Results 81 to 90 of about 1,275,517 (295)

Sarcoidosis revealed by recurrent dactylitis.

Arthritis &Rheumatology, Accepted Article.
Thomas Subervie, Thibault Willaume, Amin Maazouzi, Jacques‐Eric Gottenberg, Jean Sibilia, Noëlle Weingertner, Eden Sebbag, Marc Scherlinger   +7 more
wiley   +1 more source

Clinical progress note: Rubella

Journal of Hospital Medicine, EarlyView.
Abstract Rates of rubella infection and congenital rubella syndrome decreased significantly since the introduction of the rubella vaccine in 1969. Endemic rubella was declared eliminated in the United States in 2004, and since 2012, all rubella cases in the United States have been associated with infections acquired abroad.
Adam E. Gailani, Walter Dehority, Sophie E. Katz   +2 more
wiley   +1 more source

Interleukin (IL)‐5, Eosinophils and IL‐5 Pathway Inhibitors in Eosinophilic Granulomatosis with Polyangiitis.

Arthritis &Rheumatology, Accepted Article.
Alvise Berti, Christian Pagnoux
wiley   +1 more source

Specific phenotypes may drive an increased incidence of pediatric inflammatory bowel disease in South‐Eastern Norway

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Pediatric inflammatory bowel disease (PIBD) incidence has increased in recent decades but may be stabilizing, prompting exploration of incidence changes, disease distribution, and severity. Methods From 2017 to 2019, patients under 18 years with PIBD symptoms were recruited from nine hospitals in South‐Eastern Norway for ...
Svend Andersen, Tomm Bernklev, Ketil Størdal, Milada C. Hagen, Vendel A. Kristensen, Randi Opheim, Christine Olbjørn, Jon Rove, Emma E. Løvlund, Hans K. Holm, Batool Aballi, Marte L. Høivik, Gøri Perminow   +12 more
wiley   +1 more source

Chronic Granulomatous Disease with Disseminated Trichosporonosis : A Case Report

Siriraj Medical Journal, 2020
A case of a two year and three month old Thai boy with a history of recurrent bacterial infections since aged 2 months. A definite absence of superoxide activity in the patient' s granulocytes detected by nitroblue tetrazolium test indicated the ...
Samonmars Kanngurn, Paisal Parichatikanond, Visanu Pootong, Pakit Vichyanond   +3 more
doaj  

Papulopustular Dermatitis in X-Linked Chronic Granulomatous Disease

Frontiers in Pediatrics, 2019
Here we describe two term male infants diagnosed with X-linked CGD who present, in addition to frequent infection, with a unique papulopustular skin rash. CGD is caused by a number of genetic defects that impair phagocyte function.
Puja Sood Rajani, Maria A. Slack
doaj   +1 more source

Cow's milk protein allergy with protein‐losing enteropathy under the scope

JPGN Reports, EarlyView.
ABSTRACT Objectives Cow's milk protein allergy (CMPA) is very frequent in infants. Presentation is variable, and symptoms fluctuate in intensity. Diagnosis can be challenging as it is mostly clinical. In severe cases, patients can present with anasarca secondary to protein‐losing enteropathy (PLE).
Morgane Thorens‐Borgeat, Géraldine Blanchard‐Rohner, Salim Ramadan, Jean‐Christophe Caubet, Laetitia‐Marie Petit, Valerie McLin, Anne‐Laure Rougemont   +6 more
wiley   +1 more source

A Case Diagnosed with Chronic Granulomatous Disease Presenting with Dactylitis

Bagcilar Medical Bulletin
Chronic granulomatous disease is a rare primary immunodeficiency seen in 1/70,000-1/200,000 births. It is a monogenetic disease caused by defects in the nicotinamideadenine-dinucleotide-phosphate oxidase enzyme complex.
Selami Ulaş, Işılay Turan, Mehmet Halil Çeliksoy, Gözde Kurşun, Sezin Naiboğlu, Çiğdem Aydoğmuş   +5 more
doaj   +1 more source

Interleukin-4 Receptor Alpha Expressing B Cells Are Essential to Down-Modulate Host Granulomatous Inflammation During Schistosomasis

Frontiers in Immunology, 2018
Schistosomiasis (bilharzia) is a parasitic helminth disease that can cause severe inflammatory pathology leading to organ damage in humans. Failure of the host to regulate egg-driven granulomatous inflammation causes host morbidity during chronic ...
Hlumani Ndlovu, Hlumani Ndlovu, Hlumani Ndlovu, Hlumani Ndlovu, Justin Komguep Nono, Justin Komguep Nono, Justin Komguep Nono, Justin Komguep Nono, Nada Abdel Aziz, Nada Abdel Aziz, Nada Abdel Aziz, Nada Abdel Aziz, Natalie Eva Nieuwenhuizen, Natalie Eva Nieuwenhuizen, Natalie Eva Nieuwenhuizen, Frank Brombacher, Frank Brombacher, Frank Brombacher   +17 more
doaj   +1 more source

Digestive autoimmune diseases mimicking gastrointestinal manifestations in children with sickle cell anemia: A report of three cases

JPGN Reports, EarlyView.
ABSTRACT Sickle cell anemia (SCA) is a genetic disorder that presents with a variety of systemic complications, including gastrointestinal (GI) manifestations. These GI symptoms can overlap with those of digestive autoimmune diseases (DAD) such as inflammatory bowel disease (IBD) and autoimmune hepatitis (AIH), complicating the diagnosis and management.
Saray Mesonero Cavia, Marta García Bernal, Maria Jose López Liñan, Roger García Puig   +3 more
wiley   +1 more source