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1.
Chinese Acupuncture & Moxibustion ; (12): 81-83, 2009.
Artículo en Chino | WPRIM | ID: wpr-257127

RESUMEN

In Clinical Practice Guideline of Evidence-based Acupuncture and Moxibustion, following principles and methods of evidence-based medicine, in combination with characteristics of acupuncture and moxibustion science, primary literature quality assessment criteria and corresponding scale were stipulated and were repeatedly seeked advice from experts and proved, finally, forming the assessment criteria: (1) Evaluation criteria of literature quality for RCT; (2) Evaluation criteria of literature quality for non-randomly controlled trials; (3) Evaluation criteria of literature quality for cases-study trials.


Asunto(s)
Humanos , Terapia por Acupuntura , Bibliometría , Estudios de Casos y Controles , Ensayos Clínicos como Asunto , Estudios de Evaluación como Asunto , Medicina Basada en la Evidencia , Moxibustión , Guías de Práctica Clínica como Asunto
2.
Chinese Acupuncture & Moxibustion ; (12): 147-150, 2008.
Artículo en Chino | WPRIM | ID: wpr-292889

RESUMEN

<p><b>OBJECTIVE</b>To assess the quality of literature of clinical studies on acupuncture in treatment of herpes zoster.</p><p><b>METHODS</b>The literatures between 1994-2006 were searched by means of electronic retrieval. Type and methodology, general condition, diagnosis of diseases and enrolled and excluded criteria, assessment of sample content, treatment condition, criteria for assessment of therapeutic effects, following-up, etc. in clinical studies are evaluated according to principles and methods of clinical epidemiology and evidence-based medicine.</p><p><b>RESULTS</b>Of the 399 literatures enrolled, only 8 were authentic randomized controlled trials (RCTs), 20 quasi-randomized controlled trials, 66 non-randomized concurrent controlled trials and 277 narrative studies, 70 had clear diagnostic criteria, 16 mentioned enrolled or excluded criteria, 287 had clear criteria for therapeutic effects, 107 reported follow-up, 2 had the description of health economical index, 9 reported adverse reaction.</p><p><b>CONCLUSION</b>At present, correct randomization, concealment, blinding and placebo-control, and the RCTs with generally accepted criteria for assessment of diagnosis and therapeutic effects, safety evaluation and rational design of follow-up are needed. It is indicated by preliminary study of the literatures that blood-letting puncture and cupping at Ashi points are main methods for treatment of herpes zoster.</p>


Asunto(s)
Humanos , Terapia por Acupuntura , Bibliometría , Estudios de Seguimiento , Herpes Zóster , Diagnóstico , Terapéutica , Ensayos Clínicos Controlados Aleatorios como Asunto
3.
Chinese Medical Journal ; (24): 1638-1642, 2008.
Artículo en Inglés | WPRIM | ID: wpr-293944

RESUMEN

<p><b>BACKGROUND</b>Pelizaeus-Merzbacher disease (PMD) is a rare X-linked recessive disorder with symptoms including nystagmus, impaired motor development, ataxia, and progressive spasticity. The proteolipid protein 1 (PLP1) gene is the only pathogenic gene of PMD. Duplication of the PLP1 gene is the most frequent gene defect, accounting for 50%-70% of PMD cases, whereas point mutations in the coding sequence or the splice sites account for 10%-25% of PMD cases. This study aimed to identify PLP1 mutations in nine unrelated Chinese patients (P1-9) with PMD, and 14 subjects from the family of patient 2 were also described.</p><p><b>METHODS</b>Genomic DNA was extracted from peripheral blood samples. Gene dosage was determined using the multiplex ligation-dependent probe amplification (MLPA). All 7 exons and exon-intron boundaries of the PLP1 gene were amplified and analyzed using direct DNA sequencing.</p><p><b>RESULTS</b>Of these nine patients, there were four transitional, four classical, and one connatal PMD according to their clinical and radiological presentations. PLP1 duplications were identified in patients 1-7 with PMD. Their mothers were PLP1 duplications carriers as well. Both duplication carriers and normal genotypes of PLP1 were identified in the family members of patient 2. A c.517C > T (p. P173S) hemizygous missense mutation in exon 4 was found in patient 8 with PMD, and his mother was shown to be a heterozygote of this mutation.</p><p><b>CONCLUSIONS</b>We identified seven genomic duplications and one missense mutation (p. P173S) of the PLP1 gene in eight Chinese patients with PMD. This is the report about PLP1 mutations in PMD patients from the mainland of China.</p>


Asunto(s)
Preescolar , Femenino , Humanos , Lactante , Masculino , Duplicación de Gen , Mutación , Proteína Proteolipídica de la Mielina , Genética , Técnicas de Amplificación de Ácido Nucleico , Enfermedad de Pelizaeus-Merzbacher , Genética , Análisis de Secuencia de ADN
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