valine and Amyloid Neuropathy Type 1

valine has been researched along with Amyloid Neuropathy Type 1 in 39 studies

Research

Studies (39)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's16 (41.03)29.6817
2010's23 (58.97)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ericzon, BG; Nowak, G; Suhr, OB; Westermark, P1
Alcazar, A; Corral, I; García-Barragán, N; Jiménez-Escrig, A; Martínez-Alonso, E; Martínez-Poles, J; Martínez-Ulloa, PL; Pian, H; Vallejo, M1
Hashizume, A; Iijima, M; Ikeda, S; Katsuno, M; Kawagashira, Y; Koike, H; Nakamura, T; Nishi, R; Sobue, G1
Ando, Y; Masuda, T; Matsui, H; Misumi, Y; Nomura, T; Obayashi, K; Sasada, K; Takamatsu, K; Tasaki, M; Ueda, M; Yamashita, T1
Alves, C; Cardoso, M; Cavaco, S; Coelho, T; Fernandes, J; Kelly, JW; Martins da Silva, A; Monteiro, C; Samões, R1
Ando, Y; Ishii, T; Koike, H; Misawa, S; Sekijima, Y; Ueda, M1
Azizi, M; Barreiros, AP; Birklein, F; Emrich, T; Galle, PR; Geber, C; Heise, M; Hoppe-Lotichius, M; Lang, H; Mittler, J; Otto, G; Schad, A; Schmid, JC; Vollmar, J; Weyer, V; Zimmermann, T1
Chan, J; Coelho, T; Conceiçao, I; Cruz, MW; da Silva, AM; Grogan, DR; Kelly, JW; Labaudinière, R; Maia, LF; Packman, J; Planté-Bordeneuve, V; Schmidt, HH; Suhr, OB; Trigo, P1
Chang, HS; Liao, MF1
Gonçalves, NP; Saraiva, MJ; Teixeira-Coelho, M1
Ikeda, T; Ikeda, Y; Iwasa, K; Kayano, D; Komatsu, J; Nakamura, K; Ono, K; Sakai, K; Samuraki, M; Shibata, S; Takahashi, R; Yamada, M1
Coelho, T; Costa, V; Da Silva, AM; Faber, CG; Merkies, IS; Pruppers, MH1
Ando, Y; Ikeda, S; Machii, K; Misumi, Y; Morita, H; Obayashi, K; Ohta, M; Sekijima, Y; Takata, A; Ueda, M; Yamashita, T1
Enzan, H; Komatsu, K; Kuzume, D; Morimoto, Y; Sajima, K; Yamasaki, M1
Andreu-Serra, H; Buades-Reinés, J; Cisneros-Barroso, E; Gallego-Lezaún, C; Raya-Cruz, M; Ripoll-Vera, T; Usón-Martín, M1
Hasegawa, K; Hirata, KI; Ishibashi-Ueda, H; Kono, AK; Mori, S; Morinaga, Y; Nishii, T; Sato, C; Soga, F; Takaya, T; Tanaka, H; Watanabe, Y1
Ando, Y; Misumi, Y; Nakamura, M; Okamoto, S; Takashi, O; Uchino, M; Ueda, M; Yamashita, T1
Ando, Y; Fujitake, J; Hattori, N; Hayashi, M; Iijima, M; Katsuno, M; Kawagashira, Y; Koike, H; Mukai, E; Nakamura, T; Sobue, G; Ueda, M; Yamamoto, M1
Cunningham, ET; Roe, RH1
Abe, K; Ando, Y; Fujii, D; Kono, S; Manabe, Y; Narai, H; Omori, N; Sakai, Y; Tanaka, T; Ueda, M1
Ikeda, S; Kametani, F; Sekijima, Y; Tsuchiya-Suzuki, A; Yazaki, M1
Feng, JQ; Guo, YJ; Jiang, XM; Liu, JY; Ye, YQ; Yin, F; Zhou, CK1
Ando, Y; Horibata, Y; Jono, H; Kumabe, Y; Misumi, Y; Miura, A; Obayashi, K; Oshima, T; Uchino, M; Ueda, M; Yamashita, T1
Guo, YJ; Jiang, XM; Liu, JY; Zhang, M1
Hashimoto, R; Iijima, M; Kamei, H; Kawagashira, Y; Kiuchi, T; Koike, H; Nakamura, T; Sobue, G; Tomita, M; Watanabe, H1
Borodinsky, LN; Costa, PP; Di Egidio, M; Fiszman, ML; Katz, N; Lendoire, JC; Llesuy, SF; Repetto, MG; Ricart, KC; Riedstra, S; Saizar, RD; Sica, RE; Trigo, PL; Villa, AM1
Balan, V; Brandhagen, DJ; Douglas, DD; Mulligan, DC; Perri, RE; Rakela, J; Rosen, CB; Sharma, P; Sirven, JE; Wiesner, RH; Zeldenrust, SR1
Ando, E; Ando, Y; Haraoka, K; Inomata, Y; Nakamura, M; Okabe, H; Sasaki, Y; Tanihara, H; Terazaki, H; Uchino, M; Ueda, M; Yamashita, T1
Ikeda, S; Katayanagi, K; Takei, Y; Yoshinaga, T1
Barroso, E; Freire, A; Monteiro, E1
Beirão, I; Bravo, F; Cabrita, A; Costa, PM; Fonseca, I; Lobato, L; Mendes, P; Porto, G; Silva, M1
Arima, K; Hanyu, N; Ikeda, S; Oide, T; Yamazaki, M1
Bittencourt, PL; Clemente, C; Couto, CA; Farias, AQ; Goldberg, AC; Mies, S; Palácios, SA1
Begliomini, B; Cautero, N; Dazzi, A; De Ruvo, N; Di Benedetto, F; Diago Usò, T; Lauro, A; Masetti, M; Miller, CM; Pinna, AD; Quintini, C; Ramacciato, G; Risaliti, A; Siniscalchi, A1
Conceição, I; De Carvalho, M1
Hayashi, H; Kawata, A; Mizutani, T; Nagao, M; Uotani, K1
Cunningham, ET; Eagle, RC; Fine, HF; Fisher, Y; Roe, RH1
Furukawa, Y; Ishida, C; Kato-Motozaki, Y; Machiya, T; Morinaga, A; Nozaki, I; Ono, K; Sakajiri, K; Shibata-Hamaguchi, A; Shima, K; Yamada, M; Yanase, D1
Baranov, V; Hörstedt, P; Ippel, HJ; Lundgren, E; Olofsson, A; Wijmenga, S1

