• A clinical case of restrictive myocarditis due to senile-type amyloidosis
• A new transthyretin variant (Ser23Asn) associated with familial amyloidosis in a Portuguese patient
• A novel substitution of proline (P32L) destabilises beta2-microglobulin inducing hereditary systemic amyloidosis
• A novel substitution of proline (P32L) destabilises β2-microglobulin inducing hereditary systemic amyloidosis
• Advanced glycation end products (AGE) and the receptor for AGE are present in gastrointestinal tract of familial amyloidotic polyneuropathy patients but do not induce NF-kappaB activation
• Amyloid deposits inside myocardial fibers in transthyretin-Met30 familial amyloidotic polyneuropathy. A histological and biochemical study
• Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin)
• Amyloid in hereditary amyloid polyneuropathy is related to prealbumin
• Amyloid polyneuropathies--biochemical and genetic aspects
• Amyloidosis and the respiratory tract
• Amyloidosis of the vitreous body. Possibilities of diagnosis
• Anaesthetic management of a patient with familial amyloid polyneuropathy of the Portuguese type
• Apropos of a case of bilateral perforating corneal ulcer in a patient with Portugese amyloidosis
• Aqueous outflow system in familial amyloidotic polyneuropathy, Portuguese type
• Behind heart failure syndrome: remember AL amyloidosis. Two case-reports
• Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy
• Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant
• Birth of two healthy females after preimplantation genetic diagnosis for familial amyloid polyneuropathy
• Cardiac Amyloidosis and its New Clinical Phenotype: Heart Failure with Preserved Ejection Fraction
• Cardiovascular effects of familial amyloidotic polyneuropathy of the Portuguese type
• Cases with familiar amyloid neuropathy starting of the upper limbs and having hepatic disorder
• Cavity filling mutations at the thyroxine-binding site dramatically increase transthyretin stability and prevent its aggregation
• Clinical, Laboratory, and Imaging Profile in Patients with Systemic Amyloidosis in a Brazilian Cardiology Referral Center
• Comparison of lethal and nonlethal transthyretin variants and their relationship to amyloid disease
• Correlation between clinical, electromyographic and dysautonomic evolution of familial amyloidotic polyneuropathy of the Portuguese type
• Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence
• Detection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy
• Diagnosis of familial amyloid polyneuropathy type I in Argentina
• Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset
• Diagnostic Role of NT-proBNP in Patients with Cardiac Amyloidosis Involvement: A Meta-Analysis
• Diastolic dysfunction and left ventricular hypertrophy in familial amyloidotic polyneuropathy: a cause-effect relationship?
• Diffuse tracheo-bronchial amyloidosis
• Early detection of sympathetic myocardial denervation in patients with familial amyloid polyneuropathy type I
• Familial amyloid polyneuropathy type I (Portuguese): distribution and characterization of renal amyloid deposits
• Familial amyloid polyneuropathy. Demonstration of prealbumin in a kinship of German/English ancestry with onset in the seventh decade
• Familial amyloidosis with polyneuropathy type 1 caused by transthyretin mutation Val50Met (Val30Met): 4 cases in a non-endemic area
• Familial amyloidotic polyneuropathy --Portuguese type-- clinical and neurophysiologic course
• Familial amyloidotic polyneuropathy (Portuguese type variant I) and female pelvic floor dysfunction: a tribute to Magellan
• Familial amyloidotic polyneuropathy type 1 in Brazil is associated with the transthyretin Val30Met variant
• Familial ATTR amyloidosis: microalbuminuria as a predictor of symptomatic disease and clinical nephropathy
• Familial type I (Portuguese form) amyloidotic polyneuropathy in Majorca. Study using the TTR (Met30) genetic marker
• Female sexual and pelvic floor muscles dysfunctions in familial amyloidotic polyneuropathy (FAP-Portuguese type)
• Gastric emptying before and after liver transplantation for familial amyloidotic polyneuropathy, Portuguese type (Val30Met)
• Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: clinical and neurophysiological studies
• Genetic anticipation in Portuguese kindreds with familial amyloidotic polyneuropathy is unlikely to be caused by triplet repeat expansions
• Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype-phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden
• Identification and quantitative analysis of human transthyretin variants in human serum by Fourier transform ion-cyclotron resonance mass spectrometry
