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1 nsidered in the workup of neonatal hemolytic uremic syndrome.
2 ienced fatal chronic rejection and hemolytic uremic syndrome.
3  kinase epsilon result in atypical hemolytic-uremic syndrome.
4 c thrombocytopenic purpura and the hemolytic uremic syndrome.
5  causes severe bloody diarrhea and hemolytic uremic syndrome.
6 ar degeneration (AMD) and atypical hemolytic uremic syndrome.
7 r and renal injury and can trigger hemolytic uremic syndrome.
8 re hospitalized and 6.4% developed hemolytic uremic syndrome.
9 renal diseases, including atypical hemolytic uremic syndrome.
10 ribed in association with atypical hemolytic uremic syndrome.
11 mbomicroangiopathy called atypical hemolytic uremic syndrome.
12 hagic colitis and life-threatening hemolytic uremic syndrome.
13 es such as hemorrhagic colitis and hemolytic-uremic syndrome.
14  microangiopathy disease, atypical hemolytic uremic syndrome.
15 ers' diarrhea, gastroenteritis and hemolytic uremic syndrome.
16 re clinical manifestations such as hemolytic-uremic syndrome.
17  (EHEC) causes bloody diarrhea and hemolytic-uremic syndrome.
18 diarrhea, hemorrhagic colitis, and hemolytic uremic syndrome.
19  (pathological) effects, including hemolytic uremic syndrome.
20 nteritis, hemorrhagic colitis, and hemolytic uremic syndrome.
21  in complement regulation, such as hemolytic uremic syndrome.
22 coli cause hemorrhagic colitis and hemolytic uremic syndrome.
23      Three patients had reversible hemolytic uremic syndrome.
24 causes hemorrhagic colitis and the hemolytic uremic syndrome.
25 agic colitis, and life-threatening hemolytic uremic syndrome.
26 n cases of hemorrhagic colitis and hemolytic uremic syndrome.
27  coincidental with the symptoms of hemolytic uremic syndrome.
28 actic or therapeutic agent against hemolytic-uremic syndrome.
29 gic colitis and, less commonly, to hemolytic-uremic syndrome.
30 f CD46 is a predisposing factor to hemolytic uremic syndrome.
31 e and the life-threatening sequela hemolytic uremic syndrome.
32 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome.
33 turnal hemoglobinuria and atypical hemolytic uremic syndrome.
34 ulation and thrombosis observed in hemolytic uremic syndrome.
35 ia coli (STEC) are associated with hemolytic uremic syndrome.
36 ey failure in children who develop hemolytic uremic syndrome.
37 diarrhea, hemorrhagic colitis, and hemolytic-uremic syndrome.
38  hospitalized and 2 (9%) developed hemolytic-uremic syndrome.
39  mortality among patients with the hemolytic-uremic syndrome.
40 ings in a four-month-old male with hemolytic uremic syndrome.
41 y sera from patients with atypical hemolytic uremic syndrome.
42 sy of a child with EHEC-associated hemolytic uremic syndrome.
43 luding hemorrhagic colitis and the hemolytic uremic syndrome.
44 s the cause of bloody diarrhea and hemolytic-uremic syndrome.
45  infections, as well as sepsis and hemolytic uremic syndrome.
46 s, such as hemorrhagic colitis and hemolytic uremic syndrome.
47 en causing hemorrhagic colitis and hemolytic uremic syndrome.
48  and disseminated malignancy or in hemolytic uremic syndrome.
49 litis that sometimes progresses to hemolytic-uremic syndrome.
50 izumab after a relapse of atypical hemolytic uremic syndrome.
51 erleukin-1beta, has been linked to hemolytic uremic syndrome.
52 hat causes hemorrhagic colitis and hemolytic uremic syndrome.
53 an experimental model for atypical hemolytic uremic syndrome.
54 O157 strains (P = 0.03) developing hemolytic-uremic syndrome.
55 ology of neuronal complications in hemolytic-uremic syndrome.
56 function in patients with atypical hemolytic-uremic syndrome.
57 evelopment of the life-threatening hemolytic uremic syndrome.