Reviews

3 review(s) available for valine and Amyloid Neuropathy Type 1

ArticleYear
Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm.
    Orphanet journal of rare diseases, 2018, 01-17, Volume: 13, Issue:1

    Topics: Algorithms; Amyloid Neuropathies, Familial; Benzoxazoles; Carpal Tunnel Syndrome; Humans; Japan; Liver Transplantation; Methionine; Mutation; Valine

2018
A case of familial amyloid polyneuropathy due to Phe33Val TTR with vitreous involvement as the initial manifestation.
    Internal medicine (Tokyo, Japan), 2010, Volume: 49, Issue:12

    Topics: Amino Acid Substitution; Amyloid Neuropathies, Familial; Diagnosis, Differential; Eye Diseases; Female; Humans; Middle Aged; Phenylalanine; Prealbumin; Valine; Vitreous Body

2010
Familial amyloid polyneuropathy and liver transplantation.
    Journal of hepatology, 2004, Volume: 41, Issue:2

    Topics: Amino Acid Substitution; Amyloid; Amyloid Neuropathies, Familial; Humans; Liver; Liver Transplantation; Methionine; Mutation; Portugal; Prealbumin; Prevalence; Severity of Illness Index; Tissue Donors; Treatment Outcome; Valine

2004

Trials

2 trial(s) available for valine and Amyloid Neuropathy Type 1

ArticleYear
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy.
    Journal of neurology, 2013, Volume: 260, Issue:11

    Topics: Adult; Aged; Amyloid Neuropathies, Familial; Benzoxazoles; Disease Progression; Drug Administration Schedule; Female; Follow-Up Studies; Humans; International Cooperation; Male; Methionine; Middle Aged; Mutation; Prealbumin; Quality of Life; Time Factors; Valine; Young Adult

2013
Effects of tafamidis treatment on transthyretin (TTR) stabilization, efficacy, and safety in Japanese patients with familial amyloid polyneuropathy (TTR-FAP) with Val30Met and non-Val30Met: A phase III, open-label study.
    Journal of the neurological sciences, 2016, Mar-15, Volume: 362

