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1 Multifactorial risk factors contributing to neurodevelopmental abnormalities associated with CHD hav
3 better pathophysiologic understanding of the neurodevelopmental abnormalities observed in neonates ex
7 iduals affected by a new autosomal recessive neurodevelopmental and degenerative disorder in which th
8 CHD patients and approximately 28% with both neurodevelopmental and extra-cardiac congenital anomalie
9 ctory dysfunction is broadly associated with neurodevelopmental and neurodegenerative diseases and pr
10 ing a translational approach, which combined neurodevelopmental and neurodegenerative mouse models wi
11 Understanding the genetic factors underlying neurodevelopmental and neuropsychiatric disorders is a m
12 res are implicated in the risk for offspring neurodevelopmental and neuropsychiatric disorders, promp
15 NA methylation variation in genes related to neurodevelopmental and peroxisomal processes that play a
20 role of BPTF haploinsufficiency in syndromic neurodevelopmental anomalies and extend the clinical spe
21 brain circuitry, and has been implicated in neurodevelopmental as well as neurodegenerative disease
22 1 year, and at age 18 to 24 months' PMA and neurodevelopmental assessments at 18 to 24 months' PMA d
24 mong the most commonly implicated factors in neurodevelopmental autism spectrum disorders (ASD), char
26 th [7, 8], suggesting an association between neurodevelopmental changes and cortical organization on
30 associated CNVs and of the group of 41 other neurodevelopmental CNVs had impaired performance on the
31 iffusion imaging as part of the Philadelphia Neurodevelopmental Cohort, we demonstrate that structura
34 Intellectual disability (ID) is a prevailing neurodevelopmental condition associated with impaired co
36 Autism spectrum disorder (ASD) is a complex neurodevelopmental condition that can be reliably diagno
37 spectrum disorder (ASD) encompasses a set of neurodevelopmental conditions whose striking sex-related
38 spectrum disorders are a group of pervasive neurodevelopmental conditions with heterogeneous etiolog
39 ter organization and 2 commonly co-occurring neurodevelopmental conditions, ASD and ADHD, through bot
41 show that MAE genes are under-represented in neurodevelopmental copy number variants (CNVs) (P<2.2 x
43 nd methyl-DNA binding proteins contribute to neurodevelopmental defects and altered brain plasticity.
44 armacological treatment that may prevent the neurodevelopmental defects caused by prenatal immune act
45 e association between maternal infection and neurodevelopmental defects in progeny is well establishe
49 inant disorder that is best characterized by neurodevelopmental deficits and the presence of benign t
53 is a viable risk factor contributing to the neurodevelopmental deficits observed in autism spectrum
55 al effects and resulted in the prevention of neurodevelopmental delay in the one individual treated b
57 rome in one patient (p.Pro210Leu), to severe neurodevelopmental delay with brain atrophy (p.Ser94Arg)
58 families with HPA who exhibited progressive neurodevelopmental delay, dystonia, and a unique profile
59 sy, acquired hydrocephalus and microcephaly, neurodevelopmental delay, gastrointestinal motility prob
61 dose of bevacizumab may reduce the risk for neurodevelopmental disability or detrimental effects on
66 ostnatal period by activating a well-defined neurodevelopmental disease pathway and that this phenoty
69 use autosomal recessive neurodegenerative or neurodevelopmental disease, making yeast Vps13p an impor
71 ling progress in understanding the causes of neurodevelopmental diseases such as autism, linking gene
72 ctivity are a transdiagnostic key finding in neurodevelopmental diseases, a characterization of imagi
76 re identified among 4,760 trio probands with neurodevelopmental diseases; this is highly unlikely to
77 EMENT Pitt-Hopkins syndrome (PTHS) is a rare neurodevelopmental disorder associated with TCF4 mutatio
78 ICANCE STATEMENT Angelman syndrome (AS) is a neurodevelopmental disorder caused by loss or mutation o
80 kinase-like 5 (CDKL5) deficiency is a severe neurodevelopmental disorder caused by mutations in the C
84 endent kinase-like 5 (CDKL5) deficiency is a neurodevelopmental disorder characterized by epileptic s
85 re associated with risk for schizophrenia, a neurodevelopmental disorder characterized by excitatory/
87 Fragile X syndrome (FXS) is an undertreated neurodevelopmental disorder characterized by low intelli
89 D) is a childhood-onset neuropsychiatric and neurodevelopmental disorder characterized by the presenc
90 particular; they enable the definition of a neurodevelopmental disorder due to PSMD12 variants, expa
91 Intellectual disability (ID) is a common neurodevelopmental disorder exhibiting extreme genetic h
95 tions of microcephalin (MCPH1) can cause the neurodevelopmental disorder primary microcephaly type 1.
