Suchergebnisse - "Johnson, Stephanie R"

PubPharm (26)

11

Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY) : A novel ABCC8 mutation in a previously screened family

enthalten in: Journal of diabetes | 2018

von Johnson, S. | Leo, P. | Conwell, L. | +3

12

A novel INS mutation in a family with maturity-onset diabetes of the young : Variable insulin secretion and putative mechanisms

enthalten in: Pediatric diabetes | 2018

von Johnson, S. | McGown, I. | Oppermann, U. | +3

13

Long-term outcome of insulin pump therapy in children with type 1 diabetes assessed in a large population-based case-control study

enthalten in: Diabetologia | 2013

von Johnson, S. | Cooper, M. | Jones, T. | +1

CommentIn: Nat Rev Endocrinol. 2013 Nov;9(11):629-30. - PMID 24080733

14

Long-term outcome of insulin pump therapy in children with type 1 diabetes assessed in a large population-based case–control study

enthalten in: Diabetologia | 2013

von Johnson, S. | Cooper, M. | Jones, T. | +1

15

Long-term outcome of insulin pump therapy in children with type 1 diabetes assessed in a large population-based case–control study

enthalten in: Diabetologia | 2013

von Johnson, S. | Cooper, M. | Jones, T. | +1

16

Long-term outcome of insulin pump therapy in children with type 1 diabetes assessed in a large population-based case–control study

enthalten in: Diabetologia | 2013

von Johnson, S. | Cooper, M. | Jones, T. | +1

17

Identification and Management of Malignant Skin Lesions Among Older Adults

enthalten in: The journal for nurse practitioners | 2012

von Johnson, S. | Taylor, M.

18

Sterile abscess formation associated with depot leuprorelin acetate therapy for central precocious puberty

enthalten in: Journal of paediatrics and child health | 2012

von Johnson, S. | Nolan, R. | Grant, M. | +4

19

Sterile abscess formation associated with depot leuprorelin acetate therapy for central precocious puberty

enthalten in: Journal of paediatrics and child health | 2012

von Johnson, S. | Nolan, R. | Grant, M. | +4

20

Structural chromosome disruption of the NR3C2 gene causing pseudohypoaldosteronism type 1 presenting in infancy

enthalten in: The journal of pediatric endocrinology and metabolism | 2011

von O’Connell, S. | Johnson, S. | Lewis, B. | +8