Results 131 to 140 of about 15,911 (308)

Stability of Organic Photovoltaics: From Root Causes to Advanced Analytical Techniques

Advanced Energy Materials, EarlyView.
This review explains the causes and mechanisms of degradation in organic photovoltaics (OPVs). It explores how various factors, including heat, light, oxygen, and inherent material properties, influence OPV stability. The study categorizes degradation pathways and analyzes their impact on device performance, providing insights into the fundamental ...
Yelim Choi, Dohyun Kim, Seung Un Ryu, Hangyeol Kim, Sungryong Kim, Minjun Kim, Taiho Park   +6 more
wiley   +1 more source

Autoimmune myelofibrosis revealing a systemic lupus erythematosus

European Journal of Case Reports in Internal Medicine
Background: Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease, characterised by multi-organ affections. Haematological involvement is a common manifestation of SLE, consisting of autoimmune peripheral cytopenia.
Fatimaezzahra Bensalek, Hajar Joulal, Jaouad Yousfi, Mouna Zahlane, Leila Benjilali, Lamiaa Essaadouni   +5 more
doaj   +1 more source

Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome

, 2004
G H S Ashton, W.H. Irwin McLean, Andrew P. South, Noritaka Oyama, Frances J.D. Smith, Raouf Al-Suwaid, Abla Al Ismaily, David J. Atherton, Catherine Harwood, Irene M. Leigh, Celia Moss, Biagio Didona, Giovanna Zambruno, Annalisa Patrizi, Robin A.J. Eady, John A. McGrath   +15 more
openalex   +1 more source

Sound‐Based Assembly of Magnetically Actuated Soft Robots Toward Enhanced Release of Extracellular Vesicles

Advanced Intelligent Systems, Volume 7, Issue 3, March 2025.
Magnetic soft robots offer promise in biomedicine due to their wireless actuation and rapid response, but current fabrication methods are complex and have limited cellular compatibility. A new, contactless bioassembly strategy using hydrodynamic instabilities is introduced, enabling customizable, centimeter‐scale robots.
Wei Gao, Riccardo Tognato, Micaela Natta, Elena Della Bella, Alessandro Cianciosi, Tiziano Serra   +5 more
wiley   +1 more source

Photodistributed toxic epidermal necrolysis in association with lamotrigine and tanning bed exposure

JAAD Case Reports, 2021
Kristen Russomanno, MD, Ashley DiLorenzo, MD, Joshua Horeczko, BA, Min Deng, MD, Michael Cardis, MD, Vesna Petronic-Rosic, MD, MSc, MBA, Laura S. Johnson, MD, Helena B. Pasieka, MD, MS   +7 more
doaj  

How should we diagnose and manage photosensitivity? [PDF]

, 2014
Ibbotson, S.
core   +1 more source

Mycosis Fungoides, Sézary Syndrome, and Cutaneous B‐Cell Lymphomas: 2025 Update on Diagnosis, Risk‐Stratification, and Management

American Journal of Hematology, EarlyView.
ABSTRACT Disease Overview Primary cutaneous lymphomas are a rare and heterogeneous group of extranodal lymphomas that require the integration of clinical and histopathologic data for classification and treatment. Diagnosis Diagnosis and disease classification is based on histopathologic review and immunohistochemical staining of an appropriate skin ...
Alexandra C. Hristov, Trilokraj Tejasvi, Ryan A. Wilcox   +2 more
wiley   +1 more source

Two Genetic Effects at the IRF5/ TNPO3 Locus are Independently Associated with the Development of Specific Lupus Symptoms [PDF]

, 2013
Systemic Lupus Erythematosus (SLE) is an autoimmune disorder that can affect every tissue in the body. Single nucleotide polymorphisms (SNPs) in the IRF5 and TNPO3 genes are statistically associated with the development of SLE.
Hawtrey, Samantha
core   +1 more source

Genome‐Wide Insights and Polygenic Risk Scores in Common Epilepsies: A Narrative Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT The research of single gene‐related disorders or pathogenic copy‐number variations (CNVs) has given a significant impetus to the shift from a diagnostic work‐up focused on epileptic syndromes to genomic approaches in individuals with severe pediatric‐onset epilepsies and in developmental and epileptic encephalopathies.
Mario Mastrangelo, Simona Petrucci, Giuliana Lentini, Marco Fabiani, Maria Piane, Francesco Pisani   +5 more
wiley   +1 more source

Síndrome ADULT: descrição clínica de cinco membros da mesma família, aspectos histológicos e investigação de mutação genética no p63 [PDF]

, 2012
A ADULT (acro-dermato-ungueal-lacrimal-tooth) é uma síndrome genética humana que se manifesta clinicamente por alterações cutâneas e do desenvolvimento dos apêndices embrionários.
Caspary, Patrícia
core