Detalhe da pesquisa
1.
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24.
Nat Genet
; 14(2): 214-7, 1996 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-8841199
2.
Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries.
Neuromuscul Disord
; 10(8): 584-91, 2000 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-11053686
3.
The trigemino-cervical reflex in normal subjects.
Funct Neurol
; 16(2): 129-34, 2001.
Artigo
Inglês
| MEDLINE | ID: mdl-11495418
4.
Distal muscular dystrophy. Case reports.
Electromyogr Clin Neurophysiol
; 37(4): 201-5, 1997.
Artigo
Inglês
| MEDLINE | ID: mdl-9208214
5.
Differential diagnosis of scapuloperoneal syndrome.
Electromyogr Clin Neurophysiol
; 37(2): 73-8, 1997 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-9098670
6.
Differential diagnosis of limb girdle syndromes.
Electromyogr Clin Neurophysiol
; 36(8): 469-75, 1996 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-8985674
7.
Differential diagnosis of amyotrophic lateral sclerosis and similar syndromes.
Electromyogr Clin Neurophysiol
; 40(3): 145-9, 2000.
Artigo
Inglês
| MEDLINE | ID: mdl-10812537
8.
Differential diagnosis of chronic idiopathic polymyositis and neuromyositis.
Electromyogr Clin Neurophysiol
; 38(3): 183-7, 1998.
Artigo
Inglês
| MEDLINE | ID: mdl-9637945
9.
Differential diagnosis of myasthenic syndromes.
Electromyogr Clin Neurophysiol
; 41(1): 17-21, 2001.
Artigo
Inglês
| MEDLINE | ID: mdl-11234561
10.
Schwartz-Jampel syndrome: clinical, electromyographic and genetic studies.
Electromyogr Clin Neurophysiol
; 36(2): 91-7, 1996 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-8925786
11.
Schwartz-Jampel syndrome: clinical, electromyographic and genetic studies.
Electromyogr Clin Neurophysiol
; 36(3): 151-5, 1996.
Artigo
Inglês
| MEDLINE | ID: mdl-8737936
12.
Conduction block--the diagnostic value in the early stage of Guillain-Barre syndrome.
Electromyogr Clin Neurophysiol
; 44(6): 361-4, 2004 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-15473348
13.
Peripheral late waves in patients with hereditary motor sensory neuropathy.
Electromyogr Clin Neurophysiol
; 39(6): 345-8, 1999 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-10499204
14.
Comparative analysis between Duchenne and Becker types muscular dystrophy.
Electromyogr Clin Neurophysiol
; 39(5): 315-8, 1999.
Artigo
Inglês
| MEDLINE | ID: mdl-10422002
15.
[Features of the type of inheritance of myotonic dystrophy]. / Osobennosti tipa nasledovaniia miotonicheskoi distrofii.
Genetika
; 33(7): 1012-5, 1997 Jul.
Artigo
Russo
| MEDLINE | ID: mdl-9378280
16.
A method of n. hypoglossus conductivity measurement.
Folia Med (Plovdiv)
; 24(4): 40-2, 1982.
Artigo
Inglês
| MEDLINE | ID: mdl-6821059
17.
Spontaneous EMG volleys of "bizarre" high- and low-frequency potentials in neuromuscular disorders.
Folia Med (Plovdiv)
; 28(1): 43-7, 1986.
Artigo
Inglês
| MEDLINE | ID: mdl-3104173
18.
The diagnostic significance of the blink reflex in diseases of the central and peripheral nervous systems.
Folia Med (Plovdiv)
; 29(1): 36-40, 1987.
Artigo
Inglês
| MEDLINE | ID: mdl-2838404
19.
The electrophysiological profile of hereditary motor and sensory neuropathy-Lom.
J Neurol Neurosurg Psychiatry
; 76(6): 875-8, 2005 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-15897517
20.
A-waves in patients with novel hereditary motor and sensory neuropathy Lom.
Acta Physiol Pharmacol Bulg
; 26(1-2): 55-8, 2001.
Artigo
Inglês
| MEDLINE | ID: mdl-11693402