コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 cids in the neurological complications after acute liver failure.
2 etaminophen overdose is the leading cause of acute liver failure.
3 or the importance of these variants in human acute liver failure.
4 for regenerative therapies for APAP-induced acute liver failure.
5 es, hepatitis E may lead to life-threatening acute liver failure.
6 side analogue (fialuridine [FIAU]) developed acute liver failure.
7 damage, a paradigm for glutathione-mediated acute liver failure.
8 es of drug induced liver injury resulting in acute liver failure.
9 rum cytokine assays 12 h after initiation of acute liver failure.
10 r data in consecutive patients admitted with acute liver failure.
11 ression was reduced by recAP in ACLF but not acute liver failure.
12 ric patients with end-stage liver disease or acute liver failure.
13 atment option for prevention of ACLF but not acute liver failure.
14 Keratin variants may predict outcome of acute liver failure.
15 gan dysfunction and outcome in patients with acute liver failure.
16 dysfunction syndrome and improve outcome in acute liver failure.
17 ated injury and systemic inflammation during acute liver failure.
18 n toxicity among subjects with indeterminate acute liver failure.
19 s may be an effective treatment modality for acute liver failure.
20 ver injury (DILI), chronic liver disease, or acute liver failure.
21 ty factor shown to predispose to HAV-induced acute liver failure.
22 pathy-sparing, specific and novel therapy in acute liver failure.
23 r disease which in some instances has led to acute liver failure.
24 complications independently associated with acute liver failure.
25 enerative process in liver diseases, such as acute liver failure.
26 efit patients with non-acetaminophen-related acute liver failure.
27 s with early stage non-acetaminophen-related acute liver failure.
28 minophen (APAP) overdose is a major cause of acute liver failure.
29 bclinical cardiac injury might also occur in acute liver failure.
30 siRNA resulted in the early onset of lethal, acute liver failure.
31 e intensive care management of patients with acute liver failure.
32 y been reported for adults and children with acute liver failure.
33 ly modulated even in late-stage APAP-induced acute liver failure.
34 The treatment was not effective in acute liver failure.
35 ovel regenerative therapies for APAP-induced acute liver failure.
36 Group 3 animals declined rapidly, with acute liver failure.
37 tions that lead to generalized infection and acute liver failure.
38 therapeutic option to treat posthepatectomy acute liver failure.
39 ey contributing factor for cerebral edema in acute liver failure.
40 ining diet before azoxymethane (AOM)-induced acute liver failure.
41 hat can lead to herpes simplex virus-induced acute liver failure.
42 making in patients with paracetamol-induced acute liver failure.
43 ytokine assays showed pronounced features of acute liver failure 12 h after application of acetaminop
45 were 11 catastrophic events (early deaths or acute liver failures; 2.9 per 1000; 95% CI, 1.5-5.1); si
49 xicity accounts for 41%; among children with acute liver failure, acetaminophen was the second most c
50 from 78 patients with acetaminophen-induced acute liver failure admitted to the Royal Infirmary Edin
52 a concentrations are common in patients with acute liver failure (ALF) and are associated with hepati
53 ival was also analyzed by underlying disease-acute liver failure (ALF) and chronic liver failure.
54 eration, overwhelming liver damage can cause acute liver failure (ALF) and death without emergent liv
55 hose adults with nonacetaminophen (non-APAP) acute liver failure (ALF) and grade 1-2 hepatic encephal
56 a multicenter cohort of adult patients with acute liver failure (ALF) and in an acetaminophen (APAP)
60 yzed 217 serum samples from 69 patients with acute liver failure (ALF) collected up to 24 months post
66 paracetamol) poisoning is a leading cause of acute liver failure (ALF) in humans and induces hepatocy
68 virus (HEV) infection is a leading cause of acute liver failure (ALF) in many developing countries,
70 inophen toxicity is the most common cause of acute liver failure (ALF) in the United States and Great
83 ying autoimmune hepatitis as the etiology of acute liver failure (ALF) is potentially important, beca
87 type is the most suitable source of CBTs for acute liver failure (ALF) or chronic liver failure (CLF)
89 the central nervous system in patients with acute liver failure (ALF) present unique challenges in t
94 its rarity, it represents the major cause of acute liver failure (ALF) requiring liver transplantatio
95 eptibility to developing sepsis is common in acute liver failure (ALF) resulting in tissue damage and
96 om acetaminophen (APAP, paracetamol)-induced acute liver failure (ALF) showed significant differences
98 patients with acute liver dysfunction (e.g. acute liver failure (ALF), acute-on chronic liver failur
99 ride (LPS) and concanavalin A (ConA)-induced acute liver failure (ALF), but the mechanism by which FK
101 ransplant centers coordinate complex care in acute liver failure (ALF), for which liver transplant (L
102 injury or arrhythmias have been reported in acute liver failure (ALF), overall, the heart is conside
114 d out in a patient with dengue virus induced acute liver failure (ALF).((1)) Their report highlights
117 n of AAT can be a promising therapy to treat acute liver failure and clinical studies to explore this
118 on in 24 patients with acetaminophen-induced acute liver failure and compared with 10 healthy control
119 tor of TGFbeta1 signaling during AOM-induced acute liver failure and contributes to both liver pathol
120 tation into mice with concanavalin-A-induced acute liver failure and fatal metabolic liver disease du
126 is the most frequent precipitating cause of acute liver failure and liver transplant, but contempora
127 ara-aminophenol [APAP]) is the main cause of acute liver failure and liver transplantation in several
128 ially attractive method for the treatment of acute liver failure and liver-based metabolic disorders.
