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1 ients with CatC deficiency (Papillon-Lefevre syndrome).
2  (Diamond-Blackfan anemia, Shwachman-Diamond syndrome).
3 ory (Italy), causing the Olive Quick Decline Syndrome.
4 a female patient with estrogen insensitivity syndrome.
5 effects and its role in the cytokine release syndrome.
6 ents with COVID-19-related hyperinflammatory syndrome.
7 nsporter FLVCR2 have been reported in Fowler syndrome.
8  Frailty is a complex and prevalent clinical syndrome.
9 -molecule screen for fragile X tremor ataxia syndrome.
10 et the diagnostic criteria for more than one syndrome.
11 sease and 18 046 (56.1%) with acute coronary syndrome.
12 ocyte injury drives proteinuria or nephrotic syndrome.
13  questionnaire is widely used to assess this syndrome.
14  possible brain metabolic phenotypes of this syndrome.
15 sposition in patients with Shwachman-Diamond syndrome.
16 across the lifespan of individuals with Down syndrome.
17 ymorphic ventricular tachycardia and Brugada syndrome.
18  underaction of IO muscle and anti-elevation syndrome.
19 ith a history of physician-diagnosed Sjogren syndrome.
20 ractivity in a mouse model of Birt-Hogg-Dube syndrome.
21 constitutional inherited bone marrow failure syndrome.
22 of disease pathogenesis in this heritable HF syndrome.
23 thmogenic phenotypes associated with long-QT syndrome.
24 n podocytes to cellular damage and nephrotic syndrome.
25 ues, showing multidimensional adaptive trait syndromes.
26 study of patients with atypical parkinsonian syndromes.
27 ring SCAD among patients with acute coronary syndromes.
28 ths worldwide are caused by neurocardiogenic syndromes.
29 associated with known autosomal dominant OFC syndromes.
30 seemingly unrelated adult-onset inflammatory syndromes.
31 valuate deleterious DNMs in inherited cancer syndromes.
32 ragile X, Prader-Willi, Turner, and Williams syndromes.
33                                    Metabolic syndrome (13.5%; 44 of 326) was related to traditional m
34 e (40%), followed by sudden arrhythmic death syndrome (14%).
35 ion; p<=0.0001), particularly Guillain-Barre syndrome (25 [61%] patients).
36 1%), shock (31%), acute respiratory distress syndrome (25%), neurological events (25%), arrhythmias (
37                                        TAFRO syndrome, a clinical subtype of idiopathic multicentric
38 chanism has a crucial role in Birt-Hogg-Dube syndrome, a disorder that is caused by mutations in the
39 tly mutated in cancers and Aicardi-Goutieres syndrome, a hereditary autoimmune encephalopathy.
40 n related to Brown-Vialetto-Van Laere (BVVL) syndrome, a hereditary paediatric condition associating
41 pective multicenter cohort of acute coronary syndrome (ACS), in relation to BB use: prior to admissio
42 s, in patients with suspected acute coronary syndrome admitted to Swedish coronary care units.
43 d diseases such as atypical hemolytic uremic syndrome (aHUS) and age-related macular degeneration.
44  monogenic form of IR-prone obesity, Alstrom syndrome (ALMS).
45 , we first extracted data on myelodysplastic syndrome and acute myeloid leukaemia cases from Clinical
46 d cortisol-related disorders (e.g. Cushing's syndrome and Addison's disease).
47 genes that determine different traits of the syndrome and are held together, because recombination be
48 kely to be contributing to the cause of this syndrome and consider how they might be modified or inhi
49 osis can be considered a marker of metabolic syndrome and diabetes.
50 s with severe CRS may develop capillary leak syndrome and disseminated intravascular coagulation, wit
51 nsight into the disease mechanism of Wolfram syndrome and highlight new targets and drug candidates t
52 th versus without acute respiratory distress syndrome and in relation to complicated course, defined
53 tly associated with development of metabolic syndrome and insulin resistance, manifests when triglyce
54 mma during CpG-induced macrophage activation syndrome and is present at high levels in the circulatio
55 ciated with increased odds of acute coronary syndrome and its manifestations in individuals at high c
56 ateral pneumonia, acute respiratory distress syndrome and multiorgan dysfunction.
