Ingvast S - Search Results

1

Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.

Skoglund L, Brundin R, Olofsson T, Kalimo H, Ingvast S, Blom ES, Giedraitis V, Ingelsson M, Lannfelt L, Basun H, Glaser A. Skoglund L, et al. Among authors: ingvast s. Neurogenetics. 2009 Feb;10(1):27-34. doi: 10.1007/s10048-008-0155-z. Epub 2008 Oct 15. Neurogenetics. 2009. PMID: 18855025

2

New Alzheimer's disease locus on chromosome 8.

Giedraitis V, Hedlund M, Skoglund L, Blom E, Ingvast S, Brundin R, Lannfelt L, Glaser A. Giedraitis V, et al. Among authors: ingvast s. J Med Genet. 2006 Dec;43(12):931-5. doi: 10.1136/jmg.2006.043000. Epub 2006 Jul 6. J Med Genet. 2006. PMID: 16825432 Free PMC article.

3

Frontotemporal dementia-amyotrophic lateral sclerosis complex is simulated by neurodegeneration with brain iron accumulation.

Santillo AF, Skoglund L, Lindau M, Eeg-Olofsson KE, Tovi M, Engler H, Brundin RM, Ingvast S, Lannfelt L, Glaser A, Kilander L. Santillo AF, et al. Among authors: ingvast s. Alzheimer Dis Assoc Disord. 2009 Jul-Sep;23(3):298-300. doi: 10.1097/WAD.0b013e3181a2b76b. Alzheimer Dis Assoc Disord. 2009. PMID: 19568152

4

No evidence of PGRN or MAPT gene dosage alterations in a collection of patients with frontotemporal lobar degeneration.

Skoglund L, Ingvast S, Matsui T, Freeman SH, Frosch MP, Brundin R, Giedraitis V, Growdon JH, Hyman BT, Lannfelt L, Ingelsson M, Glaser A. Skoglund L, et al. Among authors: ingvast s. Dement Geriatr Cogn Disord. 2009;28(5):471-5. doi: 10.1159/000260046. Epub 2009 Nov 23. Dement Geriatr Cogn Disord. 2009. PMID: 19940479 Free PMC article.

5

The mutation spectrum of the bestrophin protein--functional implications.

Bakall B, Marknell T, Ingvast S, Koisti MJ, Sandgren O, Li W, Bergen AA, Andreasson S, Rosenberg T, Petrukhin K, Wadelius C. Bakall B, et al. Among authors: ingvast s. Hum Genet. 1999 May;104(5):383-9. doi: 10.1007/s004390050972. Hum Genet. 1999. PMID: 10394929

6

Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene.

Ponjavic V, Eksandh L, Andréasson S, Sjöström K, Bakall B, Ingvast S, Wadelius C, Ehinger B. Ponjavic V, et al. Among authors: ingvast s. Ophthalmic Genet. 1999 Dec;20(4):251-7. doi: 10.1076/opge.20.4.251.2270. Ophthalmic Genet. 1999. PMID: 10617923

7

Radiolabelling and positron emission tomography imaging of a high-affinity peptide binder to collagen type 1.

Rosestedt M, Velikyan I, Rosenström U, Estrada S, Åberg O, Weis J, Westerlund C, Ingvast S, Korsgren O, Nordeman P, Eriksson O. Rosestedt M, et al. Among authors: ingvast s. Nucl Med Biol. 2021 Feb;93:54-62. doi: 10.1016/j.nucmedbio.2020.11.006. Epub 2020 Nov 28. Nucl Med Biol. 2021. PMID: 33321470 Free article.

8

Gene expression analysis of human islets in a subject at onset of type 1 diabetes.

Hopfgarten J, Stenwall PA, Wiberg A, Anagandula M, Ingvast S, Rosenling T, Korsgren O, Skog O. Hopfgarten J, et al. Among authors: ingvast s. Acta Diabetol. 2014 Apr;51(2):199-204. doi: 10.1007/s00592-013-0479-5. Epub 2013 Apr 27. Acta Diabetol. 2014. PMID: 23624551 Free PMC article.

9

Human islet isolation processing times shortened by one hour: minimized incubation time between tissue harvest and islet purification.

Ståhle M, Honkanen-Scott M, Ingvast S, Korsgren O, Friberg AS. Ståhle M, et al. Among authors: ingvast s. Transplantation. 2013 Dec 27;96(12):e91-3. doi: 10.1097/01.TP.0000437562.31212.d5. Transplantation. 2013. PMID: 24342944 No abstract available.

10

Evaluation of RT-PCR and immunohistochemistry as tools for detection of enterovirus in the human pancreas and islets of Langerhans.

Skog O, Ingvast S, Korsgren O. Skog O, et al. Among authors: ingvast s. J Clin Virol. 2014 Oct;61(2):242-7. doi: 10.1016/j.jcv.2014.07.014. Epub 2014 Jul 30. J Clin Virol. 2014. PMID: 25132399 Free PMC article.

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