96 ied in previously implicated high-confidence neurodevelopmental disorder risk genes, such as CHD2, CT
97 lopment and reveal a potential mechanism for neurodevelopmental disorder risk in pregnancies complica
100 s system, we find that in Timothy syndrome-a neurodevelopmental disorder that is caused by mutations
101 are the main causes of Kleefstra syndrome, a neurodevelopmental disorder that is characterized by imp
102 Prader-Willi syndrome (PWS) is a genetic neurodevelopmental disorder that presents with hypotonia
104 f maternal UBE3A causes Angelman syndrome, a neurodevelopmental disorder with some overlapping neurol
106 ntaining 1 (HUWE1) E3 ubiquitin ligase cause neurodevelopmental disorder X-linked intellectual disabi
107 disorder (ADHD) is the most common childhood neurodevelopmental disorder, and boys are two to three t
108 rotein, disrupt brain function and cause the neurodevelopmental disorder, Glut1 deficiency syndrome (
110 cynomolgus monkeys serving as a model for a neurodevelopmental disorder, Rett syndrome (RTT), which
114 variants in 50 genes already established in neurodevelopmental disorders (46 autosomal recessive, 2
115 de novo missense mutations in patients with neurodevelopmental disorders (NDDs) and highlight 35 gen
116 ople with autism spectrum disorder and other neurodevelopmental disorders (NDDs) are behaviorally and
117 d/or sign as potential communicative acts in neurodevelopmental disorders (NDDs), are research questi
118 Altered dendritic morphology is common in neurodevelopmental disorders (NDDs), many of which show
120 -LOF to a set of 1142 de novo vari3ants from neurodevelopmental disorders and find enrichment of path
121 ng evidence that these regions contribute to neurodevelopmental disorders and outline strategies for
122 tions (PMMs) have been implicated in several neurodevelopmental disorders and overgrowth syndromes.
123 the effects of experience in the context of neurodevelopmental disorders and typical neural developm
127 ngoing efforts to understand the etiology of neurodevelopmental disorders arising from Ptchd1 deficie
129 udied interneuron subtype in the etiology of neurodevelopmental disorders characterized by NMDA recep
131 to behavioural abnormalities associated with neurodevelopmental disorders in both primate and rodent
132 o induce TH17 cells may increase the risk of neurodevelopmental disorders in the offspring of pregnan
133 sts that common pathways are altered in many neurodevelopmental disorders including autism spectrum d
134 egnancy serves as a risk factor for multiple neurodevelopmental disorders including autism spectrum d
135 evelopment has been implicated in a range of neurodevelopmental disorders including tuberous sclerosi
136 tellectual disability and in the etiology of neurodevelopmental disorders is increasingly recognized.
141 l as a key player in conditions ranging from neurodevelopmental disorders such as autism to neurodege
143 reatments for FASD and conceivably for other neurodevelopmental disorders with cognitive deficits.
144 utical agents, and can be adapted for use in neurodevelopmental disorders with genetic etiologies.
145 spectrum disorder (ASD) describes a group of neurodevelopmental disorders with high heritability, alt
146 m disorder (ASD) represents a set of complex neurodevelopmental disorders with large degrees of herit
147 this domain and the C-terminal likely cause neurodevelopmental disorders with or without seizures.
148 m disorder (ASD) is a heterogeneous group of neurodevelopmental disorders without any defined uniting
150 States, one in six children are affected by neurodevelopmental disorders, and polybrominated dipheny
151 cy is correlated with increased frequency of neurodevelopmental disorders, and this is studied in mic
153 er and infections has been linked to various neurodevelopmental disorders, but it is not yet known wh
154 tism and intellectual disability are complex neurodevelopmental disorders, debilitating millions of p
156 y complications that predispose offspring to neurodevelopmental disorders, including autism, attentio
157 n the impact of a genetic lesion linked with neurodevelopmental disorders, including mechanisms of ma
158 d8(+/del5) mice across pathways disrupted in neurodevelopmental disorders, including neurogenesis, sy
159 lead to epilepsy and are also implicated in neurodevelopmental disorders, neuropathic pain, and schi
160 that is strongly associated with the risk of neurodevelopmental disorders, particularly autism and at
161 ing neural and behavioral dysfunction across neurodevelopmental disorders, particularly autism spectr
162 s associated with the DMSs were enriched for neurodevelopmental disorders, particularly for CpG sites
163 trongly implicated in the pathophysiology of neurodevelopmental disorders, raising the question of wh
164 its in sensory systems are commonly noted in neurodevelopmental disorders, such as the Rett syndrome
165 While altered cIN development contributes to neurodevelopmental disorders, the inaccessibility of hum
166 nderstand the heterogeneity of ASD and other neurodevelopmental disorders, the relationship between q
167 A receptor have already been associated with neurodevelopmental disorders, we suggest that pathogenic
