ライフサイエンスコーパス: idiopathic

1 g 30 patients with B27-AAU, 16 patients with idiopathic AAU, and 20 patients with cataracts underwent

2 olfactory processing in patients with CA or idiopathic acquired anosmia (IA) in comparison to normos

3 pathic pulmonary fibrosis comprised 34% with idiopathic acute exacerbation (65%) being the most commo

4 Idiopathic anaphylaxis (IA) is a diagnosis of exclusion,

5 Idiopathic anaphylaxis (IA) or spontaneous anaphylaxis i

6 k = 2.0; P < .05) and more prevalent in both idiopathic anaphylaxis (n = 8 of 47; [17%; P = .006]) an

7 temic mastocytosis (SM) and venom as well as idiopathic anaphylaxis from referral centers in Italy, S

8 cal dystonia, demonstrate convergence across idiopathic and acquired dystonia, and identify a network

9 t difference in BMD values was found between idiopathic and congenital scoliosis patients (p > 0.05).

10 uted tomography (QCT) and compare the BMD of idiopathic and congenital scoliosis patients.

11 ensitive biomarkers of disease state in both idiopathic and gene-identified PD patients and that foll

12 Rationale: Idiopathic and heritable pulmonary arterial hypertension

13 differential diagnosis between inflammatory, idiopathic, and myopic CNV may be challenging.

14 Idiopathic aplastic anemia (AA) has 2 key characteristic

15 iple autoimmune diseases, including juvenile idiopathic arthritis (JIA) has earned substantial attent

16 pective study, 45 participants with juvenile idiopathic arthritis (JIA) or suspected of having JIA (s

17 itis in pediatric participants with juvenile idiopathic arthritis (JIA) or suspected of having JIA an

18 act development among patients with juvenile idiopathic arthritis (JIA)-associated uveitis treated wi

19 d: Crohn's disease (n = 8; 42%) and juvenile idiopathic arthritis (n = 6; 32%) were the commonest und

20 observed in children with systemic juvenile idiopathic arthritis (sJIA) and cytokine storm syndrome

21 mmatory disorders, such as systemic juvenile idiopathic arthritis (SJIA) and macrophage activation sy

22 nged IFN-gamma KO resemble systemic juvenile idiopathic arthritis (sJIA), a childhood immune disorder

23 ynechiae, and systemic diagnoses of juvenile idiopathic arthritis and spondyloarthropathy predict red

24 Systemic diagnosis with juvenile idiopathic arthritis and spondyloarthropathy were also a

25 The aims of treating juvenile idiopathic arthritis are to elicit treatment response to

26 h MethOtRExate for the treatment of juvenile idiopathic arthritis associated uveitis) trial (identifi

27 alised medicine in the treatment of juvenile idiopathic arthritis will be aided with international co

28 ases, such as rheumatoid arthritis, juvenile idiopathic arthritis, adult-onset Still's disease, giant

29 diseases such as sepsis or systemic juvenile idiopathic arthritis.

30 tis, spondyloarthritis and systemic juvenile idiopathic arthritis.

31 prosy, Behcet disease, and systemic juvenile idiopathic arthritis.

32 o effective treatments and care for juvenile idiopathic arthritis.

33 fferences in DNA methylation associated with idiopathic ASD (iASD), with consistent signals in both c

34 ent validation series (n = 171) enriched for idiopathic ASD (PTEN(WT), p = 5.6 x 10(-4)).

35 icing changes in ASD-related target genes in idiopathic ASD and 15q11-q13 duplication syndrome.

36 likely increase the genetic liability in an idiopathic ASD case.

37 ior cerebellum (CB), from carefully selected idiopathic ASD cases and matched controls using label-fr

38 deconvoluted OL numbers distinguished human idiopathic ASD cases from controls across three postmort

39 cial deficits in genetic, environmental, and idiopathic ASD models.

40 integrated PTHS mouse model DEGs with human idiopathic ASD postmortem brain RNA-sequencing data and

41 erapeutic target to rectify the phenotype of idiopathic ASD with polygenic abnormalities.

