ライフサイエンスコーパス: rapidly progressive

1 children and adults, and does not seem to be rapidly progressive.

2 esence of preceding MS, C9ORF72-ALS was more rapidly progressive.

3 younger than 2 months old at diagnosis with rapidly progressive abdominal disease may benefit from e

4 Amyotrophic lateral sclerosis (ALS) is a rapidly progressive, adult-onset motor neuron disease th

5 Clinically advanced and rapidly progressive AIDS-associated Kaposi sarcoma (AIDS

6 Rapidly progressive alcohol-related liver injury was see

7 Rapidly progressive Alzheimer's disease that is associat

8 ary amyloidosis, due to the development of a rapidly progressive amyloid cardiomyopathy.

9 ho harbour genetic mutations associated with rapidly progressive amyotrophic lateral sclerosis.

10 Prion diseases are a group of rapidly progressive and always fatal neurodegenerative d

11 proteins is the hallmark of the late-onset, rapidly progressive and devastating neurodegenerative di

12 l hypertension (PAH), a disorder that can be rapidly progressive and fatal despite current treatments

13 Amyotrophic lateral sclerosis is a rapidly progressive and fatal disease.

14 from abnormal liver-function test results to rapidly progressive and fatal hepatic failure.

15 yotrophic lateral sclerosis (FALS) develop a rapidly progressive and fatal motor neuron disease (MND)

16 ALS is a rapidly progressive and fatal neurodegenerative disease

17 Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and fatal neurodegenerative disorder

18 ical course in Finnish children is uniformly rapidly progressive and fatal.

19 severe crescentic transformation, leading to rapidly progressive and irreversible allograft failure.

20 The clinical course is rapidly progressive and is lethal at a very young age in

21 transition from compensated hypertrophy to a rapidly progressive and lethal cardiomyopathy.

22 d mitochondrial respiratory dysfunction, and rapidly progressive and lethal dilated cardiomyopathy.

23 the patients with Bag3opathy may have had a rapidly progressive and more severe phenotype.

24 among them that meningococcemia is rare and rapidly progressive and patients are widely dispersed ge

25 Type 1 HRS is rapidly progressive and portends a very poor prognosis a

26 Cobalt can cause a distinctive, rapidly progressive and reversible depression of cardiac

27 Clinical presentation was marked by rapidly progressive and severe visual impairment for all

28 human pathogen Pseudomonas aeruginosa causes rapidly progressive and tissue-destructive infections, s

29 ch less frequent in childhood but may have a rapidly progressive and ultimately fatal course.

30 phologic differentiation the cells underwent rapidly progressive apoptosis.

31 Thus patients with rapidly progressive AVCD are treated with a sense of urg

32 fected individuals share a core phenotype of rapidly progressive axonal sensorimotor neuropathy (mani

33 Meningococcemia is an ideal model of a rapidly progressive bacterial infection associated with

34 Cochleovestibulopathy commonly presents with rapidly progressive bilateral hearing loss and/or acute

35 e presented to the emergency department with rapidly progressive bilateral visual loss over two days.

36 erm management of corticosteroid-responsive, rapidly progressive, bilateral sensorineural hearing los

37 Rapidly progressive bone loss is one feature of EOP.

38 RF72 cases show the features of a relatively rapidly progressive, but otherwise typical, variant of a

39 f small avascular masses of tumor cells into rapidly progressive cancers is triggered by the angiogen

40 level overexpression of the beta(2)AR caused rapidly progressive cardiac failure in this model.

41 s 4 and 6, alpha-MHC403/403 mice developed a rapidly progressive cardiomyopathy with left ventricular

42 venile onset of myopathy, 8 of whom also had rapidly progressive cardiomyopathy, requiring heart tran

43 -up maximal intimal thickness, >=0.5 mm) and rapidly progressive CAV (maximal intimal thickness, >=0.

