ライフサイエンスコーパス: syndrome

1 rimary progressive aphasia, and corticobasal syndrome).

2 vioural phenotypes associated with fragile X syndrome.

3 hematologic malignancies than classic Sweet syndrome.

4 contributes to the dramatic disease Timothy Syndrome.

5 t E. coli-induced acute respiratory distress syndrome.

6 d to be the cause of the patient's nephrotic syndrome.

7 in models of Alzheimer disease and Angelman syndrome.

8 congenital malformations, and Guillain-Barre syndrome.

9 CT in patients with suspected paraneoplastic syndrome.

10 s done in 739 adults with type 1 hepatorenal syndrome.

11 ouse model of systemic inflammatory response syndrome.

12 the association of this disorder with Cowden syndrome.

13 nce definition of acute respiratory distress syndrome.

14 Cre-inducible transgene causes an autoimmune syndrome.

15 ong-term clinical outcomes for carpal tunnel syndrome.

16 ive behavioural movements observed in Dravet syndrome.

17 ociated with the increased risk of metabolic syndrome.

18 ystem risk factors for iatrogenic withdrawal syndrome.

19 d safety in patients with type 1 hepatorenal syndrome.

20 in patients with acute respiratory distress syndrome.

21 to 2 years after acute respiratory distress syndrome.

22 mous cell carcinoma in patients with Kindler syndrome.

23 s, such as those associated with pollen-food syndrome.

24 T), suggesting an immune reconstitution-like syndrome.

25 in patients stabilized after acute coronary syndrome.

26 ive subjects with acute respiratory distress syndrome.

27 ent with keratitis-ichthyosis-deafness (KID) syndrome.

28 ncidence of early acute respiratory distress syndrome.

29 erved in patients with various forms of WHIM syndrome.

30 until 5 years postacute respiratory distress syndrome.

31 ction against human Zika virus infections or syndromes.

32 r, 2 archetypical monogenic autoinflammatory syndromes.

33 neurodevelopmental disorders and overgrowth syndromes.

34 d and contribute to hereditary breast cancer syndromes.

35 he phenotypes of patients exhibiting various syndromes.

36 m understanding of such immune dysregulation syndromes.

37 site 1 (EVI) and its variant myelodysplastic syndrome 1 (MDS)/EVI encode zinc-finger proteins that ha

38 ) had at least 1 gene mutation: 37 had Lynch syndrome (13, MLH1 [including one with constitutional ML

39 Chromosome 22q11.2 deletion syndrome (22q11.2DS) is associated with a more than 20-f

40 Although 22q11.2 deletion syndrome (22q11DS) is associated with early-life behavio

41 llowed by palmar-plantar erythrodysaesthesia syndrome (87 [18%]), and vomiting (24 [5%]).

42 ZNF423 mutations are associated with Joubert Syndrome, a ciliopathy causing cerebellar vermis hypopla

43 dence of AKI in patients with acute coronary syndrome (ACS) enrolled in the MATRIX-Access (Minimizing

44 the 310 subjects, 138 had an acute coronary syndrome (ACS), 101 of whom underwent desensitizations,

45 atients with biopsy-proven PMN and nephrotic syndrome after 6 months of nonimmunosuppressive antiprot

46 In the six patients with aspiration syndrome after mechanical ventilation, and therefore wit

47 as a result of an immune reconstitution-like syndrome after starting ART.

48 l crypts and that ATM inhibition promotes GI syndrome after TBI.

49 Jagged1 knockout mice, a model for Alagille Syndrome (AGS), also display stapes and incus defects.

50 53H-CFH, linked to atypical hemolytic uremic syndrome (aHUS), was defective in C3bBb decay-accelerati

51 -liver-related non-acquired immunodeficiency syndrome (AIDS)-related (NLR-NAR) events and mortality i

52 Alloimmune-mediated lung syndromes (allo-LSs) are life-threatening complications

53 mon pediatric mitochondrial disease is Leigh syndrome, an episodic, subacute neurodegeneration that c

54 ents with stable angina or an acute coronary syndrome, an iFR-guided revascularization strategy was n

55 (95% CI 1.30-1.96; P < 0.001) for metabolic syndrome and 1.37 (1.03-1.82; P = 0.021) for type 2 diab

56 erculosis-related acute respiratory distress syndrome and 451 acute respiratory distress syndrome-oth

57 ng chromosome gains and losses, such as Down syndrome and cancer.

