ライフサイエンスコーパス: hydrocephalus

1 on, adducted thumbs, spastic paraplegia, and hydrocephalus).

2 to prenatal aqueduct stenosis and resultant hydrocephalus.

3 e-axial polydactyly, neural tube defects and hydrocephalus.

4 rupting cerebrospinal fluid flow and causing hydrocephalus.

5 may help in the diagnosis and prevention of hydrocephalus.

6 ass effect/herniation, 3) infarction, and 4) hydrocephalus.

7 levated HB-EGF can elicit VEGF induction and hydrocephalus.

8 sociated with left ventricular uncompensated hydrocephalus.

9 emorrhaging branchial arch blood vessels and hydrocephalus.

10 acranial hemorrhage without midline shift or hydrocephalus.

11 d the development of fetal non-communicating hydrocephalus.

12 n, enlargement of the lateral ventricles and hydrocephalus.

13 can result in abnormal CSF accumulation and hydrocephalus.

14 ypersecretion in a model of post-hemorrhagic hydrocephalus.

15 ng glycine accumulation, early lethality and hydrocephalus.

16 mice exhibit early vision loss and die from hydrocephalus.

17 d for E cell planar polarity and may prevent hydrocephalus.

18 hat compound genetic ablation of Dvls causes hydrocephalus.

19 luid flow through ciliary beating, can cause hydrocephalus.

20 patient, magnetic resonance imaging revealed hydrocephalus.

21 syndromic ciliopathy including dysosmia and hydrocephalus.

22 f eight displayed learning disability and/or hydrocephalus.

23 uch as Alzheimer disease and normal pressure hydrocephalus.

24 using a rat model of juvenile communicating hydrocephalus.

25 sion of 1 cm or greater, or new or worsening hydrocephalus.

26 % of patients and in 64% of 22 patients with hydrocephalus.

27 of juvenile post-haemorrhagic communicating hydrocephalus.

28 meningitis, seizures, cerebral ischemia and hydrocephalus.

29 , cleft lip with or without cleft palate, or hydrocephalus.

30 t stenosis and the development of congenital hydrocephalus.

31 enotype including ventral body curvature and hydrocephalus.

32 progenitors in the pathogenesis of neonatal hydrocephalus.

33 e a serious complication in the treatment of hydrocephalus.

34 st common indication for CT in children with hydrocephalus.

35 n be an initiating cause of noncommunicating hydrocephalus.

36 evelopment and its dysregulation may lead to hydrocephalus.

37 nge in neuronal AbetaPP expression following hydrocephalus.

38 duced hippocampal long-term potentiation and hydrocephalus.

39 d on controls and after 2, 6 and 10 weeks of hydrocephalus.

40 complexes that affect brain development and hydrocephalus.

41 uch as brainstem compression and obstructive hydrocephalus.

42 , and mice with Hydin defects develop lethal hydrocephalus.

43 renchymal compared with meningeal lesions or hydrocephalus.

44 th leptomeningeal, and 0/3 for patients with hydrocephalus.

45 NM II-B-ablated mice seem to be the cause of hydrocephalus.

46 PHP-RC phenotypes, including renal cysts and hydrocephalus.

47 A child developed hydrocephalus.

48 normal CSF flow dynamics secondary to innate hydrocephalus.

49 ion of the normally smooth mouse cortex, and hydrocephalus.

50 tudy the development of both severe and mild hydrocephalus.

51 mall-molecule therapeutics for developmental hydrocephalus.

52 athways - contributes to the pathogenesis of hydrocephalus.

53 obtained from patients with normal pressure hydrocephalus.

54 nting in Ugandan infants with postinfectious hydrocephalus.

55 ccumulation of CSF within the brain known as hydrocephalus.

56 ilibrium syndrome 2, cause severe congenital hydrocephalus.

57 Administration (FDA)-approved drugs to treat hydrocephalus.

58 phalus as well as idiopathic normal pressure hydrocephalus.

59 A few mutant mice developed hydrocephalus.

60 Twenty-six fetuses (45%) had prenatal hydrocephalus.

61 of an enhancing suprasellar mass lesion and hydrocephalus.

62 (1.2%), club foot (1%), hypospadias (0.6%), hydrocephalus (0.6%), cleft lip or palate (0%), and obst

63 yes with glaucoma (4.6%) (3 uveitis, 1 prior hydrocephalus, 1 uveitis and pars plana vitrectomy, and

64 sitivity and specificity, respectively, were hydrocephalus (100% and 100%), clubfoot (100% and 99.8%)

65 dian age, 43 years) with chronic obstructive hydrocephalus, 12 of whom went on to undergo ETV, were i

66 Acute hydrocephalus (13.6% vs 7.4%; p < 0.001) and mass effect

67 halus (16.2%) and idiopathic normal pressure hydrocephalus (14.2%) in adults.