42 ivity shared across deletions, duplications, idiopathic ASD, SZ but not ADHD.

43 from 101 CNV carriers, 755 individuals with idiopathic ASD, SZ, or ADHD and 1,072 controls.

44 Here, using BTBR mice as a model of idiopathic ASD, we assessed retinal stimulus processing

45 chronic (>12 months) of refractory vomiting (idiopathic, associated with a type 1 or 2 diabetes, or p

46 The participants were idiopathic asthenozoospermic men aged 20-45 y, with norm

47 UV is mostly idiopathic but can be associated with drugs, malignancy,

48 as consistently identified as a biomarker of idiopathic cardiac arrest (P=0.002; false discovery rate

49 immunoglobulin G purified from patients with idiopathic cardiac arrest is proarrhythmogenic by reduci

50 hought to underlie a substantial fraction of idiopathic cases, the actual molecular bases are usually

51 requency were PCG, glaucoma after congenital idiopathic cataract surgery, and glaucoma associated wit

52 s causes, 5 of 23 patients (22%) showed were idiopathic causes, and 8 of 23 patients' (35%) disease w

53 Idiopathic CD4+ T cell lymphocytopenia (ICL) is a hetero

54 howed abnormal connectivity in patients with idiopathic cervical dystonia.

55 Among the idiopathic cholangitides, the most common is primary scl

56 The idiopathic chronic cholangitides comprise a group of hep

57 The pathogenesis of idiopathic CMV disease is unknown.

58 identify dimensions contributing to complex idiopathic conditions.

59 drugs available for the treatment of chronic idiopathic constipation, but their relative efficacy is

60 iagnosis of functional constipation, chronic idiopathic constipation, or irritable bowel syndrome wit

61 e most efficacious for patients with chronic idiopathic constipation.

62 panor, or velusetrag) in adults with chronic idiopathic constipation.

63 of these therapies in patients with chronic idiopathic constipation.

64 eta gene family usage between hereditary and idiopathic CP and a positive correlation of TCRbeta rear

65 Immunophenotyping analyses in hereditary and idiopathic CP pancreases indicate differences in innate

66 ecific T cell responses in hereditary versus idiopathic CP pathogenesis, providing insights into immu

67 patients including those with hereditary and idiopathic CP undergoing total pancreatectomy with islet

68 ase in the frequency of CD68+ macrophages in idiopathic CP.

69 to 80% of patients are classified as having "idiopathic CP." Up to 50% of these individuals have muta

70 ms underlying neural disruptions observed in idiopathic developmental neuropsychiatric disorders.SIGN

71 be present in the hearts of individuals with idiopathic dilated cardiomyopathy, as well as the hearts

72 ramural pseudodiverticulosis is an uncommon, idiopathic disorder characterized by multiple small outp

73 Idiopathic epilepsy (IE) is the most common chronic neur

74 veness of performing an ILM peel for initial idiopathic ERM repairs and evaluate long-term visual and

75 y codes were used to determine patients with idiopathic ERM who received PPV with or without ILM peel

76 t can be related to congenital, acquired, or idiopathic factors that impair spermatogenesis.

77 inson's disease(1) and is also linked to its idiopathic form(2).

78 uroimaging data collected from patients with idiopathic generalised epilepsy, in which we successfull

79 ent patterns of domino-like seizure onset in Idiopathic Generalized Epilepsy (IGE) and present a nove

80 nlesional focal epilepsy and 8 patients with idiopathic generalized epilepsy.

81 to our tertiary uveitis center diagnosed as "idiopathic" had an associated identifiable cause.

82 n whole-blood samples from 359 patients with idiopathic, heritable, and drug-induced PAH and 72 age-

83 igate systems-level mechanisms implicated in idiopathic illness.