129 nificantly elevated in acetaminophen-induced acute liver failure and non-acetaminophen induced acute
130 onic hyperammonemia animal models, including acute liver failure and ornithine transcarbamylase defic
131 otoxin) is implicated in the pathogenesis of acute liver failure and several chronic inflammatory liv
132 inophen overdose is the most common cause of acute liver failure and the leading cause of chronic liv
133 ll focus on the current approach to neonatal acute liver failure and the progress made in the diagnos
134 enol [APAP]) is one of the leading causes of acute liver failure, and APAP hepatotoxicity is associat
138 me of acute respiratory distress syndrome in acute liver failure are scant and hypoxemia being a comm
139 ients with liver-based metabolic disease and acute liver failure as a potential alternative to liver
140 ceptor 9 expression in acetaminophen-induced acute liver failure being mediated both by circulating e
141 r the management of individual patients with acute liver failure, but also to improve the uniformity
143 d intracranial hypertension in patients with acute liver failure by decreasing splanchnic ammonia pro
147 n confirm that of the approximately 1600 new acute liver failure cases annually, acetaminophen hepato
150 ine seems to be beneficial for patients with acute liver failure caused by medications or herbal agen
151 lase concentrations in acetaminophen-induced acute liver failure compared with controls (p < 0.05).
152 d in all patients with acetaminophen-induced acute liver failure compared with healthy controls (p <
153 or autoimmune hepatitis) or patients without acute liver failure (controls) collected from a DILI Bio
154 and 2017 because of ALF defined by Pediatric Acute Liver Failure criteria (raised transaminases, Inte
155 atients with life-threatening liver disease (acute liver failure, decompensated cirrhosis, or severe
156 tracranial pressure monitor in acetaminophen acute liver failure did not confer a significant 21-day
157 commonly available on admission in cases of acute liver failure due to APAP overdose and should be v
159 nd stabilize the lost metabolic function for acute liver failure, end-stage and congenital liver dise
160 In these regions it is an important cause of acute liver failure, especially in pregnant women who ha
161 at Angiopoietin-2 protein was upregulated in acute liver failure explants compared with matched liver
162 imate the risk of perioperative mortality or acute liver failure for live liver donors in the United
163 ence of existing liver disease distinguishes acute liver failure from decompensated cirrhosis or acut
164 osing cholangitis, neonatal hemochromatosis, acute liver failure (from the Pediatric Acute Liver Fail
165 brain herniation are major complications of acute liver failure (fulminant hepatic failure) and a ma
166 identify information related to drug-induced acute liver failure, gastrointestinal hypomotility, cons
167 aware of common drug causes of drug-induced acute liver failure, gastrointestinal hypomotility, cons
172 1) has been shown to contribute to HE during acute liver failure; however, TGFbeta1 must be activated
173 ing 30 Argentinean patients with HAV-induced acute liver failure in a case-control, cross-sectional,
174 18-associated severe systemic infection and acute liver failure in an adult hematopoietic stem cell
176 ed model of lipopolysaccharide (LPS)-induced acute liver failure in D-galactosamine (GalN)-sensitized
177 es, who presented with recurrent episodes of acute liver failure in early infancy and are affected by
179 Because it is among the common causes of acute liver failure in intensive care units and in light
181 that ameliorates the effects of APAP-induced acute liver failure in the mouse and therefore may provi
182 rdose is a major cause of hepatotoxicity and acute liver failure in the U.S., but the pathophysiology
183 erdose is one of the most frequent causes of acute liver failure in the United States and is primaril
184 ry (DILI) is among the most common causes of acute liver failure in the United States, accounting for
190 ; APAP) overdose is the most common cause of acute liver failure in the Western world, with limited t
195 APAP) overdose is the most frequent cause of acute liver failure in young adults in the United States
196 y is associated with modulating pathology in acute liver failure, in liver regeneration, and in the m
199 ntracranial pressure monitored patients with acute liver failure, intracranial hypertension is common
200 process that occurs after liver injury, but acute liver failure is a complex and fatal disease which
205 usceptibility to development of ACLF whereas acute liver failure is likely due to direct hepatoxicity
207 mine-induced osmotic swelling, especially in acute liver failure, is a contributing factor: the osmot
208 rtality benefit, whereas in nonacetaminophen acute liver failure, it may be associated with worse out
209 s in patients with WD who have progressed to acute liver failure, leaving liver transplantation as th
211 of therapeutic hypothermia in patients with acute liver failure, multicenter, randomized, controlled
212 luded patients with nonacetaminophen-induced acute liver failure (n = 13), nonhepatic multiple organ
