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PubPharm (94)
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
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2
Comment on a recent article titled 'Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia'
enthalten in:
Journal of diabetes investigation
| 2023
von
Clissold, R.
|
Bingham, C.
|
Hattersley, A.
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3
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
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4
Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic Syndrome
enthalten in:
Transplantation
| 2023
von
Glover, E.
|
Smith-Jackson, K.
|
Brocklebank, V.
| +60
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5
A case of acute tubulointerstitial nephritis following administration of the Oxford-AstraZeneca COVID-19 vaccine : a case report
enthalten in:
BMC nephrology
| 2023
von
Williams, S.
|
Holwill, S.
|
Clissold, R.
| +1
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6
A case of acute tubulointerstitial nephritis following administration of the Oxford-AstraZeneca COVID-19 vaccine: a case report
enthalten in:
BMC nephrology
| 2023
von
Williams, S.
|
Holwill, S.
|
Clissold, R.
| +1
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7
Monoallelic pathogenic ALG5 variants cause atypical polycystic kidney disease and interstitial fibrosis
enthalten in:
American journal of human genetics
| 2022
von
Lemoine, H.
|
Raud, L.
|
Foulquier, F.
| +23
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8
A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis
enthalten in:
Kidney international
| 2021
von
Mehrotra, R.
|
Stanaway, I.
|
Jarvik, G.
| +101
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9
IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank
enthalten in:
Kidney international reports
| 2020
von
Sukcharoen, K.
|
Sharp, S.
|
Thomas, N.
| +9
CommentIn: Kidney Int Rep. 2020 Aug 05;5(10):1627-1629. - PMID 33104093
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10
Familial interstitial nephritis : 42 years from case series to genetic diagnosis
enthalten in:
Clinical nephrology
| 2019
von
Clissold, R.
|
Bingham, C.
|
Shaw-Smith, C.
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Nephrology, dialysis, transplantation
10
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7
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45
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26
Research Support, Non-U.S. Gov't
22
138674-15-4
22
Hepatocyte Nuclear Factor 1-beta
16
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HNF1B protein, human
9
DNA-Binding Proteins
9
Transcription Factors
5
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4
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126548-29-6
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17q12 deletion
3
A3ULP0F556
3
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HNF-1beta
3
HNF1A protein, human
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Hepatocyte Nuclear Factor 1
3
Hepatocyte Nuclear Factor 1-alpha
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2020-
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