Christen HJ - Search Results

1

Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.

Donner K, Ollikainen M, Ridanpää M, Christen HJ, Goebel HH, de Visser M, Pelin K, Wallgren-Pettersson C. Donner K, et al. Among authors: christen hj. Neuromuscul Disord. 2002 Feb;12(2):151-8. doi: 10.1016/s0960-8966(01)00252-8. Neuromuscul Disord. 2002. PMID: 11738357

2

Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome).

Heyer R, Ehrich J, Goebel HH, Christen HJ, Hanefeld F. Heyer R, et al. Among authors: christen hj. Brain Dev. 1986;8(6):614-9. doi: 10.1016/s0387-7604(86)80009-2. Brain Dev. 1986. PMID: 3103478

3

A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome.

Müller JS, Abicht A, Christen HJ, Stucka R, Schara U, Mortier W, Huebner A, Lochmüller H. Müller JS, et al. Among authors: christen hj. Neuromuscul Disord. 2004 Nov;14(11):744-9. doi: 10.1016/j.nmd.2004.06.010. Neuromuscul Disord. 2004. PMID: 15482960

4

Immunohistochemistry of primary central nervous system malignant rhabdoid tumors: report of five cases and review of the literature.

Behring B, Brück W, Goebel HH, Behnke J, Pekrun A, Christen HJ, Kretzschmar HA. Behring B, et al. Among authors: christen hj. Acta Neuropathol. 1996;91(6):578-86. doi: 10.1007/s004010050470. Acta Neuropathol. 1996. PMID: 8781656

5

Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndrome.

Göhlich-Ratmann G, Baethmann M, Lorenz P, Gärtner J, Goebel HH, Engelbrecht V, Christen HJ, Lenard HG, Voit T. Göhlich-Ratmann G, et al. Among authors: christen hj. Am J Med Genet. 1998 Sep 23;79(3):161-7. doi: 10.1002/(sici)1096-8628(19980923)79:3<161::aid-ajmg2>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9788554

6

Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study.

Kurian MA, Li Y, Zhen J, Meyer E, Hai N, Christen HJ, Hoffmann GF, Jardine P, von Moers A, Mordekar SR, O'Callaghan F, Wassmer E, Wraige E, Dietrich C, Lewis T, Hyland K, Heales S Jr, Sanger T, Gissen P, Assmann BE, Reith ME, Maher ER. Kurian MA, et al. Among authors: christen hj. Lancet Neurol. 2011 Jan;10(1):54-62. doi: 10.1016/S1474-4422(10)70269-6. Epub 2010 Nov 25. Lancet Neurol. 2011. PMID: 21112253 Free PMC article.

7

Multiple sclerosis in childhood: report of 15 cases.

Hanefeld F, Bauer HJ, Christen HJ, Kruse B, Bruhn H, Frahm J. Hanefeld F, et al. Among authors: christen hj. Brain Dev. 1991 Nov;13(6):410-6. doi: 10.1016/s0387-7604(12)80038-6. Brain Dev. 1991. PMID: 1810154

8

[Progressive ataxia and distal muscular atrophy--differential diagnostic considerations on Roussy-Lévy syndrome].

Aksu F, Christen HJ, Hanefeld F. Aksu F, et al. Among authors: christen hj. Klin Padiatr. 1986 Mar-Apr;198(2):114-8. doi: 10.1055/s-2008-1026864. Klin Padiatr. 1986. PMID: 3702272 German.

9

Multiple sclerosis in early childhood.

Bauer HJ, Hanefeld F, Christen HJ. Bauer HJ, et al. Among authors: christen hj. Lancet. 1990 Nov 10;336(8724):1190. doi: 10.1016/0140-6736(90)92802-o. Lancet. 1990. PMID: 1978044 No abstract available.

10

Foix-Chavany-Marie (anterior operculum) syndrome in childhood: a reappraisal of Worster-Drought syndrome.

Christen HJ, Hanefeld F, Kruse E, Imhäuser S, Ernst JP, Finkenstaedt M. Christen HJ, et al. Dev Med Child Neurol. 2000 Feb;42(2):122-32. doi: 10.1017/s0012162200000232. Dev Med Child Neurol. 2000. PMID: 10698330 Free article. Review.

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