58 vein thrombosis (1), priapism (1), hemolytic uremic syndrome (1), diaphragm perforation (2), colonic
59 ve been reported--3167 without the hemolytic-uremic syndrome (16 deaths) and 908 with the hemolytic-u
60 drome (16 deaths) and 908 with the hemolytic-uremic syndrome (34 deaths)--indicating that this strain
61                                    Hemolytic uremic syndrome, a life-threatening disease often accomp
62  FH and MCP are linked to atypical hemolytic uremic syndrome, a type of thrombotic microangiopathy (T
63 ent of colitis and/or signs of the hemolytic uremic syndrome after oral infection with Escherichia co
64                Complement mediated hemolytic uremic syndrome (aHUS) accounts for a significant propor
65 ns predispose patients to atypical hemolytic uremic syndrome (aHUS) and other disorders arising from
66  causally associated with atypical hemolytic uremic syndrome (aHUS) and related glomerulopathies.
67  therapy in patients with atypical hemolytic uremic syndrome (aHUS) are remarkable in contrast to the
68 een well characterized in atypical hemolytic uremic syndrome (aHUS) but have been less well described
69             Patients with atypical hemolytic uremic syndrome (aHUS) develop a thrombotic microangiopa
70  assay that could convert atypical hemolytic uremic syndrome (aHUS) from a diagnosis of exclusion int
71  shares similarities with atypical hemolytic uremic syndrome (aHUS) in the underlying pathomechanisms
72                           Atypical hemolytic uremic syndrome (aHUS) is a genetic ultrarare renal dise
73                           Atypical hemolytic uremic syndrome (aHUS) is a genetic, life-threatening di
74                           Atypical hemolytic uremic syndrome (aHUS) is a rare disease with a high rec
75                           Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microa
76                           Atypical hemolytic uremic syndrome (aHUS) is a renal disease associated wit
77                           Atypical hemolytic uremic syndrome (aHUS) is a severe thrombotic microangio
78                           Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (
79                           Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy c
80                           Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy w
81                           Atypical hemolytic uremic syndrome (aHUS) is an orphan disease with a high
82                           Atypical hemolytic-uremic syndrome (aHUS) is associated with genetic comple
83                           Atypical hemolytic uremic syndrome (aHUS) is characterized by complement at
84                           Atypical hemolytic uremic syndrome (aHUS) is characterized by dysregulated
85                           Atypical hemolytic uremic syndrome (aHUS) is characterized by genetic and a
86                           Atypical hemolytic uremic syndrome (aHUS) is classically described to resul
87       The pathogenesis of atypical hemolytic uremic syndrome (aHUS) is strongly linked to dysregulati
88                           Atypical hemolytic uremic syndrome (aHUS) is usually characterized by uncon
89 mplement C3 identified in atypical hemolytic uremic syndrome (aHUS) patients cause dysregulation in t
90 tic microangiopathy (TMA) atypical hemolytic uremic syndrome (aHUS) resulted in the successful introd
91  glomerulopathy (C3G) and atypical hemolytic uremic syndrome (aHUS) strongly associate with inherited
92 of ADAMTS13 activity, and atypical hemolytic uremic syndrome (aHUS), a disease of complement overacti
93 escribed in patients with atypical hemolytic uremic syndrome (aHUS), a rare condition characterized b
94                           Atypical hemolytic uremic syndrome (aHUS), a rare form of thrombotic microa
95 ribed in association with atypical hemolytic uremic syndrome (aHUS), also confers high risk of age-re
96 cular degeneration (AMD), atypical hemolytic uremic syndrome (aHUS), and membranoproliferative glomer
97  reportedly contribute to atypical hemolytic uremic syndrome (aHUS), but incomplete penetrance sugges
98                        In atypical hemolytic uremic syndrome (aHUS), mutations clustering toward the
99 ereas R53H-CFH, linked to atypical hemolytic uremic syndrome (aHUS), was defective in C3bBb decay-acc
100 nt dysregulation leads to atypical hemolytic uremic syndrome (aHUS), while ADAMTS13 deficiency causes
101  hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS).
102  she developed postpartum atypical hemolytic uremic syndrome (aHUS).
103 al to the pathogenesis of atypical hemolytic uremic syndrome (aHUS).
104 ngiopathy (TMA), known as atypical hemolytic uremic syndrome (aHUS).
105 renal diseases, including atypical hemolytic uremic syndrome and C3 glomerulopathies, and age-related
106  postdiarrheal sequelae, including hemolytic uremic syndrome and central nervous system (CNS) abnorma
107 he United States and can result in hemolytic-uremic syndrome and death.
108 d with the renal diseases atypical hemolytic uremic syndrome and dense deposit disease and the ocular
109                    The outbreak of hemolytic-uremic syndrome and diarrhea caused by Shiga toxin-produ
110 vere disease, as defined by higher hemolytic uremic syndrome and hospitalization frequencies, suggest
111  implicated in the pathogenesis of hemolytic uremic syndrome and its attendant endothelial cell (EC)
112  affected with late-onset atypical hemolytic uremic syndrome and symptoms of glomerulonephritis.
