Joubert Sendromunun Nöroradyolojik Açıdan Değerlendirilmesi: Olgu Sunumu
Abstract
Keywords
References
- Blair IP, Gibson RR, Bennett CL, Chance PF. Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1. Am J Med Genet 2002; 107: 190-196.
- Joubert M, Eisenring JJ, Robb JP, Andermann F. Familial agenesis of cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia and retardation. Neurology 1969; 19: 813-825.
- Saraiva JM, Baraitser M. Joubert syndrome : a review. Am J Med Genet 1992; 43:726-731.
- Chance PF, Cavalier L, Satran D, et al. Clinical nosologic and genetic aspects of Joubert and related syndromes. J Child Neurol 1999; 14:660-666.
- Saar K, Al-Gazali L, Sztriha l, et al. Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity. Am J Hum Genet 1999; 65:1666-1667.
- Saito Y, Ito M, Ozawa Y, et al. Changes of neurotransmitters in the brainstem of patients with respiratory-pattern disorders during childhood. Neuropediatrics 1999; 30:133-140.
- Yachnis AT, Rorke LB. Neuropathology of Joubert syndrome. J Child Neurol 1999; 14:655-659.
- Barreirinho MS, Teixeira J, Moreira NC, et al. Joubert’s syndrome: report of 12 cases. Rev Neurol 2001; 32: 812-817.
Details
Primary Language
Turkish
Subjects
-
Journal Section
-
Authors
Hanefi Yıldırım
This is me
Ayşe Murat
This is me
Mustafa Aydın
This is me
Derya Benzer
This is me
Publication Date
June 1, 2005
Submission Date
July 29, 2014
Acceptance Date
-
Published in Issue
Year 2005 Volume: 10 Number: 3