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1 anging from hemorrhagic colitis to hemolytic uremic syndrome.
2 erleukin-1beta, has been linked to hemolytic uremic syndrome.
3 hat causes hemorrhagic colitis and hemolytic uremic syndrome.
4 an experimental model for atypical hemolytic uremic syndrome.
5 O157 strains (P = 0.03) developing hemolytic-uremic syndrome.
6 ology of neuronal complications in hemolytic-uremic syndrome.
7 function in patients with atypical hemolytic-uremic syndrome.
8 evelopment of the life-threatening hemolytic uremic syndrome.
9 nsidered in the workup of neonatal hemolytic uremic syndrome.
10 ienced fatal chronic rejection and hemolytic uremic syndrome.
11 kinase epsilon result in atypical hemolytic-uremic syndrome.
12 c thrombocytopenic purpura and the hemolytic uremic syndrome.
13 causes severe bloody diarrhea and hemolytic uremic syndrome.
14 ar degeneration (AMD) and atypical hemolytic uremic syndrome.
15 r and renal injury and can trigger hemolytic uremic syndrome.
16 re hospitalized and 6.4% developed hemolytic uremic syndrome.
17 renal diseases, including atypical hemolytic uremic syndrome.
18 ribed in association with atypical hemolytic uremic syndrome.
19 hagic colitis and life-threatening hemolytic uremic syndrome.
20 es such as hemorrhagic colitis and hemolytic-uremic syndrome.
21 microangiopathy disease, atypical hemolytic uremic syndrome.
22 ers' diarrhea, gastroenteritis and hemolytic uremic syndrome.
23 re clinical manifestations such as hemolytic-uremic syndrome.
24 (EHEC) causes bloody diarrhea and hemolytic-uremic syndrome.
25 diarrhea, hemorrhagic colitis, and hemolytic uremic syndrome.
26 (pathological) effects, including hemolytic uremic syndrome.
27 iated with hemorrhagic colitis and hemolytic uremic syndrome.
28 nteritis, hemorrhagic colitis, and hemolytic uremic syndrome.
29 in complement regulation, such as hemolytic uremic syndrome.
30 coli cause hemorrhagic colitis and hemolytic uremic syndrome.
31 Three patients had reversible hemolytic uremic syndrome.
32 causes hemorrhagic colitis and the hemolytic uremic syndrome.
33 agic colitis, and life-threatening hemolytic uremic syndrome.
34 n cases of hemorrhagic colitis and hemolytic uremic syndrome.
35 coincidental with the symptoms of hemolytic uremic syndrome.
36 actic or therapeutic agent against hemolytic-uremic syndrome.
37 gic colitis and, less commonly, to hemolytic-uremic syndrome.
38 f CD46 is a predisposing factor to hemolytic uremic syndrome.
39 e and the life-threatening sequela hemolytic uremic syndrome.
40 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome.
41 share features with human atypical hemolytic uremic syndrome.
42 ulation and thrombosis observed in hemolytic uremic syndrome.
43 ia coli (STEC) are associated with hemolytic uremic syndrome.
44 ey failure in children who develop hemolytic uremic syndrome.
45 diarrhea, hemorrhagic colitis, and hemolytic-uremic syndrome.
46 hospitalized and 2 (9%) developed hemolytic-uremic syndrome.
47 mortality among patients with the hemolytic-uremic syndrome.
48 loody diarrhea, renal failure, and hemolytic uremic syndrome.
49 y sera from patients with atypical hemolytic uremic syndrome.
50 mbomicroangiopathy called atypical hemolytic uremic syndrome.
51 turnal hemoglobinuria and atypical hemolytic uremic syndrome.
52 ings in a four-month-old male with hemolytic uremic syndrome.
53 HR5 genes are reported in atypical hemolytic uremic syndrome.
54 sy of a child with EHEC-associated hemolytic uremic syndrome.
55 luding hemorrhagic colitis and the hemolytic uremic syndrome.
56 s the cause of bloody diarrhea and hemolytic-uremic syndrome.
57 infections, as well as sepsis and hemolytic uremic syndrome.
58 s, such as hemorrhagic colitis and hemolytic uremic syndrome.
59 es such as hemorrhagic colitis and hemolytic uremic syndrome.