44 ed in the diagnostic workup of patients with rapidly progressive central nervous system syndromes, pa

45 ations include structural abnormalities (eg, rapidly progressive cerebellar atrophy), myopathies (inc

46 mutations in the ABCD1 gene, which lead to a rapidly progressive cerebral inflammatory demyelination

47 genetically engineered mouse model develops rapidly progressive chemosensitive neuroblastoma and lac

48 Meningococcal disease is a rapidly progressive childhood infection of global import

49 The affected individuals presented with rapidly progressive childhood retinal degeneration, card

50 on of manganese in these patients results in rapidly progressive childhood-onset parkinsonism-dystoni

51 mon in adolescent and young adults and has a rapidly progressive clinical course and poor outcome due

52 vations, we hypothesize that during ACS, the rapidly progressive clinical course that can occur is ca

53 a more aggressive large cell lymphoma with a rapidly progressive clinical course.

54 neoplasm with cutaneous manifestations and a rapidly progressive clinical course.

55 e children who died at our institution after rapidly progressive clinical deterioration from this inf

56 e right ventricular failure is a complex and rapidly progressive clinical syndrome, whereby the right

57 A 62-year-old man presented with rapidly progressive cognitive decline associated with at

58 While the severe type I mouse model has a rapidly progressive condition mimicking type I SMA in hu

59 e a clinical spectrum ranging from a severe, rapidly progressive congenital or early infantile enceph

60 All four patients had a rapidly progressive course and have become mute and non-

61 le in different individuals, spanning from a rapidly progressive course to a long-term asymptomatic i

62 ho fail to respond to steroids or who have a rapidly progressive course.

63 nterferon alpha-2a and ribavirin may trigger rapidly progressive CR in patients with therapeutic immu

64 ce of congenital scoliosis is critical, as a rapidly progressive curve may lead to significant deform

65 ly surgical treatment is often necessary for rapidly progressive curves.

66 al for microRNA (miRNA) processing, leads to rapidly progressive DCM, heart failure, and postnatal le

67 Nephrogenic systemic fibrosis (NSF) is a rapidly progressive, debilitating condition that causes

68 1KI/KI/Reep1-/- mice exhibit early onset and rapidly progressive declines in several motor function t

69 Patients with ALS suffer from rapidly progressive degeneration of motor neurons ultima

70 the differential diagnosis of patients with rapidly progressive dementia (RPD).

71 Clinically characterized by rapidly progressive dementia and accounting for 85% of h

72 acterized by organic sleep related symptoms, rapidly progressive dementia and sympathetic symptoms.

73 An early and accurate in vivo diagnosis of rapidly progressive dementia remains challenging, despit

74 on-time MR images in an elderly patient with rapidly progressive dementia represents a specific findi

75 ed with HIV clade B, some patients develop a rapidly progressive dementia that if untreated results i

76 eutzfeldt-Jakob disease (sCJD) presents as a rapidly progressive dementia which is usually fatal with

77 Rapidly progressive dementia, altered behavior, and cere

78 Four of the patients developed rapidly progressive dementia, and the other 2 patients h

79 The classic triad of symptoms consists of: rapidly progressive dementia, myoclonus and typical elec

80 sporadic Creutzfeldt-Jakob disease (sCJD), a rapidly progressive dementia.

81 sporadic Creutzfeldt-Jakob disease (sCJD), a rapidly progressive dementia.

