Results 41 to 50 of about 1,167,883 (229)

Extensive abdominal wall ulceration as a late manifestation of antiphospholipid syndrome: a case report

Journal of Medical Case Reports, 2018
Background Antiphospholipid syndrome is an autoimmune disorder characterized by the presence of antiphospholipid antibodies and commonly presents with vascular thromboembolic phenomena, thrombocytopenia, and obstetric complications.
Yogesh Sharma, Karen Humphreys, Campbell Thompson   +2 more
doaj   +1 more source

Bilateral adrenal infarction and insufficiency associated with antiphospholipid syndrome and surgery: a case report

International Journal of Emergency Medicine, 2023
Background Antiphospholipid syndrome causes systemic arterial and venous thromboses due to the presence of antiphospholipid antibodies. Adrenal insufficiency is a rare complication of antiphospholipid syndrome that may result in fatal outcomes if left ...
Yoshihito Iijima, Masahito Ishikawa, Nozomu Motono, Hidetaka Uramoto   +3 more
doaj   +1 more source

Patients with Essential thrombocythaemia have an increased prevalence of antiphospholipid antibodies which may be associated with thrombosis [PDF]

, 2002
A significant proportion of patients with Essential Thrombocythaemia (ET) have thrombotic complications which have an important impact upon the quality, and duration of their life.
Machin, S.J., C.N. Harrison, P. Carr, Mackie, I., Donohoe, S., S.J. Machin, S. Donohoe, I. Mackie, M. Dave, Harrison, C.N., Dave, M., Carr, P.   +11 more
core   +1 more source

Building a Framework for Sexual and Reproductive Health Care in the Rheumatology Context: Content and Approaches

Arthritis Care &Research, EarlyView.
People with systemic autoimmune and rheumatic diseases (SARDs) are at higher risk than the general population of experiencing adverse pregnancy and perinatal outcomes such as preeclampsia, intrauterine growth restriction, and maternal and/or fetal death.
Mehret Birru Talabi, Sonya Borrero
wiley   +1 more source

Diagnosis of antiphospholipid syndrome in routine clinical practice. [PDF]

, 2013
The updated international consensus criteria for definite antiphospholipid syndrome (APS) are useful for scientific clinical studies. However, there remains a need for diagnostic criteria for routine clinical use.
Hills, J, Cohen, H, Gardiner, C, Machin, SJ   +3 more
core  

Development and validation of LUPIN: a patient-centred self-administered tool to assess disease activity and patient-reported outcomes in systemic lupus erythematosus

RMD Open
Objective To develop and validate LUPIN, a self-administered, patient-centred questionnaire codesigned by patients and lupus specialists to assess disease activity and patient-reported outcomes in systemic lupus erythematosus (SLE).Methods LUPIN and the ...
, Zahir Amoura, Thierry Martin, Anne-Sophie Korganow, Marianne Rivière, Xavier Mariette, Christophe Richez, Jacques-Eric Gottenberg, Laurent Perard, Patricia Senet, Denis Wahl, Jean Sibilia, Christian Agard, Marc André, Perrine Smets, François Chasset, Marc Scherlinger, Elisabeth Diot, Mickaël Martin, Gilles Blaison, Nadine Magy-Bertrand, Baptiste Hervier, Daniel Wendling, Jean-François Viallard, Arnaud Hot, Mathieu Puyade, Amélie Servettaz, Roland Jaussaud, Christophe Deligny, Audrey Gorse, Jean-François Kleinmann, Pauline Orquevaux, Pascal Roblot, Ludivine Lebourg, Estelle Jean, Thomas Moulinet, Loïc Raffray, Frederic Renou, Sarah Permal, Antonin Folliasson, Raphaëlle Rybak, Sabine Malivoir, Clara Baverez, Nicolas Baillet, Julien Campagne, Nicolas Girszyn, Cécile Fermont, Emmanuelle David, Benjamin Dervieux, Estibaliz Llazaro, Irène MACHELART, Julie Le Scanff, Ludovic Ttrefond, Ronan Pasquer   +53 more
doaj   +1 more source

A probable case of catastrophic antiphospholipid syndrome: Should high-dose steroids be given in the setting of polymicrobial sepsis?

SAGE Open Medical Case Reports, 2019
In this clinical vignette, we present a case of a 59-year-old woman with catastrophic antiphospholipid syndrome likely triggered by polymicrobial sepsis.
Shanna Ariane Tucker, Justin Choi, Dhruv Khullar   +2 more
doaj   +1 more source

What nephrolopathologists need to know about antiphospholipid syndrome-associated nephropathy: Is it time for formulating a classification for renal morphologic lesions? [PDF]

Journal of Nephropathology, 2014
Context: Antiphospholipid syndrome (APS) is a systemic autoimmune disorder which commonly affects kidneys. Evidence Acquisitions: Directory of Open Access Journals (DOAJ), Google Scholar, PubMed (NLM), LISTA (EBSCO) and Web of Science have been searched.
Muhammed Mubarak, Hamid Nasri
doaj   +1 more source

Mucocutaneous Disease Activity and Damage Accrual in Systemic Lupus Erythematosus: Analyses From the Asia‐Pacific Lupus Collaboration Longitudinal Cohort Study

Arthritis Care &Research, EarlyView.
Objective This research article aims to describe the prevalence, associations, and health‐related quality of life (HRQoL) impact of mucocutaneous features of systemic lupus erythematosus (SLE). Methods Data from the Asia‐Pacific Lupus Collaboration cohort were analyzed (2013–2021).
Amanda M. Saracino, Yanjie Hao, Dylan Hansen, Yi‐Hsing Chen, Alberta Hoi, Vera Golder, Jiacai Cho, Aisha Lateef, Worawit Louthrenoo, Laniyati Hamijoyo, Shue Fen Luo, Yeong‐Jian Jan Wu, Sandra Navarra, Leonid Zamora, Chak Sing Lau, Shirley Chan, Zhanguo Li, Hai‐hong Yao, Sargunan Sockalingam, B. M. D. B. Basnayake, Yasuhiro Katsumata, Masayoshi Harigai, Zhuoli Zhang, Jun Kikuchi, Yuko Kaneko, Tsutomu Takeuchi, Madelynn Chan, Sang‐Cheol Bae, Fiona Goldblatt, Sean O'Neill, Geraldine Hassett, Kristine Ng, Nicola Tugnet, Mark Sapsford, Yih Jia Poh, Michael Tee, Cherica Tee, Naoaki Ohkubo, Yoshiya Tanaka, Rangi Kandane‐Rathnayake, Eric Morand, Shereen Oon, Mandana Nikpour   +42 more
wiley   +1 more source

Oral surgery in patients with antiphospholipid syndrome [PDF]

, 2019
Antiphospholipid syndrome (APS) is a systemic autoimmune disorder characterized by recurrent thrombosis, other associated autoimmune disease, and/or obstetrical morbidity along with persistent production of antiphospholipid antibodies.
Okuyama, Kohei, Naruse, Tomofumi, Yutori, Hirokazu, Umeda, Masahiro, Yanamoto, Souichi   +4 more
core   +1 more source