Suchergebnisse - "Duncan, Emma L"

PubPharm (115)

31

PET detectives : Molecular imaging for phaeochromocytomas and paragangliomas in the genomics era

enthalten in: Clinical endocrinology | 2021

von Ryder, S. | Love, A. | Duncan, E. | +1

32

A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the young

enthalten in: JCI insight | 2021

von Graff, S. | Johnson, S. | Leo, P. | +10

33

Unilateral hydrocephalus from a gangliocytoma-somatotrophinoma : first reported case

enthalten in: Endocrinology, diabetes & metabolism case reports | 2021

von Ryder, S. | Robusto, J. | Robertson, T. | +2

34

A woman with visual loss, amenorrhoea and polyuria : the first reported case of nodular lymphocyte-predominant Hodgkin lymphoma presenting with hypopituitarism

enthalten in: Endocrinology, diabetes & metabolism case reports | 2021

von Seymour, M. | Robertson, T. | Papacostas, J. | +4

35

Attributes and predictors of long COVID

enthalten in: Nature medicine | 2021

von Sudre, C. | Murray, B. | Varsavsky, T. | +30

ErratumIn: Nat Med. 2021 Jun;27(6):1116. - PMID 34045738

36

Gene Testing in Everyday Clinical Use : Lessons from the Bone Clinic

enthalten in: Journal of the Endocrine Society | 2021

von Duncan, E.

CommentOn: J Endocr Soc. 2020 Oct 07;4(12):bvaa148. - PMID 33195954

37

Multiple Endocrine Tumors Associated with Germline MAX Mutations : Multiple Endocrine Neoplasia Type 5?

enthalten in: The Journal of clinical endocrinology and metabolism | 2021

von Seabrook, A. | Harris, J. | Velosa, S. | +17

38

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

enthalten in: Human molecular genetics | 2020

von Martin, E. | Enriquez, A. | Sparrow, D. | +31

39

The Musculoskeletal Knowledge Portal : Making Omics Data Useful to the Broader Scientific Community

enthalten in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2020

von Kiel, D. | Kemp, J. | Rivadeneira, F. | +8

CommentIn: J Bone Miner Res. 2020 Sep;35(9):1623-1625. - PMID 32845524

40

Characteristics of Early Paget's Disease in SQSTM1 Mutation Carriers : Baseline Analysis of the ZiPP Study Cohort

enthalten in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2020

von Cronin, O. | Subedi, D. | Forsyth, L. | +36