Meschede D - Search Results

1

Smith-Lemli-Opitz syndrome: treatment with cholesterol and bile acids.

Ullrich K, Koch HG, Meschede D, Flotmann U, Seedorf U. Ullrich K, et al. Among authors: meschede d. Neuropediatrics. 1996 Apr;27(2):111-2. doi: 10.1055/s-2007-973760. Neuropediatrics. 1996. PMID: 8737829 No abstract available.

2

Smith-Lemli-Opitz syndrome diagnosed by using time-of-flight secondary-ion mass spectrometry.

Seedorf U, Fobker M, Voss R, Meyer K, Kannenberg F, Meschede D, Ullrich K, Horst J, Benninghoven A, Assmann G. Seedorf U, et al. Among authors: meschede d. Clin Chem. 1995 Apr;41(4):548-52. Clin Chem. 1995. PMID: 7720244

3

Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies.

Meschede D, Louwen F, Nippert I, Holzgreve W, Miny P, Horst J. Meschede D, et al. Am J Med Genet. 1998 Dec 4;80(4):330-4. doi: 10.1002/(sici)1096-8628(19981204)80:4<330::aid-ajmg6>3.0.co;2-7. Am J Med Genet. 1998. PMID: 9856559

4

Azoospermia and segmentation abnormalities of the cervicothoracic spine ('MURCS in the male').

Meschede D, Kliesch S, Horst J, Nieschlag E. Meschede D, et al. Clin Dysmorphol. 1998 Jan;7(1):59-60. Clin Dysmorphol. 1998. PMID: 9546833

5

Congenital heart disease in the 48,XXYY syndrome.

Meschede D, Nekarda T, Kececioglu D, Löser H, Vogt J, Miny P, Horst J. Meschede D, et al. Clin Genet. 1995 Aug;48(2):100-2. doi: 10.1111/j.1399-0004.1995.tb04064.x. Clin Genet. 1995. PMID: 7586648

6

[The Kallmann syndrome. Its pathophysiology and clinical picture].

Meschede D, Behre HM, Nieschlag E, Horst J. Meschede D, et al. Dtsch Med Wochenschr. 1994 Oct 21;119(42):1436-42. doi: 10.1055/s-2008-1058857. Dtsch Med Wochenschr. 1994. PMID: 7956761 Review. German. No abstract available.

7

Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself.

Scheuvens R, Begemann M, Soellner L, Meschede D, Raabe-Meyer G, Elbracht M, Schubert R, Eggermann T. Scheuvens R, et al. Among authors: meschede d. Clin Genet. 2017 Jul;92(1):45-51. doi: 10.1111/cge.12958. Epub 2017 Mar 8. Clin Genet. 2017. PMID: 28032339

8

Isochromosome Xq in Klinefelter syndrome: report of 7 new cases.

Arps S, Koske-Westphal T, Meinecke P, Meschede D, Nieschlag E, Harprecht W, Steuber E, Back E, Wolff G, Kerber S, Held KR. Arps S, et al. Among authors: meschede d. Am J Med Genet. 1996 Sep 6;64(4):580-2. doi: 10.1002/(SICI)1096-8628(19960906)64:4<580::AID-AJMG10>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8870925

9

Low-level sex chromosome mosaicism in female partners of couples undergoing ICSI therapy does not significantly affect treatment outcome.

Sonntag B, Meschede D, Ullmann V, Gassner P, Horst J, Nieschlag E, Behre HM. Sonntag B, et al. Among authors: meschede d. Hum Reprod. 2001 Aug;16(8):1648-52. doi: 10.1093/humrep/16.8.1648. Hum Reprod. 2001. PMID: 11473957

10

Seminal plasma characteristics as indicators of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in men with obstructive azoospermia.

von Eckardstein S, Cooper TG, Rutscha K, Meschede D, Horst J, Nieschlag E. von Eckardstein S, et al. Among authors: meschede d. Fertil Steril. 2000 Jun;73(6):1226-31. doi: 10.1016/s0015-0282(00)00516-1. Fertil Steril. 2000. PMID: 10856487

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results