57 reated patients, grade >= 3 cytokine release syndrome and neurotoxicity occurred in 7% and 31%, respe
58 imination between acute respiratory distress syndrome and nonacute respiratory distress syndrome pati
59 ecific small interfering RNA in treating KID syndrome and other dominant genetic conditions.
60 cy at identifying multiple organ dysfunction syndrome and predicting new or progressive multiple orga
61 n, progressing to acute respiratory distress syndrome and shock.
62 he prevalence of TKOS in sudden infant death syndrome and sudden unexplained death in the young is un
63 is linked to both acute respiratory distress syndrome and systemic hypercoagulability.
64 n of central nervous system lesions in Leigh syndrome and their biological evolution in view of their
65 ial fibrillation and a recent acute coronary syndrome and those undergoing percutaneous coronary inte
66 use of this outbreak of hantavirus pulmonary syndrome and to reconstruct person-to-person transmissio
67 ating disordered energy metabolism metabolic syndrome and type 2 diabetes.
68  With Atrial Fibrillation and Acute Coronary Syndrome and/or Percutaneous Coronary Intervention), pat
69 findings associated with Fregoli and Capgras syndromes and compare these with the proposed neural sub
70 ip between HTT repeat expansions and FTD/ALS syndromes and indicate that genetic screening of FTD/ALS
71 l damage (preeclampsia, eclampsia, and HELLP syndrome), and postoperative complications in patients u
72 sk of PAD events or VTE after acute coronary syndrome, and if such effects are related to levels of l
73 ort contributes to the pathogenesis of Barth syndrome, and more generally, showcases the utility of y
74  should be used for bronchiolitis obliterans syndrome; and the addition of newer treatment options fo
75 h can progress to acute respiratory distress syndrome (ARDS) in the most severe form, while children
76  air pollution on acute respiratory distress syndrome (ARDS) is limited, and most studies focus on AR
77 agonists in a rat acute respiratory distress syndrome (ARDS) model utilizing the PaO(2)/FiO(2)-ratio
78 nts who died from acute respiratory distress syndrome (ARDS) secondary to influenza A(H1N1) infection
79 irst event in the acute respiratory distress syndrome (ARDS).
80  patients without acute respiratory distress syndrome (ARDS).
81  life-threatening acute respiratory distress syndrome (ARDS).
82  life-threatening acute respiratory distress syndrome (ARDS).
83          Many treatments for irritable bowel syndrome are available to those with the disease.
84 thmias, heart failure, and nonfatal coronary syndromes are also common.
85 e and treatment for leukaemia predisposition syndromes are scarce and recommendations are largely bas
86                         The beta-thalassemia syndromes are the most prevalent genetic disorder global
87 SLT patients (with Bartter, Gitelman or EAST Syndromes) are recruited.
88 ortant to note that we should consider PFAPA syndrome as a differential diagnosis when we meet with t
89 e methods in patients with neurodegenerative syndromes as referenced to neuropathologic findings.
90                    Individuals with Angelman syndrome (AS) are characterized by severe cognitive impa
91 rategies to treat individuals with metabolic syndrome, as RXR heterodimerizes with multiple nuclear r
92  with those of histology in a case of Hurler syndrome-associated keratopathy.
93 on causes the severe ciliopathy Bardet-Biedl syndrome (BBS).
94               Werner Syndrome (WS) and Bloom Syndrome (BS) are disorders of DNA damage repair caused
95 oronary intervention (PCI) or acute coronary syndrome but with increased risk of bleeding.
96 ty, type 2 diabetes, hypertension, metabolic syndrome), but the mechanism underlying these associatio
97 itive Examination for Older Adults with Down Syndrome (CAMCOG-DS).
