4884226 13367520 2613237 2360796 11261421 14404854 13593935 4952599 7018469 1729888 19644733 8990019[uid] - Search Results

Year	Number of Results
1956	1
1958	1
1959	1
1967	1
1969	1
1981	1
1989	1
1990	1
1992	1
1997	1
2001	1
2009	1
2024	0

1

The genetic amyloidoses with particular reference to hereditary neuropathic amyloidosis, type II (Indiana or Rukavina type).

Mahloudji M, Teasdall RD, Adamkiewicz JJ, Hartmann WH, Lambird PA, McKusick VA. Mahloudji M, et al. Medicine (Baltimore). 1969 Jan;48(1):1-37. Medicine (Baltimore). 1969. PMID: 4884226 Review. No abstract available.

2

Familial primary systemic amyloidosis: an experimental, genetic and clinical study.

BLOCK WD, CURTIS AC, RUKAVINA JG. BLOCK WD, et al. J Invest Dermatol. 1956 Sep;27(3):111-31. doi: 10.1038/jid.1956.84. J Invest Dermatol. 1956. PMID: 13367520 Free article. No abstract available.

3

Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification.

Nichols WC, Liepnieks JJ, McKusick VA, Benson MD. Nichols WC, et al. Genomics. 1989 Oct;5(3):535-40. doi: 10.1016/0888-7543(89)90020-7. Genomics. 1989. PMID: 2613237

4

Diagnosis of Maryland/German familial amyloidotic polyneuropathy using allele-specific, enzymatically amplified, genomic DNA.

Mendell JR, Jiang XS, Warmolts JR, Nichols WC, Benson MD. Mendell JR, et al. Ann Neurol. 1990 May;27(5):553-7. doi: 10.1002/ana.410270516. Ann Neurol. 1990. PMID: 2360796

5

Transthyretin-associated neuropathic amyloidosis. Pathogenesis and treatment.

Hund E, Linke RP, Willig F, Grau A. Hund E, et al. Neurology. 2001 Feb 27;56(4):431-5. doi: 10.1212/wnl.56.4.431. Neurology. 2001. PMID: 11261421 Review.

6

Vitreous opacities diagnostic of familial primary amyloidosis.

KAUFMAN HE, THOMAS LB. KAUFMAN HE, et al. N Engl J Med. 1959 Dec 17;261:1267-71. doi: 10.1056/NEJM195912172612503. N Engl J Med. 1959. PMID: 14404854 No abstract available.

7

Primary familial amyloidosis.

KAUFMAN HE. KAUFMAN HE. AMA Arch Ophthalmol. 1958 Dec;60(6):1036-43. doi: 10.1001/archopht.1958.00940081056009. AMA Arch Ophthalmol. 1958. PMID: 13593935 No abstract available.

8

Primary familial amyloidosis.

Wong VG, McFarlin DE. Wong VG, et al. Arch Ophthalmol. 1967 Aug;78(2):208-13. doi: 10.1001/archopht.1967.00980030210015. Arch Ophthalmol. 1967. PMID: 4952599 No abstract available.

9

Amyloid in hereditary amyloid polyneuropathy is related to prealbumin.

Dalakas MC, Engel WK. Dalakas MC, et al. Arch Neurol. 1981 Jul;38(7):420-2. doi: 10.1001/archneur.1981.00510070054008. Arch Neurol. 1981. PMID: 7018469

10

A specific test for transthyretin 122 (Val----Ile), based on PCR-primer-introduced restriction analysis (PCR-PIRA): confirmation of the gene frequency in blacks.

Jacobson DR. Jacobson DR. Am J Hum Genet. 1992 Jan;50(1):195-8. Am J Hum Genet. 1992. PMID: 1729888 Free PMC article.

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