Results 21 to 30 of about 4,865,556 (281)

Cyanosis With Dysautonomia Mimics Raynaud Disease. [PDF]

J Clin Rheumatol, 2020
Soloway AM, DePace NL, Colombo J, Soloway S.   +3 more
europepmc   +2 more sources

Computed Tomography (CT)-Guided Percutaneous Thoracic Sympathetic Chain Radiofrequency Thermocoagulation for Raynaud Disease. [PDF]

Med Sci Monit, 2019
Huang H, Qiu W, Chen Q, Sun K, Huang B.
europepmc   +2 more sources

Qualitative Interviews to Assess the Content Validity and Usability of the Electronic Raynaud Diary in Patients with Systemic Sclerosis

ACR Open Rheumatology, 2023
Objective To better understand the symptoms and impacts of Raynaud phenomenon (RP) in patients with systemic sclerosis (SSc) and to evaluate the content validity and usability of a new electronic patient‐reported outcome (PRO) measure for RP: the Raynaud
Robyn T. Domsic, Robin Pokrzywinski, Larissa Stassek, Wade W. Benton, Christa‐Lynn Vampola, Daniel E. Furst, Lorinda Chung, Virginia Steen, Maureen D. Mayes, Ami A. Shah, Jerry A. Molitor, Kelly Oliver, Vivek Nagaraja, Dinesh Khanna   +13 more
doaj   +1 more source

Characteristics Of Systemic Sclerosis Patients In Zagazig University Hospitals; A Cross Sectional Study. [PDF]

Zagazig University Medical Journal, 2023
Background: Systemic Sclerosis (SSc) is a chronic connective tissue disease with multi-organ involvement characterized by immune activation, inflammation, widespread small-vessel vasculopathy, progressive interstitial and vascular fibrosis in the skin ...
Alaa El-Safty, manal yossef, Amal Abdul-Sattar   +2 more
doaj   +1 more source

Dystrophic calcifications and Raynaud’s phenomenon in an eight-year old girl [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2014
Introduction. Dystrophic calcifications are the most common subtype of skin calcinosis. Tumorous soft tissue calcium deposits usually contain hydroxyapatite and amorphous calcium phosphate.
Grebeldinger Slobodan P., Tomić Jelena M., Vijatov-Đurić Gordana V., Radojčić Branka S., Vučković Nada M., Ćulafić Jelena N.   +5 more
doaj   +1 more source

Osteonecrosis of carpal bones in systemic sclerosis [PDF]

Romanian Journal of Rheumatology, 2021
Background. Systemic sclerosis (SSc) is a rare chronic disease, with unknown aetiology and complex pathogenesis. The hand is often implied in the main clinical findings, being affected primarily by the vascular component (Raynaud phenomenon, digital ...
Alexandra Chitac, Codrina Ancuta
doaj   +1 more source

Anti–Jo-1–Positive Antisynthetase Syndrome and Myocarditis: An Underrecognized Clinical Presentation

Annals of Internal Medicine: Clinical Cases, 2023
Antisynthetase syndrome is a distinct entity of overlap myositis in adults and is characterized by muscle weakness, arthritis, mechanic's hands, interstitial lung disease, and Raynaud phenomenon.
Rania Al Asmar, Rabia Cheema, Samera Vaseer, Ira Targoff, Mary Beth Humphrey   +4 more
doaj   +1 more source

Antisynthetase Syndrome with Severe Interstitial Lung Disease in Pregnancy

Case Reports in Anesthesiology, 2021
Antisynthetase syndrome is a rare multisystem autoimmune disorder which clinically manifests with myositis, arthritis, interstitial lung disease, Raynaud phenomenon, and skin hyperkeratosis. Lung involvement represents the most severe form of disease and
Catalina I. Dumitrascu, David A. Olsen, Katherine W. Arendt, Carl H. Rose, Emily E. Sharpe   +4 more
doaj   +1 more source

Raynaud Phenomenon of the Nipple: A Clinical Case Report

Journal of Family and Reproductive Health, 2023
Objective: In Raynaud's phenomenon of the nipple there is a change in color, accompanied by pain or discomfort during breastfeeding. Case report: A 29-years old female patient, breastfeeding, develops a severe bilateral nipple pain during and after ...
Carolina Quental, Daniel Bertoluci Brito, João Mendes Sobral, Ana Mafalda Macedo   +3 more
doaj   +1 more source

Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. [PDF]

, 2010
The unparalleled collection of clinical data and biomaterials within the EHDN's REGISTRY can expedite the search for disease modifiers (genetic and environmental) of age at onset and disease progression that could be harnessed for the development of ...
Handley, Olivia J, Landwehrmeyer, G Bernhard, Aileen K Ho, Bisson, Jonathan Ian, Schwenke C, David Craufurd, Dunnett, Stephen B., Handley, Olivia, Investigators of the European Huntington's Disease Network, The, DI MARIA, EMILIO, Craufurd D, Dunnett, SB, Carsten Schwenke, the investigators of the European Huntington's Disease Network, Craufurd, David, Edward Wild, Landwehrmeyer, GB, Busse, Monica, Rosser, Anne Elizabeth, Olivia J Handley, Romano Silvia., Tabrizi SJ, Ho, Aileen K., Wild, E, Landwehrmeyer GB, Craufurd, D, Tabrizi, SJ, Tabrizi, Sarah J., Handley, OJ, Rickards, Hugh, Dunnett, Stephen, Ho, Aileen K, Orth, Michael, Ho, AK, Wild, Edward, Stephen B. Dunnett, Sarah J Tabrizi, Wild, EJ, Landwehrmeyer, G. Bernhard, Naji, Jenny, Landwehrmeyer, G. Bernhard, Wild E, Investigators of the European Huntington's Disease Network, Handley, Olivia J., Orth, M, Ellison-Rose, Lynda, Tabrizi, Sarah J, Price, Kathleen, Ho AK, ABBRUZZESE, GIOVANNI, Schwenke, C, Ho, A, Orth M, Handley OJ, Schwenke, Carsten, Dunnett SB, Dunnett, Stephen B, Michael Orth, G. Bernhard Landwehrmeyer   +59 more
core   +1 more source