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1 with dilation of the CSF-filled ventricles (ventriculomegaly).
2 partial agenesis of the corpus callosum, and ventriculomegaly.
3 of lower neuropsychological functioning with ventriculomegaly.
4 hypoplasia, optic nerve hypoplasia and mild ventriculomegaly.
5 es, including corpus callosum hypoplasia and ventriculomegaly.
6 lar zone (SVZ), subarachnoid hemorrhage, and ventriculomegaly.
7 instem and cerebellum hypoplasia, as well as ventriculomegaly.
8 Brain MRI revealed cerebellar hypoplasia and ventriculomegaly.
9 l hypoplasia, hippocampal malformations, and ventriculomegaly.
10 arly lethal phenotypic variant showed severe ventriculomegaly.
11 pia, consistent with a CMS diagnosis, but no ventriculomegaly.
12 emorrhage, periventricular leukomalacia, and ventriculomegaly.
13 cal volumes and is associated with secondary ventriculomegaly.
14 frequent monogenic causes of CH and primary ventriculomegaly.
15 luding impaired spermatogenesis and cerebral ventriculomegaly.
16 odeficient AAV-NKCC1-NT51 failed to mitigate ventriculomegaly.
17 ay and relative macrocephaly associated with ventriculomegaly.
18 yndrome), diseases frequently occurring with ventriculomegaly.
19 ydrocephalus mouse model resulted in reduced ventriculomegaly.
20 hemorrhage, periventricular leukomalacia, or ventriculomegaly (17.5 percent vs. 23.9 percent, P=0.03)
21 maging include a thin corpus callosum (90%), ventriculomegaly (65%) often with colpocephaly, and peri
22 o find that Kidins220 deficient mice develop ventriculomegaly accompanied by water dyshomeostasis and
25 enatal steroid tended to have lower risks of ventriculomegaly and an echolucent lesion than their pee
26 evident in newborn cranial ultrasound scans (ventriculomegaly and an echolucent lesion) and of cerebr
27 for CH, demonstrate a genetic association of ventriculomegaly and ASD, and help explain neurodevelopm
28 s who shared a phenotype comprising cerebral ventriculomegaly and echogenic kidneys with histopatholo
30 by a reduction in brain matter and secondary ventriculomegaly and is a major cause of developmental d
31 ed viral (AAV)-NKCC1 prevented blood-induced ventriculomegaly and led to persistently increased CSF c
32 7-retromer-AQP4 pathway is involved in human ventriculomegaly and open novel therapeutic perspectives
33 le, we show that the male fertility defects, ventriculomegaly and pituitary abnormalities are only pr
36 essive spastic paraparesis with accompanying ventriculomegaly and thinning of the corpus callosum, co
37 ormly present, whereas cerebellar dysplasia, ventriculomegaly, and arachnoid cysts are nearly invaria
39 facial dysmorphisms, palatal abnormalities, ventriculomegaly, and hypogonadism as well as additional
40 layed speech, varying degrees of spasticity, ventriculomegaly, and ICH/cerebral calcifications, the l
41 ne fetuses (56%, P < .05) with isolated mild ventriculomegaly, and in 24 of 31 fetuses (77%, P < .05)
42 han 10 probands, studies of mild or moderate ventriculomegaly, and studies using genetic tests other
43 aracterized by variable presence of cerebral ventriculomegaly, aqueductal stenosis, developmental del
44 which MR imaging has proved useful, such as ventriculomegaly, arachnoid cysts, and abdominal masses,
45 s, calculated total ventricular volumes, and ventriculomegaly as documented in the electronic medical
46 he TMEM67 homozygous mutant rats have severe ventriculomegaly as well as severe polycystic kidney dis
47 supplementation with formate prevented both ventriculomegaly, as assessed at prenatal stages, and po
48 odevelopment of children with isolated fetal ventriculomegaly, associated with altered cortical devel
49 toparietal regions most severely, as well as ventriculomegaly, bilateral white matter signal changes,
50 the disease with the major manifestation of ventriculomegaly caused by the accumulation of high amou
51 rate parenchymal rarefaction, severe to mild ventriculomegaly, cerebellar hypoplasia with brainstem d
52 icrocephaly, a reduction in cerebral volume, ventriculomegaly, cerebellar hypoplasia, lissencephaly w
53 identify studies: congenital hydrocephalus, ventriculomegaly, cerebral ventriculomegaly, primary ven
54 ion of the fluid-filled cerebral ventricles (ventriculomegaly) characterizes hydrocephalus and is fre
55 dentified, in the largest assembled cerebral ventriculomegaly cohort (2697 parent-proband trios), an
57 24 [20 males/4 females]) with isolated fetal ventriculomegaly, compared with 10 controls (n = 10 [6 m
58 mental disorders (TADD)', featuring variable ventriculomegaly, congenital hydrocephalus and other str
59 71 in unrelated children exhibiting variable ventriculomegaly, congenital hydrocephalus, developmenta
60 f brain morphology with leukoencephalopathy, ventriculomegaly, cortical abnormalities, and intracrani
