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The Medical Journal of Australia
|
October 22, 2013
Primary amenorrhoea with hypertension: undiagnosed 17-α-hydroxylase deficiency
Fiona L Britten, Kimberly B Ulett, Emma L Duncan, et al.
The Lancet. Child & Adolescent Health
|
December 18, 2021
Long COVID in children - Authors' reply
Erika Molteni, Sunil S Bhopal, Robert C Hughes, et al.
Pharmacoepidemiology and Drug Safety
|
September 2, 2014
Osteoporosis medication dispensing for older Australian women from 2002 to 2010: influences of publications, guidelines, marketing activities and policy
Geeske Peeters, Susan E Tett, Emma L Duncan, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
May 13, 2021
A woman with visual loss, amenorrhoea and polyuria: the first reported case of nodular lymphocyte-predominant Hodgkin lymphoma presenting with hypopituitarism
Matthew Seymour, Thomas Robertson, Jason Papacostas, et al.
Rheumatology (Oxford, England)
|
August 14, 2025
Identification of a novel TGFB1 variant in a patient with Camurati-Engelmann disease responsive to alendronate
Neelam Hassan, Celia L Gregson, Michael Oldridge, et al.
Pediatric Diabetes
|
April 11, 2018
A novel INS mutation in a family with maturity-onset diabetes of the young: Variable insulin secretion and putative mechanisms
Stephanie R Johnson, Ivan McGown, Udo Oppermann, et al.
Nutrients
|
April 12, 2022
Is Secretory Activation Delayed in Women with Type Two Diabetes? A Pilot Study
Fiona L Britten, Ching T Lai, Donna T Geddes, et al.
Experimental Gerontology
|
February 13, 2003
A novel putative collaborator of p19ARF
Renu Wadhwa, Takashi Sugihara, Md Kamrul Hasan, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 22, 2003
Site and gender specificity of inheritance of bone mineral density
Emma L Duncan, Lon R Cardon, Janet S Sinsheimer, et al.
Journal of Diabetes
|
May 5, 2018
Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): A novel ABCC8 mutation in a previously screened family
Stephanie R Johnson, Paul Leo, Louise S Conwell, et al.
Page
of 16
Search research articles
Search
Showing results (21-30 of 156) with videos related to
Sort By:
Page
of 16
The Medical Journal of Australia
|
October 22, 2013
Primary amenorrhoea with hypertension: undiagnosed 17-α-hydroxylase deficiency
Fiona L Britten, Kimberly B Ulett, Emma L Duncan, et al.
The Lancet. Child & Adolescent Health
|
December 18, 2021
Long COVID in children - Authors' reply
Erika Molteni, Sunil S Bhopal, Robert C Hughes, et al.
Pharmacoepidemiology and Drug Safety
|
September 2, 2014
Osteoporosis medication dispensing for older Australian women from 2002 to 2010: influences of publications, guidelines, marketing activities and policy
Geeske Peeters, Susan E Tett, Emma L Duncan, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
May 13, 2021
A woman with visual loss, amenorrhoea and polyuria: the first reported case of nodular lymphocyte-predominant Hodgkin lymphoma presenting with hypopituitarism
Matthew Seymour, Thomas Robertson, Jason Papacostas, et al.
Rheumatology (Oxford, England)
|
August 14, 2025
Identification of a novel TGFB1 variant in a patient with Camurati-Engelmann disease responsive to alendronate
Neelam Hassan, Celia L Gregson, Michael Oldridge, et al.
Pediatric Diabetes
|
April 11, 2018
A novel INS mutation in a family with maturity-onset diabetes of the young: Variable insulin secretion and putative mechanisms
Stephanie R Johnson, Ivan McGown, Udo Oppermann, et al.
Nutrients
|
April 12, 2022
Is Secretory Activation Delayed in Women with Type Two Diabetes? A Pilot Study
Fiona L Britten, Ching T Lai, Donna T Geddes, et al.
Experimental Gerontology
|
February 13, 2003
A novel putative collaborator of p19ARF
Renu Wadhwa, Takashi Sugihara, Md Kamrul Hasan, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 22, 2003
Site and gender specificity of inheritance of bone mineral density
Emma L Duncan, Lon R Cardon, Janet S Sinsheimer, et al.
Journal of Diabetes
|
May 5, 2018
Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): A novel ABCC8 mutation in a previously screened family
Stephanie R Johnson, Paul Leo, Louise S Conwell, et al.
Page
of 16