58 but has other findings not described in this syndrome and common in OTCS.

59 composite of systemic inflammatory response syndrome and dysfunction of at least 1 organ system of t

60 utic approach for treatment of the metabolic syndrome and dyslipidemia, while avoiding systemic toxic

61 for Alzheimer's disease, especially for Down syndrome and EGCG which inhibits Dyrk1A may have potenti

62 nk between ZIKV infection and Guillain-Barre syndrome and fetal neurological defects, including micro

63 BC and MACE was consistent in acute coronary syndrome and non-acute coronary syndrome presentations (

64 Systemic Inflammatory Response Syndrome and quick Sequential Organ Failure Assessment s

65 and CCL2 mRNAs), and attenuated the wasting syndrome and severity of colitis ( approximately 70% red

66 Participants with clinical Rett syndrome and those with MECP2 mutations without the clin

67 previously described in patients with MEN 2A syndrome and to discuss the association of this disorder

68 Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS/TEN) are ra

69 lar diseases affecting the anterior (dry eye syndrome) and posterior (age-related macular degeneratio

70 ients with glaucoma, 1 patient with Stickler syndrome, and 1 patient with an IOL exchange at 8 months

71 ty patients (83%) developed cytokine release syndrome, and eight (33%) developed neurotoxicity, which

72 oral-facial-digital syndrome, Meckel-Gruber syndrome, and Joubert syndrome exhibiting a range of cil

73 te kidney injury, acute respiratory distress syndrome, and need for vasopressors.

74 lure, and hospitalization for acute coronary syndrome, and the incidence of acute pancreatitis, pancr

75 Organization criteria for serrated polyposis syndrome, and their relatives have similar risks for col

76 using the Structured Interview for Prodromal Syndromes, and for attention-deficit/hyperactivity, subs

77 tial and complete remission of the nephrotic syndrome; and a composite of doubling of serum creatinin

78 isolated from patients with antiphospholipid syndrome (APS) display higher avidity binding to FXa wit

79 RATIONALE: Acute respiratory distress syndrome (ARDS) is caused by widespread endothelial barr

80 IONALE: Following acute respiratory distress syndrome (ARDS), joblessness is common but poorly unders

81 ult patients with acute respiratory distress syndrome (ARDS).

82 in patients with acute respiratory distress syndrome (ARDS).

83 ich provoke the onset and progression of the syndrome are largely unknown.

84 mentation to patients with fat malabsorption syndromes as well as patients with other metabolic abnor

85 Angelman syndrome (AS) is a neurogenetic disorder caused by delet

86 ur bank we determine the prevalence of Lynch syndrome, associated cancer risks and pathogenicity of s

87 ested and digested samples towards metabolic syndrome-associated enzymes (alpha-amylase, alpha-glucos

88 gene expression and the epigenetics of Goltz syndrome-associated mutations and the local effects of A

89 verall survival and bronchiolitis obliterans syndrome at 2 years.

90 Bosma arhinia microphthalmia syndrome (BAMS) is an extremely rare and striking condit

91 lesion can cause a complex neuropsychiatric syndrome based on that lesion's unique pattern of functi

92 ted children with acute respiratory distress syndrome (Berlin).

93 blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).

94 The first patient was diagnosed with Bartter syndrome (BS) >30 years ago.

95 be beneficial in acute respiratory distress syndrome, but cooling causes shivering and increases met

96 prove outcomes for patients with hepatorenal syndrome, but trials have reported variable efficacy.

97 he developmental disorder Beckwith Wiedemann Syndrome (BWS) and with several cancers.

98 fter induction of acute respiratory distress syndrome by hydrochloric acid instillation, animals unde

99 ssociated immune reconstitution inflammatory syndrome (C-IRIS), upon initiation of antiretroviral the

100 g panel incorporated 38 inherited arrhythmia syndrome candidate genes and another 33 genes not previo

101 patients with cryopyrin-associated periodic syndromes (CAPS) and familial Mediterranean fever, 2 arc

102 y known as the cryopyrin-associated periodic syndromes (CAPS).

103 roximately 70% of autosomal-dominant Robinow syndrome cases remain molecularly unsolved.

104 ndrome is a rare colon cancer predisposition syndrome caused by a duplication of a noncoding sequence

105 Delirium is a common and serious psychiatric syndrome caused by an underlying medical condition.

106 mages neurons, explaining pathology of human syndromes caused by betaIII spectrin mutations.

