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Year Number of Results
1968 1
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1982 1
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1984 1
1985 3
1986 1
1987 1
1988 1
1989 6
1990 5
1991 7
1992 4
1993 5
1994 2
1995 12
1996 6
1997 6
1998 9
1999 8
2000 11
2001 5
2002 4
2003 4
2004 8
2005 4
2006 4
2007 5
2008 3
2009 2
2010 9
2011 2
2012 5
2013 3
2014 8
2015 3
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2018 3
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2020 2
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205 results

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Page 1
Cutaneous Manifestations of Scleroderma and Scleroderma-Like Disorders: a Comprehensive Review.
Ferreli C, Gasparini G, Parodi A, Cozzani E, Rongioletti F, Atzori L. Ferreli C, et al. Clin Rev Allergy Immunol. 2017 Dec;53(3):306-336. doi: 10.1007/s12016-017-8625-4. Clin Rev Allergy Immunol. 2017. PMID: 28712039 Review.
Scleroderma refers to an autoimmune connective tissue fibrosing disease, including three different subsets: localized scleroderma, limited cutaneous systemic sclerosis, and diffuse cutaneous systemic sclerosis with divergent patterns of organ involvement, autoantibo …
Scleroderma refers to an autoimmune connective tissue fibrosing disease, including three different subsets: localized scleroderma, limited …
Cutaneous deposits.
Molina-Ruiz AM, Cerroni L, Kutzner H, Requena L. Molina-Ruiz AM, et al. Am J Dermatopathol. 2014 Jan;36(1):1-48. doi: 10.1097/DAD.0b013e3182740122. Am J Dermatopathol. 2014. PMID: 23249837 Review.
There are 5 broad categories of cutaneous deposits. The first group includes calcium salts, bone, and cartilage. The second category includes the hyaline deposits that may be seen in the dermis in several metabolic disorders, such as amyloidosis, gout, porphyria, an …
There are 5 broad categories of cutaneous deposits. The first group includes calcium salts, bone, and cartilage. The second category …
Acute Porphyrias.
Besur S, Schmeltzer P, Bonkovsky HL. Besur S, et al. J Emerg Med. 2015 Sep;49(3):305-12. doi: 10.1016/j.jemermed.2015.04.034. Epub 2015 Jul 7. J Emerg Med. 2015. PMID: 26159905 Review.
Porphyrias are classified into two major categories: 1) the acute or inducible porphyrias and 2) the chronic cutaneous porphyrias. The acute hepatic porphyrias are further classified into acute intermittent porphyria (AIP), hereditary cop
Porphyrias are classified into two major categories: 1) the acute or inducible porphyrias and 2) the chronic cutaneous
The cutaneous porphyrias.
Schulenburg-Brand D, Katugampola R, Anstey AV, Badminton MN. Schulenburg-Brand D, et al. Dermatol Clin. 2014 Jul;32(3):369-84, ix. doi: 10.1016/j.det.2014.03.001. Epub 2014 May 5. Dermatol Clin. 2014. PMID: 24891059 Review.
The porphyrias are a group of mainly inherited disorders of heme biosynthesis where accumulation of porphyrins and/or porphyrin precursors gives rise to 2 types of clinical presentation: cutaneous photosensitivity and/or acute neurovisceral attacks. The cutaneous
The porphyrias are a group of mainly inherited disorders of heme biosynthesis where accumulation of porphyrins and/or porphyrin precu …
The porphyrias.
Bloomer JR, Bonkovsky HL. Bloomer JR, et al. Dis Mon. 1989 Jan;35(1):1-54. doi: 10.1016/0011-5029(89)90003-5. Dis Mon. 1989. PMID: 2645098 Review.
The porphyrias are metabolic disorders in which there are excessive accumulation and excretion of porphyrins and porphyrin precursors. ...The precise cause of the neurologic dysfunction has not been defined, but the likely possibilities are overproduction of delta-aminolev …
The porphyrias are metabolic disorders in which there are excessive accumulation and excretion of porphyrins and porphyrin precursors …
[Neurocutaneous porphyrias].
Frank J. Frank J. Hautarzt. 2016 Mar;67(3):221-5. doi: 10.1007/s00105-015-3745-3. Hautarzt. 2016. PMID: 26743053 Review. German.
Variegate porphyria and hereditary coproporphyria are referred to as neurocutaneous porphyrias because affected patients can develop both cutaneous symptoms on light-exposed body sites and potentially life-threatening acute neurovisceral symptoms, thereby mim …
Variegate porphyria and hereditary coproporphyria are referred to as neurocutaneous porphyrias because affected patients can d …
Porphyrias.
Puy H, Gouya L, Deybach JC. Puy H, et al. Lancet. 2010 Mar 13;375(9718):924-37. doi: 10.1016/S0140-6736(09)61925-5. Lancet. 2010. PMID: 20226990 Review.
Seven porphyrias are the result of a partial enzyme deficiency, and a gain of function mechanism has been characterised in a new porphyria. ...Cutaneous porphyrias present with either acute painful photosensitivity or skin fragility and blisters. ...
Seven porphyrias are the result of a partial enzyme deficiency, and a gain of function mechanism has been characterised in a new p
[The cutaneous porphyrias].
Cuny JF. Cuny JF. Ann Dermatol Venereol. 2019 Feb;146(2):143-159. doi: 10.1016/j.annder.2018.12.005. Epub 2019 Jan 30. Ann Dermatol Venereol. 2019. PMID: 30709634 Review. French.
The porphyrias are a group of metabolic disorders resulting from an innate abnormality in haem biosynthesis, and the clinical settings of which vary according to the genetic enzyme abnormality in question. ...The clinical classification distinguishes between acute porph
The porphyrias are a group of metabolic disorders resulting from an innate abnormality in haem biosynthesis, and the clinical setting …
Erythropoietic protoporphyria.
Lecha M, Puy H, Deybach JC. Lecha M, et al. Orphanet J Rare Dis. 2009 Sep 10;4:19. doi: 10.1186/1750-1172-4-19. Orphanet J Rare Dis. 2009. PMID: 19744342 Free PMC article. Review.
Erythropoietic protoporphyria (EPP) is an inherited disorder of the haem metabolic pathway characterised by accumulation of protoporphyrin in blood, erythrocytes and tissues, and cutaneous manifestations of photosensitivity. EPP has been reported worldwide, with prevalence …
Erythropoietic protoporphyria (EPP) is an inherited disorder of the haem metabolic pathway characterised by accumulation of protoporphyrin i …
205 results