98                         Non-colorectal Lynch syndrome cancers were reported in 36 participants who re
99                The increased risk of dry eye syndrome, cataracts, glaucoma, episcleritis and scleriti
100 c arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tach
101 pe 1 (NF1) is a common cancer predisposition syndrome caused by mutations in the NF1 tumor suppressor
102                                         Down syndrome cell adhesion molecules (dscam and dscaml1) are
103 hemophagocytic lymphohistiocytosis is a rare syndrome characterized by immune dysregulation and hyper
104              Cachexia, a devastating wasting syndrome characterized by severe weight loss with specif
105  have recently been associated with CAKUTHED syndrome, characterized by multiple congenital defects i
106 diatric Adolescent Acquired Immunodeficiency Syndrome Clinical Trials [IMPAACT] P1060); 183 age-match
107 nd magnetic resonance studies from our Leigh syndrome cohort to provide a detailed description of cen
108 ew or progressive multiple organ dysfunction syndrome, compared to the objective assessment of multip
109                                   Despite HF syndrome complexities, evidence of significant sympathet
110 enniality and annuality should be considered syndromes comprised of many interacting traits, and that
111 immunothrombosis in severe acute respiratory syndrome corona virus 2 pneumonia is linked to both acut
112 cluding SARS-CoV and Middle East respiratory syndrome coronavirus (MERS-CoV).
113 veys measuring anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) antibodies prov
114 ad 180,458 cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and 9,385 reported d
115 n a new pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and an existing pand
116 ce of antibodies to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the risk of subs
117 nd vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are being expedited
118           Tests for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) based on reverse tra
119 COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in China and
120                     Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in December
121 The rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has elicited an equa
122                 The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in thou
123 past infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have many uses for p
124 vent infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in an older populati
125 revious exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in populations, and
126 19) or detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the environment a
127                     Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections and the r
128 of introductions of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) into Scotland using
129      Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is initiated by viru
130                     Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for m
131                     Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of an o
132 ture.IMPORTANCE The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the etiological a
133 ldren infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is unknown.
134 fective vaccine for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may be required to e
135                 The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has devasta
136  workers during the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic.
137 eliminary data from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia patients i
138 age, and sex and on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) prevalence and the c
139 or the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA in respiratory s
140  antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein, used
141  of airway cells by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that results in exce
142  earliest sustained severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) transmission network
143                 The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus is causing a g
144 his pathogen, named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), causes a pathogenic
145 OVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in late 201
146 ission dynamics for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), in order to inform
147 he causative agent, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a member of the
148                     Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent
149 e disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsib
150 s who may carry the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), while striving to f
151 nfections caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
152 rior infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
153 ng the emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
154 e to infection with severe acute respiratory syndrome coronavirus 2 during the coronavirus disease 20
155 sitive findings for severe acute respiratory syndrome coronavirus 2 from nasopharyngeal swab and cere
156 een associated with severe acute respiratory syndrome coronavirus 2 illness, but it remains unclear w
157  may be observed in severe acute respiratory syndrome coronavirus 2 infected patients, even in the ab
158 e 2019 out of 1,788 severe acute respiratory syndrome coronavirus 2 positive cases, rendering an over
159 ients infected with severe acute respiratory syndrome coronavirus 2 requiring venovenous extracorpore
160 and splatters), for severe acute respiratory syndrome coronavirus 2 transmission, has challenged care
161  chain reaction for severe acute respiratory syndrome coronavirus 2 was positive in 33.6%, whereas im
162  pandemic caused by severe acute respiratory syndrome coronavirus 2, resulting in significant morbidi
163 members exposure to severe acute respiratory syndrome coronavirus 2.
164  viruses, including severe acute respiratory syndrome coronavirus, human immunodeficiency virus 1, he
165 responses following severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection increase t
166 lls with SARS-CoV-2, Middle East respiratory syndrome CoV (MERS-CoV), bat CoV HKU5 expressing the SAR
167  old with confirmed severe acute respiratory syndrome-CoV-2 disease who were admitted to an ICU durin
168                             Cytokine release syndrome (CRS) is a life-threatening treatment-related t
169 e adverse events, including cytokine release syndrome (CRS).
170 tion is now firmly linked to congenital Zika syndrome (CZS), including fetal microcephaly.
