Lannfelt L - Search Results

1

The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation.

Nilsberth C, Westlind-Danielsson A, Eckman CB, Condron MM, Axelman K, Forsell C, Stenh C, Luthman J, Teplow DB, Younkin SG, Näslund J, Lannfelt L. Nilsberth C, et al. Among authors: lannfelt l. Nat Neurosci. 2001 Sep;4(9):887-93. doi: 10.1038/nn0901-887. Nat Neurosci. 2001. PMID: 11528419

2

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid.

Mullan M, Crawford F, Axelman K, Houlden H, Lilius L, Winblad B, Lannfelt L. Mullan M, et al. Among authors: lannfelt l. Nat Genet. 1992 Aug;1(5):345-7. doi: 10.1038/ng0892-345. Nat Genet. 1992. PMID: 1302033

3

The Swedish mutation causes early-onset Alzheimer's disease by beta-secretase cleavage within the secretory pathway.

Haass C, Lemere CA, Capell A, Citron M, Seubert P, Schenk D, Lannfelt L, Selkoe DJ. Haass C, et al. Among authors: lannfelt l. Nat Med. 1995 Dec;1(12):1291-6. doi: 10.1038/nm1295-1291. Nat Med. 1995. PMID: 7489411

4

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

5

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.

6

Schizophrenia and APP gene mutations.

Jönsson E, Forsell C, Lannfelt L, Sedvall G. Jönsson E, et al. Among authors: lannfelt l. Biol Psychiatry. 1995 Jan 15;37(2):135-6. doi: 10.1016/0006-3223(94)00211-K. Biol Psychiatry. 1995. PMID: 7718679 No abstract available.

7

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

8

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

9

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.

10

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

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