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

Year Number of Results
1983 1
1984 1
1985 2
1986 1
1987 2
1991 1
1992 1
1993 1
1994 1
1996 1
1998 1
1999 1
2001 1
2003 3
2005 1
2006 2
2007 2
2008 2
2009 2
2010 3
2011 1
2014 2
2015 1
2018 3
2019 2
2020 3
2021 5
2022 2
2023 3
2024 0

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50 results

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Page 1
Treatment in Juvenile Scleroderma.
Zulian F, Tirelli F. Zulian F, et al. Curr Rheumatol Rep. 2020 Jun 26;22(8):45. doi: 10.1007/s11926-020-00910-x. Curr Rheumatol Rep. 2020. PMID: 32591919 Review.
RECENT FINDINGS: According to the recent recommendations for Pediatric Rheumatology in Europe (SHARE), systemic treatment in localized scleroderma is needed when there is a risk for disability, such as in generalized or pansclerotic morphea and progressive linear sclero …
RECENT FINDINGS: According to the recent recommendations for Pediatric Rheumatology in Europe (SHARE), systemic treatment in localized scler …
Autoimmunity in Segmental Vitiligo.
Speeckaert R, Lambert J, Bulat V, Belpaire A, Speeckaert M, van Geel N. Speeckaert R, et al. Front Immunol. 2020 Oct 27;11:568447. doi: 10.3389/fimmu.2020.568447. eCollection 2020. Front Immunol. 2020. PMID: 33193342 Free PMC article. Review.
Systemic autoimmune diseases are less frequently associated compared to non-segmental vitiligo (NSV), but localized skin disorders - in particular linear morphea - have been repeatedly observed in patients with SV. The inflammatory response is documented on a clinical leve …
Systemic autoimmune diseases are less frequently associated compared to non-segmental vitiligo (NSV), but localized skin disorders - in part …
Interventions for morphea.
Albuquerque JV, Andriolo BN, Vasconcellos MR, Civile VT, Lyddiatt A, Trevisani VF. Albuquerque JV, et al. Cochrane Database Syst Rev. 2019 Jul 16;7(7):CD005027. doi: 10.1002/14651858.CD005027.pub5. Cochrane Database Syst Rev. 2019. PMID: 31309547 Free PMC article.
This RCT included children and adults with active morphea (circumscribed morphea, linear scleroderma (with trunk/limb variant and head variant), generalised morphea, or mixed morphea), who received phototherapy five times a week, for eight weeks. ...AUTHORS' CONCLUS …
This RCT included children and adults with active morphea (circumscribed morphea, linear scleroderma (with trunk/limb variant …
Hair disorders associated with autoimmune connective tissue diseases.
Cassano N, Amerio P, D'Ovidio R, Vena GA. Cassano N, et al. G Ital Dermatol Venereol. 2014 Oct;149(5):555-65. Epub 2014 Jun 30. G Ital Dermatol Venereol. 2014. PMID: 24975949 Review.
Hair disorders are frequently observed in various systemic diseases, including autoimmune connective tissue diseases (CTDs), with predilection of lupus erythematosus (LE), followed by dermatomyositis (DM) and scleroderma. ...In DM, the involvement of the scalp is common, a …
Hair disorders are frequently observed in various systemic diseases, including autoimmune connective tissue diseases (CTDs), with pre …
Linear alopecia in pediatrics: RCM and dermoscopy reveal diagnostic cues.
Wang Y, Chen L, Qin B, Li Q. Wang Y, et al. Skin Res Technol. 2023 Nov;29(11):e13523. doi: 10.1111/srt.13523. Skin Res Technol. 2023. PMID: 38009024 Free PMC article.
BACKGROUND: Alopecia areata (AA), trichotillomania (TM), nevus sebaceous (NS), and linear scleroderma en coup de sabre (LSCS) can all present with a patch of linear alopecia, making diagnosis challenging. ...Both NS and LSCS patients exhibited an absence of follicul …
BACKGROUND: Alopecia areata (AA), trichotillomania (TM), nevus sebaceous (NS), and linear scleroderma en coup de sabre (LSCS) …
