Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Janani Devaraja"'
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
An 11-year-old girl presented with acute lower limb weakness, dehydration, hypernatraemia and secondary rhabdomyolysis on a background of an 8-month history of polyuria. Radiological investigations revealed a suprasellar tumour which was diagnosed on
Externí odkaz:
https://doaj.org/article/0800ca21ee3c408e9615915b52f8ac64
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2020)
This case report describes a family pedigree of a mother and her children with an E227K mutation in the KCNJ11 gene. People with this particular gene mutation typically present with transient neonatal diabetes; with more than half the cohort relapsin
Externí odkaz:
https://doaj.org/article/3d9a3651c7594ae49e34cbbfece01375
Publikováno v:
JBMR Plus, Vol 4, Iss 11, Pp n/a-n/a (2020)
ABSTRACT Adults with type 1 diabetes mellitus (T1DM) are at risk of premature osteoporosis and fractures. The onset of T1DM typically starts during childhood and adolescence. Thus, the effects of DM on the skeleton may be established during this peri
Externí odkaz:
https://doaj.org/article/abf79a1f7407454388c0163f89ebee5f
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports
Summary An 11-year-old girl presented with acute lower limb weakness, dehydration, hypernatraemia and secondary rhabdomyolysis on a background of an 8-month history of polyuria. Radiological investigations revealed a suprasellar tumour which was diag
Publikováno v:
Abstracts.
Publikováno v:
Abstracts.
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2020)
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2020)
Summary This case report describes a family pedigree of a mother and her children with an E227K mutation in the KCNJ11 gene. People with this particular gene mutation typically present with transient neonatal diabetes; with more than half the cohort
Autor:
Richard Jacques, Carolyn Clark, Margaret Paggiosi, Nick Bishop, Janani Devaraja, Paul Dimitri
Publikováno v:
Bone Abstracts.
Publikováno v:
Archives of Disease in Childhood; 2021 Supplement, Vol. 106, pA1-A501, 1213p