|1.||Akiyama, Masashi: 4 articles (09/2014 - 11/2003)|
|2.||Shimizu, Hiroshi: 3 articles (02/2010 - 11/2003)|
|3.||Uchida, Yoshikazu: 2 articles (01/2012 - 02/2010)|
|4.||Nakajima, Kimiko: 2 articles (01/2012 - 02/2010)|
|5.||Sano, Shigetoshi: 2 articles (01/2012 - 02/2010)|
|6.||Chabrol, B: 1 article (04/2015)|
|7.||Angelini, Corrado: 1 article (04/2015)|
|8.||Milh, M: 1 article (04/2015)|
|9.||Boulay, C: 1 article (04/2015)|
|10.||Bollini, G: 1 article (04/2015)|
10/01/2010 - "Dorfman-Chanarin syndrome is a rare neutral lipid storage disorder characterized by ichthyosis, lipid vacuolations in peripheral leucocytes, and multisystem involvement. "
02/01/2010 - "Epidermal triglyceride levels are correlated with severity of ichthyosis in Dorfman-Chanarin syndrome."
11/01/2008 - "CGI-58 is the causative molecule underlying Dorfman-Chanarin syndrome, a neutral lipid storage disease exhibiting apparent clinical features of ichthyosis. "
01/01/2007 - "We believe that patients with ichthyosis should be evaluated bearing in mind the possibility of Dorfman-Chanarin syndrome. "
07/01/2006 - "Dorfman-Chanarin syndrome is a rare, autosomal recessive disorder characterized by congenital ichthyosis and presence of intracellular lipid droplets in most tissues. "
10/01/2008 - "Dorfman-Chanarin syndrome with cirrhosis."
11/01/2010 - "A 27-year-old Japanese man underwent liver transplantation because of uncompensated cirrhosis due to Dorfman-Chanarin syndrome (DCS). "
05/01/2004 - "Steatohepatitis and unsuspected micronodular cirrhosis in Dorfman-Chanarin syndrome with documented ABHD5 mutation."
|3.||Exfoliative Dermatitis (Erythroderma)
10/01/2011 - "Dorfman-Chanarin syndrome (DCS), which is also known as neutral lipid storage disease, is a rare autosomal recessive inherited lipid storage disease with congenital ichthyotic erythroderma. "
05/01/2008 - "Dorfman-Chanarin syndrome is a rare, autosomal recessive inherited lipid storage disease with congenital ichthyotic erythroderma due to an acylglycerol recycling defect. "
01/01/2000 - "Dorfman-Chanarin syndrome is a rare, autosomal recessive inherited lipid storage disease with congenital ichthyotic erythroderma due to an acylglycerol recycling defect. "
01/01/2007 - "To report the case of a boy with Dorfman-Chanarin syndrome with rickets. "
01/01/2007 - "Rickets with Dorfman-Chanarin syndrome."
04/01/2015 - "[Vitamin D deficiency rickets complicating Dorfman-Chanarin syndrome]."
|5.||Muscular Diseases (Myopathy)
11/01/2008 - "Opposed-phase MR imaging of lipid storage myopathy in a case of Chanarin-Dorfman disease."
11/01/2008 - "Chanarin-Dorfman disease (CDD) is a rare genetic disorder characterized by ichthyosis, myopathy, central nervous system disturbances, and intracellular lipid storage in muscle fibers, hepatocytes, and granulocytes. "
04/01/2015 - "Other metabolic myopathies with massive lipid storage and weakness are carnitine deficiency, neutral lipid storage-myopathy (NLSD-M), besides RR-MADD. "