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Journal Abstract Search
284 related items for PubMed ID: 19250403
1. Chanarin-Dorfman syndrome: clinical features of a rare lipid metabolism disorder. Selimoglu MA, Esrefoglu M, Gul M, Gungor S, Yildirim C, Seyhan M. Pediatr Dermatol; 2009; 26(1):40-3. PubMed ID: 19250403 [Abstract] [Full Text] [Related]
2. Chanarin-Dorfman syndrome with eccrine gland vacuolation: a case report. Pahwa M, Kar R, Singh A, Goel A, Ramesh V, Jain R. Int J Dermatol; 2008 Dec; 47(12):1257-9. PubMed ID: 19126011 [Abstract] [Full Text] [Related]
3. Chanarin Dorfman syndrome: a case report with novel nonsense mutation. Gupta N, Gothwal S, Satpathy AK, Missaglia S, Tavian D, Das P, Timila D, Kabra M. Gene; 2016 Jan 10; 575(2 Pt 1):359-62. PubMed ID: 26353074 [Abstract] [Full Text] [Related]
4. Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome. Pujol RM, Gilaberte M, Toll A, Florensa L, Lloreta J, González-Enseñat MA, Fischer J, Azon A. Br J Dermatol; 2005 Oct 10; 153(4):838-41. PubMed ID: 16181472 [Abstract] [Full Text] [Related]
5. Neutral lipid storage disease with unusual presentation: report of three cases. Singh S, Sharma S, Agarwal S, Nangia A, Chander R, Varghese B. Pediatr Dermatol; 2012 Oct 10; 29(3):341-4. PubMed ID: 21575048 [Abstract] [Full Text] [Related]
6. [Dorfman-Chanarin syndrome--a neutral lipid storage disease]. Wollenberg A, Schaller M, Röschinger W, Schirren CG, Wolff H. Hautarzt; 1997 Oct 10; 48(10):753-8. PubMed ID: 9441170 [Abstract] [Full Text] [Related]
7. Dorfman-Chanarin syndrome: a rare neutral lipid storage disease. Mitra S, Samanta M, Sarkar M, Chatterjee S. Indian J Pathol Microbiol; 2010 Oct 10; 53(4):799-801. PubMed ID: 21045422 [Abstract] [Full Text] [Related]
8. Images of interest. Hepatobiliary and pancreatic: Dorfman-Chanarin syndrome. Doganci T, Gurakar F, Karaduman A, Orhan D, Caglar M. J Gastroenterol Hepatol; 2005 Jan 10; 20(1):156. PubMed ID: 15610464 [No Abstract] [Full Text] [Related]
9. Education and imaging. Hepatology: Chanarin-Dorfman syndrome, a rare cause of fatty liver and steatohepatitis. Kazemi MH, Taghavi SA, Eshraghian A, Talebzadeh M, Hamidpour L. J Gastroenterol Hepatol; 2015 May 10; 30(5):803. PubMed ID: 25865863 [No Abstract] [Full Text] [Related]
10. Dorfman-Chanarin syndrome (neutral lipid storage disease). A case report. Bañuls J, Betlloch I, Botella R, Sevila A, Morell A, Román P. Clin Exp Dermatol; 1994 Sep 10; 19(5):434-7. PubMed ID: 7955510 [Abstract] [Full Text] [Related]
11. Dorfman-Chanarin syndrome in a Turkish kindred: conductor diagnosis requires analysis of multiple eosinophils. Wollenberg A, Geiger E, Schaller M, Wolff H. Acta Derm Venereol; 2000 Sep 10; 80(1):39-43. PubMed ID: 10721832 [Abstract] [Full Text] [Related]
12. Dorfman-Chanarin syndrome: morphologic studies and presentation of new cases. Srebrnik A, Brenner S, Ilie B, Messer G. Am J Dermatopathol; 1998 Feb 10; 20(1):79-85. PubMed ID: 9504676 [Abstract] [Full Text] [Related]
13. Dorfman-Chanarin syndrome: a rare neutral lipid storage disease. Tullu MS, Muranjan MN, Save SU, Deshmukh CT, Khubchandani SR, Bharucha BA. Indian Pediatr; 2000 Jan 10; 37(1):88-93. PubMed ID: 10745395 [No Abstract] [Full Text] [Related]
14. Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parents. Durdu M, Missaglia S, Moro L, Tavian D. BMC Med Genet; 2018 May 29; 19(1):88. PubMed ID: 29843625 [Abstract] [Full Text] [Related]
18. Renal involvement as a rare complication of Dorfman-Chanarin syndrome: a case report. Aksu G, Kalkan Ucar S, Bulut Y, Aydinok Y, Sen S, Anal O, Simsek Gosen D, Darcan S, Coker M, Kutukculer N. Pediatr Dermatol; 2008 May 29; 25(3):326-31. PubMed ID: 18577036 [Abstract] [Full Text] [Related]