Mycophenolate mofetil for methotrexate-resistant juvenile localized scleroderma.
Martini G, Saggioro L, Culpo R, Vittadello F, Meneghel A, Zulian F. Martini G, et al. Rheumatology (Oxford). 2021 Mar 2;60(3):1387-1391. doi: 10.1093/rheumatology/keaa392. Rheumatology (Oxford). 2021. PMID: 32978631 Free PMC article.
No significant difference in demographics, follow-up duration and treatment before diagnosis was observed between groups. The most represented clinical subtypes in the MMF-group were pansclerotic morphea and mixed subtype (P = 0.008 and P = 0.029, respectively), and lin …
No significant difference in demographics, follow-up duration and treatment before diagnosis was observed between groups. The most re …
Neuroimaging findings of linear scleroderma of the head and face: a case report.
Meng L, Wang Q. Meng L, et al. J Int Med Res. 2022 Jan;50(1):3000605211066002. doi: 10.1177/03000605211066002. J Int Med Res. 2022. PMID: 35040339 Free PMC article.
Linear scleroderma of the head and face is a rare connective tissue disorder characterized by linear depressed scarring in the frontoparietal area of the face. ...The imaging findings suggested a disrupted fiber tract and decreased relative cerebral blood flow. Our …
Linear scleroderma of the head and face is a rare connective tissue disorder characterized by linear depressed scarring in the …
Juvenile localized scleroderma: A single-centre experience from India.
Jindal AK, Handa S, Loganathan SK, Sudhakar M, Kaushik A, Suri D, Pandiarajan V, Rawat A, Gupta A, De D, Mahajan R, Singh S. Jindal AK, et al. J Eur Acad Dermatol Venereol. 2023 Mar;37(3):598-604. doi: 10.1111/jdv.18765. Epub 2022 Dec 3. J Eur Acad Dermatol Venereol. 2023. PMID: 36413107
Median age of disease onset was 5 years, and median age at diagnosis was 8 years. Commonest subtype was linear scleroderma (57 patients, 67.7%) followed by plaque morphoea and generalized morphoea. ...Using linear regression analysis, administration of dexamethasone …
Median age of disease onset was 5 years, and median age at diagnosis was 8 years. Commonest subtype was linear scleroderma (57 …
Disease course and long-term outcome of juvenile localized scleroderma: Experience from a single pediatric rheumatology Centre and literature review.
Martini G, Fadanelli G, Agazzi A, Vittadello F, Meneghel A, Zulian F. Martini G, et al. Autoimmun Rev. 2018 Jul;17(7):727-734. doi: 10.1016/j.autrev.2018.02.004. Epub 2018 May 3. Autoimmun Rev. 2018. PMID: 29729451 Review.
At least one disease relapse occurred in 22.2% of patients and first flare was observed 20 months after first treatment discontinuation. Mild tissue damage was observed in more than half of patients, in 25.4% was moderate and in 23.0% severe; 19.8% presented a funct …
At least one disease relapse occurred in 22.2% of patients and first flare was observed 20 months after first treatment discontinuati …
Overlap between linear scleroderma, progressive facial hemiatrophy and immune-inflammatory encephalitis in a paediatric cohort.
De Somer L, Morren MA, Muller PC, Despontin K, Jansen K, Lagae L, Wouters C. De Somer L, et al. Eur J Pediatr. 2015 Sep;174(9):1247-54. doi: 10.1007/s00431-015-2532-6. Epub 2015 Apr 8. Eur J Pediatr. 2015. PMID: 25851111
Linear scleroderma en coup the sabre (LSCS), progressive facial hemiatrophy (PFH) and autoimmune encephalitis are distinct clinical entities, although patients with overlapping features have been reported. ...CONCLUSION: Our patient cohort brings more arguments to c …
Linear scleroderma en coup the sabre (LSCS), progressive facial hemiatrophy (PFH) and autoimmune encephalitis are distinct cli …
50 results