82 ly distinguishing treatable from untreatable rapidly progressive dementias and for future therapeutic

83 Because many rapidly progressive dementias are treatable, it is param

84 onditions that typically develop over years, rapidly progressive dementias can develop subacutely ove

85 Creutzfeldt-Jakob disease (CJD) and nonprion rapidly progressive dementias is important and sometimes

86 l adrenoleukodystrophy (CALD) is an X-linked rapidly progressive demyelinating disease leading to dea

87 tic fatal demyelinating disease, because its rapidly progressive demyelination in the nervous system

88 nephritis (GN) is a devastating disease with rapidly progressive deterioration in kidney function, wh

89 ial electrodiagnostic testing demonstrated a rapidly progressive diffuse sensory motor axonopathy, an

90 ve genetic defect in a pair of siblings with rapidly progressive dilated cardiomyopathy and death in

91 The cardiac defect results in a severe and rapidly progressive dilated cardiomyopathy.

92 Patients with CML in accelerated phase have rapidly progressive disease and are characteristically u

93 ic T lymphocytes (CTL) in an individual with rapidly progressive disease and high levels of viremia.

94 ffers the opportunity to treat patients with rapidly progressive disease and where autologous CAR-T-c

95 isease with no need for immediate therapy to rapidly progressive disease associated with therapeutic

96 nknown and understudied reasons some develop rapidly progressive disease at the menopause.

97 By contrast, rapidly progressive disease correlated with persistent a

98 tients with multiple sclerosis who display a rapidly progressive disease course and in whom potent ph

99 ommon c.745G>A mutation generally had a less rapidly progressive disease course than the 17 cases wit

100 of these enzymes were strikingly reduced in rapidly progressive disease in homozygous cystic mice an

101 ciency virus (SIV)-infected macaques develop rapidly progressive disease in the apparent absence of d

102 54, B*55, and B*56--has been associated with rapidly progressive disease in white patients with human

103 ity of some M. tuberculosis strains to cause rapidly progressive disease may relate to their intrinsi

104 apse, and all patients in this group died of rapidly progressive disease postrelapse.

105 nti-CTLA4 monoclonal antibody developed more rapidly progressive disease than sham-treated mice, wher

106 r, nearly one third of patients experience a rapidly progressive disease with a dismal outcome.

107 ent and incomplete response with evidence of rapidly progressive disease within 2.5 months posttransp

108 enotypic spectrum from infancy (early onset, rapidly progressive disease) to childhood/adolescence an

109 /null mice are normal, Pkd1RC/null mice have rapidly progressive disease, and Pkd1RC/RC animals devel

110 PC1 and PC2 in the kidney exhibited severe, rapidly progressive disease, illustrating the importance

111 nteresting feature of plague is that it is a rapidly progressive disease, suggesting that Y. pestis e

112 melanoma, a subset of patients will develop rapidly progressive disease.

113 th the possible exception of a subgroup with rapidly progressive disease.

114 ected, static CTL response in a patient with rapidly progressive disease.

115 of the identical mutation causes severe and rapidly progressive disease.

116 erapy, except in cases of visceral crisis or rapidly progressive disease.

117 A rapidly progressive disorder termed consumptive coagulop

118 ung development, with a phenotype comprising rapidly progressive distal airspace dilation, impaired g

119 y young age at onset, early weight loss, and rapidly progressive dopa-responsive parkinsonism, follow

120 7-year-old Italian boy with childhood-onset rapidly progressive encephalomyopathy and stroke-like ep

121 isability in the mother of a girl with RS to rapidly progressive encephalopathy in her brother.

122 Acute necrotizing encephalopathy (ANE) is a rapidly progressive encephalopathy that can occur in oth

123 High-risk neuroblastomas are rapidly progressive; even with intensive myeloablative c

124 omal acid alpha-glucosidase (Gaa), manifests rapidly progressive fatal cardiac and skeletal myopathy

125 BV-positive B lymphocytes and often follow a rapidly progressive fatal clinical course.

126 Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, fatal and transmissible neurodegene

127 ant differential regulation in patients with rapidly progressive fibrosis.

128 e of the highest-expressing line developed a rapidly progressive fibrotic dilated cardiomyopathy and

129 body titers did not differ between cats with rapidly progressive FIV disease and long-term survivors.