171 ion for pediatric acute respiratory distress syndrome did not require the presence of bilateral infil
172                Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic sy
173 l deficits in the Ts65Dn mouse model of Down syndrome (DS), translation to human clinical trials to i
174 h autism (ASD), schizophrenia (SZ), and Down syndrome (DS).
175 rging model of COVID-related cardiometabolic syndrome encompassing events before, during the acute ph
176            We report that parental metabolic syndrome epigenetically reprograms members of the TGF-be
177 sions in England for types of acute coronary syndrome from Jan 1, 2019, to May 24, 2020, that were re
178                                    Fragile X syndrome (FXS) is caused by inactivation of the FMR1 gen
179                                    Fragile X syndrome (FXS), the most common monogenetic cause of ASD
180 tors that are known to promote the metabolic syndrome generally cause pro-inflammatory alterations in
181 f the directly measured iron on the clinical syndrome has not been assessed.
182 ure similar to that of macrophage activation syndrome/hemophagocytic lymphohistiocytosis.
183                       Hypoplastic left heart syndrome (HLHS) is a complex congenital heart disease ch
184 LHS/TGA" fetuses with hypoplastic left heart syndrome (HLHS) or transposition of the great arteries (
185 ere dengue hemorrhagic fever or dengue shock syndrome; however, the complexities of DENV immunopathog
186 flammatory diet is associated with metabolic syndrome, hypertension, abdominal obesity, and hypertrig
187   Mutations in CUBN cause Imerslund-Grasbeck syndrome (IGS), which is characterized by intestinal mal
188 ytokine storm and acute respiratory distress syndrome implicated in the most severe cases.
189 ric disorder termed multisystem inflammatory syndrome in children (MIS-C) emerged.
190 e epidemic, a novel multisystem inflammatory syndrome in children (MIS-C) emerged.
191                   A multisystem inflammatory syndrome in children (MIS-C) is associated with coronavi
192 hanges indicate the development of nephrotic syndrome in mice bearing the Asah1 podocyte-specific gen
193 nic variant in the gene associated with Lowe syndrome in one child, and an average of 1.8 reportable
194 y phenotypic spectrum, reminiscent of Noonan syndrome in some subjects.
195  is usually designated macrophage activation syndrome in those settings.
196 ar blight, root rot, fruit rot and crown rot syndromes in squash (Cucurbita moschata), is a devastati
197 s with anemia and lower-risk myelodysplastic syndromes in whom erythropoiesis-stimulating agent thera
198 estigated the epidemiology of the "alpha-Gal syndrome" in the United States and sought additional evi
199 hogenesis in patients with obesity/metabolic syndrome, in which the GRK2-mediated signaling can be a
200                      The top 3 prevalent ARI syndromes included: viral upper respiratory tract infect
201 he 2002 outbreak of severe acute respiratory syndrome, including the system of cell entry, which is t
202 in patients with mutant IDH2 myelodysplastic syndromes, including in those who have had previous ther
203 ost, as is seen in the macrophage activation syndrome induced by severe infections, including in infe
204 endocrinopathy, enteropathy, X-linked (IPEX) syndrome is a lethal disease caused by mutations in a tr
205 loid-related proteinemia inflammatory (PAMI) syndrome is a novel genetic disorder, causing hypercalpr
206 oclonal gammopathy, and skin changes (POEMS) syndrome is a rare multisystem disease resulting from an
207                Multiple evanescent white dot syndrome is a rare self-limiting condition of the outer
208 romeric Instability Facial Anomalies (ICF) 4 syndrome is a severe disease with increased mortality ca
209          Keratitis-ichthyosis-deafness (KID) syndrome is a severe, untreatable condition characterize
210                                    Metabolic syndrome is a significant risk factor for several common
211 an recognition of acute respiratory distress syndrome is associated with both systemic and respirator
212         The neurodevelopmental disorder Rett syndrome is caused by mutations in the gene Mecp2 Misexp
213     Survival from acute respiratory distress syndrome is improving, and outcomes beyond mortality may
214 ation in exon 2.Since an adult case of PFAPA syndrome is likely to be made misunderstanding for infec
215                                The metabolic syndrome is prevalent in developed nations and accounts
216 thogen that causes acquired immunodeficiency syndrome, is distinct from the more prevalent HIV-1 in s
217 significantly from that of Johanson-Blizzard syndrome (JBS), which is caused by bi-allelic variants i
218                                      Joubert syndrome (JBTS) is a recessive neurodevelopmental ciliop
219               Patients with the neurological syndrome known as body integrity dysphoria express a des
220 ) more often agreed that living with Sjogren syndrome made every day a challenge (adjusted odds ratio
221                    Consideration of clinical syndrome may help improve the accuracy of ATN designatio
222 iologies, a range of other movement disorder syndromes may also present with SIBs, even though this c
223           Risk of developing myelodysplastic syndrome (MDS) is significantly increased in both multip
224 ly ill patients with Middle East respiratory syndrome (MERS), accounting for time-varying confounders
225 ks of SARS-CoV-1 and Middle East respiratory syndrome (MERS), the development of therapeutic antibodi
226  of plant-based diets and incident metabolic syndrome (MetS) and components of MetS.
