Results 121 to 130 of about 68,298 (256)

Amoxicillin-Induced Hypersensitivity Versus Viral Exanthem in Epstein-Barr Virus Infection: A Paediatric Case Series. [PDF]

Cureus
Viegas M, Mendes J, Lemos S, Maia E, Rubino G.   +4 more
europepmc   +1 more source

Case Report of a Dermatologic Reaction to Wound Closure Strips and Liquid Adhesive. [PDF]

J Educ Teach Emerg Med
Asghar A, Smith T, Underwood M, Kim TY.
europepmc   +1 more source

Epigenetic mechanisms and therapeutic innovations in chronic pain‐associated neuropsychiatric co‐morbidities

British Journal of Pharmacology, EarlyView.
Abstract Chronic pain, marked by nociceptive sensitization and maladaptive neuroplasticity, affects 30% of the global population with escalating socioeconomic burdens. Epidemiological data show a 2‐3‐fold increase in neuropsychiatric co‐morbidities among individuals with chronic pain, where epigenetic dysregulation serves as a key mechanism linking ...
Kai Zhang, Sijia Zhu, Na Xing, Zhen Zhou, Jiayi Chen, Tianen Si, Mingrui Li, Lin Jia, Yousef Rastegar‐Kashkooli, Tom J. Wang, Wei Zhu, Jing Li, Chao Jiang, Junmin Wang, Moxin Wu, Xiaoping Yin, Weidong Zang, Jian Wang, Songxue Su   +18 more
wiley   +1 more source

Hyaluronidase Use in Aesthetic Medicine: Formulations, Safety, and Clinical Practice. [PDF]

J Clin Med
Arrigoni F, Belletti S, Caboni S, Cavallini M, Cordovana A, Lazzari R, Papagni MF.   +6 more
europepmc   +1 more source

Case Report: Late Hypersensitivity Reaction to Hydroxyurea in a Patient With Myeloproliferative Disorder. [PDF]

Case Rep Hematol
Kahlon N, Baddam S, Kaur H, Singh P, Qureshi Z, Gowda AM.   +5 more
europepmc   +1 more source

Expansion of the Phenotypic and Genotypic Spectrum for PRKAR1B‐Related Marbach–Schaaf Neurodevelopmental Syndrome: A Case Series

Clinical Genetics, EarlyView.
Comprehensive clinical description of 12 subjects with pathogenic PRKAR1B variants, including two heterozygous deletions supporting haploinsufficiency as a possible mechanism of disease, providing valuable insight into the pathophysiology of MASNS and setting a framework upon which to design future mechanistic studies of PKA signaling in brain ...
Sebastian Burkart, Tarik Guzeloglu, Ana R. Soares, Irene Valenzuela, Eduardo F. Tizzano, David Gómez‐Andres, Laurent Pasquier, Marine Legendre, Camille Berges, Julien Thevenon, Marjolaine Gauthier, Caleb Heid, Elly Ranum, Joseph Shen, Michelle Frees, Michael W. Schmidtke, Caro Pilar, Christian P. Schaaf   +17 more
wiley   +1 more source

Case Report: Management of a delayed type III hypersensitivity reaction with acute kidney injury in a dog after administration of human serum albumin with immunoadsorption. [PDF]

Front Vet Sci
Sänger F, Nagel F, Herges S, Weber K, Dörfelt R.   +4 more
europepmc   +1 more source

Unusual Disease‐Progression in Two Siblings With Xeroderma Pigmentosum Group G

Clinical Genetics, EarlyView.
Protein truncation mutations in the gene for XPG nuclease cause a very severe clinical phenotype. Two siblings have splicing mutations, which result in in‐frame deletions and a less severe phenotype.
Elena Botta, Heather Fawcett, Donata Orioli, Hiva Fassihi, Alan R. Lehmann   +4 more
wiley   +1 more source

Hypersensitivity Reactions Associated With Aesthetic Botulinum Toxin A Injections: A Case Series. [PDF]

Cureus
Buchholz E, Wanitphakdeedecha R, Jaturawichanant S, Pattanapran K, Corduff N.   +4 more
europepmc   +1 more source

Genetic Insights Into Allergic Contact Dermatitis: Reassessing the Role of LCE3C_LCE3B Deletion

Contact Dermatitis, EarlyView.
This study found no significant association between the LCE3C_LCE3B deletion and allergic contact dermatitis or polysensitisation in Tunisian patients, suggesting that other genetic or environmental factors may contribute to disease susceptibility. ABSTRACT Background Allergic contact dermatitis (ACD) is a multifactorial inflammatory skin disorder ...
Zeineb Ben Lamine, Amen Moussa, Marwa Bouhoula, Razene Gerisha, Sarra Sabbagh, Imen Kacem, Asma Aloui, Souheil Chatti, Aicha Brahem, Ramzi Zemni, Foued Ben Hadj Slama   +10 more
wiley   +1 more source