The diagnosis and classification of scleroderma (systemic sclerosis)

scientific article published on February 1988

The diagnosis and classification of scleroderma (systemic sclerosis) is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1136/PGMJ.64.748.121
P932PMC publication ID2428791
P698PubMed publication ID3050937
P5875ResearchGate publication ID20105220

P2093author name stringMiller M
Barnett AJ
Littlejohn GO
P2860cites workMULTIPLE TELANGIECTASIA, RAYNAUD'S PHENOMENON, SCLERODACTYLY, AND SUBCUTANIOUS CALCINOSIS: A SYNDROME MIMICKING HEREDITARY HEMORRHAGIC TELANGIECTASIAQ34257322
The systemic involvement in sclerodermaQ43739773
Scleroderma (Progressive Systemic Sclerosis): progress and course based on a personal series of 118 casesQ44530975
THE CLINICAL SIGNIFICANCE OF THE ANTICENTROMERE ANTIBODYQ59032616
Association of Antibodies to Ribonucleoprotein and Sm Antigens with Mixed Connective-Tissue Disease, Systemic Lupus Erythematosus and Other Rheumatic DiseasesQ66888389
Differentiation and characterization of autoantibodies and their antigens in sjögren's syndromeQ67442594
The anticentromere antibody: disease specificity and clinical significanceQ70383558
Clinical and laboratory associations of anticentromere antibody in patients with progressive systemic sclerosisQ71002244
Diagnostic potential of in vivo capillary microscopy in scleroderma and related disordersQ71154365
Diversity of antinuclear antibodies in progressive systemic sclerosis. Anti-centromere antibody and its relationship to CREST syndromeQ72611213
Scleroderma; based on a study of over 150 casesQ73642800
AcrosclerosisQ75823729
Acrosclerosis: a disease sui generis or a variety of diffuse sclerodermaQ78588309
Progressive Systemic Sclerosis Sine SclerodermaQ79064145
Systemic scleroderma, A clinical study of 727 casesQ79087145
Prognostic significance of Raynaud's phenomenon and other clinical characteristics of systemic scleroderma. A study of 271 casesQ79229206
Diffuse systemic scleroderma. A comparison with acrosclerosisQ79431871
Scleroderma. 1. Clinical features, course of illness and response to treatment in 61 casesQ93788109
AcrosclerosisQ93899768
P433issue748
P407language of work or nameEnglishQ1860
P1104number of pages5
P304page(s)121-125
P577publication date1988-02-01
P1433published inPostgraduate Medical JournalQ7234294
P1476titleThe diagnosis and classification of scleroderma (systemic sclerosis)
P478volume64

Reverse relations

cites work (P2860)
Q37402787A TGFbeta-responsive gene signature is associated with a subset of diffuse scleroderma with increased disease severity
Q34567867Are There Clinical Differences in Limited Systemic Sclerosis according to Extension of Skin Involvement?
Q33320557Autoantibodies in systemic sclerosis (scleroderma): clues for clinical evaluation, prognosis and pathogenesis
Q37905787Capturing the heterogeneity in systemic sclerosis with genome-wide expression profiling
Q37689570Diagnosis and classification of systemic sclerosis
Q28070002Enigmatic insight into collagen
Q37998968Extracorporeal photopheresis: clinical use so far.
Q39177903Extrahepatic Manifestations of Primary Biliary Cholangitis
Q52889034Quantification of cutaneous sclerosis with a skin elasticity meter in patients with generalized scleroderma.
Q36806259Vascular leak is a central feature in the pathogenesis of systemic sclerosis
Q79423262[Classification criteria of scleroderma]

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