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Melasma: a clinicopathological study of 43 cases.
Melasma is a symmetrical hypermelanosis of the exposed skin characterized by brown macules on the sun-exposed areas of the skin. The present study was carried out on 43 patients to analyze theExpand
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Congenital Langerhans cell histiocytosis: the self-healing variety.
Congenital self-healing Langerhans cell histiocytosis (CSHLCH) is a rare variant of Langerhans cell histiocytosis, presenting at birth or in the neonatal period with cutaneous lesions that involuteExpand
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Clear cell syringoma--association with diabetes mellitus.
Clear cell syringomas are rare histological variants of syringoma and are clinically indistinguishable from ordinary syringomas. We report a case of clear cell syringoma associated with diabetesExpand
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Multiple eccrine hidrocystomas: report of two cases treated unsuccessfully with atropine ointment.
Eccrine hidrocystomas are rare, benign, cystic lesions with a lining that resembles that of the eccrine sweat gland and may be solitary or multiple. Multiple eccrine hidrocystomas occur predominantlyExpand
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Development and Validation of a Reversed Phase HPLC Method for Simultaneous Determination of Curcumin and Piperine in Human Plasma for Application in Clinical Pharmacological Studies
Abstract A sensitive and specific HPLC method was developed for the simultaneous determination of curcumin and piperine in human plasma in view of the potential therapeutic application of curcuminExpand
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Odontotrichodysplasia: A Case Report with a Review of Conditions Combining Ectodermal Dysplasia (Subgroup 1–2) with Skin Manifestations
We report a 5‐year‐old girl with partial anodontia, hypotrichosis, hyperpigmentation of the skin, absence of pilosebaceous structures, and long thin fingers. There has as yet been, to the best of ourExpand
Penetrating injury of the brachial artery
A case of penetrating injury of the brachial artery by an uncommon foreign body was managed by resection and end-to-end anastomosis of the vessel. Patency was restored and recovery was uneventful.
Hereditary onycho-osteo dysplasia syndrome.
We report a two and a half year old male child with dystrophy of all the nails, absent patellae and iliac horns. In addition he had dysmorphic facial features, sparing of lunula and bilateral halluxExpand