84 The final diagnosis was MS in 57%, idiopathic in 29%, MOG-IgG-associated disorder in 5%, AQ

85 fantile nystagmus (19 with albinism, 17 with idiopathic infantile nystagmus, and 6 with achromatopsia

86 evelop a molecular analysis to identify male idiopathic infertility using genome wide alterations in

87 MS is a chronic idiopathic inflammatory demyelinating disease of the cen

88 Idiopathic inflammatory myopathies (IIM) involve chronic

89 Inclusion body myositis is an idiopathic inflammatory myopathy and the most common myo

90 movement and can occur as an isolated trait (idiopathic INS, IINS) or as part of multisystem disorder

91 s for pulmonary hypertension associated with idiopathic interstitial pneumonia (PH-IIP).

92 ced pseudotumor cerebri (PTC-T) and those of idiopathic intracranial hypertension (IIH) are absent in

93 understand retinal changes in patients with idiopathic intracranial hypertension (IIH) using fundus

94 he cause cannot be identified (also known as idiopathic intracranial hypertension), and secondary pse

95 after GPi DBS in patients with inherited or idiopathic isolated dystonia to evaluate the effects of

96 following DBS in patients with inherited or idiopathic isolated dystonia.

97 f life (HRQoL) in patients with inherited or idiopathic isolated dystonia.

98 o within brain ventricles is associated with idiopathic-like scoliosis across diverse genetic models.

99 genetic studies using zebrafish have linked idiopathic-like scoliosis to irregularities in motile ci

100 scospondin (sspo) mutants develop late-onset idiopathic-like spinal curvatures in the absence of obvi

101 ic activation patterns often occurred during idiopathic LVS-VAs, which could mislead the catheter abl

102 Determining which factors influence idiopathic macular hole (MH) size is important because i

103 ups: eyes from control subjects (n = 4) with idiopathic macular holes (IMH) and eyes from test subjec

104 to sperm parameters in an Estonian cohort of idiopathic male factor infertility subjects.

105 have the potential to lead to a therapy for idiopathic male infertility in the clinic, and could ope

106 D (MCD), the latter of which is divided into idiopathic MCD (iMCD), human herpes virus-8 (HHV8)-assoc

107 linking might inhibit degrading processes in idiopathic melting or in ocular inflammatory diseases of

108 bility and MLD (beta = 0.29; P = 0.002), and idiopathic MH duration (beta = 0.23; P = 0.004) explaine

109 opathic MH was correlated significantly with idiopathic MH size and may explain some of the variabili

110 fellow eye to evaluate its relationship with idiopathic MH size and postoperative outcomes.

111 ompared to determine their relationship with idiopathic MH size and postoperative visual acuity (VA)

112 e and may explain some of the variability in idiopathic MH size observed between individuals.

113 etrical within individuals and may influence idiopathic MH size.

114 iameter (MLD) and base diameter (BD) defined idiopathic MH size.

115 the fellow eye in patients with a unilateral idiopathic MH was correlated significantly with idiopath

116 Using a series of patients with unilateral idiopathic MHs, we examined the foveal floor size of the

117 Idiopathic multicentric Castleman disease (iMCD) is a he

118 Idiopathic multicentric Castleman disease (iMCD) is a ra

119 Idiopathic multicentric Castleman disease (iMCD) is a ra

120 TAFRO syndrome, a clinical subtype of idiopathic multicentric Castleman disease (iMCD), consis

121 onal consensus as a first-line treatment for idiopathic multicentric Castleman disease on the basis o

122 the life-long use required by patients with idiopathic multicentric Castleman disease.

123 Cardiovascular diseases, especially idiopathic myocardial fibrosis, is one of the most signi

124 ed comparative study of patients affected by idiopathic, myopic or traumatic stage 4 MH (minimum diam

125 The most common final diagnosis was idiopathic (n = 46, 43.0%), followed by tuberculosis (n

126 Idiopathic nephrotic syndrome (INS) describes a group of

127 cently been described as unifying feature in idiopathic nephrotic syndromes (INS).