68 dren, and tumours (24.6%), post-haemorrhagic hydrocephalus (16.2%) and idiopathic normal pressure hyd

69 Hydrocephalus (17.4%) was the commonest MRI finding.

70 included raised intracranial pressure (42%), hydrocephalus (30%), neurological deficits (27%; 6% deve

71 , 51.9-100.0), fever (89.8%, 79.8-95.2), and hydrocephalus (86.1%, 68.6-94.6).

72 ase, results in aberrant CSF circulation and hydrocephalus, a common disorder of the CNS.

73 Pard3 depletion results in hydrocephalus, a defect often associated with abnormal c

74 in both, the Reelin pathway and Lis1 exhibit hydrocephalus, a phenotype that is suppressed by mutatio

75 L1cam knockout (L1(KO)) mice have hydrocephalus, a small cerebellum, hyperfasciculation of

76 Mendelian forms of hydrocephalus account for a small fraction of the geneti

77 Hydrocephalus also occurs in some mutants.

78 In Wistar polycystic kidney rats with hydrocephalus, alteration of migratory trajectory is det

79 port that loss of pericytic laminin leads to hydrocephalus and BBB breakdown in a small percentage (1

80 ia and tissue infarction, ultimately causing hydrocephalus and death of mutant animals.

81 dentifying molecular mechanisms for neonatal hydrocephalus and developing noninvasive treatment modal

82 tvrm360, displaying subcortical heterotopia, hydrocephalus and disorganization of retinal architectur

83 ng brain enlargement, cortical malformation, hydrocephalus and epilepsy, with phenotypic severity dep

84 f recessive mutations in familial congenital hydrocephalus and expands the locus heterogeneity of thi

85 ontributing to this Rnd3-deficiency-mediated hydrocephalus and found that Rnd3 is a regulator of Notc

86 The mice developed hydrocephalus and grossly dilated lateral ventricles, wi

87 and therapeutic options for various forms of hydrocephalus and ideopathic intracranial hypertension.

88 and therapeutic options for various forms of hydrocephalus and idiopathic intracranial hypertension.S

89 ons associated with chronic airway diseases, hydrocephalus and infertility.

90 y ciliary dyskinesia phenotypes that include hydrocephalus and laterality malformations.

91 In addition, cdc42 knockdown led to hydrocephalus and loss of photoreceptor cilia.

92 tions in the human L1CAM gene cause X-linked hydrocephalus and MASA (Mental retardation, Aphasia, Shu

93 rated primitive reflexes, epilepsy, acquired hydrocephalus and microcephaly, neurodevelopmental delay

94 nse morpholinos (MOs) led to bent body axes, hydrocephalus and oedema.

95 regimens of neurological complications (eg, hydrocephalus and paradoxical reactions) and of hyponatr

96 3) resulting in a pleiotropic phenotype with hydrocephalus and renal cystic disease in both humans an

97 onal Cep290(gt/gt) mouse that survives shows hydrocephalus and severely cystic kidneys.

98 Surgical management of hydrocephalus and space occupying hemorrhage in the post

99 s with fever and headache that progressed to hydrocephalus and status epilepticus necessitating a med

100 ve control cohort consisted of patients with hydrocephalus and suspected intracranial hypertension (n

101 hort (33% female), 48.9 (83.8) months in the hydrocephalus and suspected intracranial hypertension co

102 tudy the pathophysiology of various forms of hydrocephalus and to design therapeutic strategies in re

103 strong genetic and biochemical evidence that hydrocephalus and white spotting in B3glct mutants resul

104 ted tomographic imaging revealed obstructive hydrocephalus, and a ventriculoperitoneal shunt was plac

105 pkd2 morphant phenotypes, pronephric cysts, hydrocephalus, and body curvature.

106 g morpholinos (MOs) caused pronephric cysts, hydrocephalus, and body curvature.

107 ebrafish resulted in ventral body curvature, hydrocephalus, and cystic kidneys, similar to the effect

108 rain abnormalities (occipital encephalocele, hydrocephalus, and Dandy Walker-type cerebellar anomalie

109 hydin, a protein that, when mutated, causes hydrocephalus, and defined a unique role for hydin in ci

110 actures, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features.

