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Frontiers in Endocrinology
|
May 3, 2024
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications
Morten Krogh Herlin
Orphanet Journal of Rare Diseases
|
August 22, 2020
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update
Morten Krogh Herlin, Michael Bjørn Petersen, Mats Brännström
Disability and Rehabilitation
|
March 29, 2023
A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women's experiences and negotiations of living with an underdeveloped uterus and vagina
Amalie Hahn Jensen, Morten Krogh Herlin, Ida Vogel, et al.
Genes
|
June 2, 2021
What Is Abnormal in Normal Karyotype Acute Myeloid Leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort
Morten Krogh Herlin, Sara A Yones, Eigil Kjeldsen, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
July 23, 2024
Experiences of vaginal lengthening treatment and sexual well-being in women with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: An interview study
Amalie Hahn Jensen, Morten Krogh Herlin, Birgitta Trolle, et al.
Journal of Pediatric and Adolescent Gynecology
|
March 17, 2024
Understanding the Diagnostic Odyssey of Women with Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome in Denmark: A Qualitative Interview Study
Stina Lou, Amalie Hahn Jensen, Ida Vogel, et al.
Pediatric Dermatology
|
September 11, 2024
Phenotypes, Genetics, and Estimated Prevalence of Focal Dermal Hypoplasia (Goltz Syndrome): A Single-Center Report
Laura Krogh Herlin, Morten Krogh Herlin, Hanne Vinter, et al.
Clinical Kidney Journal
|
March 6, 2026
Acute kidney injury and chronic kidney disease in individuals with Down syndrome: a nationwide cohort study
Freja Leonore Uhd Weldingh, Morten Krogh Herlin, Ellen Hollands Steffensen, et al.
European Journal of Medical Genetics
|
January 30, 2022
Autosomal dominant sleep-related hypermotor epilepsy caused by a previously unreported CHRNA4 variant
Trine Østergaard Nielsen, Morten Krogh Herlin, Karen Markussen Linnet, et al.
Ugeskrift for Laeger
|
October 24, 2023
Thorkild Terkelsen, Thomas Folkmann Hansen, Morten Krogh Herlin, et al.
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Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Frontiers in Endocrinology
|
May 3, 2024
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications
Morten Krogh Herlin
Orphanet Journal of Rare Diseases
|
August 22, 2020
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update
Morten Krogh Herlin, Michael Bjørn Petersen, Mats Brännström
Disability and Rehabilitation
|
March 29, 2023
A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women's experiences and negotiations of living with an underdeveloped uterus and vagina
Amalie Hahn Jensen, Morten Krogh Herlin, Ida Vogel, et al.
Genes
|
June 2, 2021
What Is Abnormal in Normal Karyotype Acute Myeloid Leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort
Morten Krogh Herlin, Sara A Yones, Eigil Kjeldsen, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
July 23, 2024
Experiences of vaginal lengthening treatment and sexual well-being in women with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: An interview study
Amalie Hahn Jensen, Morten Krogh Herlin, Birgitta Trolle, et al.
Journal of Pediatric and Adolescent Gynecology
|
March 17, 2024
Understanding the Diagnostic Odyssey of Women with Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome in Denmark: A Qualitative Interview Study
Stina Lou, Amalie Hahn Jensen, Ida Vogel, et al.
Pediatric Dermatology
|
September 11, 2024
Phenotypes, Genetics, and Estimated Prevalence of Focal Dermal Hypoplasia (Goltz Syndrome): A Single-Center Report
Laura Krogh Herlin, Morten Krogh Herlin, Hanne Vinter, et al.
Clinical Kidney Journal
|
March 6, 2026
Acute kidney injury and chronic kidney disease in individuals with Down syndrome: a nationwide cohort study
Freja Leonore Uhd Weldingh, Morten Krogh Herlin, Ellen Hollands Steffensen, et al.
European Journal of Medical Genetics
|
January 30, 2022
Autosomal dominant sleep-related hypermotor epilepsy caused by a previously unreported CHRNA4 variant
Trine Østergaard Nielsen, Morten Krogh Herlin, Karen Markussen Linnet, et al.
Ugeskrift for Laeger
|
October 24, 2023
Thorkild Terkelsen, Thomas Folkmann Hansen, Morten Krogh Herlin, et al.
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