128 ve stress is a common feature of genetic and idiopathic neurological diseases that thus far have been

129 Associations were stronger in men with idiopathic NGU.

130 o delineate the molecular characteristics of idiopathic NOA and SO, we performed whole-exome sequenci

131 econdary datasets containing 12 volumes with idiopathic normal pressure hydrocephalus (iNPH) and 30 n

132 ion to clinical outcomes, with patients with idiopathic normal pressure hydrocephalus (iNPH) serving

133 Approximately 10% of dementia patients have idiopathic normal pressure hydrocephalus (iNPH), an expa

134 hotomy of a neurodegenerative NPH and a true idiopathic NPH, with the latter appearing to be rare.

135 Patients with idiopathic nystagmus syndrome often develop an abnormal

136 s abnormal head titling in patients who have idiopathic nystagmus syndrome.

137 The underlying pathophysiology of idiopathic OAB is not clearly known and the existence of

138 lysed in lung biopsies from 30 patients with idiopathic or connective tissue disease (CTD)-related IL

139 ing, compared with placebo, in patients with idiopathic or diabetic gastroparesis.

140 ant, an antagonist of NK1R, in patients with idiopathic or diabetic gastroparesis.

141 It can be idiopathic or due to different etiologies.

142 volved muscles in IOM resemble those seen in idiopathic orbital inflammation and differ from those se

143 ication and degradation has been observed in idiopathic osteoarthritis (OA), while the detailed mecha

144 nium in bone biopsy from a male patient with idiopathic osteoporosis (without indication of renal imp

145 t the cause of gastroparesis remains largely idiopathic, our findings open the possibility that a phy

146 control subjects (n = 120) and patients with idiopathic PAH (n = 260).Measurements and Main Results:

147 ese mutations occur in <25% of patients with idiopathic PAH and are rare in PAH associated with conne

148 rget genes are elevated in pre-clinical PAH, idiopathic PAH and heritable PAH with missense p.H288Y K

149 ases in specimens derived from patients with idiopathic PAH.

150 lasma BMP9 and BMP10 levels in patients with idiopathic PAH.Methods: Missense BMP9 mutant proteins we

151 alue as biomarkers of disease progression in idiopathic Parkinson's disease (iPD).

152 We also analyzed six cases of idiopathic Parkinson's disease (PD), one case of familia

153 predictive potential to discriminate between idiopathic Parkinson's disease and Parkinson's disease l

154 (r -0.66, 95% CI -0.88 to -0.20; p=0.0099), idiopathic Parkinson's disease cohort 1 (r -0.66, -0.84

155 1 (r -0.66, -0.84 to -0.36; p=0.00031), and idiopathic Parkinson's disease cohort 2 (r -0.71, -0.84

156 duals harbouring mutations in PRKN/PINK1 and idiopathic Parkinson's disease patients remain elusive.

157 , while no such association was observed for idiopathic Parkinson's disease patients.

158 age between 22 and 75 years, a diagnosis of idiopathic Parkinson's disease with over 5 years of moto

159 ing network structure in 37 individuals with idiopathic Parkinson's disease, both ON and OFF dopamine

160 eterozygous PRKN/PINK1 mutations compared to idiopathic Parkinson's disease, which is in line with pr

161 The concept of 'idiopathic' Parkinson's disease (PD) as a single entity

162 nitial characterization of EMVs derived from idiopathic patients (AHNPs) and mutant LRRK2 patients sh

163 recruited 5 pairs of MZ twins discordant for idiopathic PD and established skin fibroblast cultures t

164 t kinase 2 (LRRK2) mutations in familial and idiopathic PD has emerged.

165 e MSA samples were more potent than those of idiopathic PD in seeding aggregation.

166 Methods: Eighteen individuals with idiopathic PD in the off-medication state, 9 with FOG (a

167 an brain organoids generated from normal and idiopathic PD patients.

168 however, the etiology and pathophysiology of idiopathic PD remain unclear.

169 One hundred and four idiopathic PD, 40 LRRK2-PD, 70 GBA-PD, 196 healthy non-c

170 Nrf2 activator, and inverse risk factor for idiopathic PD, is one such candidate biomarker of PD ris

171 ropathology resembling the premotor stage of idiopathic PD.

172 Viral or idiopathic pericarditis is a frequent condition, often c

173 patterns in patients with incident viral or idiopathic pericarditis.

