Results 81 to 90 of about 2,353 (157)

Cardiac Resynchronization Therapy, Remodeling, and Outcome in Patients With Amyloid Transthyretin Cardiomyopathy. [PDF]

J Am Heart Assoc
Aimo A, Nesti M, Vergaro G, Killu AM, Bampatsias D, Tomasoni D, Forleo C, Musca F, Serenelli M, Rosenthal J, Teruya SL, Al-Shakarchi NJ, Tameze MS, Castiglione V, Nicolai A, Panichella G, Saro R, Porcari A, Sinigiani G, Fico V, Frau E, Matar R, Guaricci AI, Tini G, Cipriani A, Musumeci MB, Longhi S, Chimenti C, Metra M, Grogan M, Perfetto F, Cappelli F, Merlo M, Sinagra G, Maurer MS, Masri A, Emdin M.   +36 more
europepmc   +1 more source

Corneal lattice dystrophy type II – familial amyloid neuropathy type IV (gelsolin amyloidosis)

Einstein (São Paulo), 2008
Evandro Penteado Villar Felix, Liang Shih Jung, Geiser Souza Carvalho, Acary Souza Bulle Oliveira   +3 more
openaire   +1 more source

Clinical Utility of Serum Neurofilament Light Chain in Peripheral Neuropathy. [PDF]

Muscle Nerve
Karam C.
europepmc   +1 more source

Sixty years of experience with hereditary transthyretin amyloidosis: Insights from the Swedish transthyretin amyloidosis registry. [PDF]

J Intern Med
Stenberg L, Pilebro B, Anan I, Baranda JM, Samuelsson K, Eldhagen P, Backlund R, Wixner J.   +7 more
europepmc   +1 more source

Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy

Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy
This is an electronic version of an article published in Amyloid 2010, Vol. 17, No. 1 : Pages 32-35. Amyloid is available online at: http://informahealthcare.com/doi/pdf/10.3109/13506121003619369 We report here two patients with amyloidogenic transthyretin (ATTR) Val30Met familial amyloid polyneuropathy (FAP) who developed numbness in both hands and ...
openaire  

False negative biceps tendon sampling for detection of systemic amyloidosis: a case report. [PDF]

JSES Rev Rep Tech
Mendoza ZD, Yetter TR, Lintner DM, Trachtenberg BH, Liberman SR.   +4 more
europepmc   +1 more source

TTR Gene Screening Since the Advent of Biotherapies in France: A Nationwide Retrospective Survey Between 2018 and 2023. [PDF]

Eur J Neurol
Ait Tayeb AEK, Chazelas P, Poinsignon V, Adams D, Berthot C, Cauquil C, Dhaenens CM, Francou B, Jedraszak G, Labeyrie C, Redondo CL, Lia AS, Lopez M, Proust A, Sturtz F, Tosca L, Verstuyft C, Echaniz-Laguna A, Bouligand J.   +18 more
europepmc   +1 more source

Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157. [PDF]

J Alzheimers Dis
Holm-Mercer L, Mok TH, Sequeira D, Coysh T, Rudge P, Ramadan H, Darwent L, Campbell T, Murphy T, Smith C, Ritchie D, Brandner S, Jaunmuktane Z, Collinge J, Mead S.   +14 more
europepmc   +1 more source

Phenomenological model of transthyretin stabilization. [PDF]

Sci Rep
Lisowski B, Ulaszek S, Wiśniowska B, Bernhauerová V, Polak S.   +4 more
europepmc   +1 more source

Novel Pathogenic Variant c.258A>C, p.(Glu86Asp) in the <i>TTR</i> Gene in a Bulgarian Patient with Hereditary Transthyretin Amyloidosis. [PDF]

Genes (Basel)
Pavlova Z, Zhelyazkova S, Gospodinova M, Ormandjieva A, Todorov T, Asenov O, Chamova T, Antimov P, Mikova D, Palashev Y, Tournev I, Todorova A.   +11 more
europepmc   +1 more source