    Topics: Adult; Aged; Amyloid Neuropathies, Familial; Benzoxazoles; Body Mass Index; Echocardiography; Female; Follow-Up Studies; Humans; Japan; Male; Methionine; Middle Aged; Pharmacogenetics; Prealbumin; Valine; Young Adult

2016

Other Studies

34 other study(ies) available for valine and Amyloid Neuropathy Type 1

ArticleYear
Domino liver transplantation: full-length transthyretin in donor and recipient patients with ATTR Val30Met amyloidosis.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2017, Volume: 24, Issue:sup1

    Topics: Adult; Aged; Amyloid Neuropathies; Amyloid Neuropathies, Familial; Amyloidosis; Female; Humans; Liver Transplantation; Male; Methionine; Middle Aged; Valine

2017
A novel ATTR L32V mutation causes familial amyloid polyneuropathy in a Bolivian family.
    Journal of the peripheral nervous system : JPNS, 2017, Volume: 22, Issue:3

    Topics: Amyloid Neuropathies, Familial; Bolivia; DNA Mutational Analysis; Family Health; Female; Humans; Leucine; Middle Aged; Mutation; Neural Conduction; Prealbumin; Valine

2017
Cardiac and peripheral vasomotor autonomic functions in late-onset transthyretin Val30Met familial amyloid polyneuropathy.
    Journal of neurology, 2017, Volume: 264, Issue:11

    Topics: 3-Iodobenzylguanidine; Aged; Amyloid Neuropathies, Familial; Autonomic Nervous System Diseases; Blood Pressure; Female; Heart Diseases; Humans; Male; Methionine; Microscopy, Electron, Transmission; Middle Aged; Mutation; Prealbumin; Radionuclide Imaging; Sural Nerve; Valine; Vasoconstriction

2017
Genetic and clinical characteristics of hereditary transthyretin amyloidosis in endemic and non-endemic areas: experience from a single-referral center in Japan.
    Journal of neurology, 2018, Volume: 265, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Amyloid Neuropathies, Familial; Epidemics; Female; Humans; Japan; Male; Methionine; Middle Aged; Mutation; Prealbumin; Retrospective Studies; Statistics, Nonparametric; Valine; Young Adult

2018
Age-dependent cognitive dysfunction in untreated hereditary transthyretin amyloidosis.
    Journal of neurology, 2018, Volume: 265, Issue:2

    Topics: Adult; Age of Onset; Aging; Amyloid Neuropathies, Familial; Anxiety; Chi-Square Distribution; Cognition Disorders; Depression; Female; Humans; Male; Methionine; Middle Aged; Mutation; Neurologic Examination; Neuropsychological Tests; Prealbumin; Statistics, Nonparametric; Valine

2018
Progression of transthyretin (TTR) amyloidosis in donors and recipients after domino liver transplantation-a prospective single-center cohort study.
    Transplant international : official journal of the European Society for Organ Transplantation, 2018, Volume: 31, Issue:11

    Topics: Adult; Aged; Amyloid Neuropathies, Familial; Biopsy; Child; Databases, Factual; Disease Progression; Echocardiography; Female; Heart Rate; Humans; Liver Failure; Liver Transplantation; Living Donors; Male; Methionine; Middle Aged; Prospective Studies; Time Factors; Treatment Outcome; Valine

2018
A novel variant mutation of transthyretin Ile73Val-related amyloidotic polyneuropathy in Taiwanese.
    Acta neurologica Taiwanica, 2013, Volume: 22, Issue:2

    Topics: Action Potentials; Amyloid Neuropathies, Familial; Family Health; Female; Genetic Testing; Humans; Isoleucine; Male; Middle Aged; Mutation; Neural Conduction; Taiwan; Valine

2013
The inflammatory response to sciatic nerve injury in a familial amyloidotic polyneuropathy mouse model.
    Experimental neurology, 2014, Volume: 257

    Topics: Amyloid Neuropathies, Familial; Animals; Disease Models, Animal; Female; Functional Laterality; Ganglia, Spinal; Gene Expression Regulation; Humans; Inflammation; Locomotion; Male; Methionine; Mice; Mice, Transgenic; Mutation; Pain Measurement; Prealbumin; Schwann Cells; Sciatic Neuropathy; Time Factors; Valine

