Results 31 to 40 of about 8,722 (247)

A Qualitative Analysis of Patient Perspectives and Preferences in Lupus Management to Guide Lupus Guidelines Development

Arthritis Care &Research, EarlyView.
Objective A patient‐centered approach for chronic disease management, including systemic lupus erythematosus (SLE), aligns treatment with patients’ values and preferences, leading to improved outcomes. This paper summarizes how patient experiences, perspectives, and priorities informed the American College of Rheumatology (ACR) 2024 Lupus Nephritis (LN)
Shivani Garg, Izzy Hartel, Lisa R. Sammaritano, Anca Askanase, Bonnie L. Bermas, Maria Dall'Era, Alí Duarte‐García, Victoria P. Werth, Brad Rovin, Reem A. Mustafa, Amy S. Turner, Bené Williams, Brian L. Ung, Hiya Bhavsar, Monique C. Gore‐Massy, Nahirannette Pulido, Natacha Guerrero, Natalie M. Smith, Wambui Machua, Linda T. Hiraki, Mary Beth Son   +20 more
wiley   +1 more source

Alport Syndrome is a Partial Tubulointerstitial Disease of the Kidney

Kidney International Reports
Introduction: Recent genetic studies have shown that Alport syndrome (AS) is much more prevalent than clinically recognized, suggesting that atypical cases may phenocopy other kidney diseases.
Lisa Loderbauer, Karl X. Knaup, Daniel Reisenbüchler, Nicolas Kaiser, Stephanie Naas, Karen Schneider, Florian J. Wopperer, Antje Wiesener, Francesca Pasutto, Mario Schiffer, Christoph Daniel, Katharina A.E. Broeker, Dorit Merhof, Maike Buettner-Herold, Michael S. Wiesener   +14 more
doaj   +1 more source

Systemic lupus erythematosus with various clinical manifestations in a patient with hereditary angioedema: a case report

Allergy, Asthma & Clinical Immunology, 2022
Background Hereditary angioedema (HAE) is an inherited disease characterized by recurrent angioedema without urticaria or pruritus. The most common types of HAE are caused by deficiency or dysfunction in C1 esterase inhibitor (C1-INH-HAE).
Yusuke Ushio, Risa Wakiya, Tomohiro Kameda, Shusaku Nakashima, Hiromi Shimada, Mai Mahmoud Fahmy Mansour, Mikiya Kato, Taichi Miyagi, Koichi Sugihara, Rina Mino, Mao Mizusaki, Emi Ibuki, Norimitsu Kadowaki, Hiroaki Dobashi   +13 more
doaj   +1 more source

HEREDITARY FAMILIAL NEPHRITIS

Nihon Naika Gakkai Zasshi, 1972
HASHIMOTO, Yasuo, MORI, Mayumi, KANAZAWA, Ichiro, ISHIKAWA, Tadashi, TANAKA, Toshiyuki, DOFUKU, Ryuichi, KINUGASA, Keiji, SUGANO, Haruo, TAKUMA, Takehide   +8 more
openaire   +3 more sources

Addressing Economic Insecurities Can Improve Patient‐Reported Outcomes in Lupus

Arthritis Care &Research, EarlyView.
Objective Economic insecurities, such as food, housing, transportation, and financial challenges, are modifiable risk factors and influence patient‐reported outcomes (PROs) in systemic lupus erythematosus (SLE). We examined the following: (1) associations between economic insecurities and PROs, and (2) the impact of screening and addressing economic ...
Jay Patel, Tripti Singh, Meredith Ingersoll, Shelby Gomez, Amanda Weber, Sarah E. Panzer, Sancia Ferguson, Christie M. Bartels, Shivani Garg   +8 more
wiley   +1 more source

Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis

, 1982
Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis. The finding of a characteristic ultrastructural lesion in the glomerular basement membranes (GBM) of patients with hereditary nephritis prompted us to study and ...
Stone, William J., Johnson, H. Keith, Wilson, Curtis B., McCoy, Ralph C.   +3 more
core   +1 more source

Rheumatologic Manifestations of Patients With Type B Insulin Resistance

Arthritis Care &Research, EarlyView.
Objective The objectives of this study were to identify laboratory and clinical features associated with type B insulin resistance (TBIR), a rare condition caused by autoantibodies that inhibit the insulin receptor, most frequently occurring in the setting of systemic lupus erythematosus (SLE), and to increase awareness of this rare, life‐threatening ...
S. Amara Ogbonnaya, Sandra G. Williams, Raphael A. Kirou, Marissa Lightbourne, Rebecca J. Brown   +4 more
wiley   +1 more source

Immunohistochemical study of α1-5 chains of type IV collagen in hereditary nephritis

, 1994
Immunohistochemical study of α1-5 chains of type IV collagen in hereditary nephritis. The distribution of α1-5 chains of type IV collagen [α1-5(IV)] in the glomerular basement membrane (GBM) and epidermal basement membrane (EBM) of 23 families with ...
Yoshikawa, Norishige, Kagawa, Megumi, Yoshioka, Kazuo, Nakanishi, Koichi, Kitagawa, Kosaku, Sado, Yoshikazu, Ito, Hiroshi, Nakamura, Hajime, Iijima, Kazumoto   +8 more
core   +1 more source

Clinical Significance of Therapeutic Drug Level Monitoring for Mycophenolate in Patients With Extrarenal Systemic Lupus Erythematosus—A Systematic Review and Meta‐Analysis

Arthritis Care &Research, EarlyView.
Objective Clinical response to mycophenolic acid (MPA) is highly heterogeneous; thus, therapeutic drug level monitoring (TDM) may help improve treatment efficacy. This systematic review and meta‐analysis examined therapeutic ranges for MPA levels associated with better outcomes and safety in patients with systemic lupus erythematosus (SLE ...
Zahraa Qamhieh, Dalia Sriwi, Callie Saric, Tripti Singh, Christie M. Bartels, Shivani Garg   +5 more
wiley   +1 more source

Phacolytic uveitis associated with spontaneous rupture of anterior capsule in a patient with Alport syndrome

Iatreia, 2019
Alport syndrome is a rare genetic disorder due to mutations involving the coding genes for type IV collagen characterized by renal failure, sensorineural hearing loss and ocular abnormalities.
López Torres, Vanessa, Ramírez-Cheyne, Julián Andrés , Lozano Cruz, Edgar, Salamanca Libreros, Omar Fernando   +3 more
doaj   +1 more source