227                                       Marfan syndrome (MFS) is a connective tissue disorder that resu
228 te detection is challenging, as the clinical syndrome might be confused with either behavioural varia
229  a life-threatening multisystem inflammatory syndrome (MIS-C)(3-5).
230                                   Our Fowler syndrome model therefore defined the pathobiology of thi
231 er toevaluate the influence of the metabolic syndrome (MS) (obesity, hypertension, elevated triglycer
232                                       Noonan syndrome (NS) is a multisystemic developmental disorder
233                                    Nephrotic syndrome (NS) was the most common indication for biopsy.
234 dney tubules may vary with time in nephrotic syndrome (NS).
235 lammation, immunosuppression, and catabolism syndrome observed in adult human surgical sepsis survivo
236  T cell expansion characterized the HLH-like syndromes occurring in the murine model and in humans.
237           Frailty is a clinically recognized syndrome of decreased physiological reserve and a key co
238          However, acute respiratory distress syndrome often goes unrecognized.
239      After excluding individuals with Marfan syndrome or bicuspid aortic valve, a family history of A
240 s, hypertension, dyslipidemia, the metabolic syndrome or impaired renal function.
241 kaemia arising from previous myelodysplastic syndrome or myeloproliferative neoplasm, the presence of
242 en (12%) individuals had a diagnosis of Down syndrome or other developmental disorder, while 84 (52.5
243 piratory failure, acute respiratory distress syndrome, or multiple organ dysfunction; and direct tiss
244 y snoring through to obstructive sleep apnea syndrome (OSAS), may cause compromise of respiratory gas
245 meeting pediatric acute respiratory distress syndrome oxygenation criteria with bilateral infiltrates
246 ly unappreciated role in sHLH/cytokine storm syndrome pathogenesis by preventing macrophages from bec
247 s syndrome and nonacute respiratory distress syndrome patients (C-statistic, 0.78; 95% CI, 0.72-0.84)
248 ically ventilated acute respiratory distress syndrome patients.
249 sociated with cystic kidneys in Hajdu-Cheney syndrome patients.
250 d mucosal symptoms observed in many of these syndromes, patients are likely to present to an allergis
251                  Women with polycystic ovary syndrome (PCOS) have been shown to be less insulin sensi
252 TEN) are diagnosed with PTEN hamartoma tumor syndrome (PHTS) and are at high risk for developing brea
253 enotypic rescue in the Simpson-Golabi-Behmel syndrome preadipocyte knockout lines.
254 increasing rates of complex hematologic pain syndromes, present in up to 60% of patients with maligna
255 actin cytoskeletal regulator Wiskott Aldrich syndrome protein (WASp) has been implicated in maintenan
256                       Neural Wiskott-Aldrich syndrome protein(N-Wasp) is an actin nucleation factor t
257 pectrum of frontotemporal lobar degeneration syndromes provides a useful framework with which to unde
258                         Respiratory Distress Syndrome (RDS) is the commonest diagnosis after prematur
259 imilar to food protein-induced enterocolitis syndrome reactions.