107 r the treatment of athymic complete DiGeorge syndrome (cDGS).

108 Down syndrome cell adhesion molecule (Dscam) is expressed by

109 ) in cirrhosis is an increasingly recognized syndrome characterized by acute decompensation, organ fa

110 arents to identify the genetic etiology of a syndrome characterized by neonatal diabetes, sensorineur

111 al tubular dysfunction indicative of Fanconi syndrome, characterized by glycosuria, aminoaciduria, ca

112 g-remitting MS (RRMS) or clinically isolated syndrome (CIS) with disease onset before 18 years of age

113 individuals within 10 days of acute coronary syndrome, combination therapy seemed to be more effectiv

114 hemisphere has been linked to Guillain-Barre syndrome, congenital microcephaly, and devastating ophth

115 future research into the effect of carcinoid syndrome control on patient survival.

116 Middle East respiratory syndrome coronavirus (MERS-CoV) is an important emerging

117 Severe acute respiratory syndrome coronavirus (SARS-CoV) causes lethal disease in

118 Severe acute respiratory syndrome coronavirus (SARS-CoV) is a highly pathogenic r

119 cular mechanisms that underlie restless legs syndrome could lead to new treatment options.

120 e (SARS)-CoV and the Middle East respiratory syndrome-CoV, cause acute respiratory illness.

121 ssment score, systemic inflammatory response syndrome criteria, the National and Modified Early Warni

122 Cantu syndrome (CS) is a condition characterized by a range of

123 cancer is a major component cancer of Cowden syndrome (CS), a disorder typically associated with germ

124 Metabolic syndrome defines a cluster of interrelated risk factors

125 schizophrenia, bipolar disorder, Tourette's syndrome, dementia, alcohol-induced delusions and obsess

126 eral changing notions in the approach to G1D syndrome diagnosis and treatment, such as the perceived

127 st month of life), 44.5% had classic Bartter syndrome (diagnosis during childhood, hypercalciuria, an

128 is currently the best animal model for this syndrome, displaying functional hyperdopaminergia and ne

129 gue hemorrhagic fever (DHF) and dengue shock syndrome (DSS) occur.

130 ngue hemorrhagic fever (DHF) or dengue shock syndrome (DSS).

131 Here, we describe a family with Liddle syndrome due to a mutation in alphaENaC.

132 During the acute respiratory distress syndrome, epithelial cells, primarily alveolar type (AT)

133 or mismatch repair (MMR) deficiency in Lynch syndrome establishing a new paradigm, combinatorial chem

134 l defects overlapping with Ellis-van Creveld syndrome (EvC), a disease caused by diminished Hh signal

135 s reach, patients with complex regional pain syndrome exhibited a bias away from the affected side.

136 yndrome, Meckel-Gruber syndrome, and Joubert syndrome exhibiting a range of ciliopathic defects.

137 ) are associated with the genome instability syndrome Fanconi anemia (FA).

138 rradiation with these doses caused lethal GI syndrome, focal (5 mm) radiation of the intestine did no

139 ompletion is associated with lower metabolic syndrome for whites across all levels of childhood disad

140 nd/or polyuria), and 26.0% had Gitelman-like syndrome (fortuitous discovery of hypokalemia with hypom

141 The post-thrombotic syndrome frequently develops in patients with proximal d

142 Fragile X Syndrome (FX) is generally considered a developmental di

143 al and anatomical deficits seen in fragile X syndrome (FXS) are widely believed to result from imbala

144 cits in FXS.SIGNIFICANCE STATEMENT Fragile X Syndrome (FXS) is the most common inheritable form of in

145 Fragile X syndrome (FXS), caused by the loss of functional FMRP, i

146 knock-out mice, the mouse model of fragile X syndrome (FXS).

147 its and sensory dysfunction in the fragile X syndrome (FXS).

148 Although tendencies were reported for this syndrome, genetic variations influencing risk and diseas

149 wever, relevant pathomechanisms of nephrotic syndrome have not been studied in nephrocytes.

150 ic acidosis and stroke-like episodes (MELAS) syndrome, however, the common m.3243 A > G mutation was

151 ular rejection, and bronchiolitis obliterans syndrome; however, the significance of circulating antib

152 outbreak with >800 cases of hemolytic uremic syndrome (HUS) in Germany, including 90 children.

153 ota and clinical features of irritable bowel syndrome (IBS).

154 ar, and is a risk factor for irritable bowel syndrome (IBS).