111 BS knockout models: no overt obesity, severe hydrocephalus, and elevated blood pressure (shared by so

112 y, cerebellar hypoplasia, lissencephaly with hydrocephalus, and fetal akinesia deformation sequence (

113 haracterized by glomeruloid vasculopathy and hydrocephalus, and is almost invariably prenatally fatal

114 isease, including aberrant neuron migration, hydrocephalus, and malformations of the anterior and pos

115 n, GM hemorrhage can lead to cerebral palsy, hydrocephalus, and mental retardation.

116 ) was observed, with almost complete agyria, hydrocephalus, and multifocal dystrophic calcifications

117 opathy phenotypes, including axis curvature, hydrocephalus, and pronephric cysts, and disrupts multic

118 udy of conditions such as Alzheimer disease, hydrocephalus, and pseudotumor cerebri.

119 Early complications include rebleeding, hydrocephalus, and seizures.

120 re pronounced phenotypes, including runting, hydrocephalus, and shortened life span, recapitulating t

121 haracterized by sinusitis, male infertility, hydrocephalus, and situs inversus.

122 Patterns of brain parenchyma, hydrocephalus, and so-called middle cerebral artery (MCA

123 es of secondary intraventricular hemorrhage, hydrocephalus, and thromboembolic events were similar be

124 are crucial in the pathogenesis of neonatal hydrocephalus, and we identify new therapeutic targets f

125 herapy, pre-existing endocrine deficiencies, hydrocephalus, and younger age at CRT (< 5 years) were p

126 Ventriculomegaly and hydrocephalus are associated with loss of function of gl

127 ycystin-2, whose ablation is associated with hydrocephalus are colocalized to the ependymal cilia.

128 factors that contribute to the initiation of hydrocephalus are poorly understood.

129 JCV in aseptic meningitis and in idiopathic hydrocephalus are warranted.

130 ntricles and a minority developed idiopathic hydrocephalus as adults, but none of the transgenic mice

131 The classic understanding of hydrocephalus as the result of obstruction to bulk flow

132 new therapies and work toward understanding hydrocephalus as well as idiopathic normal pressure hydr

133 esenting a phenotypic spectrum of congenital hydrocephalus associated with 5 recessive alleles.

134 t of certain types of neonatal and childhood hydrocephalus associated with hemorrhages and infections

135 s opposed to excess glycine, is the cause of hydrocephalus associated with loss of function of the gl

136 ow-up time (OR, 1.10; 95% CI, 1.02 to 1.18), hydrocephalus at diagnosis (OR, 1.77; 95% CI, 1.09 to 2.

137 t in 22.8% (566/2,486) of examinations, with hydrocephalus being most common (11.5% [286/2,486]).

138 ice deficient in STAT1 also developed severe hydrocephalus, blood-brain barrier permeability, and inc

139 also disrupts ependymal cilia, resulting in hydrocephalus by postnatal day 4.

140 Hydrocephalus can also be acquired, mostly from patholog

141 Hydrocephalus caused by mutations in hydin likely involv

142 In hydrocephalus, cerebrospinal fluid (CSF) builds up in th

143 aemorrhagic and other forms of communicating hydrocephalus, cerebrospinal fluid flow and drainage is

144 dynamics have been implicated in congenital hydrocephalus (CH) characterized by the potentially leth

145 Congenital hydrocephalus (CH), characterized by enlarged brain vent

146 a bona fide human disease gene in congenital hydrocephalus (CH).

147 Although tumor site, hydrocephalus, chemotherapy, and cranial radiation thera

148 ic fistula, undescended testes, hypospadias, hydrocephalus, cleft lip or palate, and club foot.

149 c fistulas, undescended testes, hypospadias, hydrocephalus, cleft lip/palate, and clubfoot) was deter

150 the mice died, by 4weeks after birth, severe hydrocephalus could also be seen.

151 splay significant abnormalities that include hydrocephalus, defective myelination and reduced lifespa

152 Defects in the ependymal cilia can result in hydrocephalus, defects in the cilia in the fallopian tub

153 e minority of Cep290(ko/ko) mice that escape hydrocephalus demonstrate progressive kidney pathology.

154 tor of Yap that can cause fetal haemorrhagic hydrocephalus, deregulates Yap in the developing aqueduc

155 the mechanistic role of neuroinflammation in hydrocephalus development is unclear.

156 Inhibition of Notch activity rescued the hydrocephalus disorder in the mutant animals.

157 report a role of Rnd3 in the pathogenesis of hydrocephalus disorder.

