Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 138

Similar articles for PubMed (Select 15452860)

1.

Molecular genetics of the ichthyoses.

Richard G.

Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):32-44. Review.

PMID:
15452860
2.

Ichthyoses: differential diagnosis and molecular genetics.

Oji V, Traupe H.

Eur J Dermatol. 2006 Jul-Aug;16(4):349-59. Review.

PMID:
16935789
4.

Updated molecular genetics and pathogenesis of ichthiyoses.

Akiyama M.

Nagoya J Med Sci. 2011 Aug;73(3-4):79-90. Review.

PMID:
21928690
5.

The ichthyoses--pathogenesis and prenatal diagnosis: a review of recent advances.

Williams ML.

Pediatr Dermatol. 1983 Jul;1(1):1-24. Review.

PMID:
6208542
6.

An update on molecular aspects of the non-syndromic ichthyoses.

Akiyama M, Shimizu H.

Exp Dermatol. 2008 May;17(5):373-82. doi: 10.1111/j.1600-0625.2007.00691.x. Epub 2008 Mar 12. Review.

PMID:
18341575
7.

[The ichthyoses. Pathophysiological models of epidermal differentiation].

Hohl D, Huber M.

Hautarzt. 2013 Jan;64(1):12-21. doi: 10.1007/s00105-012-2407-y. German.

PMID:
23337961
8.

Abnormal barrier function in the pathogenesis of ichthyosis: therapeutic implications for lipid metabolic disorders.

Elias PM, Williams ML, Feingold KR.

Clin Dermatol. 2012 May-Jun;30(3):311-22. doi: 10.1016/j.clindermatol.2011.08.017.

9.

New clinico-genetic classification of trichothiodystrophy.

Morice-Picard F, Cario-André M, Rezvani H, Lacombe D, Sarasin A, Taïeb A.

Am J Med Genet A. 2009 Sep;149A(9):2020-30. doi: 10.1002/ajmg.a.32902. Review.

PMID:
19681155
10.

Ichthyosis: etiology, diagnosis, and management.

DiGiovanna JJ, Robinson-Bostom L.

Am J Clin Dermatol. 2003;4(2):81-95. Review.

PMID:
12553849
11.

The biologic basis of the ichthyoses.

McGuire J.

Dermatol Clin. 1986 Jan;4(1):67-78. Review.

PMID:
3521981
12.

Recessive ichthyosis congenita type II.

Niemi KM, Kanerva L, Kuokkanen K.

Arch Dermatol Res. 1991;283(4):211-8.

PMID:
1929537
13.

A novel in situ method for the detection of deficient transglutaminase activity in the skin.

Raghunath M, Hennies HC, Velten F, Wiebe V, Steinert PM, Reis A, Traupe H.

Arch Dermatol Res. 1998 Nov;290(11):621-7.

PMID:
9860283
14.
15.

The molecular basis of inherited disorders of keratinization.

Dunnill MG.

Hosp Med. 1998 Jan;59(1):17-22.

PMID:
9798559
16.

Ichthyoses - Part 1: Differential diagnosis of vulgar ichthyoses and therapeutic options.

Krug M, Oji V, Traupe H, Berneburg M.

J Dtsch Dermatol Ges. 2009 Jun;7(6):511-9. doi: 10.1111/j.1610-0387.2008.06969.x. Review. English, German.

PMID:
19192163
17.
18.

A recurrent mutation in the loricrin gene underlies the ichthyotic variant of Vohwinkel syndrome.

O'Driscoll J, Muston GC, McGrath JA, Lam HM, Ashworth J, Christiano AM.

Clin Exp Dermatol. 2002 May;27(3):243-6.

PMID:
12072018
19.

The expression of the 27-kd heat shock protein in keratinization disorders: an immunohistological study.

Jonak C, Metze D, Traupe H, Happle R, König A, Trautinger F.

Hum Pathol. 2005 Jun;36(6):686-93.

PMID:
16021576
20.

Reticular erythrokeratoderma: a new disorder of cornification.

Itin PH, Moschopulos M, Richard G.

Am J Med Genet A. 2003 Jul 15;120A(2):237-40.

PMID:
12833406
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk