Panventriculomegaly with a wide foramen of Magendie and large cisterna magna

Prevalence of idiopathic normal-pressure hydrocephalus

(2014) D. Jaraj et al.   NEUROLOGY

Disproportionate subarachnoid space hydrocephalus-outcome and perivascular space

(2014) Ichiro Akiguchi et al.   Annals of Clinical and Translational Neurology

Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases

(2013) Homa Adle-Biassette et al.   ACTA NEUROPATHOLOGICA

Disruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalus

(2013) Oliver K. Appelbe et al.   DEVELOPMENTAL BIOLOGY

DYX1C1 is required for axonemal dynein assembly and ciliary motility

(2013) Aarti Tarkar et al.   NATURE GENETICS

The Zebrafish Orthologue of the Dyslexia Candidate Gene DYX1C1 Is Essential for Cilia Growth and Function

(2013) Gayathri Chandrasekar et al.   PLoS One

Ciliary aplasia associated with hydrocephalus: an extremely rare occurrence

(2012) Marco Berlucchi et al.   EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY

Primary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosis

(2012) José Pedro Vieira et al.   JOURNAL OF CHILD NEUROLOGY

Familial aggregation of idiopathic normal pressure hydrocephalus: Novel familial case and a family study of the NPH triad in an iNPH patient cohort

(2012) Alexander McGirr et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia

(2012) Hannah M Mitchison et al.   NATURE GENETICS

Tubulin-dynein system in flagellar and ciliary movement

(2012) Hideo MOHRI et al.   PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES

MNS1 Is Essential for Spermiogenesis and Motile Ciliary Functions in Mice

(2012) Jian Zhou et al.   PLoS Genetics

Loss of SPEF2 Function in Mice Results in Spermatogenesis Defects and Primary Ciliary Dyskinesia1

(2011) Anu Sironen et al.   BIOLOGY OF REPRODUCTION

Familial normal pressure hydrocephalus (NPH) with an autosomal-dominant inheritance: A novel subgroup of NPH

(2011) Yoshimi Takahashi et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

The clinical spectrum of Blake’s pouch cyst: report of six illustrative cases

(2010) Erwin M. J. Cornips et al.   CHILDS NERVOUS SYSTEM

Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse

(2010) G. R. Wilson et al.   HUMAN MOLECULAR GENETICS

Situs Inversus in Dpcd/Poll–/–, Nme7–/–, and Pkd1l1–/– Mice

(2010) P. Vogel et al.   VETERINARY PATHOLOGY

Heritable essential tremor-idiopathic normal pressure hydrocephalus (ETINPH)

(2008) Jun Zhang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genetic disorders associated with macrocephaly

(2008) Charles A. Williams et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mutation of Murine Adenylate Kinase 7 Underlies a Primary Ciliary Dyskinesia Phenotype

(2008) Angeles Fernandez-Gonzalez et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

Visualization of Cerebrospinal Fluid Movement with Spin Labeling at MR Imaging: Preliminary Results in Normal and Pathophysiologic Conditions

(2008) Shinya Yamada et al.   RADIOLOGY