يعرض 1 - 10 نتائج من 507 نتيجة بحث عن '"Hereditary transthyretin amyloidosis"', وقت الاستعلام: 1.12s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Quantitative muscle ultrasound as a disease biomarker in hereditary transthyretin amyloidosis with polyneuropathy

    المؤلفون: Tan, Siew Yin, Tan, Cheng YinAff1, Aff2, IDs1007202407340y_cor2, Yahya, Mohd Azly, Low, Soon Chai, Shahrizaila, Nortina, Goh, Khean Jin

    المصدر: Neurological Sciences. 45(7):3449-3459

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  2. 2
    دورية أكاديمية
    Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy

    المؤلفون: Gentile, Luca, Mazzeo, Anna, Briani, Chiara, Casagrande, Silvia, De Luca, Marcella, Fabrizi, Gian Maria, Gagliardi, Christian, Gemelli, Chiara, Forcina, Francesca, Grandis, MarinaAff6, Aff8, Guglielmino, Valeria, Iabichella, Giacomo, Leonardi, Luca, Lozza, Alessandro, Manganelli, Fiore, Mussinelli, Roberta, My, Filomena, Occhipinti, Giuseppe, Fenu, Silvia, Russo, Massimo, Romano, Angela, Salvalaggio, Alessandro, Tagliapietra, Matteo, Tozza, Stefano, Palladini, GiovanniAff10, Aff15, Obici, LauraAff10, IDs10072024074949_cor26, Luigetti, MarcoAff14, Aff9

    المصدر: Neurological Sciences. 45(9):4563-4571

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  3. 3
    دورية أكاديمية
    Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN)

    المؤلفون: Galosi, EleonoraAff1, IDs10072024075620_cor1, Costanzo, Rocco, Forcina, Francesca, Morino, Stefania, Antonini, Giovanni, Salvetti, MarcoAff2, Aff3, Lauletta, Antonio, Luigetti, MarcoAff4, Aff5, Romano, Angela, Primiano, Guido, Guglielmino, Valeria, Fionda, Laura, Garibaldi, Matteo, Esposito, Nicoletta, Falco, Pietro, di Pietro, Giuseppe, Truini, Andrea, Leonardi, LucaAff2, Aff6

    المصدر: Neurological Sciences. :1-10

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  4. 4
    دورية أكاديمية
    Early detection of nerve involvement in presymptomatic TTR mutation carriers: exploring potential markers of disease onset

    المؤلفون: Romano, Angela, Guglielmino, Valeria, Bisogni, Giulia, Di Paolantonio, Andrea, Truini, Andrea, Minnella, Angelo MariaAff2, Aff6, Sciarrone, Maria Ausilia, Vitali, Francesca, Maceroni, MartinaAff2, Aff6, Galosi, Eleonora, Sabatelli, MarioAff2, Aff3, Luigetti, MarcoAff2, Aff1, IDs1007202307177x_cor12

    المصدر: Neurological Sciences. 45(4):1675-1684

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  5. 5
    دورية أكاديمية
    Update on Amyloid Polyneuropathy and Treatment

    المؤلفون: Živković, Sasha A.Aff1, IDs1194002400780z_cor1, Avila, J. David, Gallegos-Kattan, Cesia, Quan, Dianna

    المصدر: Current Treatment Options in Neurology. 26(3):51-66

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  6. 6
    دورية أكاديمية
    Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study

    المؤلفون: Marco Luigetti, Francesca Vitali, Angela Romano, Maria Ausilia Sciarrone, Valeria Guglielmino, Michelangelo Ardito, Andrea Sabino, Serenella Servidei, Geny Piro, Carmine Carbone, Francesca Graziani, Rosa Lillo, Pietro Manuel Ferraro, Guido Primiano

    المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)

    مصطلحات موضوعية: Hereditary transthyretin amyloidosis, Biomarkers, Growth differentiation factor-15, Uromodulin, Cystatin C, Estimated glomerular filtration rate, Medicine, Science

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/2045-2322

    URL الوصول: https://doaj.org/article/9d4ad3a470334b5a9a72305ae28d9df3

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  7. 7
    كتاب إلكتروني
    Hereditary Transthyretin Amyloidosis

    المؤلفون: Obici, LauraAff5, Panichella, GiorgiaAff6, Mussinelli, RobertaAff5

    المساهمون: Emdin, Michele, editorAff1, Vergaro, Giuseppe, editorAff2, Aimo, Alberto, editorAff3, Fontana, Marianna, editorAff4

    المصدر: Cardiac Amyloidosis : Diagnosis and Treatment. :53-67

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  8. 8
    دورية أكاديمية
    Patisiran for the treatment of patients with p.Ile88Leu hereditary transthyretin amyloidosis: an Italian real-life experience

    المؤلفون: Giacomo Urbinati, Ilaria Cani, Marco Currò Dossi, Simone Longhi, Samuela Carigi, Christian Gagliardi, Elena Biagini, Nazzareno Galiè, Pietro Cortelli, Pietro Guaraldi

    المصدر: Frontiers in Neurology, Vol 15 (2024)

    مصطلحات موضوعية: hereditary transthyretin amyloidosis, patisiran, p.Ile88Leu, TTR, familial amyloid polyneuropathy, transthyretin amyloid cardiomyopathy, Neurology. Diseases of the nervous system, RC346-429

    وصف الملف: electronic resource

    Relation: https://www.frontiersin.org/articles/10.3389/fneur.2024.1415851/full; https://doaj.org/toc/1664-2295

    URL الوصول: https://doaj.org/article/6d48eaa8280b4f93b36312858de5a918

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  9. 9
    دورية أكاديمية
    Occupational practice in patients with hereditary transthyretin amyloidosis, a qualitative study

    المؤلفون: Gayà-Barroso, AinaAff1, Aff2, González-Moreno, JuanAff1, Aff2, Rodríguez, AdriánAff1, Aff2, Ripoll-Vera, TomásAff3, Aff2, Losada-López, InésAff1, Aff2, Gili, Margarita, Paneque, MilenaAff5, Aff6, Aff7, Pérez-Martínez, Sara, Cisneros-Barroso, EugeniaAff1, Aff2, IDs13023023029643_cor9

    المصدر: Orphanet Journal of Rare Diseases. 18(1)

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  10. 10
    دورية أكاديمية
    Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study

    المؤلفون: Tsai, Cheng-HsuanAff1, Aff2, Chao, Chi-Chao, Hsieh, Sung-Tsang, Yu, An-LiAff4, Aff5, Wu, Yuan-Kun (Aden)Aff4, Aff5, Cheng, Mei-FangAff6, Aff7, Lee, Ming-Jen, Chou, Chia-Hung, Shun, Chia-TungAff9, Aff10, Hsueh, Hsueh-Wen, Jyh-Ming Juang, JimmyAff4, Aff5, Tseng, Ping-Huei, Su, Mao-YuanAff12, Aff13, IDs13023023028240_cor13, Lin, Yen-HungAff4, Aff5, IDs13023023028240_cor14

    المصدر: Orphanet Journal of Rare Diseases. 18(1)

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