Kress W - Search Results

1

[Primary failure of eruption (PFE). Clinical and molecular genetics analysis].

Stellzig-Eisenhauer A, Decker E, Meyer-Marcotty P, Rau C, Fiebig BS, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Witt E, Weber BH. Stellzig-Eisenhauer A, et al. Among authors: kress w. Orthod Fr. 2013 Sep;84(3):241-50. doi: 10.1051/orthodfr/2013055. Epub 2013 Sep 3. Orthod Fr. 2013. PMID: 23993365 French.

2

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: kress w. 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.

3

Primary failure of eruption (PFE)--clinical and molecular genetics analysis.

Stellzig-Eisenhauer A, Decker E, Meyer-Marcotty P, Rau C, Fiebig BS, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Witt E, Weber BH. Stellzig-Eisenhauer A, et al. Among authors: kress w. J Orofac Orthop. 2010 Jan;71(1):6-16. doi: 10.1007/s00056-010-0908-9. Epub 2010 Feb 5. J Orofac Orthop. 2010. PMID: 20135246 English, German.

4

Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.

Grimm T, Kress W, Meng G, Müller CR. Grimm T, et al. Among authors: kress w. Acta Myol. 2012 Dec;31(3):179-83. Acta Myol. 2012. PMID: 23620649 Free PMC article.

5

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: kress w. Am J Dis Child. 1993 Dec;147(12):1303-5. doi: 10.1001/archpedi.1993.02160360045015. Am J Dis Child. 1993. PMID: 8249949

6

Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.

Stec I, Kress W, Meng G, Müller B, Müller CR, Grimm T. Stec I, et al. Among authors: kress w. J Med Genet. 1995 Dec;32(12):930-3. doi: 10.1136/jmg.32.12.930. J Med Genet. 1995. PMID: 8825917 Free PMC article.

7

Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease.

Schuster V, Seidenspinner S, Grimm T, Kress W, Zielen S, Bock M, Kreth HW. Schuster V, et al. Among authors: kress w. Eur J Pediatr. 1994 Jun;153(6):432-7. doi: 10.1007/BF01983408. Eur J Pediatr. 1994. PMID: 7916289

8

[X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies].

Schuster V, Grimm T, Kress W, Seidenspinner S, Belohradsky BH, Müller P, Kreth HW. Schuster V, et al. Among authors: kress w. Klin Padiatr. 1995 Sep-Oct;207(5):271-6. doi: 10.1055/s-2008-1046550. Klin Padiatr. 1995. PMID: 7500602 German.

9

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. Neuromuscul Disord. 2000 Oct;10(7):478-80. doi: 10.1016/s0960-8966(00)00129-2. Neuromuscul Disord. 2000. PMID: 10996776

10

An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.

Kress W, Petersen B, Collmann H, Grimm T. Kress W, et al. Cytogenet Cell Genet. 2000;91(1-4):138-40. doi: 10.1159/000056834. Cytogenet Cell Genet. 2000. PMID: 11173846

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