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    <title>Bouchard, P.</title>
    <link>http://repub.eur.nl/res/aut/10161/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>A new LH receptor splice mutation responsible for male hypogonadism with subnormal sperm production in the propositus, and infertility with regular cycles in an affected sister (Article)</title>
      <link>http://repub.eur.nl/res/pub/29507/</link>
      <pubDate>2008-08-01T00:00:00Z</pubDate>
      <description>BACKGROUND: Inactivating LH receptor (LHR) mutations have been described so far in men as well as in women. Phenotypes in men have been variable with in nearly all cases impairment of sex differentiation or azoospermia. We report a milder reproductive phenotype both in a male patient and his sister. METHODS AND RESULTS: We describe a family that carries a homozygous mutation G→A at position -1 at the intron 10-exon 11 boundary of the LHR gene. The male patient presented with delayed puberty, micropenis and oligospermia. Two of his sisters were homozygous for the same mutation and were infertile. Surprisingly, one of them was found to have had regular ovarian cycles for years and showed normal LH values (6.5 and 10.6 mIU/ml for LH and FSH, respectively). In vitro analysis showed that this altered splicing resulted in an LHR from which eight amino acids are deleted from the extracellular domain (ΔTyr317- Ser324). In vitro expression has shown that the receptor was expressed and capable of LH-induced signaling, albeit with reduced potency (P &lt; 0.001). CONCLUSIONS: LHR mutations may represent an underestimated cause of infertility in women, in addition to being responsible for male hypogonadism with reduced spermatogenesis. </description>
    </item> <item>
      <title>Alternative approaches in IVF (Article)</title>
      <link>http://repub.eur.nl/res/pub/31839/</link>
      <pubDate>2002-02-26T00:00:00Z</pubDate>
      <description>Various new developments in clinical and basic science which may impact on IVF in the near or distant future will be discussed in this review. These key areas include the regulation of early follicle development and the extended in vitro culture of oocytes and embryos. Moreover, alternative compounds and ovarian stimulation protocols will be discussed, along with highlights in the development of the cryopreservation of excess oocytes or embryos. Finally, the health economics of IVF is addressed.</description>
    </item> <item>
      <title>Alternative approaches in IVF (Article)</title>
      <link>http://repub.eur.nl/res/pub/9863/</link>
      <pubDate>2002-01-01T00:00:00Z</pubDate>
      <description>Various new developments in clinical and basic science which may impact on
      IVF in the near or distant future will be discussed in this review. These
      key areas include the regulation of early follicle development and the
      extended in-vitro culture of oocytes and embryos. Moreover, alternative
      compounds and ovarian stimulation protocols will be discussed, along with
      highlights in the development of the cryopreservation of excess oocytes or
      embryos. Finally, the health economics of IVF is addressed.</description>
    </item> <item>
      <title>Free androgen index and leptin are the most prominent endocrine predictors of ovarian response during clomiphene citrate induction of ovulation in normogonadotropic oligoamenorrheic infertility (Article)</title>
      <link>http://repub.eur.nl/res/pub/9278/</link>
      <pubDate>2000-01-01T00:00:00Z</pubDate>
      <description>We have previously demonstrated that obese hyperandrogenic amenorrheic
      women are less likely to ovulate after clomiphene citrate (CC) medication.
      The present study was designed to identify whether additional endocrine
      screening characteristics, all potentially involved in ovarian dysfunction
      in 182 normogonadotropic oligoamenorrheic infertile women, are associated
      with ovarian response, which may improve overall prediction of
      CC-resistant anovulation. Standardized endocrine screening took place
      before initiation of CC medication (50 mg/day; increasing doses up to 150
      mg/day if required) from cycle days 3-7. Screening included serum assays
      for fasting insulin and glucose, insulin-like growth factor I (IGF-I),
      IGF-binding protein-1 (IGFBP-1), IGFBP-3, free IGF-I, inhibin B, leptin,
      and vascular endothelial growth factor. Forty-two women (22% of the total
      group) did not ovulate at the end of follow-up (a total number of 325
      cycles were analyzed). Fasting serum insulin, insulin/glucose ratio,
      IGFBP-1, and leptin were all significantly different in univariate
      analyses (P &lt; or = 0.02), comparing CC responders vs. nonresponders.
      Forward stepwise multivariate analyses in combination with factors
      reported earlier for prediction of patients remaining anovulatory after CC
      revealed a prediction model including 1) free androgen index (FAI =
      testosterone/sex hormone-binding globulin ratio), 2) cycle history
      (oligomenorrhea or amenorrhea), 3) leptin level, and 4) mean ovarian
      volume. These data suggest that decreased insulin sensitivity,
      hyperandrogenemia, and obesity, all associated with polycystic ovary
      syndrome, are prominent factors involved in ovarian dysfunction,
      preventing these ovaries from responding to stimulation by raised
      endogenous FSH levels due to CC medication. By using leptin instead of
      body mass index or waist to hip ratio, the previous model for prediction
      of patients remaining anovulatory after CC medication could be slightly
      improved (area under the curve from 0.82-0.85). This may indicate that
      leptin is more directly involved in ovarian dysfunction in these patients.
      The capability of insulin and IGFBP-1 to predict patients who remain
      anovulatory after CC disappears when FAI enters into the model due to a
      significant correlation between FAI and these endocrine parameters. This
      suggests that markers for insulin sensitivity (e.g. IGFBP-1 and insulin)
      are associated with abnormal ovarian function through its correlation with
      androgens, whereas leptin is directly involved in ovarian dysfunction.</description>
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