Lebertransplantation bei Familiärer Amyloid Polyneuropathie Fallbericht und Literaturübersicht
暂无分享,去创建一个
M. Manns | G. Oehler | R. Pichlmayr | B. Ringe | R. P. Linke | K. Altland | H. Maschek | M. Krüger
[1] D. Jenne,et al. A new isoleucine substitution of Val-20 in transthyretin tetramers selectively impairs dimer-dimer contacts and causes systemic amyloidosis. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[2] M. Benson,et al. Demonstration of mutant TTR(Ala47) in spinal fluid and its absence in plasma after liver transplantation , 1996, Neuromuscular Disorders.
[3] T. Meinertz,et al. Klinik, Diagnostik und Therapie der kardiovaskulären autonomen Neuropathie , 1996 .
[4] S. Kawasaki,et al. A case of familial amyloid polyneuropathy treated with partial liver transplantation using a graft from a living related donor. , 1995, Transplantation.
[5] M. Pepys,et al. Treatment of amyloidosis. , 1995, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[6] P. Parrilla,et al. Clinical improvement after liver transplantation for type I familial amyloid polyneuropathy , 1995, The British journal of surgery.
[7] Y. Ando,et al. Intranasal l‐threo‐3,4,‐dihydroxyphenylserine in Treating Diarrhea Associated With Familial Amyloidotic Polyneuropathy , 1995, Pharmacotherapy.
[8] T. Murakami,et al. Genetic abnormalities and pathogenesis of familial amyloidotic polyneuropathy , 1995, Pathology international.
[9] K. Yamamura,et al. Transgenic mouse model of familial amyloidotic polyneuropathy type I: its production, biological features, and usefulness. , 1995, Laboratory animal science.
[10] U. Gundel. [Liver transplantation in familial amyloidosis]. , 1995, Deutsche medizinische Wochenschrift.
[11] G. Holmgren,et al. Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate. , 1994, Journal of medical genetics.
[12] R. Simms,et al. Orthotopic liver transplantation for familial amyloidotic polyneuropathy. , 1994, Clinical transplantation.
[13] M. Nakazato,et al. Treatment of a Japanese patient with familial amyloidotic polyneuropathy with orthotopic liver transplantation. , 1994, Internal medicine.
[14] P. Parrilla,et al. [Liver transplantation for the treatment of type I familial amyloidotic polyneuropathy]. , 1993, Medicina clinica.
[15] A. Teixeira,et al. Immunoassay for Transthyretin Variants associated with Amyloid Neuropathy , 1993, Scandinavian journal of immunology.
[16] M. Saraiva,et al. Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant. , 1993, British heart journal.
[17] K. Bhatia,et al. Transthyretin gene mutations in British and French patients with amyloid neuropathy. , 1993, Journal of neurology, neurosurgery, and psychiatry.
[18] B. Wallin,et al. Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis , 1993, The Lancet.
[19] D. Adams,et al. Late‐onset familial amyloid polyneuropathy with the TTR Met 30 mutation in France , 1993, Clinical genetics.
[20] S. Heim,et al. [The value of nerve biopsy in the diagnosis of familial amyloidosis]. , 1993, Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis.
[21] L. Steen,et al. Oesophageal dysfunction in familial amyloidosis with polyneuropathy. , 1993, Clinical physiology.
[22] I. Conceição,et al. [Familial amyloidotic polyneuropathy --Portuguese type-- clinical and neurophysiologic course]. , 1993, Acta medica portuguesa.
[23] A. Cohen,et al. Advances in amyloidosis. , 1993, Current opinion in rheumatology.
[24] A. Hays,et al. Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70 , 1992, Neurology.
[25] M. Alves,et al. Octreotide--a new treatment for diarrhoea in familial amyloidotic polyneuropathy. , 1992, Journal of neurology, neurosurgery, and psychiatry.
[26] J. Kere,et al. Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family. , 1992, Genomics.
[27] Y. Ando,et al. Role of autonomic nerve functions in patients with familial amyloidotic polyneuropathy as analyzed by laser doppler flowmetry, capsule hydrograph, and cardiographic R–R interval , 1992, Muscle & nerve.
[28] V. Regnault,et al. Specific Removal of Transthyretin from Plasma of Patients with Familial Amyloidotic Polyneuropathy: Optimization of an Immunoadsorption Procedure , 1992, The International journal of artificial organs.
[29] L. Steen,et al. Bile acid malabsorption caused by gastrointestinal motility dysfunction? An investigation of gastrointestinal disturbances in familial amyloidosis with polyneuropathy. , 1992, Scandinavian journal of gastroenterology.
[30] G. Holmgren,et al. Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP‐met30) , 1991, Clinical genetics.
[31] M. R. Almeida,et al. Molecular analyses of an acidic transthyretin Asn 90 variant. , 1991, American journal of human genetics.
[32] M. L. Sales-Luis,et al. Treatment of familial amyloidotic polyneuropathy (Portuguese type) by plasma exchange. , 1991, Muscle & nerve.
[33] Y. Sakaki,et al. Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP). , 1991, Biochemistry.
[34] F. Tashiro,et al. Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I. , 1991, The American journal of pathology.
