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Year Number of Results
1946 3
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1948 1
1949 4
1957 3
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1966 2
1967 2
1968 2
1970 2
1975 2
1976 2
1977 4
1978 4
1979 3
1980 4
1981 5
1982 2
1983 4
1984 6
1985 9
1986 7
1987 8
1988 13
1989 10
1990 10
1991 6
1992 6
1993 9
1994 6
1995 8
1996 7
1997 4
1998 8
1999 5
2000 4
2001 10
2002 6
2003 4
2004 6
2005 11
2006 10
2007 11
2008 5
2009 8
2010 12
2011 10
2012 11
2013 13
2014 14
2015 9
2016 8
2017 9
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2024 5

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364 results

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Page 1
Systemic sclerosis sine scleroderma.
Kucharz EJ, Kopeć-Mędrek M. Kucharz EJ, et al. Adv Clin Exp Med. 2017 Aug;26(5):875-880. doi: 10.17219/acem/64334. Adv Clin Exp Med. 2017. PMID: 29068586 Free article. Review.
Systemic sclerosis is a rare generalized disease with scleroderma, i.e. skin thickening as one of the most common symptoms. The disease has 2 main subsets, diffuse and limited forms. The subset known as systemic sclerosis sine scleroderma (ssSSc) is a …
Systemic sclerosis is a rare generalized disease with scleroderma, i.e. skin thickening as one of the most common symptoms. Th …
Systemic Sclerosis.
Adigun R, Goyal A, Hariz A. Adigun R, et al. 2022 May 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2022 May 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 28613625 Free Books & Documents.
Scleroderma can be divided into two forms, localized Scleroderma (morphea, linear scleroderma, and scleroderma en coup de sabre), or Systemic sclerosis, which can further be classified as either limited systemic sclerosis (formerly known …
Scleroderma can be divided into two forms, localized Scleroderma (morphea, linear scleroderma, and scleroderma e …
Morphea and Eosinophilic Fasciitis: An Update.
Mertens JS, Seyger MMB, Thurlings RM, Radstake TRDJ, de Jong EMGJ. Mertens JS, et al. Am J Clin Dermatol. 2017 Aug;18(4):491-512. doi: 10.1007/s40257-017-0269-x. Am J Clin Dermatol. 2017. PMID: 28303481 Free PMC article. Review.
Morphea, also known as localized scleroderma, encompasses a group of idiopathic sclerotic skin diseases. ...In most patients with circumscribed superficial subtypes, treatment with topical therapies suffices. In more widespread disease, UVA1 phototherapy or systemic …
Morphea, also known as localized scleroderma, encompasses a group of idiopathic sclerotic skin diseases. ...In most patients with cir …
Cutaneous Manifestations, Clinical Characteristics, and Prognosis of Patients With Systemic Sclerosis Sine Scleroderma: Data From the International EUSTAR Database.
Lescoat A, Huang S, Carreira PE, Siegert E, de Vries-Bouwstra J, Distler JHW, Smith V, Del Galdo F, Anic B, Damjanov N, Rednic S, Ribi C, Bancel DF, Hoffmann-Vold AM, Gabrielli A, Distler O, Khanna D, Allanore Y; EUSTAR collaborators. Lescoat A, et al. JAMA Dermatol. 2023 Aug 1;159(8):837-847. doi: 10.1001/jamadermatol.2023.1729. JAMA Dermatol. 2023. PMID: 37378994

IMPORTANCE: Systemic sclerosis (SSc) sine scleroderma (ssSSc) is a subset of SSc defined by the absence of skin fibrosis. ...Survival rate was higher in patients with ssSSc (92.4%) compared with lcSSc (69.4%; P = .06) and dcSSc (55.5%; P < .001) after up to 15 ye

