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Pubblicazioni

AMYLOID

Rivista

Codice:

E008357

ISSN:

1350-6129

Dati Generali

Dati Generali

Pubblicazioni (67)

Ordina Pubblicazioni:

ascendente
decrescente

A multicenter phase II trial of 4'-iodo-4'deoxydoxorubicin in primary amyloidosis (AL)

Articolo

A workflow management system for the biological samples exchange within the amyloidosis network

Articolo

A workflow management system for the biological samples exchange within the amyloidosis network

Contributo in Atti di convegno

AA amyloidosis in inflammatory active malignant paraganglioma

Articolo

AMICA: an electronic patient record specifically designed for an amyloidosis network

Contributo in Atti di convegno

AMICA: an electronic patient record specifically designed for an amyloidosis network.

Articolo

ATTRv amyloidosis Italian Registry: clinical and epidemiological data

Articolo

Abnormalities in thrombin-antithrombin pathway in AL amyloidosis.

Articolo

Abnormalities in thrombin-antithrombin pathway in primary systemic amyloidosis.

Articolo

Amyloid fibril protein nomenclature: 2010 recommendations from the nomenclature committee of the International Society of Amyloidosis.

Articolo

Amyloid fibril protein nomenclature: 2012 recommendations from the Nomenclature Committee of the International Society of Amyloidosis

Articolo

Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis

Articolo

Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee

Articolo

Amyloid nomenclature 2020: update and recommendations by the International Society of Amyloidosis (ISA) nomenclature committee

Articolo

Amyloid persistence in decellularized liver: Biochemical and histopathological characterization

Articolo

An Asp to Asn mutation is a toxic trigger in beta-2 microglobulin: structure and biophysics

Articolo

Antiamyloidogenic and proamyloidogenic chaperone effects of C-reactive protein and serum amyloid P component

Articolo

As we cannot afford to renounce to new generation echocardiography in systemic amyloidosis

Articolo

Attitudes about when and how to treat patients with AL amyloidosis: an international survey

Articolo

Benefit of doxycycline treatment on articular disability caused by dialysis related amyloidosis

Articolo

Bioelectrical impedance vector analysis-derived phase angle predicts survival in patients with systemic immunoglobulin light-chain amyloidosis

Articolo

Cardiac light-chain deposition disease relapsing in the transplanted heart

Articolo

Changes in tissue proteome associated with ATTR amyloidosis: Insights into pathogenesis

Articolo

Clarification on the definition of complete haematologic response in light-chain (AL) amyloidosis

Articolo

Clinical, radiological, and biochemical features of a bilateral buttock amyloidoma emerging after 27 years of hemodialysis

Articolo

Clinical, radiological, and biochemical features of a bilateral buttock amyloidoma emerging after 27 years of hemodialysis.

Articolo

Diagnostic performance of amyloid A protein quantification in fat tissue of patients with clinical AA amyloidosis.

Articolo

Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study

Articolo

Electron and immuno-electron microscopy of abdominal fat identifies and characterizes amyloid fibrils in suspected cardiac amyloidosis

Articolo

Embryonic stem and haematopoietic progenitor cells resist to Abeta oligomer toxicity and maintain the differentiation potency in culture

Articolo

Enhanced toxicity of silver nanoparticles in transgenic Caenorhabditis elegans expressing amyloidogenic proteins

Articolo

Extended characterization of the novel co-isogenic C57BL/6J Prnp−/− mouse line

Articolo

Functional correlates of N-terminal natriuretic peptide type B (NT-proBNP) response to therapy in cardiac light chain (AL) amyloidosis

Articolo

Gender-related risk of myocardial involvement in systemic amyloidosis.

Articolo

Guidelines for high dose chemotherapy and stem cell transplantation for systemic AL amyloidosis: EHA-ISA working group guidelines

Articolo

High Tc-99m-DPD myocardial uptake in a patient with apolipoprotein AI-related amyloidotic cardiomyopathy

Articolo

Identification and quantification of urinary monoclonal proteins by capillary electrophoresis in AL amyloidosis

Articolo

In search of the most effective therapy for light chain amyloidosis

Articolo

Introducing the new editor of amyloid: the journal of protein folding disorders, Per Westermark, M.D., Ph.D.

Articolo

Light and electron microscopy immunohistochemical characterization of amyloid deposits

Articolo

Liver involvement as the hallmark of aggressive disease in light chain amyloidosis: distinctive clinical features and role of light chain type in 225 patients

Articolo

Localized oral amyloidosis of the palate

Articolo

Lysozyme amyloid: evidence for the W64R variant by proteomics in the absence of the wild type protein

Articolo

Mass spectrometry-based proteomics as a diagnostic tool when immunoelectron microscopy fails in typing amyloid deposits

Articolo

Midregional proadrenomedullin (MR-proADM) is a powerful predictor of early death in AL amyloidosis

Articolo

Misidentification of transthyretin and immunoglobulin variants by proteomics due to methyl lysine formation in formalin-fixed paraffin-embedded amyloid tissue

Articolo

Modulating the cardiotoxic behaviour of immunoglobulin light chain dimers through point mutations

Articolo

Multicenter versus single center approach to rare diseases: the model of systemic light chain amyloidosis

Articolo

Oxidative conversion of transthyretin in formalin-fixed clinical amyloid samples results in the formation of the His90Asp and His90Asn variants

Articolo

Patients with AL amyloidosis and low free light-chain burden have distinct clinical features and outcome

Articolo

Patterns of relapse after upfront bortezomib therapy in AL amyloidosis

Articolo

Plasma neurofilament light chain: an early biomarker for hereditary ATTR amyloid polyneuropathy

Articolo

Pomalidomide and dexamethasone grant rapid haematologic responses in patients with relapsed and refractory AL amyloidosis: a European retrospective series of 153 patients

Articolo

Prognostication of survival and progression to dialysis in AA amyloidosis

Articolo

Proteomic characterization of amyloid deposits in transthyretin amyloidosis associated with various mutations

Articolo

Regulated expression of amyloidogenic immunoglobulin light chains in mice

Articolo

Response to bendamustine is associated with a survival advantage in a heavily pretreated patients with AL amyloidosis

Articolo

Severity and reversibility of cardiac dysfunction and residual concentration of amyloidogenic light chain predict overall survival of patients with AL amyloidosis who attain complete response

Articolo

Structure, function and amyloidogenic propensity of apolipoprotein A-I.

Articolo

Systemic AA amyloidosis as a unique manifestation of a combined mutation of TNFRSF1A and MEFV genes

Articolo

The Diflunisal Trial: Study accrual and drug tolerance

Articolo

The concurrency of several biophysical traits links immunoglobulin light chains with toxicity in AL amyloidosis

Articolo

The role of minor salivary gland biopsy in the diagnosis of systemic amyloidosis: results of a prospective study in 62 patients

Articolo

Tissue biopsy for the diagnosis of amyloidosis: experience from some centres

Articolo

Transthyretin deposition in the eye in the era of effective therapy for hereditary ATTRV30M amyloidosis

Articolo

Urinary albumin to creatinine ratio in diagnosis and risk stratification of renal AL amyloidosis

Articolo

Vascular alterations in apolipoprotein A-I amyloidosis (Leu75Pro). A case-control study

Articolo

No Results Found

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