome
Michelle R Jones, Scott G Wilson, Ben H Mullin, et al.
American Journal of Human Genetics
|
May 24, 2008
Identification of a role for the ARHGEF3 gene in postmenopausal osteoporosis
Ben H Mullin, Richard L Prince, Ian M Dick, et al.
Clinical Endocrinology
|
June 11, 2009
A cohort study of the effects of serum osteoprotegerin and osteoprotegerin gene polymorphisms on cardiovascular mortality in elderly women
Thor Ueland, Scott G Wilson, F M Amirul Islam, et al.
Journal of the Endocrine Society
|
March 31, 2022
Functional Assessment of Calcium-Sensing Receptor Variants Confirms Familial Hypocalciuric Hypercalcemia
Benjamin H Mullin, Nathan J Pavlos, Suzanne J Brown, et al.
Clinical Endocrinology
|
February 17, 2015
Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease
Purdey Campbell, Thomas H Brix, Scott G Wilson, et al.
Fertility and Sterility
|
October 31, 2006
Polymorphism in HSD17B6 is associated with key features of polycystic ovary syndrome
Michelle R Jones, Lisa Italiano, Scott G Wilson, et al.
BMC Medical Genetics
|
December 22, 2011
A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture
Jenny Z Wang, Mandeep S Deogan, Joshua R Lewis, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 90) with videos related to
Sort By:
Page
of 9
Case Reports in Endocrinology
|
February 12, 2024
Case Presentation: Functional Assessment of a <i>CASR</i> Variant Identified in a Patient with Hypercalcaemia Confirms Familial Hypocalciuric Hypercalcaemia in the Patient and a Sister Previously Misdiagnosed with Primary Hyperparathyroidism
Bryan K Ward, Kirsten A Loffell, John P Walsh, et al.
Bone
|
May 12, 2009
Further genetic evidence suggesting a role for the RhoGTPase-RhoGEF pathway in osteoporosis
Ben H Mullin, Richard L Prince, Cyril Mamotte, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
November 3, 2009
A comparative study between corresponding structural geometric variables using 2 commonly implemented hip structural analysis algorithms applied to dual-energy X-ray absorptiometry images
Benjamin C C Khoo, Scott G Wilson, Graeme K Worth, et al.
Fertility and Sterility
|
February 6, 2008
Polymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome
Michelle R Jones, Scott G Wilson, Ben H Mullin, et al.
American Journal of Human Genetics
|
May 24, 2008
Identification of a role for the ARHGEF3 gene in postmenopausal osteoporosis
Ben H Mullin, Richard L Prince, Ian M Dick, et al.
Clinical Endocrinology
|
June 11, 2009
A cohort study of the effects of serum osteoprotegerin and osteoprotegerin gene polymorphisms on cardiovascular mortality in elderly women
Thor Ueland, Scott G Wilson, F M Amirul Islam, et al.
Journal of the Endocrine Society
|
March 31, 2022
Functional Assessment of Calcium-Sensing Receptor Variants Confirms Familial Hypocalciuric Hypercalcemia
Benjamin H Mullin, Nathan J Pavlos, Suzanne J Brown, et al.
Clinical Endocrinology
|
February 17, 2015
Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease
Purdey Campbell, Thomas H Brix, Scott G Wilson, et al.
Fertility and Sterility
|
October 31, 2006
Polymorphism in HSD17B6 is associated with key features of polycystic ovary syndrome
Michelle R Jones, Lisa Italiano, Scott G Wilson, et al.
BMC Medical Genetics
|
December 22, 2011
A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture
Jenny Z Wang, Mandeep S Deogan, Joshua R Lewis, et al.
Page
of 9