155 hogen that has been linked to Guillain-Barre syndrome in adults and congenital microcephaly in develo

156 us infection could also cause Guillain-Barre syndrome in adults.

157 therapy can cause a debilitating withdrawal syndrome in chronic users.

158 el of risk factors for iatrogenic withdrawal syndrome in critically ill children.

159 lmark of leukocyte adhesion deficiency (LAD) syndrome in humans, characterized by impaired leukocyte

160 omotes ectopic adiposity and cardiometabolic syndrome in humans.

161 ical presentation of a congenital myasthenic syndrome in one patient (p.Pro210Leu), to severe neurode

162 The identification of alpha-gal syndrome in patients with IA supports the need for routi

163 Congenital Zika syndrome in the current study had severe ocular abnormal

164 ns in patients with suspected acute coronary syndrome in which the diagnosis was adjudicated accordin

165 od disadvantage for depression and metabolic syndrome in young adulthood, across race/ethnicity.

166 associated with florid episodic CNS clinical syndromes in addition to peripheral neuropathy.

167 nt a promising target to manage inflammatory syndromes in diseases with active type I IFN signature.

168 included patients, 98 (39.2%) had aspiration syndrome, including 92 before mechanical ventilation dis

169 l that recapitulates many features of Dravet syndrome, including spontaneous seizures, premature deat

170 disease or presenting with an acute coronary syndrome, including ST-segment-elevation myocardial infa

171 ystemic lupus erythematosus (SLE), Sjogren's syndrome, inflammatory bowel disease and multiple sclero

172 The progressive relation among metabolic syndrome, insulin resistance (IR), and dementia has rece

173 Nephrotic syndrome is a common disorder in adults and children who

174 Long-QT syndrome is a potentially fatal condition for which 30%

175 Hunter syndrome is a rare but devastating childhood disease cau

176 Hereditary mixed polyposis syndrome is a rare colon cancer predisposition syndrome

177 Axenfeld-Rieger syndrome is caused by mutations in PITX2 or FOXC1 and an

178 Steroid-resistant nephrotic syndrome is characterized by podocyte dysfunction.

179 Antiphospholipid syndrome is characterized by recurrent thrombosis and ge

180 ty and even mortality, particularly when the syndrome is complicated by intracranial haemorrhage or b

181 he basis for intellectual impairment in Down syndrome is hindered by the large number of genes duplic

182 e also analyze whether this variant of Sweet syndrome is more frequently associated with hematologic

183 Phenotypic heterogeneity in Tourette syndrome is partly due to complex genetic relationships

184 Although narcotic bowel syndrome is rarely diagnosed, given the current epidemic

185 the defective gene in human Chanarin-Dorfman syndrome, is a highly conserved regulator of adipose tri

186 rophic lateral sclerosis (ALS) and fragile X syndrome, is challenging for short-read whole-genome seq

187 the developmental disorders Joubert and MORM syndromes, is essential for the function of the primary

188 round to generate a mouse model for Alagille syndrome (Jag1(Ndr/Ndr) mice).

189 a number of ciliopathies, including Joubert syndrome (JS).

190 olic disorders, including obesity, metabolic syndrome, lipodystrophy, and cachexia.

191 tients with inherited hematologic malignancy syndromes may present without classic clinical stigmata

192 imilarly, high-risk cases of myelodysplastic syndrome (MDS) showed far greater suppression of TEs tha

193 understanding of genomics in myelodysplastic syndromes (MDS) and leukemias and the limitations of pre

194 c myeloid leukemia (CML) and myelodysplastic syndromes (MDS) either sensitive or resistant to their r

195 atologic conditions, such as myelodysplastic syndromes (MDS).

196 reviously connected with oral-facial-digital syndrome, Meckel-Gruber syndrome, and Joubert syndrome e

197 Metabolic syndrome (MetS) has been associated with chronic damage

198 ne in individuals with established metabolic syndrome (MetS) or diabetes identifies CHD and ASCVD pro

199 Marfan syndrome (MFS) is a heritable connective tissue disorder

200 findings of adults and children with Marfan syndrome (MFS) recruited from 2 annual National Marfan F

201 cystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a congenital disorder characterized

202 cystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a congenital visceral myopathy chara

203 visual and olfactory sensory systems in Down syndrome model mice, which provide insight into defects

204 cluding those with basal-cell nevus (Gorlin) syndrome, need extended treatment.

