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1.
Arch Fr Pediatr ; 46(9): 675-7, 1989 Nov.
Artículo en Francés | MEDLINE | ID: mdl-2604529

RESUMEN

A case of Zollinger-Ellison due to hyperplasia of antral gastrin cells in a 11 year-old child is reported. Only 49 cases of this syndrome in children have been published. The diagnosis (gastrin stimulation test, immunohistochemical detection of endocrine cells and therapeutic strategy are outlined).


Asunto(s)
Gastrinas/sangre , Síndrome de Zollinger-Ellison/diagnóstico , Niño , Femenino , Humanos , Hiperplasia/etiología , Antro Pilórico/patología , Síndrome de Zollinger-Ellison/etiología , Síndrome de Zollinger-Ellison/terapia
3.
Sem Hop ; 58(34): 1944-6, 1982 Sep 23.
Artículo en Francés | MEDLINE | ID: mdl-6293077

RESUMEN

The effectiveness of tiapride on psychic disorders was studied in 30 chronic alcoholics by assessing four parameters: sleep disturbances, mood disorders, conduct disturbances, and tremor. In a daily dosage of 600 to 900 mg tiapride proved particularly effective on insomnia, anxiety, passivity and tremor, without adverse side-effects. This drug seems useful for controlling psychic disorders in alcoholics and for motivating acceptance of a detoxification program.


Asunto(s)
Alcoholismo/tratamiento farmacológico , Benzamidas/uso terapéutico , Clorhidrato de Tiapamilo/uso terapéutico , Adulto , Anciano , Alcoholismo/complicaciones , Femenino , Humanos , Masculino , Persona de Mediana Edad , Trastornos Neuróticos/tratamiento farmacológico , Trastornos Neuróticos/etiología , Trastornos del Sueño-Vigilia/tratamiento farmacológico , Trastornos del Sueño-Vigilia/etiología , Trastorno de la Conducta Social/tratamiento farmacológico , Trastorno de la Conducta Social/etiología , Temblor/tratamiento farmacológico , Temblor/etiología
5.
Nouv Presse Med ; 9(38): 2811-3, 1980 Oct 18.
Artículo en Francés | MEDLINE | ID: mdl-6160453

RESUMEN

Four members of the same family (2 male and 2 female) with normal thyroid function were found to have decreased total T3 and total T4, elevated response to the T3 test and low free thyroxin index. Such biological changes result from a deficiency in carrier protein and should be distinguished from nearly similar abnormalities observed in low T3 syndrome and hypothyroidism. Whilst gonosomal transmission through the X chromosome of thyroxin-binding protein deficiency seems well established, our findings show that another mechanism, i.e. dominant autosomal heredity, is practically certain.


Asunto(s)
alfa-Globulinas/deficiencia , Proteínas de Unión a Tiroxina/deficiencia , alfa-Globulinas/genética , Errores Diagnósticos , Femenino , Genes Dominantes , Humanos , Hipotiroidismo/diagnóstico , Masculino , Persona de Mediana Edad , Factores Sexuales , Proteínas de Unión a Tiroxina/genética , Triyodotironina/análisis
9.
Nouv Presse Med ; 7(36): 3233-6, 1978 Oct 21.
Artículo en Francés | MEDLINE | ID: mdl-83600

RESUMEN

The authors report the case of a 21 years old man, with sex-linked agammaglobulinemia, who presents a presumed viral hepatitis, followed two years. The evolution, does yet fear a progressive cirrhosis. About this report and analysis of literature, frequency, evolution and pathophysiologic hypothesis, particularly the lymphocyte T role, are also discussed as the problem of hepatitis prevention of these subjects, who receive gammaglobulin injections.


Asunto(s)
Agammaglobulinemia/complicaciones , Hepatitis Viral Humana/complicaciones , Cromosomas Sexuales , Adulto , Agammaglobulinemia/genética , Agammaglobulinemia/inmunología , Linfocitos B/inmunología , Ligamiento Genético , Hepatitis Viral Humana/prevención & control , Humanos , Masculino , Linfocitos T/inmunología , gammaglobulinas/uso terapéutico
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