113 iated endothelial damage: atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura.
114 ted macular degeneration, atypical hemolytic uremic syndrome, and C3 glomerulopathies.
115  implicated previously in atypical hemolytic uremic syndrome, and it abrogates C-terminal ligand bind
116  diseases such as AMD and atypical hemolytic uremic syndrome, and leads to a better understanding of
117 35 were hospitalized, 10 developed hemolytic-uremic syndrome, and none died.
118 sses, such as hemorrhagic colitis, hemolytic uremic syndrome, and septicemia.
119 emic lupus erythematosus, atypical hemolytic uremic syndrome, and the complocentric membranoglomerulo
120 es have been described in atypical hemolytic uremic syndrome, arising commonly through nonallelic hom
121 of clinical presentation (atypical hemolytic uremic syndrome as thrombotic microangiopathy), biopsy a
122 d with wild type FH19-20, atypical hemolytic uremic syndrome-associated mutants were less able to com
123 f the structural basis of familial hemolytic uremic syndrome, attributed to mutational disruption of
124  hemoglobinuria (PNH) and atypical hemolytic uremic syndrome, blocks the terminal complement pathway
125 d with E. coli O157:H7 progress to hemolytic uremic syndrome, but this figure may reach 50% if antibi
126 n (Stx) causes diarrhea-associated hemolytic uremic syndrome by damaging renal microvascular endothel
127 croangiopathies including atypical hemolytic uremic syndrome, C3 and C1q glomerulopathies, and preecl
128 large outbreak of diarrhea and the hemolytic-uremic syndrome caused by an unusual serotype of Shiga-t
129 eutrophilia is a characteristic of hemolytic uremic syndrome caused by Shiga toxin (Stx2)-producing E
130    Five patients had evidence of a hemolytic uremic syndrome concurrently with or after sirolimus tre
131                Diarrhea-associated hemolytic uremic syndrome (D(+)HUS) is caused by the ingestion of
132                Diarrhea-associated hemolytic uremic syndrome (D+HUS) is characterized by endothelial
133  Cellular injury in post-diarrheal hemolytic-uremic syndrome (D+HUS) is related to shigatoxin (Stx) b
134                Diarrhea-associated hemolytic uremic syndrome (D+HUS) is the most common cause of acut
135  serious but completely reversible hemolytic-uremic syndrome developed during the second cycle of tre
136 e patients was four years, and the hemolytic-uremic syndrome developed in eight.
137                           When the hemolytic-uremic syndrome developed, the urinary concentrations of
138 ble of the 16 children in whom the hemolytic-uremic syndrome developed.
139 ia coli causes diarrhea-associated hemolytic-uremic syndrome (DHUS), a severe renal thrombotic microa
140 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome difficult or impossible.
141 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome during pregnancy and (2) to search for r
142 nticomplement therapy for atypical hemolytic uremic syndrome during pregnancy, and implications of th
143 toxin-producing E. coli-associated hemolytic uremic syndrome during this outbreak.
144 ve or therapeutic ends, for use in hemolytic uremic syndrome-endemic areas or during future outbreaks
145 e have identified a large atypical hemolytic uremic syndrome family where a deletion has occurred thr
146 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome from 1964 to 2002 were reviewed (1) to d
147 serious long-term sequelae such as hemolytic uremic syndrome, Guillain-Barre syndrome and malnutritio
148                           Atypical hemolytic uremic syndrome has been associated with dysregulation o
149 botic thrombocytopenic purpura and hemolytic-uremic syndrome, have been reported to have a drug-induc
150 t influence the risk of developing hemolytic uremic syndrome (HUS) after Escherichia coli O157:H7 inf
151 42 cases, including 855 cases with hemolytic uremic syndrome (HUS) and 53 deaths.
152 o comprised 64.3% of patients with hemolytic uremic syndrome (HUS) and 87.5% of patients who died (P
153 x2) responsible for development of hemolytic uremic syndrome (HUS) and acute kidney injury (AKI).
