المؤلفون: Asuman ARGON, Deniz NART, Funda YILMAZ BARBET

المصدر: Türk Patoloji Dergisi, Vol 40, Iss 1, Pp 1-9 (2024)

مصطلحات موضوعية: amyloid, cardiac amyloidosis, transthyretin, hereditary amyloidosis, senile amyloidosis, Pathology, RB1-214

وصف الملف: electronic resource

العلاقة: https://turkjpath.org/pdf.php?id=2051Test; https://doaj.org/toc/1018-5615Test; https://doaj.org/toc/1309-5730Test

الوصول الحر: https://doaj.org/article/517f2aad0a7945239c90fdf35a133cd2Test

المؤلفون: Nicholas S. Hendren, James A. De Lemos, Jarett D. Berry, Julia Kozlitina, Lorena Saelices, Alan X. Ji, Zhili Shao, Chia-Feng Liu, Sonia Garg, Maryjane A. Farr, Mark H. Drazner, W. H. Wilson Tang, Justin L. Grodin

مصطلحات موضوعية: Biochemistry, Genetics, Neuroscience, Pharmacology, Sociology, Science Policy, Biological Sciences not elsewhere classified, Retinol binding protein 4, hereditary amyloidosis, transthyretin amyloidosis, prealbumin, V122I carriers

العلاقة: https://figshare.com/articles/journal_contribution/Circulating_transthyretin_and_retinol_binding_protein_4_levels_among_middle-age_V122I_i_TTR_i_carriers_in_the_general_population/25351429Test

الإتاحة: https://doi.org/10.6084/m9.figshare.25351429.v1Test
https://figshare.com/articles/journal_contribution/Circulating_transthyretin_and_retinol_binding_protein_4_levels_among_middle-age_V122I_i_TTR_i_carriers_in_the_general_population/25351429Test

المؤلفون: E. I. Safiulina, O. E. Zinovieva, N. S. Shcheglova, V. V. Rameev, Z. V. Surnina, E. N. Nikitina, O. A. Vorobieva

المصدر: Неврология, нейропсихиатрия, психосоматика, Vol 14, Iss 6, Pp 67-72 (2022)

مصطلحات موضوعية: leptomeningeal amyloidosis, transthyretin hereditary amyloidosis, mutation in the transthyretin gene, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://nnp.ima-press.net/nnp/article/view/1923Test; https://doaj.org/toc/2074-2711Test; https://doaj.org/toc/2310-1342Test

الوصول الحر: https://doaj.org/article/7d08b9bd50d84effb6057a28fa24dce7Test

المؤلفون: Stefano Tozza, Marco Luigetti, Giovanni Antonini, Anna Mazzeo, Daniele Severi, Andrea Di Paolantonio, Luca Leonardi, Massimo Russo, Angela Romano, Francesca Forcina, Luca Gentile, Maria Nolano, Consalvo Mattia, Fiore Manganelli

المصدر: Frontiers in Neurology, Vol 14 (2023)

مصطلحات موضوعية: ATTRv, hereditary amyloidosis, pain, quality of life, transthyretin, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2023.1109782/fullTest; https://doaj.org/toc/1664-2295Test

الوصول الحر: https://doaj.org/article/fc9a2d01a08646199d7f8e3d575db67aTest

المؤلفون: Schmidt, Eeva-Kaisa, Mustonen, Tuuli, Kiuru-Enari, Sari, Kivelä, Tero T., Atula, Sari

المساهمون: Department of Neurosciences, Neurologian yksikkö, HUS Neurocenter, HUS Head and Neck Center, Silmäklinikka