130 irus load is 1 to 2 logs higher in cats with rapidly progressive FIV disease than in long-term surviv

131 al Alzheimer's disease clinical subtypes-the rapidly progressive form (r-AD) and the posterior cortic

132 ing the pathogenetic mechanisms of this most rapidly progressive form of focal segmental sclerosis is

133 rovirulent virus called FrCasE that causes a rapidly progressive form of this disease.

134 Fibrosing cholestatic hepatitis (FCH) is a rapidly progressive form of viral hepatitis B that occur

135 c HDV infection commonly results in the most rapidly progressive form of viral hepatitis; it is the c

136 se requiring only brief hospitalization to a rapidly progressive, fulminant illness resulting in the

137 In this model of rapidly progressive gastritis due to H. pylori, the O ch

138 ntil age 12 years when they began developing rapidly progressive generalized dystonia.

139 s unique periodontal presentation were pain, rapidly progressive gingival recession, and significant

140 sease were 2.33 times more likely to develop rapidly progressive glaucoma disease despite significant

141 merular basement membrane (GBM) disease is a rapidly progressive glomerulonephritis (GN) resulting fr

142 lar basement membrane (GBM), usually causing rapidly progressive glomerulonephritis (GN).

143 Crescentic rapidly progressive glomerulonephritis (RPGN) represents

144 ococcal glomerulonephritis, IgA nephropathy, rapidly progressive glomerulonephritis (RPGN), and membr

145 iated vasculitis is the most common cause of rapidly progressive glomerulonephritis and immune-mediat

146 the use of PLEX to rescue organ function in rapidly progressive glomerulonephritis and lung haemorrh

147 Rapidly progressive glomerulonephritis in Goodpasture di

148 Rapidly progressing AVCD is analogous to rapidly progressive glomerulonephritis in that inner ear

149 Rapidly progressive glomerulonephritis is characterized

150 tation with full blown nephritic syndrome or rapidly progressive glomerulonephritis is uncommon and i

151 ciated vasculitis (AAV) is a common cause of rapidly progressive glomerulonephritis resulting in end-

152 e as a potential therapeutic intervention in rapidly progressive glomerulonephritis, we treated mice

153 ransplant nephritis alloantibodies mediating rapidly progressive glomerulonephritis.

154 ntigens (ANCA) is the most frequent cause of rapidly progressive glomerulonephritis.

155 ody (ANCA)-associated vasculitis (AAV), with rapidly progressive glomerulonephritis.

156 more frequently recognized in the setting of rapidly progressive glomerulonephritis.

157 pic haematuria and stable kidney function to rapidly progressive glomerulonephritis.

158 utrophil accumulation in post-infectious and rapidly progressive glomerulonephritis.

159 as a potential novel therapeutic strategy in rapidly progressive glomerulonephritis.

160 e focal segmental glomerulosclerosis (FSGS), rapidly progressive glomerulonephritis/idiopathic cresce

161 the formation of both cellular crescents in rapidly progressive GN and sclerotic lesions in FSGS.

162 otoxic serum to induce crescentic nephritis (rapidly progressive GN), this genetic inactivation of th

163 In a model of rapidly progressive GN, Notch3 expression was induced by

164 n in allografts as it can be associated with rapidly progressive graft failure.

165 HL) is characterized typically by bilateral, rapidly progressive hearing loss that responds therapeut

166 virus (EBOV) and Marburg virus (MARV) cause rapidly progressive hemorrhagic fever with high mortalit

167 es associating plaque angiogenesis with more rapidly progressive high-grade disease.

168 Children with rapidly progressive HIV-1 disease have more frequent EBV

169 ocrine cancers that are widely metastatic or rapidly progressive, however, the role of the medical on

170 dema appears to be decreasing, patients with rapidly progressive (hyperacute) liver failure, such as

171 lar mesenchymal cells of human subjects with rapidly progressive idiopathic pulmonary fibrosis (IPF).

