Lannfelt L - Search Results

1

Neuronal nicotinic receptor deficits in Alzheimer patients with the Swedish amyloid precursor protein 670/671 mutation.

Marutle A, Warpman U, Bogdanovic N, Lannfelt L, Nordberg A. Marutle A, et al. Among authors: lannfelt l. J Neurochem. 1999 Mar;72(3):1161-9. doi: 10.1046/j.1471-4159.2000.0721161.x. J Neurochem. 1999. PMID: 10037489 Free article.

2

Decreased alpha-secretase-cleaved amyloid precursor protein as a diagnostic marker for Alzheimer's disease.

Lannfelt L, Basun H, Wahlund LO, Rowe BA, Wagner SL. Lannfelt L, et al. Nat Med. 1995 Aug;1(8):829-32. doi: 10.1038/nm0895-829. Nat Med. 1995. PMID: 7585189

3

Characterization of stable complexes involving apolipoprotein E and the amyloid beta peptide in Alzheimer's disease brain.

Näslund J, Thyberg J, Tjernberg LO, Wernstedt C, Karlström AR, Bogdanovic N, Gandy SE, Lannfelt L, Terenius L, Nordstedt C. Näslund J, et al. Among authors: lannfelt l. Neuron. 1995 Jul;15(1):219-28. doi: 10.1016/0896-6273(95)90079-9. Neuron. 1995. PMID: 7619525 Free article.

4

Amyloid precursor protein mutation at codon 713 (Ala-->Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent).

Forsell C, Lannfelt L. Forsell C, et al. Among authors: lannfelt l. Neurosci Lett. 1995 Jan 23;184(2):90-3. doi: 10.1016/0304-3940(94)11176-j. Neurosci Lett. 1995. PMID: 7724053

5

Apolipoprotein epsilon 4 allele and disease progression in patients with late-onset Alzheimer's disease.

Basun H, Grut M, Winblad B, Lannfelt L. Basun H, et al. Among authors: lannfelt l. Neurosci Lett. 1995 Jan 2;183(1-2):32-4. doi: 10.1016/0304-3940(94)11107-t. Neurosci Lett. 1995. PMID: 7746480

6

Increased cerebrospinal fluid tau in patients with Alzheimer's disease.

Jensen M, Basun H, Lannfelt L. Jensen M, et al. Among authors: lannfelt l. Neurosci Lett. 1995 Feb 17;186(2-3):189-91. doi: 10.1016/0304-3940(95)11297-a. Neurosci Lett. 1995. PMID: 7777193 Clinical Trial.

7

Microsatellite D21S210 (GT-12) allele frequencies in sporadic Alzheimer's disease.

Lannfelt L, Lilius L, Viitanen M, Houlden H, Rossor M, Hardy J, Winblad B, Basun H. Lannfelt L, et al. Acta Neurol Scand. 1995 Feb;91(2):145-8. doi: 10.1111/j.1600-0404.1995.tb00422.x. Acta Neurol Scand. 1995. PMID: 7785426

8

The significance of the Swedish APP670/671 mutation for the development of Alzheimer's disease amyloidosis.

Johnston J, O'Neill C, Lannfelt L, Winblad B, Cowburn RF. Johnston J, et al. Among authors: lannfelt l. Neurochem Int. 1994 Jul;25(1):73-80. doi: 10.1016/0197-0186(94)90056-6. Neurochem Int. 1994. PMID: 7950974 Review.

9

Increased beta-amyloid release and levels of amyloid precursor protein (APP) in fibroblast cell lines from family members with the Swedish Alzheimer's disease APP670/671 mutation.

Johnston JA, Cowburn RF, Norgren S, Wiehager B, Venizelos N, Winblad B, Vigo-Pelfrey C, Schenk D, Lannfelt L, O'Neill C. Johnston JA, et al. Among authors: lannfelt l. FEBS Lett. 1994 Nov 14;354(3):274-8. doi: 10.1016/0014-5793(94)01137-0. FEBS Lett. 1994. PMID: 7957938 Free article.

10

A large Swedish family with Alzheimer's disease with a codon 670/671 amyloid precursor protein mutation. A clinical and genealogical investigation.

Axelman K, Basun H, Winblad B, Lannfelt L. Axelman K, et al. Among authors: lannfelt l. Arch Neurol. 1994 Dec;51(12):1193-7. doi: 10.1001/archneur.1994.00540240037013. Arch Neurol. 1994. PMID: 7986173

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