174 n patients presenting with apparent viral or idiopathic pericarditis.

175 ory cells from lung tissues of patients with idiopathic PH.

176 Decidua basalis sections from term (n = 10), idiopathic preterm birth (PTB; n = 8), and abruption-com

177 ivity was higher in abruption-complicated or idiopathic PTB specimens versus normal term specimens (P

178 PDGFB are higher in PAE cells isolated from idiopathic pulmonary arterial hypertension (IPAH) patien

179 s isolated from pulmonary arteries (PAAF) of idiopathic pulmonary arterial hypertension (IPAH) patien

180 in patients with pressure-overloaded RVs of idiopathic pulmonary arterial hypertension and chronic t

181 In idiopathic pulmonary arterial hypertension and chronic t

182 f galectin-3 were increased in patients with idiopathic pulmonary arterial hypertension but did not c

183 ontinuation of nintedanib was progression of idiopathic pulmonary fibrosis (51 [12%] patients continu

184 interstitial lung diseases (ILDs), including idiopathic pulmonary fibrosis (IPF) and sarcoidosis.

185 nal changes in a cohort of participants with idiopathic pulmonary fibrosis (IPF) and to evaluate the

186 Rationale: Several new drugs for idiopathic pulmonary fibrosis (IPF) are in development.

187 nic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF) are two pathological

188 Patients with idiopathic pulmonary fibrosis (IPF) can experience life-

189 Rationale: Idiopathic pulmonary fibrosis (IPF) causes considerable

190 Idiopathic pulmonary fibrosis (IPF) has a poor prognosis

191 nic Obstructive Pulmonary Disease (COPD) and Idiopathic Pulmonary Fibrosis (IPF) have contrasting cli

192 dysfunctional telomeres are at the origin of idiopathic pulmonary fibrosis (IPF) in patients mutant f

193 Idiopathic pulmonary fibrosis (IPF) is a chronic and fat

194 Idiopathic pulmonary fibrosis (IPF) is a chronic progres

195 Idiopathic pulmonary fibrosis (IPF) is a chronic progres

196 Rationale: Idiopathic pulmonary fibrosis (IPF) is a complex lung di

197 Rationale: Idiopathic pulmonary fibrosis (IPF) is a deadly disease

198 Idiopathic Pulmonary Fibrosis (IPF) is a disease with a

199 Idiopathic pulmonary fibrosis (IPF) is a disease with hi

200 Idiopathic pulmonary fibrosis (IPF) is a fatal and incur

201 Idiopathic pulmonary fibrosis (IPF) is a fatal disease o

202 Idiopathic pulmonary fibrosis (IPF) is a fatal disease w

203 Idiopathic pulmonary fibrosis (IPF) is a lung parenchyma

204 Idiopathic pulmonary fibrosis (IPF) is a progressive and

205 Idiopathic pulmonary fibrosis (IPF) is a progressive and

206 Idiopathic pulmonary fibrosis (IPF) is a progressive dis

207 Idiopathic pulmonary fibrosis (IPF) is a progressive lun

208 Idiopathic pulmonary fibrosis (IPF) is a rare and devast

209 Idiopathic pulmonary fibrosis (IPF) is a severe form of

210 Idiopathic pulmonary fibrosis (IPF) is characterized by

211 Idiopathic pulmonary fibrosis (IPF) is characterized by

212 dels; however, the role of these proteins in idiopathic pulmonary fibrosis (IPF) is not known.

213 (ILD), the risk among relatives of sporadic idiopathic pulmonary fibrosis (IPF) is not known.Objecti

214 EVERBalpha expression was increased in human idiopathic pulmonary fibrosis (IPF) lung tissue.

215 Patients with idiopathic pulmonary fibrosis (IPF) treated with PRM-151

216 ulum (ER) stress in AEC has been observed in idiopathic pulmonary fibrosis (IPF), a disease of aging.