154 mage is one of the major causes of hemolytic uremic syndrome (HUS) and acute renal failure in childre
155 histomorphologic similarities with hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic pu
156 thrombotic microangiopathy are the hemolytic-uremic syndrome (HUS) and thrombotic thrombocytopenic pu
157 thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS) are appropriately at the top of a
158 mbocytopenic purpura (TTP) and the hemolytic uremic syndrome (HUS) are both characterized by thromboc
159 :H7 causes hemorrhagic colitis and hemolytic uremic syndrome (HUS) by colonizing the gut mucosa and p
160 ypes associated with postdiarrheal hemolytic uremic syndrome (HUS) cases among children and adults in
161 a toxin 2 (Stx2) are isolated from hemolytic-uremic syndrome (HUS) cases more frequently than are str
162                                    Hemolytic uremic syndrome (HUS) caused by intestinal Shiga toxin-p
163                                    Hemolytic-uremic syndrome (HUS) caused by Shiga toxin-producing Es
164                                    Hemolytic-uremic syndrome (HUS) features episodes of small-vessel
165 scherichia coli (STEC) can lead to hemolytic-uremic syndrome (HUS) in 5 to 10% of patients.
166 n often lead to the development of hemolytic-uremic syndrome (HUS) in a small percentage of infected
167 rhea or developed life-threatening hemolytic uremic syndrome (HUS) in any of 6 closed cohorts from 4
168 ibes the epidemiology of childhood hemolytic uremic syndrome (HUS) in California, for which hospitali
169 sed an outbreak with >800 cases of hemolytic uremic syndrome (HUS) in Germany, including 90 children.
170 EC) causes hemorrhagic colitis and hemolytic-uremic syndrome (HUS) in humans.
171                       Incidents of hemolytic uremic syndrome (HUS) include a subset of patients that
172                                    Hemolytic uremic syndrome (HUS) is a potentially life-threatening
173                                    Hemolytic-uremic syndrome (HUS) is a serious complication predomin
174                                    Hemolytic-uremic syndrome (HUS) is a serious complication which is
175                                    Hemolytic uremic syndrome (HUS) is a thrombotic microangiopathy ch
176                                    Hemolytic-uremic syndrome (HUS) is a thrombotic microangiopathy th
177                                The hemolytic uremic syndrome (HUS) is a triad of microangiopathic hem
178         Mortality in postdiarrheal hemolytic-uremic syndrome (HUS) is associated with brain injury.
179                                    Hemolytic uremic syndrome (HUS) is associated with intestinal infe
180 scherichia coli O157:H7-associated hemolytic-uremic syndrome (HUS) is characterized by profound proth
181                                    Hemolytic uremic syndrome (HUS) is the cause of renal failure in 2
182                                    Hemolytic uremic syndrome (HUS) is the life-threatenig sequela of
183                      Postdiarrheal hemolytic uremic syndrome (HUS) is the most common cause of acute
184                                The hemolytic uremic syndrome (HUS) is the most common cause of acute
185                Diarrhea-associated hemolytic uremic syndrome (HUS) is the most common cause of acute
186                    Brain injury in hemolytic-uremic syndrome (HUS) may be enhanced by inflammatory cy
187                                    Hemolytic uremic syndrome (HUS) occurred in 12 patients (10 infect
188 infection with a high incidence of hemolytic uremic syndrome (HUS) occurred in Germany in May 2011.
189 2011 the largest known outbreak of hemolytic uremic syndrome (HUS) occurred in northern Germany.
190   On 22 June 2011, 8 patients with hemolytic uremic syndrome (HUS) or bloody diarrhea were reported i
191 individuals the infection leads to hemolytic uremic syndrome (HUS) or other complications.
192                                    Hemolytic-uremic syndrome (HUS) results from infection by Shiga to
193  the 62 individuals with diarrheal hemolytic uremic syndrome (HUS) seen at our institution during the
194 g agent of postdiarrhea-associated hemolytic uremic syndrome (HUS), a disorder of glomerular ischemic
195 imary cause of diarrhea-associated hemolytic uremic syndrome (HUS), a disorder of thrombocytopenia, m
196 emorrhagic colitis and can lead to hemolytic-uremic syndrome (HUS), a life-threatening condition that
197 main etiological agent that causes hemolytic uremic syndrome (HUS), a microangiopathic disease charac
198 coli O157:H7 infection can lead to hemolytic-uremic syndrome (HUS), a severe disease characterized by
199 oody diarrhea that can progress to hemolytic uremic syndrome (HUS), a systematic microvascular syndro
200  cytotoxic proteins that can cause hemolytic-uremic syndrome (HUS), a thrombotic microangiopathy, fol
201 s, the development and severity of hemolytic uremic syndrome (HUS), and adverse outcomes in STEC-infe
202 trains are responsible for causing hemolytic-uremic syndrome (HUS), and systemic administration of Sh
203                                    Hemolytic-uremic syndrome (HUS), caused by Shiga toxin (Stx)-produ
204 es to hemorrhagic colitis (HC) and hemolytic uremic syndrome (HUS), due to the expression of one or m
205  systemic complications, including hemolytic-uremic syndrome (HUS), in animal models of disease.
