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Molecular diagnosis of toxoplasmosis
Transactions of the Royal Society of Tropical Medicine and Hygiene, 2002Toxoplasmosis is an anthropozoonotic disease endemic world-wide, caused by the apicomplexan Toxoplasma gondii. Although the course of infection is generally benign, it can cause significant morbidity and mortality in the developing fetus and in immunocompromised individuals.
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Molecular diagnosis in allergy
Clinical & Experimental Allergy, 2010SummaryDevelopment and progress made in the field of recombinant allergens have allowed for the development of a new concept in allergy diagnosis, molecular diagnosis (MD), which makes it possible to identify potential disease‐eliciting molecules. Microarray‐based testing performed with a small amount of serum sample enables clinicians to determine ...
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[Molecular diagnosis of ADPKD].
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 2016Most patients with ADPKD do not need molecular genetic testing. When indicated, Sanger sequencing is the most commonly used technique. When a pathogenic mutation is not identified by Sanger, multiplex ligation-dependent probe amplification analysis (MLPA) should be performed to detect gene rearrangement (insertion or deletion).
SCOLARI, Francesco +3 more
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Serological and Molecular Diagnosis
Seminars in Liver Disease, 2006The development of serological assays to detect hepatitis B surface antigen (HBsAg) has played a major role in the diagnosis of hepatitis B virus (HBV) infection. With other hepatitis B serological assays, a diagnosis of acute or chronic HBV infection, past infection, or successful vaccination can be determined.
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Molecular diagnosis of tuberculosis.
The European respiratory journal. Supplement, 1995Rapid and sensitive tools for the diagnosis of tuberculosis are needed, due to the increased incidence of tuberculosis epidemics and the length of time required by classical diagnostic tests, especially among human immunodeficiency virus (HIV)-infected patients. In this context, the recent advances in cloning and characterization of M.
RICHELDI, Luca, BARNINI S, SALTINI C.
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Molecular Diagnosis of Genodermatoses
2012The progress of molecular genetics helps clinicians to prove or exclude a suspected diagnosis for a vast and yet increasing number of genodermatoses. This leads to precise genetic counselling, prenatal diagnosis and preimplantation genetic haplotyping for many inherited skin conditions.
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Health insurance status and cancer stage at diagnosis and survival in the United States
Ca-A Cancer Journal for Clinicians, 2022Jingxuan Zhao +2 more
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