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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1980 2
1981 1
1982 1
1985 2
1986 2
1987 1
1989 1
1990 2
1991 1
1992 4
1993 1
1994 5
1995 2
1996 2
1997 3
1998 5
1999 4
2000 3
2001 4
2002 3
2003 6
2004 6
2005 5
2006 5
2008 3
2009 2
2010 1
2011 3
2012 4
2013 10
2014 10
2015 10
2016 10
2017 11
2018 9
2019 12
2020 9
2021 10
2022 16
2023 11
2024 4

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188 results

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Page 1
Inherited ichthyosis: Non-syndromic forms.
Takeichi T, Akiyama M. Takeichi T, et al. J Dermatol. 2016 Mar;43(3):242-51. doi: 10.1111/1346-8138.13243. J Dermatol. 2016. PMID: 26945532 Review.
Included in autosomal recessive congenital ichthyosis are three of the major phenotypes (harlequin ichthyosis, lamellar ichthyosis and congenital ichthyosiform erythroderma) and three of the minor subtypes (self-healing collodion baby, acral self-healing collodion b …
Included in autosomal recessive congenital ichthyosis are three of the major phenotypes (harlequin ichthyosis, lamellar ichthyosis …
Topical tacrolimus for atopic dermatitis.
Cury Martins J, Martins C, Aoki V, Gois AF, Ishii HA, da Silva EM. Cury Martins J, et al. Cochrane Database Syst Rev. 2015 Jul 1;2015(7):CD009864. doi: 10.1002/14651858.CD009864.pub2. Cochrane Database Syst Rev. 2015. PMID: 26132597 Free PMC article. Review.
Exception is made for diseases with severe barrier defects, such as Netherton's syndrome, lamellar ichthyosis, and a few others, with case reports of a higher absorption. ...
Exception is made for diseases with severe barrier defects, such as Netherton's syndrome, lamellar ichthyosis, and a few other …
Genetic skin diseases.
Francis JS. Francis JS. Curr Opin Pediatr. 1994 Aug;6(4):447-53. doi: 10.1097/00008480-199408000-00016. Curr Opin Pediatr. 1994. PMID: 7951667 Review.
Recessive X-linked ichthyosis is characterized by a deficiency of the enzyme steroid sulfatase. A type of lamellar ichthyosis may be explained on the basis of abnormal cornified cell envelope formation, and bullous congenital ichthyosiform erythroderma (epidermolyti …
Recessive X-linked ichthyosis is characterized by a deficiency of the enzyme steroid sulfatase. A type of lamellar ichthyosis …
Autosomal recessive congenital ichthyosis.
Rodríguez-Pazos L, Ginarte M, Vega A, Toribio J. Rodríguez-Pazos L, et al. Actas Dermosifiliogr. 2013 May;104(4):270-84. doi: 10.1016/j.adengl.2011.11.021. Epub 2013 Apr 3. Actas Dermosifiliogr. 2013. PMID: 23562412 Free article. Review. English, Spanish.
The term autosomal recessive congenital ichthyosis (ARCI) refers to a group of rare disorders of keratinization classified as nonsyndromic forms of ichthyosis. This group was traditionally divided into lamellar ichthyosis (LI) and congenital ichthyosiform erythroder …
The term autosomal recessive congenital ichthyosis (ARCI) refers to a group of rare disorders of keratinization classified as nonsyndromic f …
Ichthyosis in the newborn.
Craiglow BG. Craiglow BG. Semin Perinatol. 2013 Feb;37(1):26-31. doi: 10.1053/j.semperi.2012.11.001. Semin Perinatol. 2013. PMID: 23419760 Free PMC article. Review.
Ichthyosis: etiology, diagnosis, and management.
DiGiovanna JJ, Robinson-Bostom L. DiGiovanna JJ, et al. Am J Clin Dermatol. 2003;4(2):81-95. doi: 10.2165/00128071-200304020-00002. Am J Clin Dermatol. 2003. PMID: 12553849 Review.
CARI can progress into any one of a spectrum of disorders. Lamellar ichthyosis is characterized by dark, plate (armor)-like scale. ...
CARI can progress into any one of a spectrum of disorders. Lamellar ichthyosis is characterized by dark, plate (armor)-like sc …
Secukinumab responses vary across the spectrum of congenital ichthyosis in adults.
Lefferdink R, Rangel SM, Chima M, Ibler E, Pavel AB, Kim H, Wu B, Abu-Zayed H, Wu J, Jackson K, Singer G, Choate KA, Guttman-Yassky E, Paller AS. Lefferdink R, et al. Arch Dermatol Res. 2023 Mar;315(2):305-315. doi: 10.1007/s00403-022-02325-3. Epub 2022 Feb 26. Arch Dermatol Res. 2023. PMID: 35218370 Free PMC article. Clinical Trial.
PARTICIPANTS: Twenty subjects 18 yo with genotype-confirmed epidermolytic ichthyosis, Netherton syndrome, lamellar ichthyosis, or congenital ichthyosiform erythroderma with at least moderate erythroderma. ...
PARTICIPANTS: Twenty subjects 18 yo with genotype-confirmed epidermolytic ichthyosis, Netherton syndrome, lamellar ichthyosis, …
Nail involvement in autosomal recessive congenital ichthyosis.
Zaouak A, Chamli A, Ben Mansour N, Jouini W, Fenniche S, Hammami H. Zaouak A, et al. Clin Dermatol. 2022 Jul-Aug;40(4):388-394. doi: 10.1016/j.clindermatol.2022.02.012. Epub 2022 Feb 15. Clin Dermatol. 2022. PMID: 35181410 Review.
Proposal for a 6-step approach for differential diagnosis of neonatal erythroderma.
Cuperus E, Bygum A, Boeckmann L, Bodemer C, Bolling MC, Caproni M, Diociaiuti A, Emmert S, Fischer J, Gostynski A, Guez S, van Gijn ME, Hannulla-Jouppi K, Has C, Hernández-Martín A, Martinez AE, Mazereeuw-Hautier J, Medvecz M, Neri I, Sigurdsson V, Suessmuth K, Traupe H, Oji V, Pasmans SGMA. Cuperus E, et al. J Eur Acad Dermatol Venereol. 2022 Jul;36(7):973-986. doi: 10.1111/jdv.18043. Epub 2022 Mar 15. J Eur Acad Dermatol Venereol. 2022. PMID: 35238435 Free PMC article. Review.
188 results