60 en causing hemorrhagic colitis and hemolytic uremic syndrome.
61 and disseminated malignancy or in hemolytic uremic syndrome.
62 litis that sometimes progresses to hemolytic-uremic syndrome.
63 izumab after a relapse of atypical hemolytic uremic syndrome.
64 vein thrombosis (1), priapism (1), hemolytic uremic syndrome (1), diaphragm perforation (2), colonic
65 ve been reported--3167 without the hemolytic-uremic syndrome (16 deaths) and 908 with the hemolytic-u
66 drome (16 deaths) and 908 with the hemolytic-uremic syndrome (34 deaths)--indicating that this strain
68 with the related disease atypical hemolytic uremic syndrome; 6.8% in cases versus 5.9% in controls)
69 macular degeneration and atypical hemolytic uremic syndrome, a form of thrombotic microangiopathy.
71 FH and MCP are linked to atypical hemolytic uremic syndrome, a type of thrombotic microangiopathy (T
73 -related diseases such as atypical hemolytic uremic syndrome (aHUS) and age-related macular degenerat
75 ns predispose patients to atypical hemolytic uremic syndrome (aHUS) and other disorders arising from
77 therapy in patients with atypical hemolytic uremic syndrome (aHUS) are remarkable in contrast to the
78 een well characterized in atypical hemolytic uremic syndrome (aHUS) but have been less well described
80 assay that could convert atypical hemolytic uremic syndrome (aHUS) from a diagnosis of exclusion int
81 shares similarities with atypical hemolytic uremic syndrome (aHUS) in the underlying pathomechanisms
101 mplement C3 identified in atypical hemolytic uremic syndrome (aHUS) patients cause dysregulation in t
102 tic microangiopathy (TMA) atypical hemolytic uremic syndrome (aHUS) resulted in the successful introd
103 glomerulopathy (C3G) and atypical hemolytic uremic syndrome (aHUS) strongly associate with inherited
104 of ADAMTS13 activity, and atypical hemolytic uremic syndrome (aHUS), a disease of complement overacti
105 escribed in patients with atypical hemolytic uremic syndrome (aHUS), a rare condition characterized b
107 ribed in association with atypical hemolytic uremic syndrome (aHUS), also confers high risk of age-re
108 cular degeneration (AMD), atypical hemolytic uremic syndrome (aHUS), and membranoproliferative glomer
109 nal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), and various glomerular diseases.
110 reportedly contribute to atypical hemolytic uremic syndrome (aHUS), but incomplete penetrance sugges
112 native pathway results in atypical hemolytic uremic syndrome (aHUS), the prototypes of thrombotic mic
113 ereas R53H-CFH, linked to atypical hemolytic uremic syndrome (aHUS), was defective in C3bBb decay-acc
114 nt dysregulation leads to atypical hemolytic uremic syndrome (aHUS), while ADAMTS13 deficiency causes
120 renal diseases, including atypical hemolytic uremic syndrome and C3 glomerulopathies, and age-related
121 t-driven diseases such as atypical hemolytic uremic syndrome and catastrophic antiphospholipid antibo
122 postdiarrheal sequelae, including hemolytic uremic syndrome and central nervous system (CNS) abnorma
124 d with the renal diseases atypical hemolytic uremic syndrome and dense deposit disease and the ocular
126 vere disease, as defined by higher hemolytic uremic syndrome and hospitalization frequencies, suggest
127 foodborne pathogens that can cause hemolytic uremic syndrome and infantile diarrhea, respectively.
129 iated endothelial damage: atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura.