2014
Efficacy of diflunisal on autonomic dysfunction of late-onset familial amyloid polyneuropathy (TTR Val30Met) in a Japanese endemic area.
    Journal of the neurological sciences, 2014, Oct-15, Volume: 345, Issue:1-2

    Topics: 3-Iodobenzylguanidine; Aged; Amyloid Neuropathies, Familial; Anti-Inflammatory Agents, Non-Steroidal; Autonomic Nervous System Diseases; Diflunisal; Electrocardiography; Female; Humans; Japan; Male; Methionine; Middle Aged; Mutation; Pharmacogenetics; Prealbumin; Radionuclide Imaging; Radiopharmaceuticals; Valine

2014
The Val30Met familial amyloid polyneuropathy specific Rasch-built overall disability scale (FAP-RODS(©) ).
    Journal of the peripheral nervous system : JPNS, 2015, Volume: 20, Issue:3

    Topics: Activities of Daily Living; Adult; Aged; Amyloid Neuropathies, Familial; Disability Evaluation; Female; Humans; Male; Methionine; Middle Aged; Mutation; Outcome Assessment, Health Care; Portugal; Prealbumin; Reproducibility of Results; Retrospective Studies; Severity of Illness Index; Surveys and Questionnaires; Valine

2015
A case of familial amyloid polyneuropathy (FAP ATTR Ile107Val) with proximal muscle weakness in the lower extremities.
    Rinsho shinkeigaku = Clinical neurology, 2016, 04-28, Volume: 56, Issue:4

    Topics: Aged; Amyloid Neuropathies, Familial; Electromyography; Humans; Isoleucine; Lower Extremity; Male; Muscle Weakness; Neural Conduction; Neurologic Examination; Prealbumin; Quadriceps Muscle; Valine

2016
Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease.
    Journal of the peripheral nervous system : JPNS, 2016, Volume: 21, Issue:4

    Topics: Adult; Age of Onset; Aged; Amyloid Neuropathies, Familial; Disease Progression; Female; Follow-Up Studies; Humans; Male; Methionine; Middle Aged; Mutation; Prealbumin; Retrospective Studies; Spain; Valine; Young Adult

2016
An Isolated Case of Late-onset Amyloidogenic Transthyretin Type Familial Amyloid Polyneuropathy Associated with a Mutant Transthyretin Substituting Methionine for Valine at Position 30 Showing Latent Progressive Cardiac Involvement Confirmed by Serial Ann
    Internal medicine (Tokyo, Japan), 2017, Volume: 56, Issue:2

    Topics: Aged; Amyloid Neuropathies, Familial; Asian People; Cardiomegaly; Diabetes Mellitus, Type 2; Diagnosis, Differential; Electrocardiography; Humans; Japan; Male; Methionine; Valine

2017
A rapid and sensitive prenatal diagnosis of familial amyloidotic polyneuropathy ATTR Val30Met by mass spectrometry.
    Prenatal diagnosis, 2009, Volume: 29, Issue:10

    Topics: Amniotic Fluid; Amyloid Neuropathies, Familial; Animals; Antibodies; DNA Mutational Analysis; Female; Humans; Mass Spectrometry; Methionine; Mice; Mice, Transgenic; Prealbumin; Pregnancy; Prenatal Diagnosis; Sensitivity and Specificity; Time Factors; Valine

2009
Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy.
    Journal of the neurological sciences, 2009, Dec-15, Volume: 287, Issue:1-2

    Topics: Adrenal Glands; Adult; Age Factors; Age of Onset; Aged; Amino Acid Sequence; Amino Acid Substitution; Amyloid; Amyloid Neuropathies, Familial; Coloring Agents; Congo Red; DNA Mutational Analysis; Female; Genetic Markers; Genetic Testing; Humans; Kidney; Male; Methionine; Middle Aged; Myocardium; Peripheral Nerves; Prealbumin; Staining and Labeling; Valine; Viscera; Young Adult

2009
Considering amyloidosis in patients with clinically unresponsive vitreous inflammation (Oculoleptomeningeal amyloidosis in 3 individuals with transthyretin variant Tyr69His. Vol. 44[3]).
    Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 2010, Volume: 45, Issue:1

