“…Used electron microscope to examine marginal and central skin samples from lesional and nonlesional skin from vitiligo patients and skin from healthy controls Gokhale and Mehta, 1983 40 74 vitiligo patients; number of controls not provided Examined biopsies from affected depigmented areas and contralateral unaffected areas from vitiligo patients and compared to skin biopsies from healthy control skin from corresponding sites Bose, 1994 43 5 stable type A vitiligo patients; used patients' unaffected breast skin as control Used monoclonal antibody trophectoderm specific monoclonal antibody-1 (TROMA-1) for indirect immunofluorescence to analyze biopsies from lesional skin and adjacent nonlesional skin and compared to unaffected control skin Laties and Lerner, 1975 44 28 brown-eyed Dutch belted rabbits Animal study; sympathectomy via resection of superior cervical ganglion on one side in 10 rabbits and via interrupting the preganglionic nerve trunk in the remaining 18 rabbits Al'Abadie et al, 1994 45 12 vitiligo patients (active in 7 patients, static in 2, unknown in 3), 7 healthy controls Biopsies from lesional, nonlesional, marginal, and control skin were frozen with cryospray and cut on a cryostat and subjected to fluorescence immunohistochemistry Lazarova et al, 2000 46 10 vitiligo patients, 10 controls Indirect immunofluorescence Liu et al, 1996 47 18 vitiligo patients Case control study Rateb et al, 2004 48 20 vitiligo patients ( 52 10 patients with stable facial segmental-type vitiligo and 2 groups of controls:…”