Ichthyosiform dermatoses: So many discoveries, so little progress

Journal of the American Academy of Dermatology

Volumn 51, Issue 1 SUPPL., 2004, Pages 31-34

  DiGiovanna, John J ^a,b,c  

^a BROWN UNIVERSITY   (United States)

^b NATIONAL CANCER INSTITUTE   (United States)

^c RHODE ISLAND HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

KERATIN; PYROXYLIN;

CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; CYTOSKELETON; GENE MUTATION; GENETIC COUNSELING; GENETIC DISORDER; HEARING IMPAIRMENT; HUMAN; HYPERKERATOSIS; ICHTHYOSIS; KERATINOCYTE; KERATITIS; LAMELLAR ICHTHYOSIS; NETHERTON DISEASE; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SKIN DISEASE; TEMPERATURE;

EID: 3042812660     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaad.2004.01.019     Document Type: Article

References (2)

1. DiGiovanna J.J. Ichthyosiform dermatoses. Freedberg I.M., Eisen A.Z., Wolff K., Austen K.F., Goldsmith L.A., Katz S.I. Fitzpatrick's Dermatology in General Medicine. 6th ed. 2003;481-505 McGraw Hill, New York
2. National Center for Biotechnology Information. Online Mendelian Inheritance in Man Web site. Available at www.ncbi.nlm.nih.gov. Accessed February 27, 2004.