133 implicated previously in atypical hemolytic uremic syndrome, and it abrogates C-terminal ligand bind
134 diseases such as AMD and atypical hemolytic uremic syndrome, and leads to a better understanding of
137 emic lupus erythematosus, atypical hemolytic uremic syndrome, and the complocentric membranoglomerulo
138 es have been described in atypical hemolytic uremic syndrome, arising commonly through nonallelic hom
139 of clinical presentation (atypical hemolytic uremic syndrome as thrombotic microangiopathy), biopsy a
140 d with wild type FH19-20, atypical hemolytic uremic syndrome-associated mutants were less able to com
141 f the structural basis of familial hemolytic uremic syndrome, attributed to mutational disruption of
142 hemoglobinuria (PNH) and atypical hemolytic uremic syndrome, blocks the terminal complement pathway
143 d with E. coli O157:H7 progress to hemolytic uremic syndrome, but this figure may reach 50% if antibi
144 n (Stx) causes diarrhea-associated hemolytic uremic syndrome by damaging renal microvascular endothel
145 croangiopathies including atypical hemolytic uremic syndrome, C3 and C1q glomerulopathies, and preecl
146 large outbreak of diarrhea and the hemolytic-uremic syndrome caused by an unusual serotype of Shiga-t
147 eutrophilia is a characteristic of hemolytic uremic syndrome caused by Shiga toxin (Stx2)-producing E
149 Cellular injury in post-diarrheal hemolytic-uremic syndrome (D+HUS) is related to shigatoxin (Stx) b
151 ia coli causes diarrhea-associated hemolytic-uremic syndrome (DHUS), a severe renal thrombotic microa
153 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome during pregnancy and (2) to search for r
154 nticomplement therapy for atypical hemolytic uremic syndrome during pregnancy, and implications of th
156 ve or therapeutic ends, for use in hemolytic uremic syndrome-endemic areas or during future outbreaks
157 e have identified a large atypical hemolytic uremic syndrome family where a deletion has occurred thr
158 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome from 1964 to 2002 were reviewed (1) to d
159 serious long-term sequelae such as hemolytic uremic syndrome, Guillain-Barre syndrome and malnutritio
161 botic thrombocytopenic purpura and hemolytic-uremic syndrome, have been reported to have a drug-induc
162 t influence the risk of developing hemolytic uremic syndrome (HUS) after Escherichia coli O157:H7 inf
164 x2) responsible for development of hemolytic uremic syndrome (HUS) and acute kidney injury (AKI).
165 mage is one of the major causes of hemolytic uremic syndrome (HUS) and acute renal failure in childre
166 e symptoms of the life-threatening hemolytic uremic syndrome (HUS) and are the main virulence factors
167 histomorphologic similarities with hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic pu
168 thrombotic microangiopathy are the hemolytic-uremic syndrome (HUS) and thrombotic thrombocytopenic pu
169 thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS) are appropriately at the top of a
170 mbocytopenic purpura (TTP) and the hemolytic uremic syndrome (HUS) are both characterized by thromboc
171 :H7 causes hemorrhagic colitis and hemolytic uremic syndrome (HUS) by colonizing the gut mucosa and p
172 a toxin 2 (Stx2) are isolated from hemolytic-uremic syndrome (HUS) cases more frequently than are str
177 n often lead to the development of hemolytic-uremic syndrome (HUS) in a small percentage of infected
178 rhea or developed life-threatening hemolytic uremic syndrome (HUS) in any of 6 closed cohorts from 4
179 sed an outbreak with >800 cases of hemolytic uremic syndrome (HUS) in Germany, including 90 children.
185 scherichia coli O157:H7-associated hemolytic-uremic syndrome (HUS) is characterized by profound proth
192 infection with a high incidence of hemolytic uremic syndrome (HUS) occurred in Germany in May 2011.
193 2011 the largest known outbreak of hemolytic uremic syndrome (HUS) occurred in northern Germany.
