Detalhe da pesquisa
1.
Lipid storage myopathy in Kearns-Sayre syndrome.
Neurology
; 35(11): 1582-6, 1985 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-2932655
2.
Unusual course of nemaline myopathy.
Neuromuscul Disord
; 2(5-6): 413-8, 1992.
Artigo
em Inglês
| MEDLINE | ID: mdl-1300189
3.
Follow-up study of myasthenic children after thymectomy.
J Neurol
; 217(2): 133-8, 1977 Dec 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-75259
4.
A dominant form of neuronal ceroid-lipofuscinosis. An ultrastructural study of sural nerve and peripheral lymphocytes.
J Neurol
; 226(3): 205-12, 1981.
Artigo
em Inglês
| MEDLINE | ID: mdl-6172569
5.
Is central core disease with structural core a fetal defect?
J Neurol
; 231(4): 212-9, 1984.
Artigo
em Inglês
| MEDLINE | ID: mdl-6512576
6.
Interrelationship between gene, its product and phenotype in Duchenne and Becker muscular dystrophy.
Acta Neurobiol Exp (Wars)
; 53(1): 297-303, 1993.
Artigo
em Inglês
| MEDLINE | ID: mdl-8317263
7.
Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
Electromyogr Clin Neurophysiol
; 38(2): 95-101, 1998 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-9553747
8.
[Giant-axon polyneuropathy (case report)]. / Polineuropatia z olbrzymimi aksonami (opis przypadku).
Neurol Neurochir Pol
; 17(3): 367-71, 1983.
Artigo
em Polonês
| MEDLINE | ID: mdl-6316185
9.
[Distal myopathy]. / Miopatia odsiebna.
Neurol Neurochir Pol
; 19(6): 512-5, 1985.
Artigo
em Polonês
| MEDLINE | ID: mdl-3835492
10.
[Epileptic seizures in children with myasthenia gravis]. / Napady padaczkowe u dzieci z miastenia.
Neurol Neurochir Pol
; 25(3): 326-31, 1991.
Artigo
em Polonês
| MEDLINE | ID: mdl-1961379
11.
[Satellite potentials in electromyograms in patients with Duchenne progressive muscular atrophy]. / Wystepowanie potencjalów satelitarnych w elektromiogramach chorych z dystrofia miesniowa postepujaca typu Duchenne'a.
Neurol Neurochir Pol
; 27(2): 163-73, 1993.
Artigo
em Polonês
| MEDLINE | ID: mdl-8327035
12.
[Hereditary sensorimotor neuropathy in electrophysiological studies]. / Dziedziczna czuciowo-ruchowa neuropatia w obrazie elektrofizjologicznym.
Neurol Neurochir Pol
; 32(2): 295-308, 1998.
Artigo
em Polonês
| MEDLINE | ID: mdl-9760549
13.
[Hereditary motor and sensory neuropathy. I. Principles of classification and clinical picture]. / Ruchowo-czuciowa neuropatia dziedziczna. I. Podstawy klasyfikacji, obraz kliniczny.
Neurol Neurochir Pol
; 20(1): 24-8, 1986.
Artigo
em Polonês
| MEDLINE | ID: mdl-3012388
14.
[Idiopathic juvenile osteoporosis with the symptoms suggesting nervous system damage]. / Mlodziencza osteoporoza idiopatyczna z objawami sugerujacymi uszkodzenie ukladu nerwowego.
Neurol Neurochir Pol
; 23(2): 118-20, 1989.
Artigo
em Polonês
| MEDLINE | ID: mdl-2615884
15.
[Motor-sensory hereditary neuropathy. III. Histological changes]. / Ruchowo-czuciowa neuropatia dziedziczna. III. Zmiany histologiczne.
Neurol Neurochir Pol
; 20(3): 201-6, 1986.
Artigo
em Polonês
| MEDLINE | ID: mdl-3466053
16.
[Sensorimotor hereditary neuropathy. IV. Clinical, electrophysiologic and histologic correlations. Summary of studies]. / Ruchowo-czuciowa neuropatia dziedziczna. IV. Korelacje kliniczno-elektrofizjologiczno-histologiczne. podsumowanie badan.
Neurol Neurochir Pol
; 20(4): 303-7, 1986.
Artigo
em Polonês
| MEDLINE | ID: mdl-3470625
17.
[Separation of dystrophinopathies from the group previously classified as limb-girdle muscular dystrophies]. / Wyodrebnienie dystrofinopatii z grupy dystrofii rozpoznawanych jako obreczowo-konczynowe.
Neurol Neurochir Pol
; 28(1 Suppl 1): 115-24, 1994.
Artigo
em Polonês
| MEDLINE | ID: mdl-8065538
18.
[Clinical-genetic studies of infantile and juvenile proximal spinal muscular atrophy]. / Badania kliniczno-genetyczne dzieciecego i mlodzienczego ksobnego rdzeniowego zaniku miesni.
Neurol Neurochir Pol
; 28(1 Suppl 1): 91-102, 1994.
Artigo
em Polonês
| MEDLINE | ID: mdl-8065545
19.
[Hereditary motor-sensory neuropathy. II. Electrophysiological studies]. / Ruchowo-czuciowa neuropatia dziedziczna. Czesc II. Zmiany elektrofizjologiczne.
Neurol Neurochir Pol
; 20(2): 95-100, 1986.
Artigo
em Polonês
| MEDLINE | ID: mdl-3464849
20.
[Detection of dystrophin gene mutation carrier state]. / Wykrywanie nosicielstwa mutacji genu dystrofiny.
Neurol Neurochir Pol
; 30(2): 193-9; quiz 200, 1996.
Artigo
em Polonês
| MEDLINE | ID: mdl-8756246