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D Meschede

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TOP 3
Barbara Sonntag; D Meschede; V Ullmann; Paul Gassner; Jürgen Horst; Eberhard Nieschlag; Hermann M Behre
Low-level sex chromosome mosaicism in female partners of couples undergoing ICSI therapy does not significantly affect treatment outcome.
D Meschede; S Albersmann; Jürgen Horst
The practical importance of pedigree analysis in women considering invasive prenatal diagnosis for advanced maternal age or abnormal serum screening tests.
D Meschede; Beate Lemcke; Hermann M Behre; C D Geyter; Eberhard Nieschlag; Jürgen Horst
Non-reproductive heritable disorders in infertile couples and their first degree relatives.

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All Publications

2001: Barbara Sonntag; D Meschede; V Ullmann; Paul Gassner; Jürgen Horst; Eberhard Nieschlag; Hermann M Behre
Low-level sex chromosome mosaicism in female partners of couples undergoing ICSI therapy does not significantly affect treatment outcome.
Human reproduction (Oxford, England) 2001;16(8):1648-52.
2000: D Meschede; S Albersmann; Jürgen Horst
The practical importance of pedigree analysis in women considering invasive prenatal diagnosis for advanced maternal age or abnormal serum screening tests.
Prenatal diagnosis 2000;20(11):865-9.
2000: D Meschede; Beate Lemcke; Hermann M Behre; C D Geyter; Eberhard Nieschlag; Jürgen Horst
Non-reproductive heritable disorders in infertile couples and their first degree relatives.
Human reproduction (Oxford, England) 2000;15(7):1609-12.
2000: D Meschede; Beate Lemcke; Hermann M Behre; C De Geyter; Eberhard Nieschlag; Jürgen Horst
Clustering of male infertility in the families of couples treated with intracytoplasmic sperm injection.
Human reproduction (Oxford, England) 2000;15(7):1604-8.
2000: Sigrid von Eckardstein; Trevor G Cooper; K Rutscha; D Meschede; Jürgen Horst; Eberhard Nieschlag
Seminal plasma characteristics as indicators of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in men with obstructive azoospermia.
Fertility and sterility 2000;73(6):1226-31.
2000: D Meschede; Bernd Dworniczak; Hermann M Behre; Eberhard Nieschlag; Jürgen Horst
No evidence for uniparental disomy of the sex chromosomes in idiopathic male infertility.
Molecular human reproduction 2000;6(1):1-4.
1998: D Meschede; Rita Exeler; B Wittwer; Jürgen Horst
Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p.
American journal of medical genetics 1998;80(5):443-7.
1998: D Meschede; Frank Louwen; Irmgard Nippert; Wolfgang Holzgreve; Peter Miny; Jürgen Horst
Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies.
American journal of medical genetics 1998;80(4):330-4.
1998: B Koppers; Paul Gassner; D Meschede; Jürgen Horst; Hermann M Behre; Eberhard Nieschlag
Prognostic value of male diagnostic profiles in intracytoplasmic sperm injection (ICSI).
International journal of andrology 1998;21(4):227-32.
1998: D Meschede; Beate Lemcke; Julia Stüssel; Frank Louwen; Jürgen Horst
Strong preference for non-invasive prenatal diagnosis in women pregnant through intracytoplasmic sperm injection (ICSI)
Prenatal diagnosis 1998;18(7):700-5.
1998: D Meschede; Beate Lemcke; J R Exeler; C De Geyter; Hermann M Behre; Eberhard Nieschlag; Jürgen Horst
Chromosome abnormalities in 447 couples undergoing intracytoplasmic sperm injection--prevalence, types, sex distribution and reproductive relevance.
Human reproduction (Oxford, England) 1998;13(3):576-82.
1998: D Meschede; Bernd Dworniczak; Eberhard Nieschlag; Jürgen Horst
Genetic diseases of the seminal ducts.
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 1998;52(5):197-203.
1998: D Meschede; Sabine Kliesch; Jürgen Horst; Eberhard Nieschlag
Azoospermia and segmentation abnormalities of the cervicothoracic spine ('MURCS in the male').
Clinical dysmorphology 1998;7(1):59-60.
1997: D Meschede; Bernd Dworniczak; Hermann M Behre; Sabine Kliesch; M Claustres; Eberhard Nieschlag; Jürgen Horst
CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesicles.
American journal of human genetics 1997;61(5):1200-2.
1997: D Meschede; Frank Louwen; Bernd Eiben; Jürgen Horst
Intracytoplasmic sperm injection pregnancy with fetal trisomy 9p resulting from a balanced paternal translocation.
Human reproduction (Oxford, England) 1997;12(9):1913-4.