217 The progression and severity of idiopathic pulmonary fibrosis (IPF), a fatal and irrever

218 Pathogenic fibrotic diseases, including idiopathic pulmonary fibrosis (IPF), have some of the wo

219 iven the paucity of effective treatments for idiopathic pulmonary fibrosis (IPF), new insights into t

220 In Idiopathic Pulmonary Fibrosis (IPF), there is unrelentin

221 re the genetic risk architecture observed in idiopathic pulmonary fibrosis (IPF), with key risk facto

222 efforts to identify effective therapies for idiopathic pulmonary fibrosis (IPF).

223 n's nodules and also in the fibrotic foci of idiopathic pulmonary fibrosis (IPF).

224 elaxin is considered a potential therapy for idiopathic pulmonary fibrosis (IPF).

225 n in multiple fibrotic conditions, including idiopathic pulmonary fibrosis (IPF).

226 diator that is pivotal to the development of idiopathic pulmonary fibrosis (IPF).

227 that underlies chronic lung diseases such as idiopathic pulmonary fibrosis (IPF).

228 ave identified rs2076295 in association with idiopathic pulmonary fibrosis (IPF).

229 gy of diffuse parenchymal diseases including idiopathic pulmonary fibrosis (IPF).

230 osecretory dysfunction to the development of idiopathic pulmonary fibrosis (IPF).Objectives: We sough

231 f patients with PVOD (n = 19), PAH (n = 20), idiopathic pulmonary fibrosis (n = 13), and chronic obst

232 e (PAF, 14%); chronic bronchitis (PAF, 13%); idiopathic pulmonary fibrosis (PAF, 26%); hypersensitivi

233 in the lung tissues from both patients with idiopathic pulmonary fibrosis and a mouse model of bleom

234 disorders, including dyskeratosis congenita, idiopathic pulmonary fibrosis and bone marrow failure.

235 Patients with idiopathic pulmonary fibrosis and percentage of predicte

236 In patients with idiopathic pulmonary fibrosis and preserved lung functio

237 uencing of human lungs, including those from idiopathic pulmonary fibrosis and scleroderma patients,

238 Pamrevlumab attenuated progression of idiopathic pulmonary fibrosis and was well tolerated.

239 database, we identified 8,098 patients with idiopathic pulmonary fibrosis between October 1, 2014 an

240 biomarkers to better stratify patients with idiopathic pulmonary fibrosis by risk for lung transplan

241 Idiopathic pulmonary fibrosis comprised 34% with idiopat

242 specific immune cell type from patients with idiopathic pulmonary fibrosis could identify those at hi

243 profiled monocyte counts in 45 patients with idiopathic pulmonary fibrosis from March 12, 2010, to Ma

244 Secondary analysis distinguished idiopathic pulmonary fibrosis from non-idiopathic pulmon

245 ished idiopathic pulmonary fibrosis from non-idiopathic pulmonary fibrosis ILD and used lung function

246 n for transplantation at index operation was idiopathic pulmonary fibrosis in 8 of 10 patients (1.2%

247 Idiopathic pulmonary fibrosis is a deadly disease charac

248 Idiopathic pulmonary fibrosis is a fatal disease involvi

249 Idiopathic pulmonary fibrosis is a progressive scarring

250 Idiopathic pulmonary fibrosis may be associated with inc

251 and fibroblasts have long been the focus of idiopathic pulmonary fibrosis research, the role of vari

252 sis of medical records of 7459 patients with idiopathic pulmonary fibrosis showed that patients with

253 tyrosine kinase inhibitor, in patients with idiopathic pulmonary fibrosis were assessed in two phase

254 uded ACE-IPF (Anticoagulant Effectiveness in Idiopathic Pulmonary Fibrosis) (n = 101) and an independ

255 ronic obstructive pulmonary disease, asthma, idiopathic pulmonary fibrosis, acute respiratory distres

256 Rett syndrome, inherited retinal disorders, idiopathic pulmonary fibrosis, and Charcot-Marie-Tooth d

257 onic renal disease, heart failure, diabetes, idiopathic pulmonary fibrosis, and scleroderma.

258 s of chronic diseases such as severe asthma, idiopathic pulmonary fibrosis, and systemic sclerosis.