194 On 22 June 2011, 8 patients with hemolytic uremic syndrome (HUS) or bloody diarrhea were reported i
198 the 62 individuals with diarrheal hemolytic uremic syndrome (HUS) seen at our institution during the
199 tening sequela of infection called hemolytic-uremic syndrome (HUS) than isolates that make Stx1a only
200 g agent of postdiarrhea-associated hemolytic uremic syndrome (HUS), a disorder of glomerular ischemic
201 imary cause of diarrhea-associated hemolytic uremic syndrome (HUS), a disorder of thrombocytopenia, m
202 emorrhagic colitis and can lead to hemolytic-uremic syndrome (HUS), a life-threatening condition that
203 main etiological agent that causes hemolytic uremic syndrome (HUS), a microangiopathic disease charac
204 coli O157:H7 infection can lead to hemolytic-uremic syndrome (HUS), a severe disease characterized by
205 oody diarrhea that can progress to hemolytic uremic syndrome (HUS), a systematic microvascular syndro
206 cytotoxic proteins that can cause hemolytic-uremic syndrome (HUS), a thrombotic microangiopathy, fol
207 s, the development and severity of hemolytic uremic syndrome (HUS), and adverse outcomes in STEC-infe
208 trains are responsible for causing hemolytic-uremic syndrome (HUS), and systemic administration of Sh
210 es to hemorrhagic colitis (HC) and hemolytic uremic syndrome (HUS), due to the expression of one or m
212 ative pathway, are associated with hemolytic uremic syndrome (HUS), membranoproliferative glomerulone
213 e pathogenesis of postenteropathic hemolytic uremic syndrome (HUS), most commonly caused by Shiga tox
215 h as sickle cell disease (SCD) and hemolytic uremic syndrome (HUS), pathological biophysical interact
216 n STEC isolates from patients with hemolytic-uremic syndrome (HUS), patients with less severe diarrhe
218 b pasudotox for 10 doses developed hemolytic uremic syndrome (HUS), thrombotic microangiopathy (TMA),
220 uding hemorrhagic colitis (HC) and hemolytic-uremic syndrome (HUS), which is the most common cause of
221 effects of STEC infection, such as hemolytic-uremic syndrome (HUS), zinc might be capable of preventi
243 y congenital; n = 650), glomerular-hemolytic uremic syndrome (HUS; n = 49), or glomerular-non-HUS (he
246 a cause of food-borne colitis and hemolytic-uremic syndrome in children, can be serotype O157:H7 (O1
249 toxin-producing E. coli-associated hemolytic uremic syndrome in six hospitals in Hamburg, Germany, be
251 l outbreaks of bloody diarrhea and hemolytic-uremic syndrome in the United States and worldwide.
254 ed mice developed the hallmarks of hemolytic uremic syndrome, including thrombotic microangiopathy, h
258 and autoantibody-positive form of hemolytic uremic syndrome is characterized by the presence of auto
259 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome is near term and during the postpartum p
263 2), one of the causative agents of hemolytic-uremic syndrome, is toxic to endothelial cells, includin
265 more frequent with everolimus and hemolytic uremic syndrome, lymphoproliferative disease, and protei
266 ng sequela of infection called the hemolytic uremic syndrome may develop that can lead to kidney fail
267 ted macular degeneration, atypical hemolytic uremic syndrome, membranoproliferative glomerulonephriti
268 157:H7 causes severe enteritis and hemolytic-uremic syndrome, mostly in young children and older adul
269 obinuria, cold agglutinin disease, hemolytic uremic syndrome, nephropathies, HELLP syndrome, transpla
270 us toxicity was reversible grade 3 hemolytic uremic syndrome, not requiring plasmapheresis, in two pa
272 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome occurs more commonly in women and among
273 ive regulation of the AP (atypical hemolytic-uremic syndrome) or with inadequate cleavage by ADAMTS-1
274 y-confirmed E coli O157 infection, hemolytic-uremic syndrome, or bloody diarrhea within 7 days of att
276 toxin-producing E. coli-associated hemolytic uremic syndrome outbreak in Germany, critical illness de
277 om 19 anti-FH Ab-positive atypical hemolytic uremic syndrome patients collected at the acute phase of
279 ults may also explain why atypical hemolytic uremic syndrome patients with mutations affecting domain
280 pathophysiology and progression to hemolytic uremic syndrome provides the basis for prevention, proph
284 ted with the related human disease hemolytic uremic syndrome) resulted in a striking syndrome closely
285 treptococcus pneumoniae associated hemolytic uremic syndrome (SpHUS) is defined by the occurrence of
287 of rare diseases such as atypical hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, C3
289 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome (TTP-HUS) is difficult because of lack o
290 treatment guidelines for atypical hemolytic uremic syndrome was held in Bergamo in December 2007.
291 binding sites and causing atypical hemolytic uremic syndrome, we found that it detached more uniforml
293 ns similar to those in humans with hemolytic-uremic syndrome were observed histologically in 82 of 12
295 ls in which patients with atypical hemolytic-uremic syndrome who were 12 years of age or older receiv
296 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome who were initially diagnosed during thei
298 ormalities consistent with grade 2 hemolytic uremic syndrome with peak creatinine of 1.53 to 1.66 mg/