Results 121 to 130 of about 141,957 (168)

Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly). [PDF]

Eur J Neurol
Ceccanti M, Guaraldi P, Romano A, Antonini G, Barilaro A, Briani C, Burattini M, Gianoli M, Carlini G, Cianci V, Dossi MC, Di Lisi D, Di Muzio A, Ratti A, Filosto M, Gasverde S, Gemelli C, Gentile L, Goglia M, Leonardi L, Longhi S, Lotti A, Manganelli F, Mazzeo A, Augello SM, Milella G, Novo G, Pareyson D, Fenu S, Palumbo G, Petrelli C, Poli L, Pradotto LG, Russo M, Salvalaggio A, Sciarrone MA, Sellitti L, Tagliapietra M, Tozza S, Castiglia M, Turri M, Verriello L, Chimenti C, Vitali F, Brighina F, Rini N, Inghilleri M, D'Angelo R, Abelardo D, Cambieri C, Libonati L, Moret F, Luigetti M, Di Stefano V.   +53 more
europepmc   +1 more source

p.Asp58Val Hereditary Transthyretin Amyloidosis: A Case Report and Literature Review. [PDF]

Cureus
Ramnarain J, Hosking P, Gibbs S.
europepmc   +1 more source

Disease modifying treatment of hereditary transthyretin amyloidosis with polyneuropathy in Germany - expert consensus of the German society of amyloid diseases (DGAK) and the German neurological society (DGN). [PDF]

Neurol Res Pract
Weiler M, Dohrn MF, Gingele S, Skripuletz T, Schilling M, Hagenacker T, Hund E, Sachau J, Baron R, Pernice H, Spethmann S, Khandanpour C, Carpinteiro A, Morbach C, Hahn K.   +14 more
europepmc   +1 more source

A Quantitative Assessment of Upper Limb Motor Function Across Disease Stages in Hereditary Transthyretin Amyloidosis. [PDF]

J Peripher Nerv Syst
Hamedani M, Prada V, Massucco S, Roveta E, Grandis M, Gemelli C, Schiavetti I, Signori A, Schenone C, Luigetti M, Guglielmino V, Sciarrone MA, Vitali F, Pradotto LG, Manganelli F, Tozza S, Palumbo G, Mazzeo A, Gentile L, Russo M, Luca M, D'Arma F, Pisciotta C, Fenu S, Pareyson D, Schenone A.   +25 more
europepmc   +1 more source

Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy: An Exploratory Analysis of Treatment Effect in Male and Female Patients. [PDF]

Muscle Nerve
Waddington Cruz M, Berk JL, Parman Y, Gertz M, Khella S, Weiler M, Kwoh TJ, Pola M, Reicher B, Nåtman J, Dasgupta NR, Wixner J.   +11 more
europepmc   +1 more source

Hereditary Transthyretin Amyloidosis in Austria: Clinical, Genetic, and Demographic Insights from a Nationwide Cohort. [PDF]

J Clin Med
Ermolaev N, Löscher WN, Verheyen N, Pölzl G, Ablasser K, Agis H, Binder C, Bonderman D, Cetin H, Duca F, Griedl TA, Hacker S, Höller V, Kammerlander A, Kellermair L, Kleinveld VEA, Kronberger C, Mörtl D, Poledniczek M, Reiter C, Rettl R, Schmid LM, Schwegel N, Schaumberger E, Sunder-Plassmann R, Ungericht M, Windhager R, Zimprich F, Badr Eslam R, Auer-Grumbach M.   +29 more
europepmc   +1 more source

Correlation between neuropathy severity and neurofilament light chain levels in Brazilian patients with hereditary transthyretin amyloidosis. [PDF]

Sci Rep
Ferreira P, do Amaral Martins L, Araujo Duarte L, Salvio Lemos A, Vieira Alves-Leon S, Foguel D, Waddington Cruz M.   +6 more
europepmc   +1 more source

A review of Eplontersen use in hereditary transthyretin amyloidosis. [PDF]

Neurodegener Dis Manag
Sama J, Khatri W, Markus N, Dasgupta N.
europepmc   +1 more source

A Rare Unusually Aggressive Form of Hereditary Transthyretin Amyloidosis. [PDF]

JACC Case Rep
Zhang J, Roth LR, Wees I, Phillips L, Pedretti R, Nguyen P, Saelices L, Grodin JL.   +7 more
europepmc   +1 more source