Search Results - "Jensen, Amalie Hahn"

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  1. 1

    Experiences of vaginal lengthening treatment and sexual well‐being in women with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome: An interview study by Jensen, Amalie Hahn, Herlin, Morten Krogh, Trolle, Birgitta, Vogel, Ida, Lou, Stina

    “…Objective To explore how women with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome experience dilation or surgical vaginal lengthening treatment, and their…”
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    Journal Article
  2. 2

    How are uncertain prenatal genetic results perceived and managed two years after they were received? A qualitative interview study by Lou, Stina, Jensen, Amalie Hahn, Vogel, Ida

    Published in Journal of genetic counseling (01-08-2021)
    “…Chromosomal microarray has considerably improved our ability to identify or dismiss genetic conditions in the unborn child. However, this detailed analysis…”
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    Journal Article
  3. 3

    A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women's experiences and negotiations of living with an underdeveloped uterus and vagina by Jensen, Amalie Hahn, Herlin, Morten Krogh, Vogel, Ida, Lou, Stina

    Published in Disability and rehabilitation (12-03-2024)
    “…Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by the absence or underdevelopment of the uterus and upper part of the vagina. It is usually…”
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    Journal Article
  4. 4

    Understanding the Diagnostic Odyssey of Women with Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome in Denmark: A Qualitative Interview Study by Lou, Stina, Jensen, Amalie Hahn, Vogel, Ida, Trolle, Birgitta, Herlin, Morten Krogh

    “…The diagnosis of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is often a lengthy process that typically occurs during late adolescence. To support optimized…”
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    Journal Article
  5. 5

    How are uncertain prenatal genetic results perceived and managed 2 years after they were received? A qualitative interview study by Lou, Stina, Jensen, Amalie Hahn, Vogel, Ida

    Published in Journal of genetic counseling (08-04-2021)
    “…Chromosomal microarray has considerably improved our ability to identify or dismiss genetic conditions in the unborn child. However, this detailed analysis…”
    Get full text
    Journal Article