Literature DB >> 6696655

Familial occurrence of idiopathic normal-pressure hydrocephalus.

R K Portenoy, A Berger, E Gross.   

Abstract

Shunt-responsive normal-pressure hydrocephalus developed in a 67-year-old man and in his 74-year-old sister. To our knowledge, a familial association in this disorder has not been reported previously.

Entities:  

Mesh：

Year:  1984        PMID： 6696655     DOI： 10.1001/archneur.1984.04050150117029

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


  8 in total

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

Authors:  Oliver K Appelbe; Bryan Bollman; Ali Attarwala; Lindy A Triebes; Hilmarie Muniz-Talavera; Daniel J Curry; Jennifer V Schmidt
Journal:  Dev Biol       Date:  2013-07-29       Impact factor: 3.582

Review 2.  Age-dependent changes of cerebral ventricular size. Part I: Review of intracranial fluid collections.

Authors:  E R Cardoso; M R Del Bigio; G Schroeder
Journal:  Acta Neurochir (Wien)       Date:  1989       Impact factor: 2.216

Review 3.  Genetics of human hydrocephalus.

Authors:  Jun Zhang; Michael A Williams; Daniele Rigamonti
Journal:  J Neurol       Date:  2006-06-13       Impact factor: 4.849

4.  A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.

Authors:  Hidenori Sato; Yoshimi Takahashi; Luna Kimihira; Chifumi Iseki; Hajime Kato; Yuya Suzuki; Ryosuke Igari; Hiroyasu Sato; Shingo Koyama; Shigeki Arawaka; Toru Kawanami; Masakazu Miyajima; Naoyuki Samejima; Shinya Sato; Masahiro Kameda; Shinya Yamada; Daisuke Kita; Mitsunobu Kaijima; Isao Date; Yukihiko Sonoda; Takamasa Kayama; Nobumasa Kuwana; Hajime Arai; Takeo Kato
Journal:  PLoS One       Date:  2016-11-18       Impact factor: 3.240

5.  Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPH.

Authors:  Ville E Korhonen; Seppo Helisalmi; Aleksi Jokinen; Ilari Jokinen; Juha-Matti Lehtola; Minna Oinas; Kimmo Lönnrot; Cecilia Avellan; Anna Kotkansalo; Janek Frantzen; Jaakko Rinne; Antti Ronkainen; Mikko Kauppinen; Antti Junkkari; Mikko Hiltunen; Hilkka Soininen; Mitja Kurki; Juha E Jääskeläinen; Anne M Koivisto; Hidenori Sato; Takeo Kato; Anne M Remes; Per Kristian Eide; Ville Leinonen
Journal:  Neurol Genet       Date:  2018-12-03

6.  A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report.

Authors:  Maria Santa Rocca; Gioia Piatti; Angela Michelucci; Raffaella Guazzo; Veronica Bertini; Cinzia Vinanzi; Maria Adelaide Caligo; Angelo Valetto; Carlo Foresta
Journal:  BMC Med Genet       Date:  2020-11-10       Impact factor: 2.103

7.  Diabetes is associated with familial idiopathic normal pressure hydrocephalus: a case-control comparison with family members.

Authors:  Joel Räsänen; Joel Huovinen; Ville E Korhonen; Antti Junkkari; Sami Kastinen; Simo Komulainen; Minna Oinas; Cecilia Avellan; Janek Frantzen; Jaakko Rinne; Antti Ronkainen; Mikko Kauppinen; Kimmo Lönnrot; Markus Perola; Anne M Koivisto; Anne M Remes; Hilkka Soininen; Mikko Hiltunen; Seppo Helisalmi; Mitja I Kurki; Juha E Jääskeläinen; Ville Leinonen
Journal:  Fluids Barriers CNS       Date:  2020-09-15

Review 8.  Molecular Mechanisms and Risk Factors for the Pathogenesis of Hydrocephalus.

Authors:  Jingwen Li; Xinjie Zhang; Jian Guo; Chen Yu; Jun Yang
Journal:  Front Genet       Date:  2022-01-03       Impact factor: 4.599
  8 in total

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