1997: Thilo Dörk; Bernd Dworniczak; Christa Aulehla-Scholz; Dagmar Wieczorek; I Böhm; A Mayerova; H H Seydewitz; Eberhard Nieschlag; D Meschede; Jürgen Horst; H J Pander; H Sperling; F Ratjen; Eberhard Passarge; Jörg Schmidtke; Manfred Stuhrmann
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens.
Human genetics 1997;100(3-4):365-77.
1997: D Meschede; Jürgen Horst
Sex chromosomal anomalies in pregnancies conceived through intracytoplasmic sperm injection: a case for genetic counselling.
Human reproduction (Oxford, England) 1997;12(6):1125-7.
1997: D Meschede; Jürgen Horst
The molecular genetics of male infertility.
Molecular human reproduction 1997;3(5):419-30.
1997: Manuela Simoni; Jörg Gromoll; Bernd Dworniczak; Claus Rolf; K Abshagen; Axel Kamischke; C Carani; D Meschede; Hermann M Behre; Jürgen Horst; Eberhard Nieschlag
Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia.
Fertility and sterility 1997;67(3):542-7.
1997: D Meschede; Jürgen Horst
Genetic counselling for infertile male patients.
International journal of andrology 1997;20 Suppl 3():20-30.
1996: D Meschede; Claus Rolf; D C Neugebauer; Jürgen Horst; Eberhard Nieschlag
Sperm acrosome defects in a patient with Aarskog-Scott syndrome.
American journal of medical genetics 1996;66(3):340-2.
1996: Peter H Vogt; A Edelmann; Stefan Kirsch; Octavian Henegariu; P Hirschmann; F Kiesewetter; Frank-Michael Köhn; Wolf-Bernhard Schill; S Farah; C Ramos; M Hartmann; Wolfgang Hartschuh; D Meschede; Hermann M Behre; A Castel; E Nieschlag; Wolfgang Weidner; H J Gröne; A Jung; W Engel; G Haidl
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11.
Human molecular genetics 1996;5(7):933-43.
1996: K Ullrich; H G Koch; D Meschede; U Flotmann; Udo Seedorf
Smith-Lemli-Opitz syndrome: treatment with cholesterol and bile acids.
Neuropediatrics 1996;27(2):111-2.
1995: D Meschede; Christian De Geyter; Eberhard Nieschlag; Jürgen Horst
Genetic risk in micromanipulative assisted reproduction.
Human reproduction (Oxford, England) 1995;10(11):2880-6.
1995: D Meschede; T Nekarda; D Kececioglu; H Löser; J Vogt; Peter Miny; Jürgen Horst
Congenital heart disease in the 48,XXYY syndrome.
Clinical genetics 1995;48(2):100-2.
1995: D Meschede; Hermann M Behre; Eberhard Nieschlag
Endocrine and spermatological characteristics of 135 patients with bilateral megalotestis.
Andrologia 1995;27(4):207-12.
1995: Udo Seedorf; Manfred Fobker; R Voss; K Meyer; Frank Kannenberg; D Meschede; K Ullrich; J Horst; A Benninghoven; Gerd Assmann
Smith-Lemli-Opitz syndrome diagnosed by using time-of-flight secondary-ion mass spectrometry.
Clinical chemistry 1995;41(4):548-52.
1995: Christian Jackisch; A Schwenkhagen; T Budde; Frank Louwen; D Meschede; Otmar Schober; Wolfgang Holzgreve; H P G Schneider
[Interventional therapy of inferior vena cava thrombosis in pregnancy--use of a new kind of temporary vena cava filter].
Zentralblatt für Gynäkologie 1995;117(4):181-9.
1994: D Meschede; Hermann M Behre; Eberhard Nieschlag; Jürgen Horst
[The Kallmann syndrome. Its pathophysiology and clinical picture].
Deutsche medizinische Wochenschrift (1946) 1994;119(42):1436-42.
1994: D Meschede; Ursula G Froster; Martin Bergmann; Eberhard Nieschlag
Familial pericentric inversion of chromosome 1 (p34q23) and male infertility with stage specific spermatogenic arrest.
Journal of medical genetics 1994;31(7):573-5.
1993: D Meschede; C Keck; M Zander; Trevor G Cooper; Ching-Hei Yeung; Eberhard Nieschlag
Influence of three different preparation techniques on the results of human sperm morphology analysis.
International journal of andrology 1993;16(6):362-9.
1993: D Meschede; Ursula G Froster; F Gullotta; E Nieschlag
Reproductive failure in a patient with neurofibromatosis-Noonan syndrome.
American journal of medical genetics 1993;47(3):346-51.
1993: D Meschede; Antonin Eigel; J Horst; E Nieschlag
Compound heterozygosity for the delta F508 and F508C cystic fibrosis transmembrane conductance regulator (CFTR) mutations in a patient with congenital bilateral aplasia of the vas deferens.
American journal of human genetics 1993;53(1):292-3.
1993: D Meschede; C Keck; Christian De Geyter; Antonin Eigel; Jürgen Horst; Eberhard Nieschlag
[Mutation in the cystic fibrosis transmembrane-regulator gene in bilateral congenital ductus deferens aplasia].
Deutsche medizinische Wochenschrift (1946) 1993;118(18):661-4.