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bilateral
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  “bilateral”译为未确定词的双语例句
    Study of Rb Gene Deletions in Bilateral Retinoblastomas
    双眼视网膜母细胞瘤Rb基因缺失研究
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    THE RECESSION OF BILATERAL EXTERNAL RECTUS FOR LARGE ANGLE EXOTROPIA
    双眼外直肌后徙矫正大角度外斜视
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    Detection of Heterozygous Mutations of Rb1 Gene in Bilateral Retinoblastoma Patients
    Rb1基因在双眼视网膜母细胞瘤病人体细胞中杂合性突变的检测
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    Clinical analysis of bilateral neck dissection in patients with laryngeal cancer
    喉癌患者同时双颈廓清术临床分析
短句来源
    A noval 21 base pair heterozygous deletion of Rb1 gene in a bilateral retinoblastoma patient
    Rb1基因第16内含子内21个碱基缺失1例
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  bilateral
Our approach is rooted in a dominated ergodic theorem of Mart\'{\i}n--Reyes and de la Torre which assigns $T$ a canonical family of bilateral $A_{p}$ weight sequences.
      
After surgical operation, the operation group undertook bilateral common carotid artery permanent ligation, while the other group did not.
      
The mice were pretreated with heat stress followed by ischemia/reperfusion by clipping bilateral cervical common arteries for 7 min.
      
There were 54 patients with unilateral or bilateral hyperplasia and 25 patients with adenoma according to the CT scan.
      
Numerical investigation on the dryout point of annular flow in the upward narrow annuli with bilateral heating
      
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Amblyopia is an unilateral or bilateral decrease of visual acuity caused by form vision deprivation and/or abnormal binocular interaction for which no organic lesion can be detected by physical examination of the eyes. In appropriate cases, it's reversible by therapeutic measures.The author presents 9 cases of amblyopia with various etiologic factors and demonstrates the Tesults of treatment which are cu rrently used.

弱视是形觉视力丧失及/或异常双眼作用引起的单侧或双侧视力减退,眼部检查无器质性病变,在合适的病例,治疗后可以逆转。作者报告9例不同原因的弱视和当前采用的治疗方法所取得的效果。

Post-auricular myogenic responses to clicks in normal subjects were recorded by means of averaging technic in this study. Some physiological characteristics of this evoked potential are as follows, 1) it is mainly a biphase wave of middle latency with high amplitude and the latency of the 1st peak and its intensity being 13.50± 1.43ms and 90 dB, 2) the threshold of myogenic response is about 60 dB higher than the subjective hearing threshold; 3) it is a bilateral response to stimulation of one ear; 4)...

Post-auricular myogenic responses to clicks in normal subjects were recorded by means of averaging technic in this study. Some physiological characteristics of this evoked potential are as follows, 1) it is mainly a biphase wave of middle latency with high amplitude and the latency of the 1st peak and its intensity being 13.50± 1.43ms and 90 dB, 2) the threshold of myogenic response is about 60 dB higher than the subjective hearing threshold; 3) it is a bilateral response to stimulation of one ear; 4) due to obvious individual differences, the response cannot be elicited from nearly 1/5 of the subjects in this series and 5) the response is easily fatigued and can be enhanced with concentration of attention. Authors suggest that this myogenic response be used for preliminary examination of hearing ability and brain stem function, but not for precise evaluation of hearing threshold.

用叠加技术记录33例正常人听觉诱发肌源性反应,属中潜伏期、高振幅、以双相波为主的电位;阈值明显高于听阈;反应为双侧性,有个体差异,易疲劳,欠稳定,注意力可增强反应。

This paper is a report of theclinical and pathological findings of apatient who had neurocutaneous mela-nosis involving both central nervoussystem and skin. The patient, a 33-year-old womanworker, was admitted into SichuanMedical College Hospital on July 20,1981. At birth, many pigmented neviwere found all over her body. Beforeshe was 1 year old, she had severalepisodes of fever and convulsions.After that she was quite healthy withnormal mental development. Aboutone year prior to admission, at theage of thirty-one,...

This paper is a report of theclinical and pathological findings of apatient who had neurocutaneous mela-nosis involving both central nervoussystem and skin. The patient, a 33-year-old womanworker, was admitted into SichuanMedical College Hospital on July 20,1981. At birth, many pigmented neviwere found all over her body. Beforeshe was 1 year old, she had severalepisodes of fever and convulsions.After that she was quite healthy withnormal mental development. Aboutone year prior to admission, at theage of thirty-one, she began to haverecurrent tonic-clonic seizures andoccasionally it developed into epilepticstatus. Ten months before admission,she began to have mental disturbances.In the last two months her mothernoticed that she could not see well. Physical examination revealed thatthe patient was drowsy and disorientedto time and place. Sometimes she hadhallucinations. The significant find-ings on the skin were multiple pig-mented nevi and giant melanotic patcheswith hair. They varied greatly in sizeand shape and were distributed on herscalp, face, neck, trunk and extrem-ities. One of the largest giant neviinvolved the anterior aspect of neckand chest. Funduscopic examinationrevealed bilateral papilledema. Bothupper and lower extremities weremarkedly spastic. The deep tendonreflexes were hyperactive and bilateralextensor plantar response was elicited. Lumbar puncture yielded a clearcerebrospinal fluid, with an increasedpressure of 200-300 mm H_2O, contain-ing erythrocytes 10-640, leukocytes2-10, protein 93-212 mg/dl, chloride580-590 mg/dl and glucose 40 mg/dl.A lot of melanotic cells and pigmentedmarcrophages were found in her CSF.Carotid arteriograms revealed hydro-cephalic signs. The patient continuedto deteriorate rapidly and died sevenmonths after her initial admission. At autopsy, diffuse pigmentedthickening of all meninges was animportant finding, and at the base ofthe brain, melanosis was most marked.Both lateral ventricles were moderatelydilated. Many benign melanocytes andpigmented macrophages were observedin both subarachnoid and leptomen-inges. In the leptomeninges, melano-cytes extended into the perivascularspace of Virchow-Robin. But, nomelancytes infiltration was seen inthe parenchyma. Neurocutaneous melanosis is a veryrare congenital disease. Cutaneouslesions may usually be present atbirth. Symptoms of central nervoussystem disturbance usually appear atan early age but they are rare in adultpatient. If the CNS symptoms occurwhen a patient is reaching adult, theclinical manifestations may includechronic intracranial hypertension,seizures, psychic disorder and signs ofmeningeal irritation. Death is usuallyresulted from communicating hydroce-phalus. In this case, the clinical andpathological features were compatiblewith that of neuro-cutaneotis melanosiswhich was found in three generationsin her family, e.g. her father and 3of 5 of her siblings and her niece. Allof them had pigmented nevi at birth.Therefore, the analysis of familypedigree of this patient is compatiblewith the diagnosis autosomal dominantinheritance disease. But, three of herfamily members who had been examinedfor lymphocytic chromosome werefound to be normal.

本文报告一例罕见的、典型的神经-皮肤黑色素沉着病的临床病理资料,此患者出生时即有全身多处皮肤巨痣及黑痣斑。神经系统症状于生后31年出现;表现为脑膜黑色素细胞广泛浸润脑膜及脑室系统,引起脑脊液循环吸收障碍而发生交通性脑积水所致的颅压增高症状及脑膜炎症状。患者家庭多个成员有皮肤痣发生,从家系图分析,符合常染色体显性遗传方式。

 
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