Grimm T - Search Results

1

Identification of a novel mutation in the arginine vasopressin-neurophysin II gene in familial central diabetes insipidus.

Bullmann C, Kotzka J, Grimm T, Heppner C, Jockenhövel F, Krone W, Müller-Wieland D. Bullmann C, et al. Among authors: grimm t. Exp Clin Endocrinol Diabetes. 2002 May;110(3):134-7. doi: 10.1055/s-2002-29091. Exp Clin Endocrinol Diabetes. 2002. PMID: 12012274

2

V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanisms.

Schöneberg T, Schulz A, Biebermann H, Grüters A, Grimm T, Hübschmann K, Filler G, Gudermann T, Schultz G. Schöneberg T, et al. Among authors: grimm t. Hum Mutat. 1998;12(3):196-205. doi: 10.1002/(SICI)1098-1004(1998)12:3<196::AID-HUMU7>3.0.CO;2-F. Hum Mutat. 1998. PMID: 9711877

3

A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.

Grimm T, Garshasbi M, Puettmann L, Chen W, Ullmann R, Müller-Myhsok B, Klopocki E, Herbst L, Haug J, Jensen LR, Fischer C, Nöthen M, Ludwig K, Warnke A, Ott J, Schulte-Körne G, Ropers HH, Kuss AW. Grimm T, et al. Z Kinder Jugendpsychiatr Psychother. 2020 Nov;48(6):478-489. doi: 10.1024/1422-4917/a000758. Z Kinder Jugendpsychiatr Psychother. 2020. PMID: 33172359 Free article.

4

Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.

Giess R, Holtmann B, Braga M, Grimm T, Müller-Myhsok B, Toyka KV, Sendtner M. Giess R, et al. Among authors: grimm t. Am J Hum Genet. 2002 May;70(5):1277-86. doi: 10.1086/340427. Epub 2002 Apr 9. Am J Hum Genet. 2002. PMID: 11951178 Free PMC article.

5

PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.

Decker E, Stellzig-Eisenhauer A, Fiebig BS, Rau C, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Weber BH. Decker E, et al. Among authors: grimm t. Am J Hum Genet. 2008 Dec;83(6):781-6. doi: 10.1016/j.ajhg.2008.11.006. Am J Hum Genet. 2008. PMID: 19061984 Free PMC article.

6

Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).

Kress W, Mueller-Myhsok B, Ricker K, Schneider C, Koch MC, Toyka KV, Mueller CR, Grimm T. Kress W, et al. Among authors: grimm t. Neuromuscul Disord. 2000 Oct;10(7):478-80. doi: 10.1016/s0960-8966(00)00129-2. Neuromuscul Disord. 2000. PMID: 10996776

7

Precise mapping of the brain alpha 2-adrenergic receptor gene within chromosome 4p16.

Riess O, Thies U, Siedlaczck I, Potisek S, Graham R, Theilmann J, Grimm T, Epplen JT, Hayden MR. Riess O, et al. Among authors: grimm t. Genomics. 1994 Jan 15;19(2):298-302. doi: 10.1006/geno.1994.1061. Genomics. 1994. PMID: 8188260

8

Linkage of proximal myotonic myopathy to chromosome 3q.

Ricker K, Grimm T, Koch MC, Schneider C, Kress W, Reimers CD, Schulte-Mattler W, Mueller-Myhsok B, Toyka KV, Mueller CR. Ricker K, et al. Among authors: grimm t. Neurology. 1999 Jan 1;52(1):170-1. doi: 10.1212/wnl.52.1.170. Neurology. 1999. PMID: 9921867

9

X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysis.

Schuster V, Kress W, Friedrich W, Grimm T, Kreth HW. Schuster V, et al. Among authors: grimm t. Am J Dis Child. 1993 Dec;147(12):1303-5. doi: 10.1001/archpedi.1993.02160360045015. Am J Dis Child. 1993. PMID: 8249949

10

Linkage analysis and genetic models in dyslexia--considerations pertaining to discrete trait analysis and quantitative trait analyses.

Müller-Myhsok B, Grimm T. Müller-Myhsok B, et al. Among authors: grimm t. Eur Child Adolesc Psychiatry. 1999;8 Suppl 3:40-2. doi: 10.1007/pl00010692. Eur Child Adolesc Psychiatry. 1999. PMID: 10638368

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