205 r of PCIs in patients with no acute coronary syndrome/no prior coronary artery bypass graft surgery t

206 complex genetic relationships among Tourette syndrome, obsessive-compulsive disorder (OCD), and atten

207 Grade 3-4 cytokine release syndrome occurred in 46% of patients following T cell th

208 and polygenic load associated with Tourette syndrome, OCD, and ADHD were estimated.

209 ephalopathy syndrome (RPLS), is a neurotoxic syndrome of cerebral vasoregulation classically characte

210 but not mTORC2 alone develop a Fanconi-like syndrome of glucosuria, phosphaturia, aminoaciduria, low

211 This syndrome of pre-rain green-up has long been recognized a

212 ren who experience an acquired demyelinating syndrome of the central nervous system will have a monop

213 -) mice, an animal model of 22q11.2 deletion syndrome, one of the most common genetic risk factors fo

214 were collected at acute respiratory distress syndrome onset and at 24 hours in 352 children between 2

215 At acute respiratory distress syndrome onset, neither mechanical variables nor PaO2/FI

216 scribed, such as the prevention of metabolic syndrome or type 2 diabetes.

217 New York in patients without acute coronary syndromes or previous coronary artery bypass graft surge

218 immune diseases, including primary Sjogren's syndrome (OR = 2.45 in Chinese, OR = 2.35 in European Am

219 ted with a higher incidence of the metabolic syndrome (OR=2.49; 95% CI 1.30-4.77), a steeper increase

220 nical manifestations of Birt-Hogg-Dube (BHD) syndrome, or with BMF kidney tumours as the only manifes

221 syndrome and 451 acute respiratory distress syndrome-others) with acute respiratory distress syndrom

222 ection and Natural History in Parkinson Plus Syndromes Parkinson Plus Score and the Clinical Global I

223 THODS AND A total of 135 symptomatic Brugada syndrome patients having implantable cardiac defibrillat

224 ortality and complications in acute coronary syndrome patients treated with extracorporeal circulator

225 Mutant mice developed a Bartter syndrome phenotype, characterized by renal salt loss, ma

226 d a compelling explanation for severe Hunter syndrome phenotypes.

227 udy was to investigate whether post-hospital syndrome (PHS) places patients undergoing elective herni

228 (LS) pupillary block (PB), and plateau iris syndrome (PL).

229 ull-blown immune reconstitution inflammatory syndrome (PML-IRIS).

230 .5% had a phenotype of ante/neonatal Bartter syndrome (polyhydramnios or diagnosis in the first month

231 laxity are classified as Pseudo Prune Belly syndrome (PPBS).

232 ed since posterior reversible encephalopathy syndrome (PRES) was first described in 1996.

233 Posterior reversible encephalopathy syndrome (PRES), also called the acute hypertensive ence

234 ute coronary syndrome and non-acute coronary syndrome presentations (interaction P=0.15).

235 While daily seizures are uncommon in Rett syndrome, prolonged remission is less common than in oth

236 in actin dynamics including Wiskott-Aldrich syndrome protein (WASp) were regulated by NPM-ALK.

237 e we show that deficiency of Wiskott-Aldrich syndrome protein (WASp), which signals to the actin cyto

238 The Werner syndrome protein (WRN) is a RecQ family helicase that ha

239 The Werner syndrome protein (WRN) suppresses the loss of telomeres

240 Cockayne syndrome protein B (CSB) belongs to the SWI2/SNF2 ATP-de

241 domain and an actin-binding Wiskott-Aldrich syndrome protein homology 2 (WH2) domain that is absent

242 The hydrolethalus syndrome protein HYLS-1 is the only centriolar protein k

243 Wiskott-Aldrich syndrome protein-deficient neutrophils are unable to pol

244 uterine neoplasms that develop in the HPT-JT syndrome, provide in vivo models for future studies of t

245 T)/ventricular fibrillation (VF) and Brugada syndrome-related symptoms, and 72 (group 2) having induc

246 ) and traits would be correlated to produce 'syndromes' resulting from phylogeny and environmental va

247 s meeting predefined criteria for aspiration syndrome routinely underwent telescopic plugged catheter

248 and reversible posterior leukoencephalopathy syndrome (RPLS), is a neurotoxic syndrome of cerebral va

249 Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder ch

250 Rett syndrome (RTT) is a debilitating neurological disorder c

251 Sudden arrhythmic death syndrome (SADS) describes a sudden death with negative a

252 itis C virus (HCV), Severe acute respiratory syndrome (SARS), coxsackie viruses, and rhinoviruses.

