Results 281 to 290 of about 298,517 (337)

Characterization of COVID‐19‐Associated Candidemia Among Burn Patients

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
This study investigates the distribution of Candida species isolated from burn patients with candidemia, colonization, and urinary cultures. The findings highlight the predominance of C. albicans and C. parapsilosis across different sample types, including wound colonization, blood, and urine.
Maryam Salimi   +12 more
wiley   +1 more source

Use of Dynamic Contrast‐Enhanced Magnetic Resonance Imaging Combined With Serum Carcinoembryonic Antigen and Carbohydrate Antigen 19‐9 in Predicting Colorectal Cancer Liver Metastasis

open access: yesJournal of Clinical Ultrasound, EarlyView.
The study subjects were mainly CRC patients (n = 120), all of whom underwent the same comprehensive treatment regimen and were divided into the effective treatment group (n = 86) and the ineffective treatment group (n = 34) according to efficacy after treatment.
Hong‐Bo Ji   +4 more
wiley   +1 more source

Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years. [PDF]

open access: yesGenes (Basel)
Kimizu T   +16 more
europepmc   +1 more source
Some of the next articles are maybe not open access.

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Primary Immunodeficiency and Thrombocytopenia

International Reviews of Immunology, 2021
Primary immunodeficiency (PID) or Inborn errors of immunity (IEI) refers to a heterogeneous group of disorders characterized by immune system impairment. Although patients with IEI manifest highly variable symptoms, the most common clinical manifestations are recurrent infections, autoimmunity and malignancies.
Maryam Mohtashami   +6 more
openaire   +3 more sources

The Primary Immunodeficiencies

New England Journal of Medicine, 1984
The primary immunodeficiency disorders reflect abnormalities in the development and maturation of cells of the immune system. These defects result in an increased susceptibility to infection; recurrent pyogenic infections occur with defects of humoral immunity, and opportunistic infections with defects of cell-mediated immunity.
Ralph J. Wedgwood   +2 more
openaire   +3 more sources

Primary Immunodeficiencies

Journal of Allergy and Clinical Immunology, 2010
In the last years, advances in molecular genetics and immunology have resulted in the identification of a growing number of genes causing primary immunodeficiencies (PIDs) in human subjects and a better understanding of the pathophysiology of these disorders.
openaire   +6 more sources

Primary Immunodeficiency and Rhinosinusitis

Immunology and Allergy Clinics of North America, 2020
Refractory rhinosinusitis can be related to comorbid medical conditions, including primary immunodeficiency. Given the prevalence of immunodeficiency, clinicians should have a low threshold to consider these diagnoses. This article reviews primary immunodeficiencies contributing to chronic rhinosinusitis, including a proposed diagnostic work-up and the
Camille Huwyler   +2 more
openaire   +3 more sources

Cytomegalovirus in primary immunodeficiency

Current Opinion in Infectious Diseases, 2021
Purpose of review Cytomegalovirus (CMV) infection and disease are well described in the setting of secondary immunodeficiency. Less is known about CMV in the context of primary immunodeficiencies (PIDs), where inborn errors in one or more arms of the immune system result in variable degrees of CMV susceptibility.
Charlotte Slade   +6 more
openaire   +2 more sources

Primary Immunodeficiency and the Gut

Gastroenterology Clinics of North America, 2019
This article presents the most common gastrointestinal, hepatic, and pancreatic manifestations of the primary immunodeficiency diseases, including the appropriate laboratory testing, endoscopic evaluation, and recommendations for further management.
David Schwimmer, Sarah C. Glover
openaire   +3 more sources

Classification of Primary Immunodeficiencies

New England Journal of Medicine, 1973
Primary specific immunodeficiency results from failure to manifest an efficient humoral or cellular immune response.
Henry G. Kunkel   +9 more
openaire   +3 more sources

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