Alpha 2.0
Login Register
» Authors » P Warwicker

P Warwicker

Explore the profile of P Warwicker including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 15
Citations 256
Followers 0
Related Specialties
Nephrology
General Surgery
General Medicine
Top 10 Co-Authors
T H Goodship
J A Goodship
S Watkins
R L Donne
K Farrington
J Stratton
Y Pirson
C Lambert
R F Jarrett
R A Thompson
Published In
Nephrol Dial Transplant
Br J Hosp Med
Immunogenetics
N Engl J Med
QJM
Affiliations
Soon will be listed here.
Recent Articles
1.
Familial hemolytic uremic syndrome: a privileged observation
Pirson Y, Lefebvre C, Lambert C, Warwicker P, Goodship T
Bull Mem Acad R Med Belg . 2004 Dec; 159(Pt 2):191-4. PMID: 15615092
No abstract available.
2.
Acute renal failure and metabolic disturbances in the short bowel syndrome
Banerjee A, Warwicker P
QJM . 2002 Feb; 95(1):37-40. PMID: 11834771
Background: Short bowel syndrome (SBS) describes a malabsorptive state caused by extensive loss of small intestinal length. Aim: To improve understanding of the metabolic complications of SBS. Design: Observational study...
3.
Allergic reactions to oral cyclophosphamide therapy in immunologically-mediated renal disease
Stratton J, Warwicker P, Farrington K
Nephrol Dial Transplant . 2001 Jul; 16(8):1724-5. PMID: 11477189
No abstract available.
4.
Minimal-change glomerulonephritis and chronic lymphocytic leukaemia
Spalding E, Watkins S, Warwicker P
Nephron . 2001 Jun; 88(3):283-4. PMID: 11423765
No abstract available.
5.
Desmopressin may be hazardous in thrombotic microangiopathy
Stratton J, Warwicker P, Watkins S, Farrington K
Nephrol Dial Transplant . 2001 Feb; 16(1):161-2. PMID: 11209013
No abstract available.
6.
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1
Feather S, Malcolm S, Woolf A, WRIGHT V, Blaydon D, Reid C, et al.
Am J Hum Genet . 2000 Mar; 66(4):1420-5. PMID: 10739767
Primary vesicoureteric reflux (VUR) affects 1%-2% of whites, and reflux nephropathy (RN) causes up to 15% of end-stage renal failure in children and adults. There is a 30-50-fold increased incidence...
7.
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency
Warwicker P, Donne R, Goodship J, Goodship T, Howie A, Kumararatne D, et al.
Nephrol Dial Transplant . 1999 May; 14(5):1229-33. PMID: 10344366
Background: In a recent study of three families we have found that inherited haemolytic uraemic syndrome (HUS) maps to a region of chromosome 1q containing the gene for complement factor...
8.
von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
Warwicker P, Goodship J, Goodship T
N Engl J Med . 1999 May; 340(17):1368-9. PMID: 10223877
No abstract available.
9.
Factor H--US?
Warwicker P, Goodship J, Goodship T
Nephrol Dial Transplant . 1998 Aug; 13(8):1921-3. PMID: 9719138
No abstract available.
10.
Genetic studies into inherited and sporadic hemolytic uremic syndrome
Warwicker P, Goodship T, Donne R, Pirson Y, Nicholls A, Ward R, et al.
Kidney Int . 1998 Apr; 53(4):836-44. PMID: 9551389
Hemolytic uremic syndrome (HUS) in adults carries a high morbidity and mortality, and its cause remains unknown despite many theories. Although familial HUS is rare, it affords a unique opportunity...