168 onal morphology and synaptic changes seen in neurodevelopmental disorders, while alteration in astroc
204 s an important underlying molecular cause of neurodevelopmental dysfunction, we developed and charact
205 ted long-term data on potential systemic and neurodevelopmental effects after anti-VEGF use for ROP t
206 erapeutic target to mitigate the deleterious neurodevelopmental effects of prenatal cocaine exposure
208 ults implicate social visual engagement as a neurodevelopmental endophenotype not only for autism, bu
211 impact of early vitamin A supplementation on neurodevelopmental function has not been adequately stud
213 We applied network analysis to characterize neurodevelopmental gene expression, revealing widespread
215 f mutants, we observed that most but not all neurodevelopmental genes in the Wnt/Frizzled pathway are
217 pwise manner to further our understanding of neurodevelopmental HCMV pathogenesis.IMPORTANCE HCMV bra
220 roup vs 70% in the placebo group), with mild neurodevelopmental impairment (20% in the hydrocortisone
221 e placebo group), or with moderate to severe neurodevelopmental impairment (7% in the hydrocortisone
223 primary outcome was a composite of death or neurodevelopmental impairment (NDI) at 18 to 24 months c
224 B streptococcal (GBS) disease are at risk of neurodevelopmental impairment (NDI), a burden not previo
225 eptic encephalopathy, of which 13 had severe neurodevelopmental impairment and four died in early chi
229 m infants with adverse neonatal outcomes and neurodevelopmental impairment in early childhood, with a
230 xamining the genetic and molecular bases for neurodevelopmental impairment in model mice in vivoSIGNI
232 respecified exploratory secondary outcome of neurodevelopmental impairment was based on a standardize
234 was a three-level outcome - survival without neurodevelopmental impairment, survival with neurodevelo
237 s conclude that early disruptive behavior is neurodevelopmental in nature and should be reclassified
240 bolite levels in brain homogenates from five neurodevelopmental mouse models of psychiatric disorders
242 er is a debilitating condition with possible neurodevelopmental origins but unknown neuroanatomical c
244 ctate lesions to brain development and early neurodevelopmental outcome we used multimodal brain MRI
246 ence a high rate of brain injury and adverse neurodevelopmental outcome; however, the incidence of br
248 se exposure has been associated with adverse neurodevelopmental outcomes among school-aged children;
249 roid use, respiratory support, survival, and neurodevelopmental outcomes at 18 to 24 months' PMA.
250 hout BPD at 36 weeks' PMA or respiratory and neurodevelopmental outcomes at 18 to 24 months' PMA.
251 changes in NSCs and to link these changes to neurodevelopmental outcomes in children who were exposed
253 l be essential to prevent or improve adverse neurodevelopmental outcomes in individuals surviving CHD
255 e association between neonatal pain and poor neurodevelopmental outcomes in these high-risk neonates.
256 literature describing risk factor models for neurodevelopmental outcomes in VPT/VLBW children, yet fe
262 aploinsufficiency results in a predominantly neurodevelopmental phenotype with occasional physical an
264 dividuals who underwent WES for diagnoses of neurodevelopmental phenotypes is extremely small and ach
265 elated disorders comprise a wide spectrum of neurodevelopmental phenotypes ranging from mild to sever
266 patient cohort exhibited a broad spectrum of neurodevelopmental phenotypes, comprising six patients w
269 we propose that deprivation accelerates the neurodevelopmental process of synaptic pruning and limit
270 e that maternal immune activation hits a key neurodevelopmental process, the excitatory-to-inhibitory
271 s in the transcription factor THAP1, but the neurodevelopmental processes in which THAP1 participates
273 CMV ie3, interferes pleiotropically with key neurodevelopmental processes, including neural stem cell
275 nimal model with translational relevance for neurodevelopmental psychiatric disorders such as schizop
277 in the etiopathogenesis or manifestation of neurodevelopmental, psychiatric and neurodegenerative di
278 cated in a broad range of diseases including neurodevelopmental, renal, and lung disorders, and cance
282 hat underlie this adaptive phenomenon, since neurodevelopmental studies have mainly focused on the ri
284 icate that mutations in EBF3 cause a genetic neurodevelopmental syndrome and suggest that loss of EBF
285 nt dominant mutations in RAB11B leading to a neurodevelopmental syndrome, likely caused by altered GD
289 mmation demonstrated impaired performance in neurodevelopmental testing in early life assessed via ne
291 for schizophrenia pathogenesis, but also in neurodevelopmental theories, because rodent models indic
292 Bs) and organochlorine pesticides (OCPs) are neurodevelopmental toxicants, but few studies have exami
297 irst years of life, while deviations to this neurodevelopmental trajectory likely result in alteratio
299 Rosa26 and AAVS1); (2) biallelic knockout of neurodevelopmental transcription factor genes; (3) simpl
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