[35] J. G. Monteiro,et al. Ocular changes in familial amyloidotic polyneuropathy with dense vitreous opacities , 1991, Eye.
[36] G. Holmgren,et al. Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene. , 1990, Archives of ophthalmology.
[37] M. Pepys,et al. Evaluation of systemic amyloidosis by scintigraphy with 123I-labeled serum amyloid P component. , 1990, The New England journal of medicine.
[38] Y. Sakaki,et al. Type I familial amyloid polyneuropathy. A pathological study of the peripheral nervous system. , 1990, Brain : a journal of neurology.
[39] S. Nishiguchi,et al. Transgenic mouse model of familial amyloidotic polyneuropathy. , 1989, Molecular biology & medicine.
[40] D. Huhn,et al. Immunoelectron microscopic identification of human AA-type amyloid: exploration of various monoclonal AA-antibodies, methods of fixation, embedding and of other parameters for the protein-A gold method. , 1989, Laboratory investigation; a journal of technical methods and pathology.
[41] Mutsuo Takahashi,et al. Amyloid protein of vessels in leptomeninges, cortices, choroid plexuses, and pituitary glands from patients with systemic amyloidosis. , 1989, Human pathology.
[42] Y. Sakaki,et al. Clinical features and diagnosis by recombinant DNA techniques of familial amyloid polyneuropathy in Japan. , 1989, Research communications in chemical pathology and pharmacology.
[43] M. Saraiva,et al. Simplified method for screening populations at risk for transthyretin Met30-associated familial amyloidotic polyneuropathy. , 1989, Clinical chemistry.
[44] N. Yanagisawa,et al. Peripheral nerve pathological findings in familial amyloid polyneuropathy: A correlative study of proximal sciatic nerve and sural nerve lesions , 1989, Annals of neurology.
[45] B. Olofsson,et al. Autonomic neuropathy in familial amyloidotic polyneuropathy , 1989, Acta neurologica Scandinavica.
[46] D. V. van Thiel,et al. Liver transplantation (1). , 1989, The New England journal of medicine.
[47] M. Benson,et al. Genetic amyloidosis: recent advances. , 1989, Advances in nephrology from the Necker Hospital.
[48] M. Yamada,et al. Treatment by pacemaker in familial amyloid polyneuropathy. , 1989, Chest.
[49] J. R. Wohlgethan,et al. The clinical and biochemical spectrum of hereditary amyloidosis. , 1988, Seminars in arthritis and rheumatism.
[50] N. Yanagisawa,et al. Diagnostic value of abdominal fat tissue aspirate in familial amyloid polyneuropathy , 1987, Journal of the Neurological Sciences.
[51] N. Ito,et al. Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients. , 1987, Brain : a journal of neurology.
[52] A. Banzhoff,et al. Paraffin oil protected high resolution hybrid isoelectric focusing for the demonstration of substitutions of neutral amino acids in denatured proteins: The case of four human transthyretin (prealbumin) variants associated with familial amyloidotic polyneuropathy , 1987 .
[53] J. Darnell,et al. Transcriptional control of the mouse prealbumin (transthyretin) gene: both promoter sequences and a distinct enhancer are cell specific , 1986, Molecular and cellular biology.
[54] S. Araki,et al. Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy. , 1986, Molecular biology & medicine.
[55] B. Olofsson,et al. Electrophysiologic evaluation of the cardiac conduction system and its autonomic regulation in familial amyloid polyneuropathy. , 1985, The American journal of cardiology.
[56] D. Glass,et al. Evidence against close linkage to HLA of the gene for familial amyloid polyneuropathy. , 1985, Arthritis and rheumatism.
[57] A. Cohen,et al. Esophageal manometry in familial amyloid polyneuropathy. , 1985, The American journal of medicine.
[58] T. Shows,et al. Localization of the human prealbumin gene to chromosome 18. , 1985, Biochemical and biophysical research communications.
[59] F. Kametani,et al. A variant prealbumin-related low molecular weight amyloid fibril protein in familial amyloid polyneuropathy of Japanese origin. , 1984, Biochemical and biophysical research communications.
[60] R. Linke. Monoclonal Antibodies Against Amyloid Fibril , 1984 .
[61] L. Steen,et al. Relationship between morphological findings and function of the small intestine in familial amyloidosis with polyneuropathy. , 1983, Scandinavian journal of gastroenterology.
[62] N. Yanagisawa,et al. Gastrointestinal amyloid deposition in familial amyloid polyneuropathy , 1982, Neurology.
[63] R. Linke. Immunohistochemical identification and cross reactions of amyloid fibril proteins in senile heart and amyloid in familial polyneuropathy. Lack of reactivity with cerebral amyloid in Alzheimer's disease. , 1982, Clinical neuropathology.
[64] A. Cohen,et al. Skin involvement in familial amyloidotic polyneuropathy , 1981, Neurology.
[65] M. Benson. Partial amino acid sequence homology between an heredofamilial amyloid protein and human plasma prealbumin. , 1981, The Journal of clinical investigation.
[66] C. Andrade. A PECULIAR FORM OF PERIPHERAL NEUROPATHY , 1951, Acta psychiatrica et neurologica Scandinavica.