Suchergebnisse - "Kavanagh, David"

PubPharm (590)

1

Effects of rare kidney diseases on kidney failure : a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort

enthalten in: Lancet (London, England) | 2024

von Wong, K. | Pitcher, D. | Braddon, F. | +135

2

Iptacopan in Idiopathic Immune Complex-Mediated Membranoproliferative Glomerulonephritis : Protocol of the APPARENT Multicenter, Randomized Phase 3 Study

enthalten in: Kidney international reports | 2024

von Vivarelli, M. | Bomback, A. | Meier, M. | +5

3

A Pragmatic Informatics Approach to Develop Knowledge Tools for Supporting Cardiac Surgical Patients' Mental Health Needs

enthalten in: Studies in health technology and informatics | 2024

von Smith, S. | Strodl, E. | Varnfield, M. | +5

4

Efficacy and Safety of Iptacopan in Patients With C3 Glomerulopathy

enthalten in: Kidney international reports | 2023

von Wong, E. | Nester, C. | Cavero, T. | +19

5

The National Registry of Rare Kidney Diseases (RaDaR): Description, recruitment, and cross-sectional analyses of 25,880 adults and children with rare kidney diseases in the UK

enthalten in: bioRxiv.org | 2023

von Wong, K. | Pitcher, D. | Braddon, F. | +37

6

Atypical hemolytic uremic syndrome in the era of terminal complement inhibition : an observational cohort study

enthalten in: Blood | 2023

von Brocklebank, V. | Walsh, P. | Smith-Jackson, K. | +11

CommentIn: Blood. 2023 Oct 19;142(16):1334-1335. - PMID 37856094

7

METHODS OF PRODUCING RECOMBINANT COMPLEMENT PROTEINS, VECTORS AND THERAPEUTIC USES THEREOF

enthalten in: Europäisches Patentamt | 2023

von MARCHBANK KEVIN | KAVANAGH DAVID | HARRIS CLAIRE | +1

8

XXIX International Complement Workshop Newcastle 2023

enthalten in: Immunobiology | 2023

von Marchbank, K. | Kavanagh, D. | Harris, C.

9

Cue exposure for alcohol use disorders : A commentary on Kiyak et al. (2023)

enthalten in: Addictive behaviors | 2023

von Kavanagh, D.

10

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

enthalten in: Cell genomics | 2023

von Maury, E. | Sherman, M. | Genovese, G. | +120

1
2
3
4
5
6
7
8
9
10
11
Nächster »
[59]