مصطلحات موضوعية: Gelsolin, Amyloidosis, AGel, Hereditary amyloidosis, Meretoja syndrome, Natural history, Lifespan, Relative survival, LATTICE CORNEAL-DYSTROPHY, FAMILIAL AMYLOIDOSIS, RENAL AMYLOIDOSIS, NEPHROTIC SYNDROME, MUTATION, VARIANT, POLYNEUROPATHY, POPULATION, GENE, FAF, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: The study was supported by Helsinki University Hospital. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.; Schmidt , E-K , Mustonen , T , Kiuru-Enari , S , Kivelä , T T & Atula , S 2020 , ' Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival : FIN-GAR phase II study ' , Orphanet journal of rare diseases , vol. 15 , no. 1 , 19 . https://doi.org/10.1186/s13023-020-1300-5Test; aeaab7de-333a-4d12-be52-1a993d540e88; http://hdl.handle.net/10138/563569Test; 000514644200002

الإتاحة: http://hdl.handle.net/10138/563569Test

المؤلفون: Коробкова, Наталья Викторовна, Зуева, Светлана Алексеевна, Рохленко, Ольга Валерьевна, Мозес, Вадим Гельевич, Рудаева, Елена Владимировна, Елгина, Светлана Ивановна, Мозес, Кира Борисовна, Центер, Яэль, Черных, Наталья Степановна

المصدر: Medicine in Kuzbass; Том 22, № 3 (2023): сентябрь; 75-78 ; Медицина в Кузбассе; Том 22, № 3 (2023): сентябрь; 75-78 ; 2588-0411 ; 1819-0901

مصطلحات موضوعية: TTR gene, hereditary amyloidosis, polyneuropathy, TTR-SAP, transtiretin, ген TTR, наследственный амилоидоз, полинейропатия, ТТР-САП, транстиретин

وصف الملف: text/html; application/pdf

العلاقة: http://mednauki.ru/index.php/MK/article/view/955/1658Test; http://mednauki.ru/index.php/MK/article/view/955/1694Test; http://mednauki.ru/index.php/MK/article/view/955Test

الإتاحة: http://mednauki.ru/index.php/MK/article/view/955Test

المؤلفون: V.A. Feitosa, P.D.M.M. Neves, L.B. Jorge, I.L. Noronha, L.F. Onuchic

المصدر: Brazilian Journal of Medical and Biological Research, Vol 55 (2022)

مصطلحات موضوعية: Renal amyloidosis, Amyloid typing, Proteomics, Mass spectrometry, Hereditary amyloidosis, Medicine (General), R5-920, Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100307&lng=en&tlng=enTest; http://www.scielo.br/pdf/bjmbr/v55/1414-431X-bjmbr-55-e12284.pdfTest; https://doaj.org/toc/1414-431XTest

الوصول الحر: https://doaj.org/article/21e186f0c6da4fe5ba166dcd9f272d75Test

المؤلفون: Kari Hemminki, Asta Försti

المصدر: Hemato, Vol 2, Iss 3, Pp 429-440 (2021)

مصطلحات موضوعية: incidence, hereditary amyloidosis, periodic fever syndrome, translocation (11, 14), cyclin D1, Medicine

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2673-6357/2/3/27Test; https://doaj.org/toc/2673-6357Test

الوصول الحر: https://doaj.org/article/7922cb0a6ce24b1fa8e7adf69e3d97a8Test

المؤلفون: Ivan Urits, Daniel Swanson, Michael C. Swett, Anjana Patel, Kevin Berardino, Ariunzaya Amgalan, Amnon A. Berger, Hisham Kassem, Alan D. Kaye, Omar Viswanath

المصدر: Neurology and Therapy, Vol 9, Iss 2, Pp 301-315 (2020)

مصطلحات موضوعية: Cardiac amyloidosis, Hereditary amyloidosis, Orphan drugs, Polyneuropathy, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2193-8253Test; https://doaj.org/toc/2193-6536Test

الوصول الحر: https://doaj.org/article/d4411de9a7a947deab62328df510341aTest

المؤلفون: Eeva-Kaisa Schmidt, Tuuli Mustonen, Sari Kiuru-Enari, Tero T. Kivelä, Sari Atula

المصدر: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-13 (2020)

مصطلحات موضوعية: Gelsolin, Amyloidosis, AGel, Hereditary amyloidosis, Meretoja syndrome, Natural history, Medicine

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/1ec4b274c5604c4e8dc6475a521e6a85Test