Hirayama Hastalığı (Monomelik Amyotrofi)
Öz
Anahtar Kelimeler
References
- Fetoni V, Briem E, Carrara F, Mora M, Zeviani M. Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNA gene. Neuromusculer Disorders 2004; 14: 723-726.
- Tunçbay T, Tunçbay E. Nöromüsküler Hastalıklar. İzmir: Ege Üniversitesi Basım Evi, 2000: 136-140. 3. Hirayama K,Toyokura Y, Tsubaki T. Juvenile musculer atrophy unilateral upper extremity- a new clinical entity. Psychiatr Neurol Jpn 1959; 61: 2190-2197.
- Gourie Devi M, Nalini A. Long term follow-up of 44 patients with brachial monomelic amyotrophy. Acta Neurol Scand 2003; 107: 215-220.
- Nalini A, Lokesh E, Ratnavalli E. Familial monomelic amyotrophy: a case report from India. Journal of Neurological Sciences 2004; 220: 95-98.
- Massa R, Scalise A, Iani C, Palmieri MG, Bernardi G. Delayed focal involvement of upper motor neurons in the Madras pattern of motor neuron disease. Electroencephalography and clinical Neurophysiology 1998; 109: 523-526.
- Hamano T, Mutoh T, Hirayama M, Ito K, Kimura M, and et al. MRI findings of bening monomelic amyotrophy of lower limb. J neurological Sciences 1999; 165: 184-187.
- Münchau A, Rosenkranz T. Benign Monomelic Amyotrophy of the lower limb- case report and brief review of the Literature. Eur Neurol 2000; 43: 238-240.
- Gourei Devi M, Nalini A. Sympathetic skin response in monomelic amyotrophy. Acta Neurol Scand 2001; 104: 162-166.
Details
Primary Language
Turkish
Subjects
-
Journal Section
-
Authors
Tahir Kurtuluş Yoldaş
This is me
Yıldız Çoruh
This is me
Hava Dönmez Keklikoğlua
This is me
Hayriye Gül Polat
This is me
Bülent Güven
This is me
Publication Date
August 1, 2008
Submission Date
July 29, 2014
Acceptance Date
-
Published in Issue
Year 2008 Volume: 13 Number: 4