Zobrazeno 1 - 10
of 31
pro vyhledávání: '"P G, Leser"'
Publikováno v:
Revista do Instituto de Medicina Tropical de São Paulo, Vol 33, Iss 3, Pp 213-218 (1991)
A caracterização de infecção primária recente pelo Toxoplasma gondii se apoia principalmente na presença, no soro, de anticorpos específicos IgM. Para fins diagnósticos de toxoplasmose aguda, ou de contágio recente, a possibilidade de outros
Externí odkaz:
https://doaj.org/article/54874cf77c50408fa02a704b82d08eec
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 17:459-463
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 17(6)
Publikováno v:
Revista da Associacao Medica Brasileira (1992). 41(2)
Diagnosis and follow up of paraproteinaemias require identification and typing of paraproteins. Immunoelectrophoresis is the most commonly used method, though a lengthy one and with low sensitivity. Immunofixation is more sensitive, faster and of eas
Publikováno v:
Arquivos de gastroenterologia. 31(4)
Between July 1985 and June 1990, we prospectively investigated 236 children suspected of having malabsorption syndrome. Each patient had a xylose absorption test and small intestinal biopsy. Blood samples were collected to AGA assay. The aim of the s
Publikováno v:
Revista paulista de medicina. 111(3)
In order to evaluate the pattern of ANA testing solicitation, 506 patients with ANA testing requested from July 1st. 1988 to December 31st, 1988, had their charts reviewed. These patients, randomly selected, were regularly attending the outpatient cl
Publikováno v:
Revista paulista de medicina. 111(1)
Immunological evaluation of patients with cartilage-hair hypoplasia. TYPE: Prospective and retrospective studies.Division of Allergy, Clinical Immunology and Rheumatology-Dept. of Pediatrics-"Escola Paulista de Medicina".Two children with cartilage-h
Publikováno v:
Journal of investigational allergologyclinical immunology. 2(6)
Hereditary angioedema (HA) is caused by a quantitative or qualitative deficiency of C1 esterase inhibitor (C1 INH). We present a study of nine patients with HA belonging to two different families. The symptoms started before 10 years of age in most c
Publikováno v:
Revista paulista de medicina. 110(1)
The clinical and laboratory data for 15 patients with common variable immunodeficiency (CVI) (5 females and 10 males aged 3 years and 6 months to 40 years at first examination) were evaluated. The age of onset of infectious signs and symptoms ranged
Publikováno v:
Journal of investigational allergologyclinical immunology. 2(1)
The case of a boy with congenital agammaglobulinemia is reported. In spite of regular immunoglobulin replacement therapy (fresh plasma transfusion from family donors--20 ml/kg/month), he developed chronic meningoencephalitis (ME). Besides characteris