Results 111 to 120 of about 56,795 (260)
Autoantibody in the Systemic Sclerosis (SS) [PDF]
Systemic Sclerosis (SS) is a chronic idiopathic inflammatory disease whose main hint towards autoimmunity is given by the presence of high serum levels of autoantibodies in the majority of the patients.
Andrade, Luiz Eduardo Coelho +1 more
core +2 more sources
Gastrointestinal strictures in a pediatric patient with Satoyoshi syndrome
Abstract We present a novel case of gastrointestinal strictures in a young girl with Satoyoshi syndrome (SS), highlighting multi‐system features of alopecia universalis, painful muscle cramps with dystonia, aberrant growth velocity, and skeletal abnormalities.
Katherine (Tusia) Pohoreski +5 more
wiley +1 more source
Numerous autoantibodies are implicated in the pathogenesis of autoimmune epilepsy. In the past decade, many case series reported the association of glutamic acid decarboxylase 65 (GAD 65) antibodies with epilepsy.
Mohamed AlKhaja +3 more
doaj +1 more source
Perbandingan Hasil Pemeriksaan Antinuclear Antibodies Dengan Metode Imunofluoresens Dan Metode Elisa Pada Penderita Tersangka Systemic Lupus Erythematosus Di Rumah Sakit Dokter Hasan Sadikin Bandung [PDF]
Systemic lupus erythematosus (SLE) is characterized by the presence of anti-nuclear antibodies (ANAs). The identification of ANA has considerable importance in diagnosis and management of patients with autoimmune diseases.
Martioso, P. S. (Penny)
core
Abstract Childhood obesity is rising and leading to serious co‐morbidities, among which is metabolic dysfunction‐associated steatotic liver disease (MASLD) predisposing individuals to cirrhosis. We describe a young 11‐year‐old Hispanic male who presented with hepatopulmonary syndrome secondary to cirrhotic portal hypertension from metabolic dysfunction‐
Shruti Sakhuja +6 more
wiley +1 more source
Detection of Antinuclear Antibodies in HIV-Infected Individuals
Background: The causes of autoimmune diseases (ADs) are still not clearly known, but it is believed that diseases are propelled by multiple factors including genetic, hormone and environmental factors.
Kanyanee Promsawan +10 more
doaj
Abstract Wilson disease (WD) is an autosomal recessive disorder of hepatic copper metabolism with varied clinical presentations. We describe a 15‐year‐old male referred for elevated aminotransferases, burning facial pruritis, scalp dysesthesias, and chronic bilateral lower extremity edema.
Tierra L. R. Mosher +2 more
wiley +1 more source
Se detectó la presencia de anticuerpos antinucleares mediante un método de inmunofluorescencia indirecta en uno de los 18 pacientes estudiados con anemia hemolítica autoinmune y en 3 de los 16 pacientes con púrpura trombocitopénica autoinmune.
Ana M Guerreiro Hernández +6 more
doaj
Long‐Term Dermoscopic Evolution of Reticular Erythematous Mucinosis: Case Report
ABSTRACT Reticular erythematous mucinosis is a rare dermatosis with a challenging diagnosis. To date, its dermoscopic features have not been well characterised in the literature. Only a limited number of case reports have described dermoscopic findings that may be indicative of the disorder, including the presence of dotted and linear vessels, as well ...
Grażyna Kamińska‐Winciorek +4 more
wiley +1 more source

