1.
JPMA-Journal of Pakistan Medical Association. 2004; 54 (3): 150-158
em Inglês
| IMEMR
| ID: emr-66952
2.
JPMA-Journal of Pakistan Medical Association. 2004; 54 (3): 136-141
em Inglês
| IMEMR
| ID: emr-66954
3.
Specialist Quarterly. 1994; 10 (2): 173-7
em Inglês
| IMEMR
| ID: emr-35556
4.
Specialist Quarterly. 1993; 9 (3): 299-302
em Inglês
| IMEMR
| ID: emr-31006
RESUMO
Hemolytic uremic syndrome is a rare disorder characterized by microangiopathic hemolytic anemia, thrombocytopenia and acute renal failure following viral and bacterial infections or other causes. We present a case history of young male with glucose 6 phosphate dehydrogenase deficiency and hemolytic uremic syndrome
Assuntos
Humanos , Masculino , Síndrome Hemolítico-Urêmica/complicações , Síndrome Hemolítico-Urêmica/terapia , Deficiência de Glucosefosfato Desidrogenase
5.
PJS-Pakistan Journal of Surgery. 1992; 8 (4): 114-117
em Inglês
| IMEMR
| ID: emr-26124
RESUMO
Immunoproliferative disease of the small intestine [IPSID] is an uncommon cause of chronic diarrhoea in the developed world but is a prevalent, debilitating illness that affects the younger population in the developing world. It affects adolescents and young adults of Middle Eastern and Mediterranean countries. Here we describe two cases which are the first to be reported from Pakistan