Kalimo H - Search Results

1

[CADASIL disease: a hereditary arterial disease leading to brain infarctions and dementia].

Kalimo H, Aho T, Amberla K, Baumann M, Herva R, Juvonen V, Kalimo K, Mononen H, Myllylä V, Pöyhönen M, Rinne J, Savontaus ML, Sonninen P, Sonninen V, Tuisku S, Viitanen M. Kalimo H, et al. Among authors: kalimo k. Duodecim. 1998;114(20):2041-51. Duodecim. 1998. PMID: 11717724 Review. Finnish. No abstract available.

2

CADASIL: hereditary arteriopathy leading to multiple brain infarcts and dementia.

Viitanen M, Kalimo H. Viitanen M, et al. Among authors: kalimo h. Ann N Y Acad Sci. 2000 Apr;903:273-84. doi: 10.1111/j.1749-6632.2000.tb06377.x. Ann N Y Acad Sci. 2000. PMID: 10818516 Review.

3

CADASIL: hereditary disease of arteries causing brain infarcts and dementia.

Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, Pöyhönen M, Rinne JO, Savontaus M, Tuisku S, Winblad B. Kalimo H, et al. Neuropathol Appl Neurobiol. 1999 Aug;25(4):257-65. doi: 10.1046/j.1365-2990.1999.00198.x. Neuropathol Appl Neurobiol. 1999. PMID: 10476042 Review.

4

CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.

Kalimo H, Ruchoux MM, Viitanen M, Kalaria RN. Kalimo H, et al. Brain Pathol. 2002 Jul;12(3):371-84. doi: 10.1111/j.1750-3639.2002.tb00451.x. Brain Pathol. 2002. PMID: 12146805 Free PMC article. Review.

5

Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patients.

Tuominen S, Miao Q, Kurki T, Tuisku S, Pöyhönen M, Kalimo H, Viitanen M, Sipilä HT, Bergman J, Rinne JO. Tuominen S, et al. Among authors: kalimo h. Stroke. 2004 May;35(5):1063-7. doi: 10.1161/01.STR.0000124124.69842.2d. Epub 2004 Mar 11. Stroke. 2004. PMID: 15017012

6

Insidious cognitive decline in CADASIL.

Amberla K, Wäljas M, Tuominen S, Almkvist O, Pöyhönen M, Tuisku S, Kalimo H, Viitanen M. Amberla K, et al. Among authors: kalimo h. Stroke. 2004 Jul;35(7):1598-602. doi: 10.1161/01.STR.0000129787.92085.0a. Epub 2004 May 13. Stroke. 2004. PMID: 15143298

7

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation.

Tuominen S, Juvonen V, Amberla K, Jolma T, Rinne JO, Tuisku S, Kurki T, Marttila R, Pöyhönen M, Savontaus ML, Viitanen M, Kalimo H. Tuominen S, et al. Among authors: kalimo h. Stroke. 2001 Aug;32(8):1767-74. doi: 10.1161/01.str.32.8.1767. Stroke. 2001. PMID: 11486103

8

Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Miao Q, Paloneva T, Tuominen S, Pöyhönen M, Tuisku S, Viitanen M, Kalimo H. Miao Q, et al. Among authors: kalimo h. Brain Pathol. 2004 Oct;14(4):358-64. doi: 10.1111/j.1750-3639.2004.tb00078.x. Brain Pathol. 2004. PMID: 15605982 Free PMC article.

9

[Inflammatory muscle diseases].

Kalimo H, Alanen A, Falck B, Haapasalo H, Halonen P, Kalimo K, Salonen R, Aärimaa T. Kalimo H, et al. Among authors: kalimo k. Duodecim. 1993;109(16):1373-84. Duodecim. 1993. PMID: 7720596 Review. Finnish. No abstract available.

10

[Hereditary neuropathy with liability to pressure palsies--a more common neuropathy than generally thought].

Meretoja P, Silander K, Savontaus ML, Kalimo H. Meretoja P, et al. Among authors: kalimo h. Duodecim. 1998;114(24):2569-74. Duodecim. 1998. PMID: 11757129 Review. Finnish. No abstract available.

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