172 Idiopathic pulmonary fibrosis is a rapidly progressive illness of unknown cause characteriz

173 Melioidosis pneumonia is often a rapidly progressive illness with high mortality, particu

174 All six rapidly progressive imatinib-resistant implants from fiv

175 luating the molecular etiology for isolated, rapidly progressive infantile hepatic failure.

176 specific immune responses over the course of rapidly progressive infection are not well defined.

177 nd that this inhibition did not abrogate the rapidly progressive infection in these RMs.

178 acid (AAI) nephropathy (AAN) is a common and rapidly progressive interstitial nephropathy caused by i

179 RGMc) cause juvenile hemochromatosis (JH), a rapidly progressive iron overload disorder in which expr

180 HIV-associated nephropathy (HIVAN) is a rapidly progressive kidney disease that is caused by HIV

181 A 78-year-old female was referred with rapidly progressive left ocular pain, redness, blurred v

182 However, in mouse infections, after a delay rapidly progressive lesions appeared, and purified amast

183 tosomal dominant inheritance of a late onset rapidly progressive leukodystrophy in which exome sequen

184 he clinical details of three patients with a rapidly progressive, levodopa-unresponsive bradykinetic-

185 Anaphylaxis is a rapidly progressive life-threatening disorder.

186 Anaphylaxis is a rapidly progressive life-threatening syndrome manifestin

187 ges from indolent, stable disease through to rapidly progressive, life-threatening disease.

188 Necrotizing fasciitis (NF) is a rapidly progressive, life-threatening soft-tissue infect

189 hepatitis C appears to cause more severe and rapidly progressive liver disease leading more frequentl

190 mia survivors with chronic HCV may have more rapidly progressive liver disease than has been previous

191 Chronic hepatitis D causes more rapidly progressive liver disease than HBV alone.

192 Four patients developed rapidly progressive liver failure while receiving interf

193 nuary 1995, 13 infants were transplanted for rapidly progressive liver failure.

194 with the onset of RD at 3 weeks of age and a rapidly progressive loss of photoreceptors.

195 er the next 3 months, serial audiograms show rapidly progressive loss of threshold and word recogniti

196 t-3-deleted mice to 95% oxygen caused a more rapidly progressive lung injury associated with alveolar

197 Acute myeloid leukemia (AML) is a rapidly progressive malignancy without effective therapi

198 included early lethal encephalopathies with rapidly progressive massive brain atrophy, severe develo

199 a Minnesota resident, aged 7 years, died of rapidly progressive meningoencephalitis after local fres

200 Ethylmalonic encephalopathy is a fatal, rapidly progressive mitochondrial disorder caused by ETH

201 Group 1: Three patients developed a rapidly progressive MND, less prominent symptoms of invo

202 ion of ILK in Pkd1(fl/fl) ;Pkhd1-Cre mice, a rapidly progressive model of ADPKD, decreased renal Akt/

203 mpairment and behavioral changes followed by rapidly progressive motor and gait impairment.

204 hQ200 mice is paralleled by earlier and more rapidly progressive motor deficits: progressive imbalanc

205 All bi-transgenic mice presented rapidly progressive motor deterioration, with wide-based

206 al care unit for evaluation and treatment of rapidly progressive motor weakness and encephalopathy.

207 ly Hdh(neoQ20)/Hdh(neoQ111) mice exhibited a rapidly progressive movement disorder that, in the absen

208 The approach to the diagnosis of a rapidly progressive multifocal brain disorder is discuss

209 Acute liver failure can be associated with rapidly progressive multiorgan failure and devastating c

210 otentially lethal disease that presents with rapidly progressive multiple organ thromboses.

211 There were 21 patients with rapidly progressive multiple sclerosis (MS) treated on a

212 nsthyretin-mediated (hATTR) amyloidosis is a rapidly progressive, multisystem disease that presents w

213 ine spinal muscular atrophy (HCSMA) features rapidly progressive muscle weakness that affects muscles

214 and lower motor neuron dysfunction and loss, rapidly progressive muscle weakness, wasting and death.

