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1.
J Indian Med Assoc ; 1991 Jul; 89(7): 195-7
Artigo em Inglês | IMSEAR | ID: sea-98391

RESUMO

Studies of intestinal absorptive functions in 11 hyperthyroid and 14 hypothyroid patients showed that steatorrhoea was common in hyperthyroid patients and rare in hypothyroid patients. D-xylose malabsorption was present in both the groups of thyroid disorders being more common in hypothyroid one. Occasionally vitamin B12 malabsorption was found in 2 hypothyroid patients. Jejunal mucosal changes were almost unremarkable. Both fat and carbohydrate malabsorption in both groups of patients appeared to be casually related to the thyroid dysfunction.


Assuntos
Adulto , Doença Celíaca/etiologia , Feminino , Humanos , Hipertireoidismo/complicações , Hipotireoidismo/complicações , Absorção Intestinal , Síndromes de Malabsorção/etiologia , Masculino , Pessoa de Meia-Idade
2.
Artigo em Inglês | IMSEAR | ID: sea-95349

RESUMO

Thirteen patients of duodenal ulcer, below 20 years of age, ten age and sex matched controls and 17 first probands were studied to find out (i) the special characteristics of this duodenal ulcer subtype and (ii) the serum alpha-1-antitrypsin (alpha-1-AT) activity in these patients and their first probands. Basal and maximal acid output, and serum level of alpha-1-AT were measured, and serum agar gel electrophoresis done, in the above subjects. Special characteristics like positive family history, and high basal (p less than or equal to 0.01) and maximal (p less than or equal to 0.001) acid output were noted in these patients. Serum alpha-1-AT was found to be deficient in nine patients. Five first probands also had the heterozygous level of the enzyme deficiency. Thus, patients of early onset duodenal ulcer seem to have special characteristics with alpha-1-antitrypsin deficiency in them as well as in their first probands.


Assuntos
Adolescente , Adulto , Criança , Úlcera Duodenal/sangue , Feminino , Determinação da Acidez Gástrica , Triagem de Portadores Genéticos , Humanos , Masculino , alfa 1-Antitripsina/genética , Deficiência de alfa 1-Antitripsina
9.
J Indian Med Assoc ; 1965 Aug; 45(4): 206-8
Artigo em Inglês | IMSEAR | ID: sea-98353
10.
J Indian Med Assoc ; 1964 Dec; 43(): 550-1
Artigo em Inglês | IMSEAR | ID: sea-99011
11.
J Indian Med Assoc ; 1964 Sep; 43(): 282-3
Artigo em Inglês | IMSEAR | ID: sea-103284
12.
J Indian Med Assoc ; 1964 Aug; 43(): 183-4
Artigo em Inglês | IMSEAR | ID: sea-106044
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