Falck B - Search Results

1

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.

Nokelainen P, Alanen-Kurki L, Winqvist R, Falck B, Somer H, Leisti J, Johnson K, Savontaus ML, Peltonen L. Nokelainen P, et al. Among authors: falck b. Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234. Hum Genet. 1990. PMID: 1977684

2

DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP).

Silander K, Halonen P, Sara R, Kalimo H, Falck B, Savontaus ML. Silander K, et al. Among authors: falck b. J Neurol Neurosurg Psychiatry. 1994 Oct;57(10):1260-2. doi: 10.1136/jnnp.57.10.1260. J Neurol Neurosurg Psychiatry. 1994. PMID: 7931393 Free PMC article.

3

[Facioscapulohumeral muscular dystrophy].

Halonen P, Alanen A, Falck B, Kalimo H, Kiuru A, Lang H, Savontaus ML, Sonninen V. Halonen P, et al. Among authors: falck b. Duodecim. 1990;106(17):1210-8. Duodecim. 1990. PMID: 1670542 Review. Finnish. No abstract available.

4

[Carnitine palmitoyltransferase deficiency: fatty acid utilization defect causing myopathy].

Lehtonen A, Paljärvi L, Falck B, Somer H, Kalimo H. Lehtonen A, et al. Among authors: falck b. Duodecim. 1983;99(16):1063-9. Duodecim. 1983. PMID: 6641545 Finnish. No abstract available.

5

[Peripheral myopathies in Finland--a new kind of muscular dystrophy in the leg].

Udd B, Partanen J, Halonen P, Somer H, Falck B, Hakamies L, Heikkilä H, Ingo S, Kalimo H, Laulumaa V, et al. Udd B, et al. Among authors: falck b. Duodecim. 1992;108(15):1331-8. Duodecim. 1992. PMID: 1366093 Review. Finnish. No abstract available.

6

Increased activity of serum gamma-glutamyltransferase in myotonic dystrophy.

Rönnemaa T, Alaranta H, Viikari J, Tilvis R, Falck B. Rönnemaa T, et al. Among authors: falck b. Acta Med Scand. 1987;222(3):267-73. doi: 10.1111/j.0954-6820.1987.tb10669.x. Acta Med Scand. 1987. PMID: 2892348

7

Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients.

Udd B, Partanen J, Halonen P, Falck B, Hakamies L, Heikkilä H, Ingo S, Kalimo H, Kääriäinen H, Laulumaa V, et al. Udd B, et al. Among authors: falck b. Arch Neurol. 1993 Jun;50(6):604-8. doi: 10.1001/archneur.1993.00540060044015. Arch Neurol. 1993. PMID: 8503797

8

[Neuromyotonia].

Sillanpää M, Lang H, Falck B. Sillanpää M, et al. Among authors: falck b. Duodecim. 1983;99(7):486-90. Duodecim. 1983. PMID: 6872903 Finnish. No abstract available.

9

The development of a multicenter database for reference values in clinical neurophysiology--principles and examples.

Falck B, Andreassen S, Groth T, Lang H, Melander M, Nurmi A, Puusa A, Rosenfalck A, Stålberg E, Suojanen M. Falck B, et al. Comput Methods Programs Biomed. 1991 Feb-Mar;34(2-3):145-62. doi: 10.1016/0169-2607(91)90040-z. Comput Methods Programs Biomed. 1991. PMID: 2060288

10

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.

Kuhlenbäumer G, Meuleman J, De Jonghe P, Falck B, Young P, Hünermund G, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: falck b. J Neurol. 2001 Oct;248(10):861-5. doi: 10.1007/s004150170070. J Neurol. 2001. PMID: 11697522

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