158 nt role in cell adhesion, thereby preventing hydrocephalus during mouse brain development.

159 There were no new lesions, worsening hydrocephalus, evidence of increased intracranial pressu

160 ain with diffuse parenchymal calcifications, hydrocephalus ex vacuo, and cerebellar hypoplasia.

161 cytes during early postnatal life results in hydrocephalus formation and additional defects in brain

162 NF-kappaB activation is sufficient to induce hydrocephalus formation and provides a potential mechani

163 requent association of neuroinflammation and hydrocephalus formation during brain development, namely

164 Hydrocephalus formation is a frequent complication of ne

165 In this animal model, hydrocephalus formation is specifically induced during a

166 orts on inflammation could shift our view of hydrocephalus from that of a lifelong neurosurgical diso

167 d genes and inheritance paradigms underlying hydrocephalus, grouping causal loci into functional modu

168 Hydrocephalus has many causes.

169 Studies of syndromic hydrocephalus have led to the identification of >100 cau

170 resulted in complete penetrance of perinatal hydrocephalus (HC) and severe polycystic kidney disease

171 everal ciliated organs, including the brain (hydrocephalus), heart (cardiac edema), and kidney (disor

172 f embryolethality before gestational day 11, hydrocephalus, hermaphroditism, and cystic ovaries.

173 ated gyrification and rescued the associated hydrocephalus, highlighting the interrelated role of reg

174 hm for detecting hemorrhage, mass effect, or hydrocephalus (HMH) at non-contrast material-enhanced he

175 o1 animals maintained on dox did not develop hydrocephalus; however, if taken off doxycycline at wean

176 cts have been identified in animal models of hydrocephalus; however, the relationship between HB-EGF

177 hernia or hydrocele [adult and paediatric]), hydrocephalus, hypospadias, injuries or wounds, neck mas

178 in Wnt1 cell lineages results in congenital hydrocephalus, implicating huntingtin for the first time

179 aseptic meningitis resulting in symptomatic hydrocephalus in a human immunodeficiency virus-seronega

180 ch we propose as a novel cause of congenital hydrocephalus in addition to its suggested role in corti

181 indicating that Ro1 expression also induces hydrocephalus in adults.

182 renatal stages, and postnatal development of hydrocephalus in Gldc-deficient mice.

183 We conclude that hydrocephalus in hydin mutants is caused by a central pa

184 Postinfectious hydrocephalus in infants is a major health problem in su

185 de that decorin prevented the development of hydrocephalus in juvenile rats by blocking transforming

186 ricular size demonstrated the development of hydrocephalus in kaolin-injected rats but also revealed

187 Our results show that hydrocephalus in mice lacking htt in Wnt1 cell lineages

188 , we describe the development of obstructive hydrocephalus in mice that are null for Wrp (Srgap3).

189 There were five cases of unexplained hydrocephalus in not-recently-ruptured aneurysms in the

190 ere the most common etiologies of congenital hydrocephalus in our cohort (19% and 26%, respectively).

191 Its dysregulation leads to hydrocephalus in postnatal mouse brains.

192 ystem, which may account for the presence of hydrocephalus in some patients.

193 Hydrocephalus in the elderly rat, therefore, can induce

194 BBB disruption always goes hand-in-hand with hydrocephalus in these mutants, and neither symptom is o

195 We found that hydrocephalus in this mouse model is caused by aberrant

196 ns in eight, parenchymal lesions in six, and hydrocephalus in two.

197 roles of primary cilia in brain patterning, hydrocephalus incidence, and cleft palate.

198 One-year-old male Sprague-Dawley rats had hydrocephalus induced by cisternal kaolin injection.

199 The human-specific gene hydrocephalus-inducing 2, HYDIN2, was generated by a 364

200 re, we show for the first time that hydin, a hydrocephalus-inducing gene product whose mutation impai

201 ects induced by treatment, such as seizures, hydrocephalus, infarcts, and neuroinjury.

202 g 12 volumes with idiopathic normal pressure hydrocephalus (iNPH) and 30 normal volumes from a public

203 ith patients with idiopathic normal pressure hydrocephalus (iNPH) serving as a contrast group.