215 compartment syndrome must be suspected when acute liver failure occurs in patients with subcapsular
216 Intracranial hypertension in patients with acute liver failure often can be temporarily controlled
217 were measured in sera from 37 patients with acute liver failure on admission and from 20 healthy con
218 ssion was increased in acetaminophen-induced acute liver failure on day 1 compared with healthy contr
220 vides an excellent outcome for patients with acute liver failure or complications of end-stage liver
221 te attack in acute intermittent porphyria or acute liver failure or end-stage chronic liver disease i
222 Liver failure, whether arising directly from acute liver failure or from decompensated chronic liver
223 rated in patients with acetaminophen-induced acute liver failure (p = 0.042) at the time of liver tra
225 y between children and adults, the Pediatric Acute Liver Failure (PALF) Study Group evaluated NAC in
227 cranial pressure monitoring in patients with acute liver failure, patient selection and ancillary ass
228 continuous renal replacement therapy use in acute liver failure patients and to assess its impact on
229 l, pulmonary, and endocrine complications of acute liver failure patients are provided, including the
230 liver failure and non-acetaminophen induced acute liver failure patients compared with multiple orga
234 ergent practices and a paucity of studies in acute liver failure patients, additional information was
238 early phases of human acetaminophen-induced acute liver failure, peaking on day 1 of hospital admiss
239 amine the influence of acetaminophen-induced acute liver failure plasma and endogenous DNA on Toll-li
240 ls were incubated with acetaminophen-induced acute liver failure plasma with and without deoxyribonuc
241 upon stimulation with acetaminophen-induced acute liver failure plasma, which was abrogated by prein
243 rough the critical period for survival after acute liver failure, providing promising clues of integr
244 Few conditions are known to cause recurrent acute liver failure (RALF), and in about 50% of cases, t
247 ause of liver injury in 14% of patients with acute liver failure remains unknown (indeterminate).
250 erdose represents the most frequent cause of acute liver failure, resulting in death or liver transpl
252 plantation of hiPSC-EB-HLC in a rat model of acute liver failure significantly prolonged the mean sur
254 ntation, used in nearly 30% of patients with acute liver failure, still provides a life-saving altern
255 only measured clinical variables (called the Acute Liver Failure Study Group [ALFSG] index) and compa
259 which to study acute liver failure, the U.S. Acute Liver Failure Study Group has sought to standardiz
260 similar prognostic power as the established Acute Liver Failure Study Group index (C-statistic 0.87
261 late, 0.604 alone, 0.797 with FABP1) and the Acute Liver Failure Study Group prognostic index (early,
262 sorbent assay with clinical data from the US Acute Liver Failure Study Group registry (1998-2014).
263 ions, sera from 110 subjects enrolled in the Acute Liver Failure Study Group registry with indetermin
264 measured in 187 patients enrolled in the US Acute Liver Failure Study Group registry, and correlated
265 m samples of 681 adults enrolled in the U.S. Acute Liver Failure Study Group were tested for anti-HEV
266 sis, acute liver failure (from the Pediatric Acute Liver Failure Study Group), and liver transplantat
271 potentially life-threatening complication of acute liver failure, the syndrome of abrupt loss of live
272 ovide a uniform platform from which to study acute liver failure, the U.S. Acute Liver Failure Study
273 sity for patients with acetaminophen-induced acute liver failure to develop sepsis, which may culmina
274 agement of patients with paracetamol-induced acute liver failure to identify those needing emergency
275 ly in critically ill children with pediatric acute liver failure to provide stability and bridge to t
276 nin I levels may be helpful in patients with acute liver failure, to detect unrecognized myocardial d
277 , aripiprazole for MI, and telithromycin for acute liver failure) using Medicaid Analytic eXtracts (f
278 with neostigmine diminishes liver damage in acute liver failure via the cholinergic anti-inflammator
283 lure Study Group registry with indeterminate acute liver failure were analyzed with a similar but mor
284 tes from patients with acetaminophen-induced acute liver failure were assessed for apoptosis-associat
285 nuous renal replacement therapy in pediatric acute liver failure were changed in 2011 following preli
292 responses prevail during the later stages of acute liver failure where elevated levels of M30 are lik
293 evalence of lung injury is relatively low in acute liver failure, where 21% fulfilled acute respirato
294 a greatly enhanced Th1 cytokine response and acute liver failure, which mechanistically depended on T
295 s should be administered to any patient with acute liver failure who develops signs of the systemic i
297 lar fatty infiltration of hepatocytes causes acute liver failure with coagulopathy and encephalopathy
298 ells to be transplanted intraperitoneally in acute liver failure with the advantage of avoiding immun
299 liver injury (DILI) is an important cause of acute liver failure, with limited therapeutic options.