    Topics: Adrenal Cortex Hormones; Amyloid Neuropathies, Familial; Drug Resistance; Eye Diseases; Genetic Variation; Glycine; Histidine; Humans; Inflammation; Point Mutation; Prealbumin; Tyrosine; Valine; Vitreous Body

2010
Wild-type transthyretin significantly contributes to the formation of amyloid fibrils in familial amyloid polyneuropathy patients with amyloidogenic transthyretin Val30Met.
    Human pathology, 2011, Volume: 42, Issue:2

    Topics: Abdomen; Adipose Tissue; Adult; Aged; Aged, 80 and over; Aging; Amyloid; Amyloid Neuropathies, Familial; Amyloidosis; Chromatography, High Pressure Liquid; Female; Humans; Male; Middle Aged; Mutation; Prealbumin; Spectrometry, Mass, Electrospray Ionization; Valine; Young Adult

2011
Clinical and histopathological features of familial amyloidotic polyneuropathy with transthyretin Val30Ala in a Chinese family.
    Journal of the neurological sciences, 2011, May-15, Volume: 304, Issue:1-2

    Topics: Adult; Alanine; Amyloid Neuropathies, Familial; Asian People; Fatal Outcome; Female; Humans; Male; Pedigree; Point Mutation; Prealbumin; Valine

2011
A homozygote case of familial amyloid polyneuropathy amyloidgenic transthyretin Val30Met in a non-endemic area.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2011, Volume: 18 Suppl 1

    Topics: Aged; Amyloid Neuropathies, Familial; Female; Homozygote; Humans; Methionine; Prealbumin; Valine

2011
Analysis of mitochondrial haplogroups associated with TTR Val30Ala familial amyloidotic polyneuropathy in Chinese patients.
    The International journal of neuroscience, 2012, Volume: 122, Issue:12

    Topics: Adult; Age of Onset; Aged; Alanine; Amyloid Neuropathies, Familial; Asian People; DNA, Mitochondrial; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mitochondria; Prealbumin; Valine; Young Adult

2012
Impact of aging on the progression of neuropathy after liver transplantation in transthyretin Val30Met amyloidosis.
    Muscle & nerve, 2012, Volume: 46, Issue:6

    Topics: Adult; Aging; Amyloid Neuropathies, Familial; Humans; Liver Diseases; Liver Transplantation; Longitudinal Studies; Male; Methionine; Middle Aged; Prealbumin; Valine

2012
Evidence of oxidative stress in familial amyloidotic polyneuropathy type 1.
    Archives of neurology, 2003, Volume: 60, Issue:4

    Topics: Amyloid Neuropathies, Familial; Antioxidants; Copper; Cyanogen Bromide; Erythrocytes; Genotype; Humans; Immunoblotting; Methionine; Mutation; Oxidative Stress; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Prealbumin; Reactive Oxygen Species; Superoxide Dismutase; Superoxide Dismutase-1; Valine; Zinc

2003
Outcome of liver transplantation for familial amyloidotic polyneuropathy.
    Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2003, Volume: 9, Issue:12

    Topics: Adult; Alanine; Amyloid Neuropathies, Familial; Diarrhea; Female; Glycine; Humans; Liver Transplantation; Lysine; Male; Methionine; Middle Aged; Mutation; Prealbumin; Treatment Outcome; Tyrosine; Valine

2003
A different amyloid formation mechanism: de novo oculoleptomeningeal amyloid deposits after liver transplantation.
    Transplantation, 2004, Feb-15, Volume: 77, Issue:3

    Topics: Adult; Amyloid; Amyloid Neuropathies, Familial; Central Nervous System Diseases; Cysteine; Eye; Eye Diseases; Female; Humans; Liver Transplantation; Magnetic Resonance Imaging; Male; Meninges; Methionine; Middle Aged; Mutation; Pia Mater; Postoperative Period; Prealbumin; Tyrosine; Valine

2004
Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2004, Volume: 11, Issue:1

    Topics: Aged; Amino Acid Substitution; Amyloid Neuropathies, Familial; Brain; Cerebral Veins; Homozygote; Humans; Methionine; Peripheral Nerves; Prealbumin; Spinal Cord; Valine