260                          We describe a novel syndrome, referred to as "food-induced immediate respons
261 mmatory response to severe acute respiratory syndrome-related coronavirus 2 infection has a direct im
262 association as well as isolated Klippel-Feil syndrome, renal agenesis or esophageal atresia.
263 amage in murine models for Cornelia de Lange syndrome results in an inefficient and senescent placent
264 d in the control-of severe acute respiratory syndrome (SARS) in 2003(5).
265 o made, which included Positive and Negative Syndrome Scale (PANSS) measurements.
266 in inherited cardiac arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymorph
267           The systemic inflammatory response syndrome (SIRS) frequently occurs in patients with cardi
268  bleeding; R: systemic inflammatory response syndrome (SIRS), spontaneous bacteria peritonitis (SBP),
269 of Alzheimer's disease will also localize to syndrome-specific and symptom-specific brain networks.
270 yocardial infarction or other acute coronary syndrome, stroke, or coronary revascularisation) per 1 m
271 the prevalence of complications of metabolic syndrome, such as non-alcoholic fatty liver disease.
272 rous neurological disorders and neurogenetic syndromes, such as autism spectrum disorder (ASD) and Dr
273 ssociated immune reconstitution inflammatory syndrome (TB-IRIS) when they commence antiretroviral the
274 erculosis immune reconstitution inflammatory syndrome (TB-IRIS).
275 ith a severe but heterogeneous developmental syndrome, termed syt1-associated neurodevelopmental diso
276 nt of neuromodulation therapies for Tourette syndrome that could use a closed-loop-based approach.
277 but, other than their association with Lynch syndrome, the contribution of genetic risk factors to UC
278 n its structure or function cause sick sinus syndrome, the most common reason for electronic pacemake
279                             Triadin knockout syndrome (TKOS) is a potentially lethal arrhythmia disor
280 d Tomography in Patients With Acute Coronary Syndromes) trial (NCT02061891) evaluated the outcome of
281                                Upper crossed syndrome (UCS) refers to the altered muscle activations
282 with non-ST-segment elevation acute coronary syndrome undergoing invasive treatment.
283 ive assessment of multiple organ dysfunction syndrome using Proulx criteria.
284 gnitive impairment in participants with Down syndrome was classified with the Cambridge Cognitive Exa
285 olymphoid cancers develop in Wiskott-Aldrich syndrome (WAS), an X-linked primary immunodeficiency dis
286  Strategy to Medically Manage Acute Coronary Syndromes) was a double-blind, placebo-controlled random
287 he elastin gene (ELN) causes Williams-Beuren syndrome (WBS), while single nucleotide variants in ELN
288              To assess the risk of metabolic syndrome we estimated HRs and 95% CIs using Cox proporti
289 ic mastocytosis and monoclonal MC activation syndrome were negative.
290                Patients with myelodysplastic syndromes were aged 18 years or older with an ECOG perfo
291 ogical complications, such as Guillain-Barre syndrome, were reported(13,14) together with cases of mi
292 d help mitigate the development of metabolic syndrome where EAEP and AEP skim proteins could be poten
293 dds of developing acute respiratory distress syndrome, which increased by 62% (CI, 48% to 81%; P < 0.
294 ile acids (BAs), overlapping irritable bowel syndrome with diarrhoea (IBS-D).
295 -specific epigenomic alterations seen in ICF syndrome with DNMT3B mutations.
296 Cdx2-transgenic mice develop myelodysplastic syndrome with progression to acute leukemia associated w
297 dy more than doubles the number of published syndromes with DNA methylation episignatures and, most s
298 r Blockers In Non-ST Elevated Acute Coronary Syndromes With Initial Invasive Indication [DUBIUS]; NCT
299 duced fungal pathogen that causes white-nose syndrome (WNS), survival of the species may ultimately d
300                                       Werner Syndrome (WS) and Bloom Syndrome (BS) are disorders of D

 
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