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1 sm, inguinal hernia or transverse testicular ectopia.
2  I malformation or asymptomatic for tonsilar ectopia.
3 formation and eight as asymptomatic tonsilar ectopia.
4  than in patients with asymptomatic tonsilar ectopia.
5 heterozygous mice in the absence of cellular ectopia.
6 plasia, foliation defects, and Purkinje cell ectopia.
7 iation, agranularity, and Purkinje cell (PC) ectopia.
8  30%, and the appearance of multiple retinal ectopias.
9 a greater likelihood of cerebellar tonsillar ectopia (30.7%; P < .002 and P < .001, respectively) and
10 (decentration, tilt, rotation) and pupillary ectopia (4.5 mm iris aperture) were varied upon each vir
11                                              Ectopia also contains astrocytes, positive for glial fib
12 f actin regulatory proteins, causes neuronal ectopias, alters intralayer positioning in the cortical
13 ing cerebellar hypoplasia with Purkinje cell ectopia and disruption of neuronal layers in the cerebra
14                                 Granule cell ectopia and hypoplasia are also associated with the brea
15 helial cell development, resulting in thymic ectopia and hypoplasia.
16 opically produces GABA INs, leading to their ectopias and a thinner cortical plate due to diminished
17              The subpial and paraventricular ectopias and connecting cell streams are comprised of po
18 inner limiting membrane led to small retinal ectopias and subsequent changes in the optic nerve.
19 ct behavioral differences between those with ectopias and their non-ectopic littermates.
20 ed clusters of neurons in layer I of cortex (ectopias) and those without.
21 erior cerebellar morphogenesis, granule cell ectopia, and hypoplasia.
22 g to basement membrane degradation, neuronal ectopia, and laminar disruption.
23        During cortical development, neuronal ectopias are associated with severe disorganization of r
24 emonstrates that the GABA INs comprising the ectopias are from a cortical Emx1 lineage generated in t
25  flow in patients with asymptomatic tonsilar ectopia averaged 62%.
26       These usually appear as focal cortical ectopias, but also include other abnormalities, such as
27 rmation and those with asymptomatic tonsilar ectopia by using a neurosurgeon's overall clinical deter
28 s suggestive of thoraco-abdominal variety of ectopia cardis.
29  as muscle-eye-brain disease, exhibit neural ectopias caused by overmigration of neurons.
30                              Molecular layer ectopia, clusters of misplaced cells in layer I of the n
31                 Mutants exhibit granule cell ectopia concomitant with foliation defects.
32                  These results indicate that ectopia contain cells of different lineages with diverse
33 ent interneuronal subtypes demonstrates that ectopia contain nonpyramidal cells immunoreactive for ca
34  midline fusion resulting in a cleft palate, ectopia cordis, and a large omphalocele.
35 ound evaluation of either of an omphalocele, ectopia cordis, distal sternal defect, pericardial defec
36 or studies showed that mice with neocortical ectopias demonstrated working memory impairments compare
37 2 mutation causes neocortical and cerebellar ectopias dependent on Dab1, a key signaling protein in t
38 tachment developed in only 1 eye and macular ectopia developed in 5 eyes.
39       Neither retinal detachment nor macular ectopia developed in any of the IVB-treated eyes.
40 d urinary tract, including ureteric bud (UB) ectopia, double ureters/collecting systems, delayed prim
41 ams arising from an aberrant paraventricular ectopia found throughout dTel.
42                    We show that cells within ectopia have membrane properties of both pyramidal and a
43            Unlike several other models of UB ectopia, hypersensitivity of p53(-/-) WD to GDNF is not
44  venous blood hormone levels; (b) hypoplasia-ectopia in 32 patients requiring lifelong TRT; (c) nonvi
45                                       Thymic ectopia in Hoxa3(+/-)Pax1(-/-) compound mutants is due t
46 s within and surrounding layer I neocortical ectopia in NXSMD/EiJ mice.
47 ss of the mouse Gpr56 gene leads to neuronal ectopia in the cerebral cortex, a cobblestone-like corti
48  functional Pax6 protein, have large subpial ectopias in dTel and ventral telencephalon connected by
49                              Intracerebellar ectopias in the chimera were composed exclusively of mut
50 esting different origins for extracerebellar ectopias in these regions.
51 ingeal fibroblasts elicited similar cortical ectopias in vivo and altered laminin organization in vit
52 universal, novel phenotype: profound retinal ectopia, in which retinal tissue was often found in the
53  in neurons alone did not result in cortical ectopias, indicating that fak deletion from glia is requ
54                                     However, ectopia induced by Otx2 differentiated and dispersed as
55 d in fibrillin microfibril biogenesis, cause ectopia lentis (EL) and EL et pupillae.