• Identification of asymptomatic forms of type I amyloid neuropathy
• Identification of carriers of a variant plasma prealbumin (transthyretin) associated with familial amyloidotic polyneuropathy type I
• Images in cardiology: Intracellular cardiac amyloidosis in familiar amyloid polyneuropathy of the Portuguese type
• Is lower urinary tract dysfunction an early marker of Portuguese type familial amyloidotic polyneuropathy in women? Preliminary results
• Kidney and anemia in familial amyloidosis type I
• Liver transplantation does not prevent the development of life-threatening arrhythmia in familial amyloidotic polyneuropathy, Portuguese-type (ATTR Val30Met) patients
• Liver transplantation for familial amyloid polyneuropathy
• Liver transplantation restores endocrine cells in patients with familial amyloidotic polyneuropathy
• Long-term follow-up of survival of liver transplant recipients with familial amyloid polyneuropathy (Portuguese type)
• Lower urinary tract dysfunction in familial amyloidotic polyneuropathy, Portuguese type
• Massive leptomeningeal amyloidosis associated with a Val30Met transthyretin gene
• Molecular characterisation of a kindred with MEN2A and clinical implications
• Molecular genetics of amyloid neuropathy in Europe
• Myocardiopathy caused by Portuguese-type familial amyloidotic polyneuropathy. Sequential morphologic and functional study of 60 patients
• Neuro-paralytic keratitis in familial Portuguese amyloidosis of the Corino-Andrade type
• Neurophysiological evaluation of sexual dysfunction in familial amyloidotic polyneuropathy--Portuguese type
• Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy-type I (Portuguese, Andrade)
• Orthotopic liver transplantation for familial Portuguese amyloidosis
• Outcome of exercise electrocardiography in familial amyloidotic polyneuropathy patients, Portuguese type, under evaluation for liver transplantation
• Partial amino acid sequence homology between an heredofamilial amyloid protein and human plasma prealbumin
• Plasma catecholamines and postural hypotension in familial amyloidotic polyneuropathy of the Portuguese type
• Portuguese type amyloidosis in an Irish patient
• Portuguese-type amyloid neuropathy in an English family
• Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M)
• Portuguese-type familial amyloidotic polyneuropathy: presentation of a case
• Prealbumin variants in the amyloid fibrils of Swedish familial amyloidotic polyneuropathy
• Preimplantation genetic diagnosis for familial amyloidotic polyneuropathy (FAP)
• Prenatal diagnosis of hereditary amyloidosis in a Portuguese family
• Prenatal diagnosis of hereditary amyloidosis in a Portuguese family living in France
• Progression of cardiomyopathy after liver transplantation in patients with familial amyloidotic polyneuropathy, Portuguese type
• Pseudohypertrophic myopathy caused by cysticercosis. Report of a case
• Pulmonary amyloidosis: radiographic finding of nodular opacities in a heavy smoker
• Pure neural leprosy or amyloid neuropathy? Systematic review and clinical case report
• Purpura: primary systemic amyloidosis manifestation
• Quantified sensory abnormalities in early genetically verified transthyretin amyloid polyneuropathy
• Regional differences and similarities of familial amyloidotic polyneuropathy (FAP) presentation in Brazil
• Renal involvement in leprosy
• Scintigraphic and Echocardiographic Study of Patients with Pathogenic or Probably Pathogenic Variants of the TTR Gene without Overt Cardiac Involvement
• Speckle Tracking and Transthyretin Amyloid Cardiomyopathy
• Structure of Met30 variant of transthyretin and its amyloidogenic implications
• Studies on plasma transthyretin (prealbumin) in familial amyloidotic polyneuropathy, Portuguese type
• Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease
• The clinical and biochemical spectrum of hereditary amyloidosis
• The heart in Portuguese amyloidosis
• The long-term impact of liver transplantation on kidney function in familial amyloidotic polyneuropathy patients
• The natural history of cardiac involvement in Portuguese-type familial amyloid polyneuropathy
• Tissue Doppler imaging in different locations of the mitral annulus: all different or all the same?
• Treatment of familial amyloidotic polyneuropathy (Portuguese type) by plasma exchange
• Two-tiered DNA-based diagnosis of transthyretin amyloidosis reveals two novel point mutations
• Type I familial amyloid polyneuropathy and pontine haemorrhage
• Type I familial amyloidotic polyneuropathy (Japanese type)
• Usefulness of labial salivary gland biopsy in familial amyloid polyneuropathy Portuguese type
• Wild-type cardiac amyloidosis with a negative bone scintigraphy: A case report