61 CSF, which often leads to hydrocephalus and ventriculomegaly, currently lacks effective treatments.
62 opathological study revealed megalencephaly, ventriculomegaly, cytomegaly and extensive vacuolization
64 ctrum of antiquitin deficiency extended from ventriculomegaly detected on foetal ultrasound, through
66 r early identification and quantification of ventriculomegaly due to either posthemorrhagic ventricul
67 ears to mediate hypoxia-induced brain injury ventriculomegaly during early postnatal development.
68 caused by the presence of megalencephaly and ventriculomegaly, (febrile) seizures and autism-like beh
69 lomegaly, cerebral ventriculomegaly, primary ventriculomegaly, fetal ventriculomegaly, prenatal ventr
72 normal cortical formation, cerebral atrophy, ventriculomegaly, hydrocephaly, and cerebellar abnormali
74 tal Zika virus infections were similar, with ventriculomegaly in 16 of 17 (94%) and 27 of 28 (96%) in
75 ular mechanism underlying the development of ventriculomegaly in a genetic subset of patients with AS
76 e to create automated algorithms that detect ventriculomegaly in adult hydrocephalus shunt malfunctio
79 arenchyma are an under-appreciated driver of ventriculomegaly in multiple forms of communicating hydr
81 urodevelopmental outcomes and persistence of ventriculomegaly in some post-surgical patients highligh
82 o association of oxygen delivery (except for ventriculomegaly in the BDG group) or carbon dioxide rea
83 t assembled cohort of patients with cerebral ventriculomegaly, including neurosurgically-treated cong
84 uch an algorithm could automatically predict ventriculomegaly indicative of shunt failure in a real-l
85 lethality craniofacial and skeletal defects, ventriculomegaly, infertility and pituitary anomalies.
86 cognized to have neurologic effects, such as ventriculomegaly, intraventricular adhesions, subependym
90 ospinal fluid (CSF)-filled brain ventricles (ventriculomegaly) is a defining feature of congenital hy
91 sive expansion of the CSF-filled ventricles (ventriculomegaly), is the most common reason for brain s
92 tal hydrocephalus, characterized by cerebral ventriculomegaly, is among the most common and least und
93 tal hydrocephalus, characterized by cerebral ventriculomegaly, is one of the most common reasons for
95 , including intrauterine growth restriction, ventriculomegaly, microcephaly, lissencephaly, and exten
96 culomegaly, fetal ventriculomegaly, prenatal ventriculomegaly, molecular analysis, genetic cause, gen
97 The most common abnormal brain findings were ventriculomegaly (n = 16, 59.2%) and corpus callosum abn
98 l abnormality (e.g. large cysts, significant ventriculomegaly; n = 240) were analysed with Statistica
99 ture of DS, exhibiting brachycephalic skull, ventriculomegaly, neurodevelopmental delay, hyperactivit
101 n of Bbs1 mutant brain neuroanatomy revealed ventriculomegaly of the lateral and third ventricles, th
102 itoneal shunt, and the other two only showed ventriculomegaly on MRI scan without neurological deteri
104 roencephaly, periventricular calcifications, ventriculomegaly, pachygyria, cerebellar hypoplasia, por
105 and p.Asn800Lys, and one child with cerebral ventriculomegaly, periventricular heterotopias, echogeni
107 iculomegaly, primary ventriculomegaly, fetal ventriculomegaly, prenatal ventriculomegaly, molecular a
108 al hydrocephalus, ventriculomegaly, cerebral ventriculomegaly, primary ventriculomegaly, fetal ventri
110 n or postnatal everolimus treatment corrects ventriculomegaly, rescues cortical deficits and increase
113 luid (CSF)-filled brain ventricles (cerebral ventriculomegaly), the cardinal feature of congenital hy
114 pathogenesis of developmental brain injury, ventriculomegaly was also observed in mice lacking the e
119 rapeutic potential for reducing fibrosis and ventriculomegaly was tested using a rat model of juvenil
122 T2-weighted imaging, focal tissue loss, and ventriculomegaly were all more commonly detected in BDG
123 genital cataracts, hypotonia, prenatal-onset ventriculomegaly, white-matter abnormalities, hypoplasti
124 more, VEGF infusions into the rats result in ventriculomegaly with an increase of SVZ neuroblast in r