Tietze HU - Search Results

1

Severe skeletal dysplasia caused by undiagnosed hypothyroidism.

Hüffmeier U, Tietze HU, Rauch A. Hüffmeier U, et al. Among authors: tietze hu. Eur J Med Genet. 2007 May-Jun;50(3):209-15. doi: 10.1016/j.ejmg.2007.02.002. Epub 2007 Mar 12. Eur J Med Genet. 2007. PMID: 17433800

2

Genotype-phenotype correlations in Noonan syndrome.

Zenker M, Buheitel G, Rauch R, Koenig R, Bosse K, Kress W, Tietze HU, Doerr HG, Hofbeck M, Singer H, Reis A, Rauch A. Zenker M, et al. Among authors: tietze hu. J Pediatr. 2004 Mar;144(3):368-74. doi: 10.1016/j.jpeds.2003.11.032. J Pediatr. 2004. PMID: 15001945

3

Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9.

Wirth J, Wagner T, Meyer J, Pfeiffer RA, Tietze HU, Schempp W, Scherer G. Wirth J, et al. Among authors: tietze hu. Hum Genet. 1996 Feb;97(2):186-93. doi: 10.1007/BF02265263. Hum Genet. 1996. PMID: 8566951

4

Short stature, mental retardation and multiple dysmorphisms in two unrelated females: one or two different syndromes or none?

Pfeiffer RA, Kapferer L, Tietze HU. Pfeiffer RA, et al. Among authors: tietze hu. Genet Couns. 1996;7(3):213-7. Genet Couns. 1996. PMID: 8897043

5

Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.

Trautmann U, Pfeiffer RA, Seufert-Satomi U, Tietze HU. Trautmann U, et al. Among authors: tietze hu. J Med Genet. 1993 Apr;30(4):330-1. doi: 10.1136/jmg.30.4.330. J Med Genet. 1993. PMID: 8487285 Free PMC article.

6

[Extensive subdural hematoma with brain edema and brain death. Sequela of late manifestation of vitamin K deficiency].

Ries M, Tietze HU, Scharf J. Ries M, et al. Among authors: tietze hu. Monatsschr Kinderheilkd. 1993 Jan;141(1):26-9. Monatsschr Kinderheilkd. 1993. PMID: 8446113 German.

7

[The Zimmermann-Laband syndrome].

Pfeiffer RA, Seemanova E, Süss J, Müssig D, Tietze HU. Pfeiffer RA, et al. Among authors: tietze hu. Klin Padiatr. 1992 Jan-Feb;204(1):1-5. doi: 10.1055/s-2007-1025313. Klin Padiatr. 1992. PMID: 1740896 German.

8

Prevalence of autoantibodies to endocrine organs in girls with Ullrich-Turner syndrome aged 5-14 years.

Glück M, Attanasio A, Speer U, Butenandt O, Tietze HU, Scherbaum WA. Glück M, et al. Among authors: tietze hu. Horm Res. 1992;38(3-4):114-9. doi: 10.1159/000182525. Horm Res. 1992. PMID: 1306841

9

[Osteoglophonic skeletal dysplasia--a variant of generalized fibrous dysplasia? Case report and review of the literature].

Stöss H, Sieber E, Tietze HU. Stöss H, et al. Among authors: tietze hu. Pathologe. 1991 May;12(3):161-6. Pathologe. 1991. PMID: 1876584 Review. German. No abstract available.

10

Pseudohypoaldosteronism in eight families: different forms of inheritance are evidence for various genetic defects.

Kuhnle U, Nielsen MD, Tietze HU, Schroeter CH, Schlamp D, Bosson D, Knorr D, Armanini D. Kuhnle U, et al. Among authors: tietze hu. J Clin Endocrinol Metab. 1990 Mar;70(3):638-41. doi: 10.1210/jcem-70-3-638. J Clin Endocrinol Metab. 1990. PMID: 2137831

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