…
IMPORTANCE: Systemic sclerosis (SSc) sine scleroderma (ssSSc) is a subset of SSc defined by the absence of skin fibrosis. ...S …
Scleroderma-like Disorders.
Sharma A. Sharma A. Curr Rheumatol Rev. 2018 Apr 20;14(1):22-27. doi: 10.2174/1573397113666170612091419. Curr Rheumatol Rev. 2018. PMID: 28606036 Review.
It could be localized to skin and subcutaneous tissue, or may involve the internal organs too in systemic sclerosis. OBJECTIVE: There are disorders that can cause hardening and tightening of skin and mimic scleroderma but are rarely associated with Raynaud phenomeno …
It could be localized to skin and subcutaneous tissue, or may involve the internal organs too in systemic sclerosis. OBJECTIVE: There …
New ACR EULAR guidelines for systemic sclerosis classification.
Johnson SR. Johnson SR. Curr Rheumatol Rep. 2015 May;17(5):32. doi: 10.1007/s11926-015-0506-3. Curr Rheumatol Rep. 2015. PMID: 25874345
The new criteria build upon previous criteria by incorporating important elements (proximal scleroderma, sclerodactyly, digital pits, pulmonary fibrosis, Raynaud's phenomenon, and scleroderma specific autoantibodies). ...Undoubtedly, this will lead to a parad …
The new criteria build upon previous criteria by incorporating important elements (proximal scleroderma, sclerodactyly, digita …
Scleroderma and IgG4-related disease.
Reddi DM, Cardona DM, Burchette JL, Puri PK. Reddi DM, et al. Am J Dermatopathol. 2013 Jun;35(4):458-62. doi: 10.1097/DAD.0b013e318276cbac. Am J Dermatopathol. 2013. PMID: 23563250
To our knowledge, the presence of IgG4-positive cells has not been well characterized in scleroderma. A retrospective review of scleroderma and related disorders (calcinosis, raynaud's syndrome, esophageal dysmotility, sclerodactyly, telangiectasia (CREST) sy …
To our knowledge, the presence of IgG4-positive cells has not been well characterized in scleroderma. A retrospective review of sc …
Pediatric morphea.
Browning JC. Browning JC. Dermatol Clin. 2013 Apr;31(2):229-37. doi: 10.1016/j.det.2012.12.002. Epub 2013 Feb 1. Dermatol Clin. 2013. PMID: 23557652 Review.
Morphea is differentiated from systemic sclerosis (scleroderma) based on the absence of sclerodactyly, Raynaud phenomenon, and nail-fold capillary changes. ...Unlike morphea, systemic sclerosis has organ involvement, particularly gastrointestinal, pulm …
Morphea is differentiated from systemic sclerosis (scleroderma) based on the absence of sclerodactyly, Raynaud phenomen …
Clinical aspects of systemic and localized scleroderma.
van den Hoogen FH, de Jong EM. van den Hoogen FH, et al. Curr Opin Rheumatol. 1995 Nov;7(6):546-50. doi: 10.1097/00002281-199511000-00014. Curr Opin Rheumatol. 1995. PMID: 8579977 Review.
Esophageal dysmotility is not specific for systemic sclerosis but occurs in other connective tissue diseases as well. Peripheral macrovascular disease was shown to be increased in patients with limited cutaneous sclerosis; signs of autonomic dysfunction were found in patie …
Esophageal dysmotility is not specific for systemic sclerosis but occurs in other connective tissue diseases as well. Peripheral macr …
The diagnosis and classification of scleroderma (systemic sclerosis).
Barnett AJ, Miller M, Littlejohn GO. Barnett AJ, et al. Postgrad Med J. 1988 Feb;64(748):121-5. doi: 10.1136/pgmj.64.748.121. Postgrad Med J. 1988. PMID: 3050937 Free PMC article. Review.
Difficulty in the diagnosis of the disease scleroderma may occur at the early stage prior to the development of obvious skin sclerosis. ...Various terms have been used to denote subdivisions of scleroderma. These include acrosclerosis, diffuse scleroderma and …
Difficulty in the diagnosis of the disease scleroderma may occur at the early stage prior to the development of obvious skin sclerosi …
364 results