204 duals treated for idiopathic normal pressure hydrocephalus (iNPH), 37 patients clinically diagnosed w

205 tia patients have idiopathic normal pressure hydrocephalus (iNPH), an expansion of the cerebrospinal

206 a motile ciliopathy that is characterized by hydrocephalus internus, chronic destructive airway disea

207 Hydrocephalus is a common disorder of cerebral spinal fl

208 Hydrocephalus is a common neurological disorder that lea

209 Congenital hydrocephalus is an important birth defect, the genetics

210 lo-peritoneal shunt failure in children with hydrocephalus is coherent with the valid principles of r

211 nsertion of a ventriculoperitoneal shunt for hydrocephalus is one of the commonest neurosurgical proc

212 Hydrocephalus is one of the most prevalent form of devel

213 cause Mendelian diseases in which congenital hydrocephalus is the main or sole clinical feature, 2 X-

214 Hydrocephalus is the most common developmental disabilit

215 Hydrocephalus is the most common neurosurgical disorder

216 however, the relationship between HB-EGF and hydrocephalus is unclear.

217 lluminated numerous pathways associated with hydrocephalus, it has also highlighted the fact that the

218 However, in persons with West syndrome or hydrocephalus, it might be impossible to unravel whether

219 associated with ciliary dysfunction, such as hydrocephalus, kidney cysts and situs inversus.

220 polycystin 2 knockdown induces kidney cysts, hydrocephalus, left/right asymmetry defects, and strong

221 One parenchymal and two hydrocephalus lesions, however, developed after diagnosi

222 s and NSCs-derived ependymal cells developed hydrocephalus-like characteristics, including enlarged v

223 the organismal level, Rad50(+/46) exhibited hydrocephalus, liver tumorigenesis, and defects in primi

224 r (acquired, preterm birth, West syndrome or hydrocephalus), making differentiation between acquired

225 Homozygous mice have PCD characterized by hydrocephalus, male infertility, and mucus accumulation.

226 e patients and patients with normal pressure hydrocephalus may have a higher risk of developing glauc

227 luated after 7 to 14 days postinfection, and hydrocephalus, micromyelia, and muscular loss were obser

228 Congenital hydrocephalus, most commonly involving aqueduct stenosis

229 he megalencephaly-polymicrogyria-polydactyly-hydrocephalus (MPPH) syndrome.

230 nd megalencephaly-polymicrogyria-polydactyly-hydrocephalus (MPPH) syndromes are sporadic overgrowth d

231 develop severe PCD-associated phenotypes of hydrocephalus, mucociliary clearance defects in the uppe

232 We describe a neonate who presented with hydrocephalus, necrotizing cellulitis, systemic inflamma

233 Idiopathic normal pressure hydrocephalus (NPH) remains both oversuspected on clinic

234 iate patients with suspected normal pressure hydrocephalus (NPH) who respond to CSF drainage from pat

235 valuate CSF hydrodynamics in normal pressure hydrocephalus (NPH), Chiari type I malformations (CMI),

236 unt-responsive patients with normal-pressure hydrocephalus (NPH; mean age, 75 years; age range, 58-87

237 humans is linked to nonsyndromic congenital hydrocephalus (NSCH).

238 zygous mutations manifest slowly progressing hydrocephalus, observed during the postnatal period and

239 wn in zebrafish replicates all WWS features (hydrocephalus, ocular defects, and muscular dystrophy),

240 controlled trial, we included patients with hydrocephalus of any aetiology undergoing insertion of t

241 che history, and initial evaluation revealed hydrocephalus of unclear etiology.

242 Atxn1L(-/-) mice have hydrocephalus, omphalocele, and lung alveolarization def

243 ted anomaly, in 1 case it was accompanied by hydrocephalus only, in the remaining 6 cases RES was an

244 e posterior fossa oedema causing obstructive hydrocephalus or brainstem compression.

245 eletion using Nestin-CreER(T2) did not cause hydrocephalus or prevent the formation of ciliated epend

246 individuals with Bell palsy, normal pressure hydrocephalus, or Tourette syndrome).

247 utation that caused VACTERL association with hydrocephalus, or VACTERL-H.

248 a defects including abnormal body curvature, hydrocephalus, otolith defects and abnormal renal, head

249 th meningeal versus parenchymal lesions, and hydrocephalus (P=0.015).

250 dynamics and role of ciliary dysfunction in hydrocephalus pathogenesis.

251 The Mg isotopic composition of the CSF from hydrocephalus patients ranged between -0.65 and 0.30 per

252 otopic analysis was carried out for CSF from hydrocephalus patients using only 5 muL of sample.

253 bearing functional ties to a reported mouse hydrocephalus phenotype associated with Ccdc85c.