215 a new recessive mouse mutation that causes a rapidly progressive muscular dystrophy and a neonatal fo

216 A case of fatal ehrlichiosis with rapidly progressive myocarditis and multiorgan failure f

217 A 69-yr-old retired fisherman with rapidly progressive necrotizing fasciitis from Photobact

218 Deletion of CSPalpha produces rapidly progressive neurodegeneration in mice, presumabl

219 port defects have also been observed in more rapidly progressive neurodegeneration, such as that obse

220 Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disease of motor n

221 lateral sclerosis is a relatively common and rapidly progressive neurodegenerative disease that, in t

222 y form of X-linked adrenoleukodystrophy is a rapidly progressive neurodegenerative disease, as devast

223 c lateral sclerosis (ALS) is one of the most rapidly progressive neurodegenerative diseases of unknow

224 ion diseases are universally fatal and often rapidly progressive neurodegenerative diseases.

225 Prion disease is a rapidly progressive neurodegenerative disorder caused by

226 Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disorder due to se

227 zheimer's disease and Parkinson disease, are rapidly progressive neurodegenerative disorders caused b

228 n levels induce SMA pathology by instigating rapidly progressive neurodegenerative pathways in lower

229 l (COFS) syndrome is a recessively inherited rapidly progressive neurologic disorder leading to brain

230 An acute and rapidly progressive neurologic syndrome developed in thr

231 ro-oculo-facio-skeletal (COFS) syndrome is a rapidly progressive neurological disorder leading to bra

232 SF RT-QuIC testing in 2,141 patients who had rapidly progressive neurological disorders, determined d

233 The latter develop rapidly progressive neurological signs around 20 days an

234 retrograde signaling pathways correlate with rapidly progressive neuronal cell death.

235 besity and nutrition in the development of a rapidly progressive nonalcoholic steatohepatitis phenoty

236 imeric murine oncornavirus FrCas(E) causes a rapidly progressive noninflammatory spongiform encephalo

237 Rapidly progressive OA occurred only in tanezumab-treate

238 To explore an anatomic basis for rapidly progressive OA, this observational study compare

239 We describe 2 Greek siblings who developed a rapidly progressive oculopharyngeal somatic syndrome, at

240 Infection by Ebola virus causes rapidly progressive, often fatal, symptoms of fever, hem

241 f knowledge about the mechanisms involved in rapidly progressive osteoarthritis are also discussed an

242 of NGF inhibitors also increased the risk of rapidly progressive osteoarthritis in a small percentage

243 istration of the same antibodies in the more rapidly progressive P301S tauopathy model not only reduc

244 31-year-old Caucasian female presented with rapidly progressive painful proptosis of the right eye a

245 Highly aggressive Burkitt lymphoma (BL) with rapidly progressive painful proptosis of the right eye i

246 nerative disease characterized clinically by rapidly progressive paralysis leading ultimately to deat

247 nical course of CMT4J, including asymmetric, rapidly progressive paralysis, in two siblings.

248 imeric murine oncornavirus FrCas(E) causes a rapidly progressive paralytic disease associated with sp

249 neurodegenerative disorder characterized by rapidly progressive parkinsonism-dystonia in childhood.

250 Rapidly progressive PDAC was observed in the setting of

251 This report describes a case of rapidly progressive periodontal tissue breakdown and bon

252 rly-onset periodontitis (G-EOP, encompassing rapidly progressive periodontitis and generalized juveni

253 by hyperkeratosis of the palms and soles and rapidly progressive periodontitis resulting in loss of d

254 s sarcoidosis of the jaw bones that mimicked rapidly progressive periodontitis.

255 nderstanding of the etiology of juvenile and rapidly progressive periodontitis.

