Rietschel M - Search Results

1

Heterogeneity in proximal spinal muscular atrophy.

Zerres K, Rudnik-Schöneborn S, Rietschel M. Zerres K, et al. Among authors: rietschel m. Lancet. 1990 Sep 22;336(8717):749-50. doi: 10.1016/0140-6736(90)92243-b. Lancet. 1990. PMID: 1975919 No abstract available.

2

Pregnancy and spinal muscular atrophy.

Rudnik-Schöneborn S, Zerres K, Ignatius J, Rietschel M. Rudnik-Schöneborn S, et al. Among authors: rietschel m. J Neurol. 1992 Jan;239(1):26-30. doi: 10.1007/BF00839207. J Neurol. 1992. PMID: 1541965 Review.

3

Clinical variability of autosomal dominant spinal muscular atrophy.

Rietschel M, Rudnik-Schöneborn S, Zerres K. Rietschel M, et al. J Neurol Sci. 1992 Jan;107(1):65-73. doi: 10.1016/0022-510x(92)90210-c. J Neurol Sci. 1992. PMID: 1578236

4

No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.

Kausch K, Müller CR, Grimm T, Ricker K, Rietschel M, Rudnik-Schöneborn S, Zerres K. Kausch K, et al. Among authors: rietschel m. Hum Genet. 1991 Jan;86(3):317-8. doi: 10.1007/BF00202419. Hum Genet. 1991. PMID: 1997389

5

MASA syndrome: clinical variability and linkage analysis.

Rietschel M, Friedl W, Uhlhaas S, Neugebauer M, Heimann D, Zerres K. Rietschel M, et al. Am J Med Genet. 1991 Oct 1;41(1):10-4. doi: 10.1002/ajmg.1320410104. Am J Med Genet. 1991. PMID: 1951449

6

No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.

Gerbitz KD, Paprotta A, Obermaier-Kusser B, Rietschel M, Zerres K. Gerbitz KD, et al. Among authors: rietschel m. FEBS Lett. 1992 Dec 21;314(3):251-5. doi: 10.1016/0014-5793(92)81482-2. FEBS Lett. 1992. PMID: 1361456 Free article.

7

Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: a new syndrome?

Zerres K, Rietschel M, Rietschel E, Majewski F, Meinecke P. Zerres K, et al. Among authors: rietschel m, rietschel e. J Med Genet. 1992 Apr;29(4):269-71. doi: 10.1136/jmg.29.4.269. J Med Genet. 1992. PMID: 1316441 Free PMC article.

8

Impact of schizophrenia-risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals.

Markov V, Krug A, Krach S, Jansen A, Eggermann T, Zerres K, Stöcker T, Shah NJ, Nöthen MM, Treutlein J, Rietschel M, Kircher T. Markov V, et al. Among authors: rietschel m. Hum Brain Mapp. 2010 Feb;31(2):266-75. doi: 10.1002/hbm.20862. Hum Brain Mapp. 2010. PMID: 19650139 Free PMC article.

9

Association of the DTNBP1 genotype with cognition and personality traits in healthy subjects.

Kircher T, Markov V, Krug A, Eggermann T, Zerres K, Nöthen MM, Skowronek MH, Rietschel M. Kircher T, et al. Among authors: rietschel m. Psychol Med. 2009 Oct;39(10):1657-65. doi: 10.1017/S0033291709005388. Epub 2009 Apr 1. Psychol Med. 2009. PMID: 19335929

10

Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals.

Markov V, Krug A, Krach S, Whitney C, Eggermann T, Zerres K, Stöcker T, Shah NJ, Nöthen MM, Treutlein J, Rietschel M, Kircher T. Markov V, et al. Among authors: rietschel m. Neuroimage. 2009 Oct 1;47(4):2016-22. doi: 10.1016/j.neuroimage.2009.05.067. Epub 2009 Jun 1. Neuroimage. 2009. PMID: 19497374

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