259 tolerability of nintedanib in patients with idiopathic pulmonary fibrosis, and this was analysed in

260 an FDA approved anti-fibrotic drug to treat idiopathic pulmonary fibrosis, has been shown to amelior

261 ts are now available for adult patients with idiopathic pulmonary fibrosis, no clinical trials have b

262 ro-fibrotic responses in a cellular model of idiopathic pulmonary fibrosis, supporting the potential

263 as shortened telomeres are risk factors for idiopathic pulmonary fibrosis, where repetitive injury t

264 s a novel, safe, and effective treatment for idiopathic pulmonary fibrosis.

265 r of response to nintedanib in patients with idiopathic pulmonary fibrosis.

266 could slow, stop, or reverse progression of idiopathic pulmonary fibrosis.

267 ll (AEC2) dysfunction in the pathogenesis of idiopathic pulmonary fibrosis.

268 5 patients), following acute exacerbation of idiopathic pulmonary fibrosis.

269 re upregulated in samples from patients with idiopathic pulmonary fibrosis.

270 pirfenidone and nintedanib in patients with idiopathic pulmonary fibrosis.

271 oblasts of fibrotic lungs from patients with idiopathic pulmonary fibrosis.

272 nuclear cell (PBMC) samples of patients with idiopathic pulmonary fibrosis.

273 ed as potential targets for the treatment of idiopathic pulmonary fibrosis.

274 onse to pro-fibrotic stimuli, which fails in idiopathic pulmonary fibrosis.

275 hort telomere syndromes manifest as familial idiopathic pulmonary fibrosis; they are the most common

276 Endothelial colony-forming cells from idiopathic pulmonary hypertensive patients showed upregu

277 essing Parkinson's disease and patients with idiopathic rapid eye movement sleep behaviour disorder (

278 ment (n = 2), corticobasal syndrome (n = 1), idiopathic rapid-eye-movement sleep behavior disorder (n

279 Isolated (or idiopathic) rapid eye movement sleep behavior disorder (

280 genotyping of SNCA was performed in isolated/idiopathic RBD (iRBD, n = 1,076), Parkinson disease (PD,

281 The prevalence of idiopathic RBD at alpha-synucleinopathy diagnosis was 3.

282 median nerve were performed on patients with idiopathic restless legs syndrome (iRLS) who were not cu

283 The fourth patient had bilateral idiopathic retinochoroiditis.

284 Furthermore, by establishing idiopathic RPL patient-specific human trophoblast stem c

285 t of unexplained recurrent pregnancy losses (idiopathic RPLs) is associated with impaired TEAD4 expre

286 Comparison of 22q11DS-psychosis to idiopathic schizophrenia (ENIGMA-Schizophrenia Working G

287 verlap between 22q11DS-associated psychosis, idiopathic schizophrenia, and other severe neuropsychiat

288 with similar neuroanatomic abnormalities to idiopathic schizophrenia.

289 Adolescent idiopathic scoliosis (AIS) affects 3% to 4% of children

290 Adolescent idiopathic scoliosis (AIS) is a prevalent spinal deformi

291 g spinal deformity progression in adolescent idiopathic scoliosis (AIS) remain poorly understood.

292 Adolescent idiopathic scoliosis is the most prevalent spine deformi

293 enetic influence on stone formation in these idiopathic stone formers remains considerable and twin s

294 tis with uveitis (6/52, 11.5%), and juvenile idiopathic uveitis (4/52, 7.7%).

295 Idiopathic uveitis is frequently the most common diagnos

296 Idiopathic ventricular arrhythmias commonly originate fr

297 n human diseases including Brugada syndrome, idiopathic ventricular arrhythmias, and epileptic enceph

298 nts without structural heart disease (mainly idiopathic ventricular fibrillation and Brugada syndrome

299 the foveal avascular zone (FAZ) in eyes with idiopathic vitreomacular traction (VMT) after ocriplasmi

300 NGU was considered idiopathic when Neisseria gonorrhoeae, Chlamydia trachom