56        The corneas of patients with MFS with ectopia lentis (EL) were significantly flatter and with
57 mutations cause autosomal recessive isolated ectopia lentis (IEL) and ectopia lentis et pupillae.
58 minant FBN1 mutations cause IEL or syndromic ectopia lentis (Marfan syndrome and Weill-Marchesani syn
59  fibrillin-1, is genetically associated with ectopia lentis and alterations in height.
60  the secreted metalloprotease ADAMTS17 cause ectopia lentis and short stature in humans with Weill-Ma
61 port a genetic basis for a syndromic form of ectopia lentis and the role of aspartyl hydroxylation in
62 of dislocation in patients with a history of ectopia lentis due to Marfan syndrome, idiopathic causes
63 n patients were examined, including one with ectopia lentis et pupillae.
64  recessive isolated ectopia lentis (IEL) and ectopia lentis et pupillae.
65 ely studied in horses, few reports of equine ectopia lentis exist and no genetic investigations have
66 h suggests a possible link to other forms of ectopia lentis given that many of the genes implicated i
67 ons were among the most consistent features (ectopia lentis in 86%, myopia in 80%).
68 syndrome and primary open angle glaucoma and ectopia lentis in dogs.
69                                              Ectopia lentis in humans and other species is reported t
70                    Given the role of FBN1 in ectopia lentis in humans and other species, FBN1 should
71 th FBN1:p.(Ala882Val) as the likely cause of ectopia lentis in this foal, the first genetic explanati
72 ith a dominant mode of inheritance, of which ectopia lentis is a common feature.
73                                              Ectopia lentis is the dislocation of the natural crystal
74 wise healthy four-year-old boy with isolated ectopia lentis whose partial lens dislocation was captur
75 t presents a unique presentation of isolated ectopia lentis with anterior lens dislocation and pupill
76 dissections, dislocation of the ocular lens (ectopia lentis) and skeletal abnormalities that are char
77 viewed, 6 (35%) had hereditary or idiopathic ectopia lentis, 5 (29%) had Marfan syndrome, 2 (12%) wer
78 pmental abnormalities including microcornea, ectopia lentis, and early onset of cone-rod dystrophy.
79  comparable in revised Ghent systemic score, ectopia lentis, and most phenotypic features, including
80 estations include bilateral iris hypoplasia, ectopia lentis, corectopia, ectropion uveae, and catarac
81 rome (MFS) presented with subluxated lenses (ectopia lentis, EL).
82 nterior segment dysgenesis, Marfan syndrome, ectopia lentis, neurofibromatosis, retinal hemangioblast
83 etardation and other disabilities (including ectopia lentis, osteoporosis, and thromboembolism) in pa
84 d bilateral microcornea, childhood cataract, ectopia lentis, rhegmatogenous retinal detachment, and c
85 e postsurgical aphakia, subluxated cataract, ectopia lentis, traumatic subluxation, and decentered IO
86 lar features including microspherophakia and ectopia lentis.
87 lar anterior segment dysgenesis, myopia, and ectopia lentis.
88 nique for visual rehabilitation in pediatric ectopia lentis.
89  same features as those in family 2, without ectopia lentis.
90 opathology of the globes was consistent with ectopia lentis.
91 the integrity of zonules, such as uveitis or ectopia lentis; (6) eyes with extreme myopia or long axi
92                Interestingly, the cerebellar ectopia occurs in the absence of any significant alterat
93  leading to disruption of the pia-arachnoid, ectopia of fibroblasts in the cortex, and reactive glios
94  the neural-meningeal boundary, resulting in ectopia of meningeal fibroblasts in the cerebral cortex
95 ghout the diffuse cell zone and resulting in ectopia of mesenchyme-derived fibroblasts in the upper h
96 t component to the environment can cause the ectopia of wild-type Purkinje cells.
97  these defects are due primarily to cellular ectopia or the absence of Reelin.
98 two in association with atypical phenotypes: ectopia pupillae (displaced pupils) and congenital nysta
99 al evidence to demonstrate that cells within ectopia receive input from cells within layers I, upper
100                              The presence of ectopias resulted in better Morris maze learning for sta
101 n the pial basement membrane underlie neural ectopia seen in those congenital muscular dystrophies (C
102 these irregularities result in small retinal ectopias that extend from the retina into the interstiti
103 tinal detachment, cataract, macular dragging/ectopia, vitreous or retinal hemorrhage, glaucoma, and e
104 itors of the rhombic lip and that cerebellar ectopia were derived from granule neuron precursors (GNP
105                      We found that brainstem ectopia were derived from neuronal progenitors of the rh
106     The granule cells of the extracerebellar ectopias were almost entirely derived from Unc5h3/Unc5h3

 
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