2004
Kidney and anemia in familial amyloidosis type I.
    Kidney international, 2004, Volume: 66, Issue:5

    Topics: Adult; Aged; Amyloid Neuropathies, Familial; Anemia; Autonomic Nervous System Diseases; Case-Control Studies; Cross-Sectional Studies; Erythropoietin; Female; Heterozygote; Humans; Kidney Failure, Chronic; Male; Methionine; Middle Aged; Mutation; Portugal; Prealbumin; Prevalence; Retrospective Studies; Valine

2004
Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family--a follow-up autopsy report.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2004, Volume: 11, Issue:3

    Topics: Amino Acid Substitution; Amyloid Neuropathies, Familial; Family; Humans; Japan; Male; Methionine; Middle Aged; Pedigree; Point Mutation; Prealbumin; Spinocerebellar Ataxias; Tomography, X-Ray Computed; Valine

2004
Phenotypic expression of familial amyloid polyneuropathy in Brazil.
    European journal of neurology, 2005, Volume: 12, Issue:4

    Topics: Adult; Age Factors; Age of Onset; Amyloid Neuropathies, Familial; Body Mass Index; Brazil; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Mutation; Neurologic Examination; Phenotype; Prealbumin; Valine

2005
Liver transplantation for familial amyloid polyneuropathy non-VAL30MET variants: are cardiac complications influenced by prophylactic pacing and immunosuppressive weaning?
    Transplantation proceedings, 2005, Volume: 37, Issue:5

    Topics: Adult; Aged; Amino Acid Substitution; Amyloid Neuropathies, Familial; Drug Administration Schedule; Female; Genetic Variation; Graft Rejection; Humans; Immunosuppressive Agents; Liver Transplantation; Male; Methionine; Middle Aged; Mutation; Prealbumin; Retrospective Studies; Tacrolimus; Valine

2005
Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal.
    Muscle & nerve, 2007, Volume: 35, Issue:1

    Topics: Adult; Age of Onset; Amino Acid Sequence; Amino Acid Substitution; Amyloid Neuropathies, Familial; Autonomic Nervous System Diseases; Female; Genetic Predisposition to Disease; Geography; Humans; Inheritance Patterns; Longitudinal Studies; Male; Methionine; Middle Aged; Mutation; Neuralgia; Peripheral Nervous System Diseases; Portugal; Prospective Studies; Sex Distribution; Valine

2007
Trigger finger as an initial manifestation of familial amyloid polyneuropathy in a patient with Ile107Val TTR.
    Internal medicine (Tokyo, Japan), 2007, Volume: 46, Issue:8

    Topics: Age of Onset; Aged; Amino Acid Substitution; Amyloid Neuropathies, Familial; Carpal Tunnel Syndrome; Female; Humans; Isoleucine; Male; Middle Aged; Prealbumin; Trigger Finger Disorder; Valine

2007
Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.
    Ophthalmology, 2007, Volume: 114, Issue:11

    Topics: Adult; Amyloid; Amyloid Neuropathies, Familial; DNA Mutational Analysis; Eye Diseases; Glycine; Humans; Intraocular Pressure; Magnetic Resonance Imaging; Male; Meninges; Ocular Hypertension; Point Mutation; Prealbumin; Trabeculectomy; Valine; Ventriculoperitoneal Shunt; Vitrectomy; Vitreous Body

2007
Epidemiology of familial amyloid polyneuropathy in Japan: Identification of a novel endemic focus.
    Journal of the neurological sciences, 2008, Jul-15, Volume: 270, Issue:1-2

    Topics: Adult; Age of Onset; Aged; Amyloid Neuropathies, Familial; Amyloidosis; Female; Humans; Japan; Male; Methionine; Middle Aged; Molecular Epidemiology; Mutation; Prealbumin; Registries; Retrospective Studies; Valine

2008
Capture of a dimeric intermediate during transthyretin amyloid formation.
    The Journal of biological chemistry, 2001, Oct-26, Volume: 276, Issue:43

    Topics: Amyloid; Amyloid Neuropathies, Familial; Anilino Naphthalenesulfonates; Asparagine; Dimerization; Fluorescent Dyes; Glutamic Acid; Guanidine; Humans; Models, Molecular; Mutation; Prealbumin; Protein Binding; Protein Denaturation; Protein Folding; Protein Structure, Secondary; Recombinant Proteins; Staining and Labeling; Temperature; Thyroxine; Valine

2001