254 and the CSF spaces in both posthaemorrhagic hydrocephalus (PHH) and postinfectious hydrocephalus (PI

255 Posthemorrhagic hydrocephalus (PHH), an expansion of the cerebral ventri

256 hagic hydrocephalus (PHH) and postinfectious hydrocephalus (PIH).

257 f permanent shunt dependency for aresorptive hydrocephalus post-ICH.

258 ed with worse intellectual outcome; however, hydrocephalus requiring CSF diversion and mutism differe

259 mas can cause life-threatening symptoms--eg, hydrocephalus, requiring surgery.

260 rowth, epilepsy, dysplastic gyrification and hydrocephalus (Roy et al., 2015).

261 Four anatomical patterns of hydrocephalus secondary to congenital Toxoplasma gondii

262 traventricular extension of haemorrhage with hydrocephalus, seizures, venous thrombotic events, hyper

263 been shown to be associated with congenital hydrocephalus, severe intellectual disability, aphasia,

264 nvolving Ugandan infants with postinfectious hydrocephalus showed no significant difference between e

265 er DALY), general surgery ($82.32 per DALY), hydrocephalus surgery ($108.74 per DALY), and ophthalmic

266 h large ventricles, causing macrocephaly and hydrocephalus suspicion, and all cases exhibited partial

267 se megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH, OMIM 603387).

268 ospinal fluid (CSF) of children with TBM and hydrocephalus taken on admission and over 3 weeks were a

269 A subset of patients developed hydrocephalus that required cerebrospinal fluid (CSF) di

270 At primary diagnosis, he presented with hydrocephalus that required ventriculoperitoneal shunt p

271 To determine if defects in Hydin cause hydrocephalus through a mechanism involving cilia, we co

272 ng from agenesis of the corpus callosum with hydrocephalus to cystic formations, abnormal hippocampi,

273 stenosis, lumbar disc herniation, childhood hydrocephalus, trauma mortality, and the occurrence of s

274 ale with Loeys-Dietz syndrome and congenital hydrocephalus treated with a ventriculoperitoneal shunt,

275 shunt infection is a common complication of hydrocephalus treatment, creating grave neurological con

276 points; altered mental status, three points; hydrocephalus, two points; infratentorial PICH, two poin

277 ded secondary intraventricular hemorrhage or hydrocephalus upon follow-up CT, thromboembolic events b

278 or children that have received treatment for hydrocephalus varies.

279 or association with intracranial evidence of hydrocephalus, vasogenic edema, central venous thrombosi

280 fetal ultrasound indicates severe symptoms (hydrocephalus, ventricular dilation), treatment is conti

281 DR (0.85 vs. 0.63; P<0.001), posthemorrhagic hydrocephalus was associated with shallower cup (331 vs.

282 West syndrome and/or hydrocephalus was identified in 21 patients (7%), and in

283 Hydrocephalus was induced by a single basal cistern inje

284 6q22.2 and implicated in autosomal recessive hydrocephalus was inserted into the 1q21.1 region during

285 (6%) both an acquired cause and West and/or hydrocephalus was present.

286 Although the etiology of hydrocephalus was studied before, the effects of ethanol

287 ary cilia without the confounding effects of hydrocephalus, we stereotaxically targeted elimination o

288 MCA pseudofeeders and hydrocephalus were risk factors for both severe cardiac

289 PHP-RC phenotypes, including renal cysts and hydrocephalus, which is rescued by a Wnt inhibitor and b

290 y thus be one determining factor for chronic hydrocephalus, which leads to atrophy of subcortical str

291 In addition, we observed highly penetrant hydrocephalus, white spotting and soft tissue syndactyly

292 enetic deletion developed severe obstructive hydrocephalus with enlargement of the lateral and third

293 Finally, the hydrocephalus with hop gait (hyh) mouse, which harbors a

294 The mouse alpha-SNAP mutant hyh (hydrocephalus with hop gait) shows enhanced binding and

295 Here we show that alpha-SNAP hypomorph, hydrocephalus with hopping gait, Napa(hyh/hyh) mice harb

296 Hydrocephalus with shunt placement was associated with i

297 proximately 50% develop lethal communicating hydrocephalus with striking dilation of the lateral, thi

298 the genetic etiology of familial congenital hydrocephalus with the assumption that these cases repre

299 artery anomalies, pulmonary valve stenosis, hydrocephalus) with trends in malformations that are unl

300 ent knockdown of hrg-1 in zebrafish leads to hydrocephalus, yolk tube malformations and, most strikin