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Items: 18

1.

Risk of cancer among Finnish multiple sclerosis patients.

Hongell K, Kurki S, Sumelahti ML, Soilu-Hänninen M.

Mult Scler Relat Disord. 2019 Aug 5;35:221-227. doi: 10.1016/j.msard.2019.08.005. [Epub ahead of print]

PMID:
31404761
2.

Epstein-barr virus and multiple sclerosis risk in the finnish maternity cohort.

Munger KL, Hongell K, Cortese M, Åivo J, Soilu-Hänninen M, Surcel HM, Ascherio A.

Ann Neurol. 2019 Sep;86(3):436-442. doi: 10.1002/ana.25532. Epub 2019 Jul 3.

PMID:
31226219
3.

Efficacy and safety outcomes in vitamin D supplement users in the fingolimod phase 3 trials.

Hongell K, Silva DG, Ritter S, Meier DP, Soilu-Hänninen M.

J Neurol. 2018 Feb;265(2):348-355. doi: 10.1007/s00415-017-8697-3. Epub 2017 Dec 14.

PMID:
29243005
4.

25-Hydroxyvitamin D deficiency and risk of MS among women in the Finnish Maternity Cohort.

Munger KL, Hongell K, Åivo J, Soilu-Hänninen M, Surcel HM, Ascherio A.

Neurology. 2017 Oct 10;89(15):1578-1583. doi: 10.1212/WNL.0000000000004489. Epub 2017 Sep 13.

5.

Vitamin D Status During Pregnancy and Risk of Multiple Sclerosis in Offspring of Women in the Finnish Maternity Cohort.

Munger KL, Åivo J, Hongell K, Soilu-Hänninen M, Surcel HM, Ascherio A.

JAMA Neurol. 2016 May 1;73(5):515-9. doi: 10.1001/jamaneurol.2015.4800.

6.

Chromosome survey of seals in the Baltic Sea in 1988-1992.

Hongell K.

Arch Environ Contam Toxicol. 1996 Oct;31(3):399-403.

PMID:
8854834
7.

A duplication within the critical fertility region of X chromosome in a mentally retarded woman with normal menarche.

Knuutila S, Heinonen K, Hongell K, Varonen S, Simell O.

Hereditas. 1984;101(2):253-5. No abstract available.

8.

Trisomy 13 in the mouse.

Hongell K, Gropp A.

Teratology. 1982 Aug;26(1):95-104.

PMID:
7135263
9.

A chromosome survey of 1062 mentally retarded patients. Evaluation of a long-term study at the Rinnekoti institution, Finland.

Gripenberg U, Hongell K, Knuutila S, Kähkönen M, Leisti J.

Hereditas. 1980;92(2):223-8. No abstract available.

10.
11.

Two cases of an abnormal short arm of chromosome 8 (8p+) associated with mental retardation.

Hongell K, Knuutila S, Westermarck T.

Clin Genet. 1978 Feb;13(2):237-40.

PMID:
627113
12.

Free trisomy 9P in elderly woman.

Gripenberg U, Hongell K, Iivanainen M, Kivimäki T.

Ann Genet. 1977 Mar;20(1):36-40.

PMID:
302671
13.

Long-lived photoproducts of porphyropsin in the retina of the crucian carp (Carassius carassius).

Donner KO, Hemilä S, Hongell K, Reuter T.

Vision Res. 1974 Dec;14(12):1359-70. No abstract available.

PMID:
4446366
14.

Australia antigen in Down's syndrome patients with Robertsonian translocation.

Tevaluoto-Aarnio M, Hongell K.

Med Biol. 1974 Feb;52(1):70-1. No abstract available.

PMID:
4283654
15.

A Gq deletion in a girl with Down's syndrome.

Hongell K, Airaksinen E.

Hum Hered. 1972;22(1):80-5. No abstract available.

PMID:
4260912
16.

Down's syndrome. Incidence of translocations in Finland.

Hongell K, Gripenberg U, Iivanainen M.

Hum Hered. 1972;22(1):7-14. No abstract available.

PMID:
4260911
17.

Neurological aspects of mental retardation associated with chromosome aberrations.

Iivanainen M, Gripenberg U, Hongell K.

Acta Paediatr Scand Suppl. 1970;206:Suppl 206:100+. No abstract available.

PMID:
5276922
18.

[Chromosome abnormalities].

Hongell K.

Katilolehti. 1968 Dec;73(12):524-30. Finnish. No abstract available.

PMID:
5191616

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