253 (CoVs), such as the severe acute respiratory syndrome (SARS)-CoV and the Middle East respiratory synd

254 0.06-0.26) against severe acute respiratory syndrome (SARS).

255 on mutations in the Shwachman-Bodian-Diamond syndrome (sbds) gene.

256 support volume in patients with short bowel syndrome (SBS) with intestinal failure, increasing intes

257 t one of the following Positive and Negative Syndrome Scale (PANSS) items: P1 (delusions), P2 (concep

258 among patients with Middle East respiratory syndrome severe acute respiratory infection from other e

259 Alcohol withdrawal syndrome severity was defined by CIWA-Ar score as minima

260 Severe fever with thrombocytopenia syndrome (SFTS) is an emerging viral disease for which t

261 Sudden infant death syndrome (SIDS), the leading cause of postneonatal infan

262 the Structured Interview for Psychosis-Risk Syndromes (SIPS), and rated these according to MacArthur

263 d removed the systemic inflammatory response syndrome (SIRS) criteria from the sepsis definition.

264 he validated Short Questionnaire for Dry Eye Syndrome (SQDES) as a previous diagnosis of DED by a cli

265 Short QT syndrome (SQTS) is a rare condition characterized by abn

266 Steroid-resistant nephrotic syndrome (SRNS), a heterogeneous disorder of the renal g

267 Primary Sjogren's syndrome (SS) is a common chronic autoimmune disease cha

268 icate asymptomatic carriage or a less severe syndrome, such as upper respiratory infection).

269 hort of long-term acute respiratory distress syndrome survivors, better annual physical and quality o

270 hundred fifty-six acute respiratory distress syndrome survivors.

271 its testing in Finnish patients with RIDDLE syndrome symptoms.

272 isk of TB immune reconstitution inflammatory syndrome (TB-IRIS), in Cape Town, South Africa.

273 d as a model for human testicular dysgenesis syndrome (TDS).

274 sk-taking behaviors constituted a behavioral syndrome that significantly differed between urban and f

275 Syndromes that do not fall easily into one of these thre

276 sent review will outline the spectrum of LMN syndromes that may develop in adulthood and provide a fr

277 Fragile X syndrome, the most common known monogenic cause of autis

278 ts with a high likelihood of the BAP1 cancer syndrome through personal and family history and TBSE fo

279 jury that can range from a fully recoverable syndrome to one that leads to chronic remodeling and dil

280 g event (also known as a clinically isolated syndrome) to multiple sclerosis.

281 r1 knock-out (KO) mice, a model of Fragile-X Syndrome, to test the E/I imbalance theory.

282 tine Leukocidin toxin (PVL), and toxic shock syndrome toxin-1 (tst) genes.

283 ent Patterns and Events After Acute Coronary Syndrome (TRANSLATE-ACS) study between April 1, 2010, an

284 Among infants with the neonatal abstinence syndrome, treatment with sublingual buprenorphine result

285 Toxic shock syndrome (TSS) is caused by staphylococcal and streptoco

286 mes administered for presumptive toxic shock syndrome (TSS), but its frequency of use and efficacy ar

287 Usher syndrome type III (USH3) characterized by progressive lo

288 dominant haploinsufficiency Saethre-Chotzen syndrome (typically associated with craniosynostosis), s

289 Acute respiratory distress syndrome was induced by repeated lung lavages and injuri

290 ogic symptoms reminiscent of Wiskott-Aldrich syndrome (WAS).

291 at we suggest calling, "astronaut ophthalmic syndrome." We maintain that this condition is geneticall

292 rome-others) with acute respiratory distress syndrome were admitted.

293 se with MECP2 mutations without the clinical syndrome were recruited through the Rett Natural History

294 owed no phylogenetic signal, suggesting that syndromes were environmentally determined.

295 without ST-segment elevation acute coronary syndrome, were randomly assigned to radial or femoral ac

296 This paper introduces a "blue pyjama syndrome" (whereby wearing hospital pyjamas results in a

297 es of glucocorticoid excess, such as Cushing syndrome, which are associated with frank dyslipidemia.

298 und in >80% of patients with myelodysplastic syndrome with ring sideroblasts (MDS-RS).

299 ria also include definitions for variant PSP syndromes with different patterns of movement, language,

300 nfatal myocardial infarction, acute coronary syndrome without myocardial infarction, coronary revascu