256 The patient presented with rapidly progressive peripheral field loss and photopsias

257 Within 31 months, six imatinib-resistant rapidly progressive peritoneal implants (metastatic foci

258 ing this autoregulatory mechanism produces a rapidly progressive phenotype and dose-dependent lethali

259 ith digenic animals exhibiting phenotypes of rapidly progressive PKD and early lethality resembling c

260 ely progressive PKD), kidneys from cpk mice (rapidly progressive PKD), and human autosomal dominant P

261 Our findings suggest that rapidly progressive pneumoconiosis in these miners was a

262 Recent recognition of rapidly progressive pneumoconiosis in younger miners, ma

263 fication scheme to determine if criteria for rapidly progressive pneumoconiosis were confirmed.

264 deficiency (MoCD) is characterised by early, rapidly progressive postnatal encephalopathy and intract

265 A severe, rapidly progressive, predominantly length dependent axon

266 eness, and between patients with typical and rapidly progressive presentations of neurodegenerative d

267 promotes both reactivation TB from LTBI and rapidly progressive primary TB following recent exposure

268 ) with associated necrotizing fasciitis is a rapidly progressive process that kills 30-60% of patient

269 ossible to recognise that some patients with rapidly progressive psychiatric symptoms or cognitive im

270 Four patients required reoperation for rapidly progressive pulmonary homograft stenosis; in all

271 o Jan 31, 2009, in patients with metastatic, rapidly progressive, radioiodine-refractory differentiat

272 that develop a severe glomerulosclerosis and rapidly progressive renal disease overexpress IL-4 in vi

273 en 20 years since the first description of a rapidly progressive renal disease that is associated wit

274 nction test results were normal, but she had rapidly progressive renal failure.

275 SP-B gene (121ins2) and is characterized by rapidly progressive respiratory failure immediately afte

276 aques and end-stage pulmonary fibrosis, with rapidly progressive respiratory failure.

277 of ocular involvement and the potential for rapidly progressive retinal vascular abnormalities and d

278 Of these patients, 15 had a severe rapidly progressive sensorimotor PN (9 were wheelchair d

279 ymphomatous ONI is rare and characterized by rapidly progressive severe visual impairment.

280 respiratory distress syndrome (ARDS) that is rapidly progressive, severe, and refractory to conventio

281 cocci (CoNS) that is responsible for severe, rapidly progressive skin and soft tissue infections and

282 riant of Friend MuLV (F-MuLV) which causes a rapidly progressive spongiform neurodegenerative disease

283 le cardiac monitor that alerts patients with rapidly progressive ST-segment deviation.

284 All developed rapidly progressive tetraplegia.

285 unction measurements showed USH3A to be more rapidly progressive than USH2A.

286 diabetic guinea pigs resulted in severe and rapidly progressive tuberculosis (TB) with a shortened s

287 olochic acid nephropathy is characterized by rapidly progressive tubulointerstitial nephritis culmina

288 ogic and clinical features, characterized by rapidly progressive tumors with high rates of extranodal

289 y healthy child who developed acute, severe, rapidly progressive vanishing bile duct syndrome shortly

290 Rapidly progressive vasculopathy by IVUS, defined as an

291 l follow-up of 5.9 years, more patients with rapidly progressive vasculopathy died, as compared with

292 Rapidly progressive vasculopathy was defined as the chan

293 2 (2.1%) of 76 patients without (p = 0.003) rapidly progressive vasculopathy.

294 t report of organ donation in a patient with rapidly progressive ventilator-dependent ALS.

295 In a young child with bilateral rapidly progressive vision loss and macular disturbance,

296 N) is a disorder characterized by severe and rapidly progressive visual loss when caused by a mutatio

297 ozygous Tk2 mutant (Tk2(-/-)) mice developed rapidly progressive weakness after age 10 days and died

298 disorder characterized by motor neuron loss, rapidly progressive weakness and early death has been co

299 The disease is rapidly progressive with loss of ambulation after a medi

300 onsistent with humoral rejection, and showed rapidly progressive xenograft failure.