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1.
Hum Immunol ; 55(1): 59-65, 1997 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9328791

RESUMO

The DRB, DQA, and DQB subregions of the major histocompatibility complex (MHC) were investigated by polymerase chain reaction and sequence-specific oligonucleotide probe hybridization (PCR/SSO) in 103 multiple sclerosis (MS) patients and 101 healthy controls from Turkey. Significant differences were detected between MS and control populations in the frequencies of DRB1*1501 [29 vs. 14, p = 0.02, odds ratio (OR) = 2.4], DRB1*04 (35 vs. 18, p = 0.01, OR = 2.3), DQB1*0302 (30 vs. 15, p = 0.02, OR = 2.3), DQB1*0602 (27 vs. 10, p = 0.005, OR = 3.2), DQB1*0501 (10 vs. 24, p = 0.01, OR = 0.3), DQA1*0101 (16 vs. 31, p = 0.02, OR = 0.4), and DQA1*0103 (7 vs. 19, p = 0.02, OR = 0.3). These results confirm the proposed positive association of the Dw2 (DRB1*1501 DQA1*0102 DQB1*0602) haplotype with MS in Caucasians in our Turkish population (25 vs. 8, p = 0.003, OR = 3.7). Furthermore, the "putative" haplotype supposed to be more frequent in the MS population of Mediterranean countries, namely DRB1*04 DQA1*03 DQB1*0302, is also associated with MS in Turkey (29 vs. 12, p = 0.006, OR = 2.9). The presence of two different haplotypic associations in MS emphasizes the complexity of the genetic susceptibility to MS in different populations.


Assuntos
Antígenos HLA-DQ/genética , Antígenos HLA-DR/genética , Esclerose Múltipla/imunologia , Adulto , Alelos , Frequência do Gene , Genótipo , Cadeias alfa de HLA-DQ , Cadeias beta de HLA-DQ , Cadeias HLA-DRB1 , Haploidia , Humanos , Esclerose Múltipla/epidemiologia , Esclerose Múltipla/genética , Turquia/epidemiologia
2.
Muscle Nerve ; 17(12): 1416-30, 1994 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-7969242

RESUMO

Electrophysiological findings of 27 males with industrial n-hexane polyneuropathy (HPNP) are presented. The results of needle electromyography and nerve conduction studies were compatible with primarily axonal polyneuropathy with secondary segmental demyelination. Motor conduction velocities were the slowest in distal regions of the nerves. In the proximal nerve segments, which were partly tested by magnetic stimulation of the nerve roots, this slowing was much less pronounced. The reduction in mean motor conduction velocities in the forearm segments of ulnar nerves was more than 30% in comparison to the control group means. This reduction was only 10% in the neck-axilla segments. We think that this finding is a reflection of the distal axonopathy process. Central motor conduction times calculated by transcranial magnetic stimulation and spinal nerve root stimulation were found to be prolonged in HPNP patients, indicating that descending motor pathways are affected in human HPNP.


Assuntos
Sistema Nervoso Central/fisiopatologia , Doenças Desmielinizantes/induzido quimicamente , Hexanos/intoxicação , Condução Nervosa/efeitos dos fármacos , Neurotoxinas/intoxicação , Nervos Periféricos/fisiopatologia , Adolescente , Adulto , Idoso , Sistema Nervoso Central/efeitos dos fármacos , Sistema Nervoso Central/fisiologia , Criança , Doenças Desmielinizantes/fisiopatologia , Eletromiografia , Eletrofisiologia/métodos , Feminino , Humanos , Magnetismo , Masculino , Pessoa de Meia-Idade , Neurônios Motores/efeitos dos fármacos , Neurônios Motores/fisiologia , Nervos Periféricos/efeitos dos fármacos , Nervos Periféricos/fisiologia , Nervo Fibular/efeitos dos fármacos , Nervo Fibular/fisiologia , Nervo Fibular/fisiopatologia , Valores de Referência , Nervo Tibial/efeitos dos fármacos , Nervo Tibial/fisiologia , Nervo Tibial/fisiopatologia , Nervo Ulnar/efeitos dos fármacos , Nervo Ulnar/fisiologia , Nervo Ulnar/fisiopatologia
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