87 related articles for article (PubMed ID: 2564248)
1. Genetic amyloidosis: recent advances.
Benson MD; Wallace MR
Adv Nephrol Necker Hosp; 1989; 18():129-37. PubMed ID: 2564248
[TBL] [Abstract][Full Text] [Related]
2. Outcome of liver transplantation for familial amyloidotic polyneuropathy.
Sharma P; Perri RE; Sirven JE; Zeldenrust SR; Brandhagen DJ; Rosen CB; Douglas DD; Mulligan DC; Rakela J; Wiesner RH; Balan V
Liver Transpl; 2003 Dec; 9(12):1273-80. PubMed ID: 14625827
[TBL] [Abstract][Full Text] [Related]
3. Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M).
Lobato L
J Nephrol; 2003; 16(3):438-42. PubMed ID: 12832749
[TBL] [Abstract][Full Text] [Related]
4. Prenatal detection of a gene for hereditary amyloidosis.
Nichols WC; Padilla LM; Benson MD
Am J Med Genet; 1989 Dec; 34(4):520-4. PubMed ID: 2516414
[TBL] [Abstract][Full Text] [Related]
5. Progression of cardiomyopathy and neuropathy after liver transplantation in a patient with familial amyloidotic polyneuropathy caused by tyrosine-77 transthyretin variant.
García-Herola A; Prieto M; Pascual S; Berenguer M; López-Viedma B; Mir J; Vilchez JJ; Berenguer J
Liver Transpl Surg; 1999 May; 5(3):246-8. PubMed ID: 10226117
[TBL] [Abstract][Full Text] [Related]
6. Amyloidotic polyneuropathy in a Jewish family. Evidence for the genetic heterogeneity of the lower limb familial amyloidotic neuropathies.
Gafni J; Fischel B; Reif R; Yaron M; Pras M
Q J Med; 1985 Apr; 55(216):33-44. PubMed ID: 3859886
[TBL] [Abstract][Full Text] [Related]
7. Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy.
Nakazato M; Sasaki H; Furuya H; Sakaki Y; Kurihara T; Matsukura S; Kangawa K; Matsuo H
Ann Neurol; 1987 Jun; 21(6):596-8. PubMed ID: 3037992
[TBL] [Abstract][Full Text] [Related]
8. Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family.
Wallace MR; Conneally PM; Long GL; Benson MD
Am J Med Genet; 1986 Oct; 25(2):335-41. PubMed ID: 2877582
[TBL] [Abstract][Full Text] [Related]
9. Diagnosis of familial amyloidotic polyneuropathy in France.
Satier F; Nichols WC; Benson MD
Clin Genet; 1990 Dec; 38(6):469-73. PubMed ID: 1981182
[TBL] [Abstract][Full Text] [Related]
10. [Identification of genetic carriers in familial amyloidosis with polyneuropathy is possible with the DNA technic].
Holmgren G; Drugge U; Lundgren E; Sandgren O; Steen L
Lakartidningen; 1988 Nov; 85(44):3677-9. PubMed ID: 2904519
[No Abstract] [Full Text] [Related]
11. Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy.
Yoshioka K; Sasaki H; Yoshioka N; Furuya H; Harada T; Kito S; Sakaki Y
Mol Biol Med; 1986 Aug; 3(4):319-28. PubMed ID: 3022107
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs.
Furuya H; Yoshioka K; Sasaki H; Sakaki Y; Nakazato M; Matsuo H; Nakadai A; Ikeda S; Yanagisawa N
J Clin Invest; 1987 Dec; 80(6):1706-11. PubMed ID: 3479441
[TBL] [Abstract][Full Text] [Related]
13. Restriction fragment length polymorphism analysis of mutated transthyretin in vitreous amyloidosis.
Sandgren O; Holmgren G; Lundgren E; Steen L
Arch Ophthalmol; 1988 Jun; 106(6):790-2. PubMed ID: 2897192
[TBL] [Abstract][Full Text] [Related]
14. Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy.
Maeda S; Mita S; Araki S; Shimada K
Mol Biol Med; 1986 Aug; 3(4):329-38. PubMed ID: 3022108
[TBL] [Abstract][Full Text] [Related]
15. Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis.
Wallace MR; Dwulet FE; Williams EC; Conneally PM; Benson MD
J Clin Invest; 1988 Jan; 81(1):189-93. PubMed ID: 2891727
[TBL] [Abstract][Full Text] [Related]
16. [Application to transthyretin analysis].
Ueda M; Ando Y
Rinsho Byori; 2006 Jun; 54(6):601-8. PubMed ID: 16872010
[TBL] [Abstract][Full Text] [Related]
17. New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online.
Misrahi AM; Plante V; Lalu T; Serre L; Adams D; Lacroix DC; Saïd G
Hum Mutat; 1998; 12(1):71. PubMed ID: 10627135
[TBL] [Abstract][Full Text] [Related]
18. Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
Holmgren G; Bergström S; Drugge U; Lundgren E; Nording-Sikström C; Sandgren O; Steen L
Clin Genet; 1992 Jan; 41(1):39-41. PubMed ID: 1353008
[TBL] [Abstract][Full Text] [Related]
19. [Two sibling patients with late-onset familial amyloidotic polyneuropathy and atypical clinical manifestations].
Matsushima K; Kotoh H; Takagi S; Okabe T; Shinohara Y
Rinsho Shinkeigaku; 1992 May; 32(5):538-40. PubMed ID: 1458734
[TBL] [Abstract][Full Text] [Related]
20. Human transthyretin (prealbumin) gene and molecular genetics of familial amyloidotic polyneuropathy.
Sakaki Y; Yoshioka K; Tanahashi H; Furuya H; Sasaki H
Mol Biol Med; 1989 Apr; 6(2):161-8. PubMed ID: 2693890
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]