206 ative pathway, are associated with hemolytic uremic syndrome (HUS), membranoproliferative glomerulone
207 e pathogenesis of postenteropathic hemolytic uremic syndrome (HUS), most commonly caused by Shiga tox
208  complicated by potentially lethal hemolytic uremic syndrome (HUS), particularly in children.
209 h as sickle cell disease (SCD) and hemolytic uremic syndrome (HUS), pathological biophysical interact
210 n STEC isolates from patients with hemolytic-uremic syndrome (HUS), patients with less severe diarrhe
211                                    Hemolytic-uremic syndrome (HUS), the life-threatening complication
212 b pasudotox for 10 doses developed hemolytic uremic syndrome (HUS), thrombotic microangiopathy (TMA),
213                                    Hemolytic uremic syndrome (HUS), which is caused by Shiga toxin-pr
214 uding hemorrhagic colitis (HC) and hemolytic-uremic syndrome (HUS), which is the most common cause of
215 effects of STEC infection, such as hemolytic-uremic syndrome (HUS), zinc might be capable of preventi
216 ere hospitalized, including 4 with hemolytic uremic syndrome (HUS).
217 22% of these individuals developed hemolytic-uremic syndrome (HUS).
218 r the serious disease consequence, hemolytic-uremic syndrome (HUS).
219 oli (EHEC) O26 causes diarrhea and hemolytic uremic syndrome (HUS).
220 ess and sometimes life-threatening hemolytic uremic syndrome (HUS).
221 li O157:H7 is the leading cause of hemolytic uremic syndrome (HUS).
222 ng-term prognosis of children with hemolytic uremic syndrome (HUS).
223 thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS).
224 oli (STEC) is the leading cause of hemolytic-uremic syndrome (HUS).
225 renal inflammation associated with hemolytic-uremic syndrome (HUS).
226  coli are the most common cause of hemolytic-uremic syndrome (HUS).
227 en shown to predispose to atypical hemolytic uremic syndrome (HUS).
228 nized cause of bloody diarrhea and hemolytic-uremic syndrome (HUS).
229 coli cause the diarrhea-associated hemolytic uremic syndrome (HUS).
230 n cause diarrhea, colitis, and the hemolytic uremic syndrome (HUS).
231 d that it may increase the risk of hemolytic uremic syndrome (HUS).
232 munosuppressive regimen to develop hemolytic uremic syndrome (HUS).
233 57:H7 are the most common cause of hemolytic uremic syndrome (HUS).
234  is associated with development of hemolytic uremic syndrome (HUS).
235  causes serious illness, including hemolytic-uremic syndrome (HUS).
236 outcomes of waitlisted adults with hemolytic uremic syndrome (HUS).
237 cing Escherichia coli (STEC) cause hemolytic uremic syndrome (HUS).
238 kidney-damaging sequela called the hemolytic uremic syndrome (HUS).
239 tery, hemorrhagic colitis (HC) and hemolytic uremic syndrome (HUS).
240 causes hemorrhagic colitis and the hemolytic-uremic syndrome (HUS).
241                We report a case of hemolytic uremic syndrome in a 69-year-old woman due to Shiga toxi
242 TEC) O146:H28 infection leading to hemolytic uremic syndrome in a neonate.
243  a cause of food-borne colitis and hemolytic-uremic syndrome in children, can be serotype O157:H7 (O1
244 diarrhea, hemorrhagic colitis, and hemolytic uremic syndrome in humans.
245 causes hemorrhagic colitis and the hemolytic-uremic syndrome in humans.
246 toxin-producing E. coli-associated hemolytic uremic syndrome in six hospitals in Hamburg, Germany, be
247 s can trigger episodes of atypical hemolytic uremic syndrome in susceptible patients.
248 l outbreaks of bloody diarrhea and hemolytic-uremic syndrome in the United States and worldwide.
249 inant cause of bloody diarrhea and hemolytic uremic syndrome in the United States.
