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Academic Journal

Arginine: A potential prophylactic supplement for transthyretin amyloidosis.

  • Authors : Fukunari A; Department of Amyloidosis Research, Faculty of Pharmaceutical Sciences, Nagasaki International University, Huis Ten Bosch, Sasebo, Nagasaki, Japan. Electronic address: .; Matsushita H

Subjects: Arginine*/Arginine*/Arginine*/chemistry ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/prevention & control ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/drug therapy Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Dec 10; Vol. 737, pp. 150770. Date of Electronic Publication: 2024 Sep 30.Publisher: Elsevier Country of Publication: United States NLM ID: 0372516 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

ATTRv-V30M amyloid fibrils from heart and nerves exhibit structural homogeneity.

  • Authors : Nguyen BA; Center for Alzheimer's and Neurodegenerative Diseases, University of Texas Southwestern Medical Center (UTSW), Dallas, TX 75390, USA; Department of Biophysics, University of Texas Southwestern Medical Center (UTSW), Dallas, TX 75390, USA

Subjects: Prealbumin*/Prealbumin*/Prealbumin*/chemistry ; Prealbumin*/Prealbumin*/Prealbumin*/metabolism ; Prealbumin*/Prealbumin*/Prealbumin*/genetics Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Structure (London, England : 1993) [Structure] 2024 Dec 05; Vol. 32 (12), pp. 2244-2250.e3. Date of Electronic Publication: 2024 Oct 17.Publisher: Cell Press Country of Publication: United States NLM ID: 101087697 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

T2-relaxometry in a large cohort of hereditary transthyretin amyloidosis with polyneuropathy.

  • Authors : Poncelet A; Amyloidosis Center Heidelberg, Heidelberg University Hospital, Heidelberg, Germany.; Department of Neuroradiology, Heidelberg University Hospital, Heidelberg, Germany.

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/pathology ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/diagnostic imaging Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2024 Dec; Vol. 31 (4), pp. Publisher: Taylor & Francis Country of Publication: England NLM ID: 9433802 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Altered connectivity of central autonomic network: effects of dysautonomia in hereditary transthyretin amyloidosis with polyneuropathy.

  • Authors : Su TJ; Department of Biomedical Engineering, National Yang Ming Chiao Tung University, Taipei, Taiwan.; Lin CJ

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/physiopathology ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/complications ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2024 Dec; Vol. 31 (4), pp. Publisher: Taylor & Francis Country of Publication: England NLM ID: 9433802 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Clinical and molecular insights into A97S variants in hereditary transthyretin amyloid polyneuropathy in South China.

  • Authors : Wang Q; Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.; Wang M

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/pathology ; Prealbumin*/Prealbumin*/Prealbumin*/genetics Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2024 Dec; Vol. 31 (4), pp. Publisher: Taylor & Francis Country of Publication: England NLM ID: 9433802 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Clinical differential factors in patients with hereditary transthyretin amyloidosis with Val142Ile and Ser43Asn mutations.

  • Authors : Castellar-Leones SM; Department of Physical Medicine and Rehabilitation, Facultad de Medicina, Universidad Nacional de Colombia, Carrera 30 No.45-03. Edificio 471, Piso 5to, Of. 513-A, Bogotá, Colombia. .; Research Center for Physiatry and Electrodiagnostics, (CIFEL), Bogotá, Colombia. .

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/pathology ; Mutation*/Mutation*/Mutation*/genetics Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Dec 20; Vol. 19 (1), pp. 474. Date of Electronic Publication: 2024 Dec 20.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

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Academic Journal

CRISPR-Cas9 Gene Editing with Nexiguran Ziclumeran for ATTR Cardiomyopathy.

  • Authors : Fontana M; From the National Amyloidosis Centre, University College London, Royal Free Hospital (M.F., Y.R., J.D.G.), and Richmond Pharmacology (J.T.) - both in London; Brigham and Women's Hospital, Boston (S.D.S.), and Intellia Therapeutics, Cambridge (J.K., L.W., R.R., D.L., D.S., J.O., A.H., P.Z., Y.X., A.L., A.S.) - both in Massachusetts

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/blood ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/complications ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics Amyloidosis, Hereditary, Transthyretin-Related

  • Source: The New England journal of medicine [N Engl J Med] 2024 Dec 12; Vol. 391 (23), pp. 2231-2241. Date of Electronic Publication: 2024 Nov 16.Publisher: Massachusetts Medical Society Country of Publication: United States NLM ID: 0255562 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis.

  • Authors : Canciello G; Department of Advanced Biomedical Sciences, University Federico II of Naples, Naples, Italy.; Tozza S

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/pathology ; Mutation*/Mutation*/Mutation*/genetics Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Dec 05; Vol. 19 (1), pp. 458. Date of Electronic Publication: 2024 Dec 05.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

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Academic Journal

Hereditary Transthyretin Amyloidosis in Patients Referred to a Genetic Testing Program.

  • Authors : Bhatt K; Department of Medicine, Division of Cardiology Emory University Atlanta GA.; Delgado DH

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/diagnosis ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/epidemiology Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Journal of the American Heart Association [J Am Heart Assoc] 2024 Dec 03; Vol. 13 (23), pp. e033770. Date of Electronic Publication: 2024 Nov 22.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101580524 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Brain MRI in patients with V30M hereditary transthyretin amyloidosis.

  • Authors : Sousa L; Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal.; Unidade Corino de Andrade, Centro Hospitalar Universitário de Santo António, Porto, Portugal.

Subjects: Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/diagnostic imaging ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/genetics ; Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/Amyloid Neuropathies, Familial*/pathology Amyloidosis, Hereditary, Transthyretin-Related

  • Source: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2024 Dec; Vol. 31 (4), pp. Publisher: Taylor & Francis Country of Publication: England NLM ID: 9433802 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 of  1,470 results for ""Prealbumin""