Results 151 to 160 of about 65,412,535 (160)
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Hereditary deficiency of C2 in association with linear scleroderma 'en coup de sabre'.
Archives of dermatology, 1986A 32-year-old man suffering from linear frontoparietal scleroderma was found to have low (less than 10% normal) serum classical pathway activity although C1q, C3, C4, C5, and total alternative pathway activity was normal. Addition of purified C2 led to complete restoration of the total hemolytic activity of the classical pathway.
R F, Hulsmans +3 more
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Treatment of linear scleroderma “en coup de sabre” with AlloDerm tissue matrix
Otolaryngology–Head and Neck Surgery, 2008Jon, Robitschek +2 more
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Treatment of Linear Scleroderma (En Coup De Sabre) With Dermal Fat Grafting.
Journal of Cutaneous Medicine and Surgery, 2016Mehmet Akif ÇAKMAK +2 more
exaly
Correction of Facial Linear Scleroderma ‘Coup De Sabre’ With BoneSource®
Journal of Plastic, Reconstructive and Aesthetic Surgery, 2009Jun Hee Byeon
exaly
Linear scleroderma en coup de sabre and frontal lobe epilepsy
Archives of Disease in Childhood, 2012J. E. Wieringa +2 more
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FRONTAL LINEAR SCLERODERMA (EN COUP DE SABRE) ASSOCIATED WITH CENTRAL SEROUS CHORIORETINOPATHY
RETINAL Cases & Brief Reports, 2007Martine, Mauget-Faÿsse +3 more
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Alopecia With Perineural Lymphocytes: A Clue to Linear Scleroderma En Coup De Sabre
Journal of Cutaneous Pathology, 2012Lynne J Goldberg +2 more
exaly
Images in paediatrics: Linear scleroderma en coup de sabre and frontal lobe epilepsy.
Archives of disease in childhood, 2013Wieringa, J.E. +2 more
openaire +3 more sources