Herediter Basınca Duyarlı Nöropati Olgusu
Öz
Anahtar Kelimeler
Kaynakça
- De Jong JGY. Over families met hereditaire dispositie tat het optreden van neurritiden gecorreleered met migraine. Psychiatr Neurol B (Amst) 1947;40:6.
- Chance PF. İnherited demyelinating neuropathy. Charcot-marie- tooth disease and related disorders. İn Roserberg RN, prusiner SB, Di Mauro S, et al. eds. The molecular and genetic basis of neurological disease. Oxford; Butter worth-Heinemann, 1996;807-16.
- Kumar N, Muley S, Pakim AS et al. Phenotypic variability in hereditary neuropathy with liability to pressure palsy (HNPP). (abstract) Neurology 1998:50;A 73.
- Mouon P, Tardieu BS, Gouider R, et al. Spectrum of clinical and electrophysiological features in HNPP patients with the 17p 11.2 deletion Neurology 1999;52;1440-6.
- Chance P, Alderson MK, Lepping KA, et al. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 1993;72;143-51.
- Nelis E, Van Broeckhoven C, De Longhe P et al. Estimation of the mutation frequencies in charcot-marie-tooth disease type 1 and hereditary neuropathy with liability to pressure palsies. A european collaborative study. Eur J Hum Genet 1996;4;25-33.
- E.P Bosch, H.Mitsumoto. Disorders of peripheral nerves. Herediter Neuropathy with Liability to Pressure Palsies. Neurology in Clinical Practice Volume 2.1996;1902.
- Parman Y.G. Ailevi Basınca Duyarlılık Nöropatisi. Herediter Nöropatiler. Türkiye KlinikleriNöroloji Dergisi Nöromuskuler Hastalıklar Özel Sayısı. 2005;1;22: 36.
Ayrıntılar
Birincil Dil
Türkçe
Konular
-
Bölüm
-
Yazarlar
Semra Bilge
Bu kişi benim
Ülgen Kökeş
Bu kişi benim
Meral Çınar
Bu kişi benim
Tuğba Eyiipgil
Bu kişi benim
Yayımlanma Tarihi
1 Nisan 2009
Gönderilme Tarihi
20 Şubat 2015
Kabul Tarihi
-
Yayımlandığı Sayı
Yıl 2009 Cilt: 16 Sayı: 2