Lang H - Search Results

1

Gene deletions in X-linked muscular dystrophy.

Lindlöf M, Kiuru A, Kääriäinen H, Kalimo H, Lang H, Pihko H, Rapola J, Somer H, Somer M, Savontaus ML, et al. Lindlöf M, et al. Among authors: lang h. Am J Hum Genet. 1989 Apr;44(4):496-503. Am J Hum Genet. 1989. PMID: 2929594 Free PMC article.

2

[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: lang h. Duodecim. 1990;106(17):1210-8. Duodecim. 1990. PMID: 1670542 Review. Finnish. No abstract available.

3

Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.

Saviranta P, Lindlöf M, Lehesjoki AE, Kalimo H, Lang H, Sonninen V, Savontaus ML, de la Chapelle A. Saviranta P, et al. Among authors: lang h. Am J Hum Genet. 1988 Jan;42(1):84-8. Am J Hum Genet. 1988. PMID: 2892402 Free PMC article.

4

X-linked myopathy with excessive autophagy: a new hereditary muscle disease.

Kalimo H, Savontaus ML, Lang H, Paljärvi L, Sonninen V, Dean PB, Katevuo K, Salminen A. Kalimo H, et al. Among authors: lang h. Ann Neurol. 1988 Mar;23(3):258-65. doi: 10.1002/ana.410230308. Ann Neurol. 1988. PMID: 2897824

5

Two cases of Dandy-Walker syndrome and chronic polyneuropathy.

Riikonen R, Lang H, Kalimo H, Röyttä M, Donner M. Riikonen R, et al. Among authors: lang h. Pediatr Neurosci. 1989;15(4):188-94. doi: 10.1159/000120467. Pediatr Neurosci. 1989. PMID: 2485913

6

Minicore myopathy with dominant inheritance.

Paljärvi L, Kalimo H, Lang H, Savontaus ML, Sonninen V. Paljärvi L, et al. Among authors: lang h. J Neurol Sci. 1987 Jan;77(1):11-22. doi: 10.1016/0022-510x(87)90202-4. J Neurol Sci. 1987. PMID: 3806134

7

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration.

Hirvasniemi A, Lang H, Lehesjoki AE, Leisti J. Hirvasniemi A, et al. Among authors: lang h. J Med Genet. 1994 Mar;31(3):177-82. doi: 10.1136/jmg.31.3.177. J Med Genet. 1994. PMID: 8014963 Free PMC article.

8

Leber's hereditary optic neuroretinopathy, a mitochondrial disease?

Nikoskelainen E, Hassinen IE, Paljärvi L, Lang H, Kalimo H. Nikoskelainen E, et al. Among authors: lang h. Lancet. 1984 Dec 22;2(8417-8418):1474. doi: 10.1016/s0140-6736(84)91669-6. Lancet. 1984. PMID: 6151084 No abstract available.

9

[Pompe's disease or glycogen storage disease].

Vanto T, Salmi TT, Kalimo H, Lang H, Näntö V, Berlin M, Penttinen R. Vanto T, et al. Among authors: lang h. Duodecim. 1982;98(9):709-16. Duodecim. 1982. PMID: 7049663 Finnish. No abstract available.

10

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. Among authors: lang h. 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

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