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2.
J Indian Med Assoc ; 1992 May; 90(5): 134-5
Artículo en Inglés | IMSEAR | ID: sea-103421
3.
Artículo en Inglés | IMSEAR | ID: sea-26124

RESUMEN

High incidence of alpha thalassaemias (estimated from detection of Hb Bart's from cord blood), Hb constant spring (CS) and high A2 beta thalassaemia trait (estimated from normal adult subjects) were detected in 12.6, 15 and 8 per cent people of coastal Orissa (with less than 5% tribal population) respectively. Quantitation of Hb Bart's suggest that the alpha thalassaemia could be any of the genotypes such as, -alpha/alpha alpha, -alpha/-alpha, --/alpha alpha and alpha alpha/alpha alpha cs. Both heterozygotes and homozygotes for Hb CS were identified.


Asunto(s)
Sangre Fetal/química , Hemoglobinas Anormales/análisis , Humanos , India/epidemiología , Prevalencia , Talasemia/epidemiología
4.
J Indian Med Assoc ; 1991 Apr; 89(4): 91-2
Artículo en Inglés | IMSEAR | ID: sea-99938

RESUMEN

Estimation of serum iron, total iron binding capacity (TIBC) and transferrin saturation was performed in 62 apparently healthy male medical students. All had haemoglobin over 140 g/1. Low serum iron, elevated level of TIBC and transferrin saturation under 20% indicating iron deficiency state was found in 2 subjects. Elevated values of TIBC was found in 25 (40.32%) students as evidence of latent iron deficiency. Such high prevalence of iron deficiency in an affluent group indicates widespread iron deficiency in the general population.


Asunto(s)
Adulto , Humanos , Hierro/sangre , Masculino , Transferrina/metabolismo
5.
Artículo en Inglés | IMSEAR | ID: sea-20182

RESUMEN

Haemoglobin fractionation in 27 subjects with sickle cell trait revealed 12 (44%) with sickle cell haemoglobin less than 35 per cent (23.4-34.2%, mean 30.4 +/- 3.3%) suggesting an association of alpha thalassaemia. Electrophoresis of 91 samples of cord blood revealed demonstrable amounts of haemoglobin Bart's in 7 (7.7%); six between 5 and 10 per cent and one with less than 2 per cent. It appeared that the six infants with higher amounts of haemoglobin Bart's were homozygous for alpha-thalassaemia + (-a/-a) genotypes and one was heterozygous for alpha-thalassaemia + (-a/aa) Results of haemoglobin electrophoresis done on 2754 blood samples analysed from hospital records, retrospectively did not reveal haemoglobin-H and haemoglobin Constant Spring in any of the samples.


Asunto(s)
Anemia de Células Falciformes/sangre , Sangre Fetal/análisis , Hemoglobina A/análisis , Hemoglobina Falciforme/análisis , Hemoglobinas Anormales/análisis , Humanos , Recién Nacido , Rasgo Drepanocítico/sangre , Talasemia/diagnóstico
10.
Indian Pediatr ; 1986 Mar; 23(3): 217-21
Artículo en Inglés | IMSEAR | ID: sea-12343
11.
Indian J Chest Dis Allied Sci ; 1985 Apr-Jun; 27(2): 124-6
Artículo en Inglés | IMSEAR | ID: sea-29883
16.
Indian J Chest Dis Allied Sci ; 1983 Jan-Mar; 25(): 76-8
Artículo en Inglés | IMSEAR | ID: sea-29784
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