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PedAM

Pediatric Disease Annotations & Medicines




Disease infertility
Phenotype C0028960|oligozoospermia
Sentences 7
PubMedID- 23713244 Objective: to explore the optimal treatment selection for treating varicocele (vc) male infertility patients accompanied with oligozoospermia or azoospermia of different chinese medical syndrome types by comparing the efficacies of integrative medicine.
PubMedID- 21559371 To determine the involvement of copy number variants (cnvs) in the origin of male infertility, patients with idiopathic severe oligozoospermia (n = 89), sertoli-cell-only syndrome (scos, n = 37)) and controls with normozoospermia (n = 100) were analysed by array-cgh using the 244a/400k array sets (agilent technologies).
PubMedID- 22594646 On the basis of analysis of 480 controls and 524 infertility patients with azoospermia or oligozoospermia, we observed that one intronic snp in mlh1 (rs4647269) and two non-synonymous snps in pms2 (rs1059060, ser775asn) and msh5 (rs2075789, pro29ser) were associated with increased susceptibility to poor sperm production.
PubMedID- 21355452 The secondary infertility couple with oligozoospermia underwent icsi two times.
PubMedID- 24457837 In phenotypically normal individuals, female carriers of ccrs are frequently identified after giving birth to malformed babies or suffering from repeated miscarriages;2 whereas, most of the male carriers of ccrs are detected due to infertility problems arising from oligozoospermia or azoospermia.
PubMedID- 24303009 The first stage included 96 idiopathic male infertility with oligozoospermia and 96 healthy controls.
PubMedID- 22411295 Methods: a total of 51 subjects visiting the university infertility clinic with normozoospermic parameters, oligozoospermia and teratozoospermia were included.

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