Literature DB >> 15235220

Development of hydrocephalus in a patient with Joubert syndrome.

F Genel, F Atlihan, D Ozdemir, S Targan.   

Abstract

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Mesh：

Year:  2004        PMID： 15235220

Source DB:  PubMed          Journal:  J Postgrad Med        ISSN： 0022-3859            Impact factor:   1.476


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  5 in total

Review 1.  Joubert Syndrome and related disorders.

Authors:  Francesco Brancati; Bruno Dallapiccola; Enza Maria Valente
Journal:  Orphanet J Rare Dis       Date:  2010-07-08       Impact factor: 4.123

Review 2.  Clinical and molecular features of Joubert syndrome and related disorders.

Authors:  Melissa A Parisi
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

3.  Late-onset hydrocephalus in a child with Joubert syndrome: a case report.

Authors:  M K Fehrenbach; U Nestler; J Meixensberger; M K Bernhard; A Merkenschlager; S Weise; M Krause
Journal:  Childs Nerv Syst       Date:  2018-03-05       Impact factor: 1.475

Review 4.  Joubert syndrome: insights into brain development, cilium biology, and complex disease.

Authors:  Dan Doherty
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636

5.  KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.

Authors:  Anna A W M Sanders; Erik de Vrieze; Anas M Alazami; Fatema Alzahrani; Erik B Malarkey; Nasrin Sorusch; Lars Tebbe; Stefanie Kuhns; Teunis J P van Dam; Amal Alhashem; Brahim Tabarki; Qianhao Lu; Nils J Lambacher; Julie E Kennedy; Rachel V Bowie; Lisette Hetterschijt; Sylvia van Beersum; Jeroen van Reeuwijk; Karsten Boldt; Hannie Kremer; Robert A Kesterson; Dorota Monies; Mohamed Abouelhoda; Ronald Roepman; Martijn H Huynen; Marius Ueffing; Rob B Russell; Uwe Wolfrum; Bradley K Yoder; Erwin van Wijk; Fowzan S Alkuraya; Oliver E Blacque
Journal:  Genome Biol       Date:  2015-12-29       Impact factor: 13.583
  5 in total

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