Almqvist E - Search Results

1

Screening of amyloid precursor protein gene mutation (APP 717 Val-->Ile) in Swedish families with Alzheimer's disease.

Almqvist E, Lake S, Axelman K, Johansson K, Winblad B. Almqvist E, et al. J Neural Transm Park Dis Dement Sect. 1993;6(2):151-6. doi: 10.1007/BF02261009. J Neural Transm Park Dis Dement Sect. 1993. PMID: 8117412

2

Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in Sweden.

Lannfelt L, Viitanen M, Johansson K, Axelman K, Lilius L, Almqvist E, Winblad B. Lannfelt L, et al. Among authors: almqvist e. Neurosci Lett. 1993 Apr 16;153(1):85-7. doi: 10.1016/0304-3940(93)90083-w. Neurosci Lett. 1993. PMID: 8510829

3

A comparison of multiplex and simplex families with Alzheimer's disease/senile dementia of Alzheimer type within a well defined population.

Alafuzoff I, Almqvist E, Adolfsson R, Lake S, Wallace W, Greenberg DA, Winblad B. Alafuzoff I, et al. Among authors: almqvist e. J Neural Transm Park Dis Dement Sect. 1994;7(1):61-72. doi: 10.1007/BF02252663. J Neural Transm Park Dis Dement Sect. 1994. PMID: 8579770

4

Geographical distribution of haplotypes in Swedish families with Huntington's disease.

Almqvist E, Andrew S, Theilmann J, Goldberg P, Zeisler J, Drugge U, Grandell U, Tapper-Persson M, Winblad B, Hayden M, et al. Almqvist E, et al. Hum Genet. 1994 Aug;94(2):124-8. doi: 10.1007/BF00202856. Hum Genet. 1994. PMID: 8045558

5

Linkage of G8 (D4S10) in two Swedish families with Huntington's disease.

Holmgren G, Almqvist EW, Anvret M, Conneally M, Hobbs W, Mattsson B, Wahlström J, Winblad B, Gusella JF. Holmgren G, et al. Among authors: almqvist ew. Clin Genet. 1987 Nov;32(5):289-94. doi: 10.1111/j.1399-0004.1987.tb03292.x. Clin Genet. 1987. PMID: 2961484

6

Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic status.

Wahlin TB, Lundin A, Bäckman L, Almqvist E, Haegermark A, Winblad B, Anvret M. Wahlin TB, et al. Among authors: almqvist e. Am J Med Genet. 1997 Dec 19;73(3):356-65. doi: 10.1002/(sici)1096-8628(19971219)73:3<356::aid-ajmg24>3.0.co;2-h. Am J Med Genet. 1997. PMID: 9415699

7

A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.

Xiang F, Almqvist EW, Huq M, Lundin A, Hayden MR, Edström L, Anvret M, Zhang Z. Xiang F, et al. Among authors: almqvist ew. Am J Hum Genet. 1998 Nov;63(5):1431-8. doi: 10.1086/302093. Am J Hum Genet. 1998. PMID: 9792871 Free PMC article.

8

[A prognostic test of Huntington disease--detailed interviews with persons at risk].

Mattsson B, Almqvist EW. Mattsson B, et al. Among authors: almqvist ew. Lakartidningen. 1990 Oct 3;87(40):3204-6. Lakartidningen. 1990. PMID: 2146453 Swedish. No abstract available.

9

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.

Kremer B, Almqvist E, Theilmann J, Spence N, Telenius H, Goldberg YP, Hayden MR. Kremer B, et al. Among authors: almqvist e. Am J Hum Genet. 1995 Aug;57(2):343-50. Am J Hum Genet. 1995. PMID: 7668260 Free PMC article.

10

Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease.

Telenius H, Almqvist E, Kremer B, Spence N, Squitieri F, Nichol K, Grandell U, Starr E, Benjamin C, Castaldo I, et al. Telenius H, et al. Among authors: almqvist e. Hum Mol Genet. 1995 Feb;4(2):189-95. doi: 10.1093/hmg/4.2.189. Hum Mol Genet. 1995. PMID: 7757066 Free article.

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