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A novel variant of familial glucocorticoid deficiency prevalent among the Irish Traveler population.
Published in:
2008
By:
- O'Riordan, Stephen M P;
- Lynch, Sally A;
- Hindmarsh, Peter C;
- Chan, Li F;
- Clark, Adrian J L;
- Costigan, Colm
Publication type:
journal article
The value of in vitro studies in a case of neonatal diabetes with a novel Kir6.2-W68G mutation.
Published in:
Clinical Case Reports, 2015, v. 3, n. 10, p. 884, doi. 10.1002/ccr3.370
By:
- O'Connell, Susan M.;
- Proks, Peter;
- Kramer, Holger;
- Mattis, Katia K.;
- Sachse, Gregor;
- Joyce, Caroline;
- Houghton, Jayne A. L.;
- Ellard, Sian;
- Hattersley, Andrew T.;
- Ashcroft, Frances M.;
- O'Riordan, Stephen M. P.
Publication type:
Article
Management of cystic fibrosis-related diabetes in children and adolescents.
Published in:
Pediatric Diabetes, 2009, v. 10, p. 43, doi. 10.1111/j.1399-5448.2009.00587.x
By:
- O'Riordan, Stephen M. P.;
- Robinson, Paul D.;
- Donaghue, Kim C.;
- Moran, Antoinette
Publication type:
Article
Management of cystic fibrosis-related diabetes.
Published in:
Pediatric Diabetes, 2008, v. 9, n. 4pt1, p. 338, doi. 10.1111/j.1399-5448.2008.00437.x
By:
- O'Riordan, Stephen M. P.;
- Robinson, Paul D.;
- Donaghue, Kim C.;
- Moran, Antoinette
Publication type:
Article
Validation of continuous glucose monitoring in children and adolescents with cystic fibrosis: a prospective cohort study.
Published in:
2009
By:
- O'Riordan SM;
- Hindmarsh P;
- Hill NR;
- Matthews DR;
- George S;
- Greally P;
- Canny G;
- Slattery D;
- Murphy N;
- Roche E;
- Costigan C;
- Hoey H;
- O'Riordan, Stephen M P;
- Hindmarsh, Peter;
- Hill, Nathan R;
- Matthews, David R;
- George, Sherly;
- Greally, Peter;
- Canny, Gerard;
- Slattery, Dubhfeasa
Publication type:
journal article
Validation of Continuous Glucose Monitoring in Children and Adolescents With Cystic Fibrosis.
Published in:
Diabetes Care, 2009, v. 32, n. 6, p. 1020, doi. 10.2337/dc08-1925
By:
- George, Sherly;
- Greally, Peter;
- Canny, Gerard;
- Costigan, Colm;
- Slattery, Dubhfeasa;
- Murphy, Nuala;
- Hindmarsh, Peter;
- O'Riordan, Stephen M. P.;
- Hill, Nathan R.;
- Matthews, David R.;
- Roche, Edna;
- Hoey, Hilary
Publication type:
Article
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency.
Published in:
Clinical Endocrinology, 2009, v. 71, n. 2, p. 171, doi. 10.1111/j.1365-2265.2008.03511.x
By:
- Li F. Chan;
- Metherell, Louise A.;
- Krude, Heiko;
- Ball, Colin;
- O'Riordan, Stephen M. P.;
- Costigan, Colm;
- Lynch, Sally A.;
- Savage, Martin O.;
- Cavarzere, Paolo;
- Clark, Adrian J. L.
Publication type:
Article

Found: 7

A novel variant of familial glucocorticoid deficiency prevalent among the Irish Traveler population.

The value of in vitro studies in a case of neonatal diabetes with a novel Kir6.2-W68G mutation.

Management of cystic fibrosis-related diabetes in children and adolescents.

Management of cystic fibrosis-related diabetes.

Validation of continuous glucose monitoring in children and adolescents with cystic fibrosis: a prospective cohort study.

Validation of Continuous Glucose Monitoring in Children and Adolescents With Cystic Fibrosis.

Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency.