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  1. Home
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Browsing by Author "P.K. Nigam"

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    PublicationArticle
    Bilateral nevus fuscocaeruleus ophthalmomaxillaris
    (1985) P.K. Nigam; P.K. Singh; G. Singh
    [No abstract available]
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    PublicationArticle
    Glucose tolerance studies in lichen planus
    (1987) P.K. Nigam; Lata Sharma; J.K. Agrawal; Gurmohan Singh; S.K. Khurana
    A study of glucose tolerance and insulin response to oral glucose was carried out in 56 consecutive histologically confirmed cases of lichen planus. 30.3% patients showed abnormal glucose tolerance. The pattern of insulin response was similar to that seen in type 11 diabetes. Insulin/glucose ratio showed the same relationship as seen in type II diabetes. These results reinforce the possibility of glucose intolerance in lichen planus patients. However, no correlation between glucose tolerance abnormalities and duration and distribution of lesions was observed. © 1987 S. Karger AG, Basel.
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    Humoral immuno-deficiency in lichen planus
    (1988) P.K. Nigam; G. Singh; L. Sharma; S.K. Khurana
    [No abstract available]
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    Linear porokeratosis
    (1987) G. Singh; P.K. Nigam; M. Kumar
    [No abstract available]
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    PublicationLetter
    Plasma insulin response to oral glycaemic stimulus in lichen planus
    (1988) P.K. Nigam; G. Singh; J.K. Agrawal
    [No abstract available]
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    Rifampicin induced uterine bleeding
    (1988) P.K. Nigam; P.K. Singh; G. Singh; M. Kumar
    A case of uterine bleeding after intake of rifampicin is reported in a 35-year-old female. Provocation test was also positive. The underlying mechanism whether it was a hypersensitivity phenomenon like fixed drug eruption or due to induction of uterine acyl-hydrolase enzyme, is not clear. Uterine bleeding has not been observed as a side-effect of rifampicin in the past.
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    Terry's nails in a case of leprosy
    (1986) P.K. Singh; P.K. Nigam; G. Singh
    A case of Terry's nails following the onset of Borderline Tuberculoid leprosy without any other involvement in a 40 year male is reported. This condition is, however, well known in cirrhosis of liver, of which there was no evidence in this patient.
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