Zhonghua yi xue za zhi
-
Zhonghua yi xue za zhi · May 2016
[3.0 T MR diffusion tentor imaging in the differential diagnosis of breast mass lesions].
To investigate the differential diagnostic value of DTI parameters in breast mass lesions by comparing apparent diffusion coefficient (ADC), fractional aniotropy (FA) and maximum eigenvalue (λ1)of normal glandular tissue, benign lesions and malignant lesions. ⋯ ADC and λ1 is helpful to differentiate malignant from benign in mass lesions.
-
Zhonghua yi xue za zhi · May 2016
[Anterior retropharyngeal debridement combined with posterior atlantoaxial fusion for atlantoaxial Tuberculosis].
To evaluate the clinical efficacy of anterior debridement combined with posterior atlantoaxial fusion for atlantoaxial Tuberculosis. ⋯ The treatment of anterior retropharyngeal debridement combine with atlantoaxial fusion, and local anti-tuberculosis drug using intraoperative, not only could obtain reliable clinical efficacy, completly removal of lesions, but also obtain strong stability, which plays an important role in the treatment of atlantoaxial Tuberculosis.
-
Zhonghua yi xue za zhi · May 2016
[Factors influencing glucose metabolism in young obese subjects with obstructive sleep apnea hypopnea syndrome].
To explore the factors influencing glucose metabolism in young obese subjects with obstructive sleep apnea hypopnea syndrome (OSAHS). ⋯ OSAHS worsens glucose metabolism and compensatory pancreatic β-cell function in young obese subjects, which could probably be attributed to sleep apnea related oxygen desaturation during sleep.
-
Zhonghua yi xue za zhi · Apr 2016
[Mutation screening of 433 families with Duchenne/Becker muscular dystrophy].
Mutation analysis of unrelated families with Duchenne/Becker muscular dystrophy (DMD/BMD) was performed to investigate the characteristic of DMD gene mutation, especially the distribution pattern of point mutation of DMD gene in Chinese population. ⋯ Inexpensive and efficient genetic/prenatal diagnosis of DMD/BMD may be plausible by MLPA analysis, NGS, and Sanger sequencing. Most of the mutations identified in this study led to a predictable premature stop codon or splicing defects, resulting in defective function of dystrophin.