نتایج جستجو برای: hepatic amyloidosis

تعداد نتایج: 104741  

Journal: :Circulation-cardiovascular Imaging 2021

Background: Systemic amyloidosis is characterized by amyloid deposition that can involve virtually any organ. Splenic and hepatic occurs in certain types, some patients but not others, may influence prognosis treatment. SAP (serum P component) scintigraphy uniquely able to identify quantify the liver spleen, thus informing clinical management, it only available 2 centers globally. The aims of t...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2002
Cécile Vigneau Jean-Philippe Haymann Noujoud Khoury Jean-Daniel Sraer Eric Rondeau

A 33-year-old black male, was referred to our department in 1981 for the following symptoms consistent with typical SCLS: several episodes of shock with generalized oedema; diffuse pain; and transient anuria. A monoclonal gammapathy of undetermined significance (MGUS) was discovered at that time. Three years later, he had minimal proteinuria (monoclonal component). Femoral artery superficializa...

Journal: :International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association 1967
N Carvalho M P Azevedo A C Marques

Relatively little interes t is evident in the study of visceral manifes tations of leprosy, in spi te of their clinical importance ( 1), The liver might be expected to be the organ most freguently affected; it is responsible for plasma protein alterations, e.g. , effective albumin reduction and globulin increase, Histologic reports show that hepatic lesions in lepromatous leprosy are characteri...

Journal: :Military Medical and Pharmaceutical Journal of Serbia 2009

2015
Cassandra Chaptini Genevieve Casey Adam G. Harris Dedee F. Murrell Lynne Gordon

Fig 1. Squamous cell carcinoma identified after multiple biopsy specimens of poorly healing area over left E pidermolysis bullosa (EB) consists of a heterogeneous group of autosomal dominant or recessive disorders, characterized by epithelial fragility. In dystrophic EB, patients have a genetic defect in the gene encoding collagen VII, COL7A1. Generalized severe recessive dystrophic EB (RDEB) i...

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