250 ed mice developed the hallmarks of hemolytic uremic syndrome, including thrombotic microangiopathy, h
251                                    Hemolytic uremic syndrome is a disease characterized by hemolytic
252                           Atypical hemolytic-uremic syndrome is a genetic, life-threatening, chronic
253                                The hemolytic-uremic syndrome is a thrombotic complication of Escheric
254                                    Hemolytic uremic syndrome is a triad of microangiopathic hemolytic
255  and autoantibody-positive form of hemolytic uremic syndrome is characterized by the presence of auto
256 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome is near term and during the postpartum p
257                           Atypical hemolytic uremic syndrome is often associated with mutations in ge
258 ife-threatening sequela called the hemolytic uremic syndrome is unpredictable.
259 tients with the autoimmune form of hemolytic uremic syndrome, is involved in B cell regulation.
260 mbotic microangiopathy, and in the hemolytic-uremic syndrome, is not established.
261 2), one of the causative agents of hemolytic-uremic syndrome, is toxic to endothelial cells, includin
262 y tract, which can precipitate the hemolytic-uremic syndrome, is unknown.
263 ly infected with EHEC O153 develop hemolytic-uremic syndrome-like disease.
264  more frequent with everolimus and hemolytic uremic syndrome, lymphoproliferative disease, and protei
265 ng sequela of infection called the hemolytic uremic syndrome may develop that can lead to kidney fail
266 157:H7 causes severe enteritis and hemolytic-uremic syndrome, mostly in young children and older adul
267 us toxicity was reversible grade 3 hemolytic uremic syndrome, not requiring plasmapheresis, in two pa
268 a coli serotype O104:H4-associated hemolytic uremic syndrome occurred in Northern Germany.
269 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome occurs more commonly in women and among
270 ive regulation of the AP (atypical hemolytic-uremic syndrome) or with inadequate cleavage by ADAMTS-1
271 y-confirmed E coli O157 infection, hemolytic-uremic syndrome, or bloody diarrhea within 7 days of att
272 O157:H7 can cause bloody diarrhea, hemolytic uremic syndrome, or even death.
273 toxin-producing E. coli-associated hemolytic uremic syndrome outbreak in Germany, critical illness de
274 om 19 anti-FH Ab-positive atypical hemolytic uremic syndrome patients collected at the acute phase of
275 ted with increasing frequency from hemolytic uremic syndrome patients in Germany.
276 ults may also explain why atypical hemolytic uremic syndrome patients with mutations affecting domain
277 pathophysiology and progression to hemolytic uremic syndrome provides the basis for prevention, proph
278              The Oklahoma TTP-HUS (hemolytic uremic syndrome) Registry enrolled 70 consecutive patien
279                                          The uremic syndrome remains poorly understood despite the wi
280                       A reversible hemolytic uremic syndrome requiring plasmapheresis was observed in
281 ted with the related human disease hemolytic uremic syndrome) resulted in a striking syndrome closely
282  February 2001 using the key words hemolytic uremic syndrome, risk factor, antibiotics, and Escherich
283 treptococcus pneumoniae associated hemolytic uremic syndrome (SpHUS) is defined by the occurrence of
284           The children in whom the hemolytic-uremic syndrome subsequently developed had significantly
285                                    Hemolytic uremic syndrome, the leading cause of kidney failure in
286                             In the hemolytic-uremic syndrome, thrombin generation (probably due to ac
287  of rare diseases such as atypical hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, C3
288 en that causes bloody diarrhea and hemolytic uremic syndrome throughout the world.
289 hrombotic thrombocytopenic purpura-hemolytic uremic syndrome (TTP-HUS) is difficult because of lack o
290 hrombotic thrombocytopenia purpura/hemolytic uremic syndrome (TTP/HUS) case involved a patient who un
291  treatment guidelines for atypical hemolytic uremic syndrome was held in Bergamo in December 2007.
292 toxin-producing E. coli-associated hemolytic uremic syndrome were admitted to eight ICUs.
293 ns similar to those in humans with hemolytic-uremic syndrome were observed histologically in 82 of 12
294                      Patients with hemolytic uremic syndrome were significantly more likely to be inf
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
297                                 In hemolytic uremic syndrome with brain involvement symptoms develop
298 ormalities consistent with grade 2 hemolytic uremic syndrome with peak creatinine of 1.53 to 1.66 mg/
299 ks of gastrointestinal illness and hemolytic uremic syndrome worldwide.
300 esponsible for bloody diarrhea and hemolytic-uremic syndrome worldwide.

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