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Detection of a new mutation (T1140C) in a patient with Hunter syndrome from Guangdong, China
      
This study identified mutations of the idurnate-2-sulfatase (IDS) gene in a patient with Hunter syndrome, and established a basis for the diagnosis of the prenatal gene of Hunter syndrome.
      
The patient is a hemizygote, and his mother is a heterozygote.
      
It is possible that this mutation severely impairs enzymatic activity and is the underlying basis for the pathology seen in this patient with Hunter syndrome.
      
A patient suffered from GERD without esophageal symptoms, which was diagnosed and treated as bronchial asthma during his five emergency admissions.
      
The patient was being treated for as long as two years.
      
One patient's pancreas was unresectable, two patients underwent a total pancreatectomy, 42 patients had a pancreatecoduodenectomy and five patients had distal pancreatectomy.
      
Transient intraocular pressure elevation occurred in one patient (6.25%) of all the 16 eyes and intraocular pressure returned to the normal after a transient treatment with antiglaucoma medication.
      
The plasma aldosterone concentration (PAC) and plasma renin activity (PRA) levels were measured by radioimmunoassay in 902 hypertensive patients from out-patient clinics or hospitals.
      
All the patients had early percutaneous coronary intervention and were followed up for 6-12 months by telephone or in the out-patient department.
      
Mathematical modeling of tuberculosis propagation and patient detection
      
Proposed was a submodel enabling objective estimation of the patient detection system on the basis of individualized database.
      
These estimates corroborated the assumption of a substantial nonuniformity of the Russian regions in terms of tuberculosis morbidity and efficiency of patient detection.
      
For example, the rates of patient detection can differ by the factor of five through six.
      
High level of Con A-induced secretion was also detected in a patient with hereditary deficiency of GP IIb-IIIa.
      
The average tissue carnitine levels in the patient group were found to be lower compared with the control group but the difference was not statistically significant (p >amp;gt; 0.05).
      
Here we describe the self-association kinetics of human monoclonal immunoglobulin light chains λ (GRY) isolated from urine of a patient with multiple myeloma.
      
Depending on the patient, the IgGs exhibit various pH optima of proteolytic activity.
      
Detection of the env MMTV-homologous sequences in mammary carcinoma patient intestine lymphoid tissue
      
Detection of the env MMTV-homologous sequences in mammary carcinoma patient intestine lymphoid tissue
      
 

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