Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Morten Herlin"'
Publikováno v:
European Medical Journal Rheumatology, Vol 1, Iss 1, Pp 73-83 (2014)
Juvenile idiopathic arthritis (JIA) is a multifactorial disease with a pathogenesis which remains inexplicable. However, genome-wide association studies brought forward within recent years have discovered several new susceptibility genes, and accumul
Externí odkaz:
https://doaj.org/article/a8d8ce0b7a9d4d9eb2a9bf6fd6b99c81
Publikováno v:
Herlin, M K, Petersen, M B & Brännström, M 2020, ' Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update ', Orphanet Journal of Rare Diseases, vol. 15, 214 . https://doi.org/10.1186/s13023-020-01491-9
Herlin, M K, Petersen, M B & Brännström, M 2020, ' Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome : a comprehensive update ', Orphanet Journal of Rare Diseases, vol. 15, no. 1, 214 . https://doi.org/10.1186/s13023-020-01491-9
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-16 (2020)
Orphanet Journal of Rare Diseases
Herlin, M K, Petersen, M B & Brännström, M 2020, ' Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome : a comprehensive update ', Orphanet Journal of Rare Diseases, vol. 15, no. 1, 214 . https://doi.org/10.1186/s13023-020-01491-9
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-16 (2020)
Orphanet Journal of Rare Diseases
Background Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, also referred to as Müllerian aplasia, is a congenital disorder characterized by aplasia of the uterus and upper part of the vagina in females with normal secondary sex characteristics and
Autor:
Birgitta Trolle, Laura Krogh Jørgensen, Anne-Mette Bay Bjørn, Morten Herlin, Michael B. Petersen
Publikováno v:
Herlin, M, Bay Bjørn, A-M, Jørgensen, L K, Trolle, B & Petersen, M B 2018, ' Treatment of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser syndrome in Denmark : a nationwide comparative study of anatomical outcome and complications ', Fertility and Sterility, vol. 110, no. 4, pp. 746-753 . https://doi.org/10.1016/j.fertnstert.2018.05.015
Herlin, M, Bay Bjørn, A M, Jørgensen, L K, Trolle, B & Petersen, M B 2018, ' Treatment of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser syndrome in Denmark : a nationwide comparative study of anatomical outcome and complications ', Fertility and Sterility, vol. 110, no. 4, pp. 746-753 . https://doi.org/10.1016/j.fertnstert.2018.05.015
Herlin, M, Bay Bjørn, A M, Jørgensen, L K, Trolle, B & Petersen, M B 2018, ' Treatment of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser syndrome in Denmark : a nationwide comparative study of anatomical outcome and complications ', Fertility and Sterility, vol. 110, no. 4, pp. 746-753 . https://doi.org/10.1016/j.fertnstert.2018.05.015
Objective: To compare the long-term anatomical outcome and complications in treatments of vaginal agenesis in Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome.Design: A historical comparative follow-up study using medical chart reviews.Setting: Public
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c6e14ceb7797afa53e7979ffd5b6408
https://vbn.aau.dk/da/publications/9dcc320b-6487-44ed-add1-9f8b0a2f0471
https://vbn.aau.dk/da/publications/9dcc320b-6487-44ed-add1-9f8b0a2f0471
Publikováno v:
Ugeskrift for laeger. 179(13)
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital anomaly characterized by uterovaginal agenesis in females with normal secondary sex characteristics and normal karyotype (46,XX). The prevalence of MRKH syndrome is one in 5,000 live fem
Publikováno v:
Herlin, M, Bjørn, A-M B, Rasmussen, M, Trolle, B & Petersen, M B 2016, ' Prevalence and patient characteristics of Mayer-Rokitansky-Küster-Hauser syndrome : a nationwide registry-based study ', Human Reproduction, vol. 31, no. 10, pp. 2384-90 . https://doi.org/10.1093/humrep/dew220
Herlin, M, Bjørn, A-M B, Rasmussen, M, Trolle, G B & Petersen, M B 2016, ' Prevalence and patient characteristics of Mayer-Rokitansky-Küster-Hauser syndrome : a nationwide registry-based study ', Human reproduction (Oxford, England), vol. 31, no. 10, pp. 2384-2390 . https://doi.org/10.1093/humrep/dew220
Herlin, M, Bjørn, A-M B, Rasmussen, M, Trolle, G B & Petersen, M B 2016, ' Prevalence and patient characteristics of Mayer-Rokitansky-Küster-Hauser syndrome : a nationwide registry-based study ', Human reproduction (Oxford, England), vol. 31, no. 10, pp. 2384-2390 . https://doi.org/10.1093/humrep/dew220
STUDY QUESTION: What is the prevalence of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome?SUMMARY ANSWER: The prevalence of MRKH syndrome in Denmark is 1 in 4982 (95% confidence interval (CI): 4216-5887) live female births.WHAT IS KNOWN ALREADY: The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e888360005abd3f8222202cea7c8daf
https://vbn.aau.dk/da/publications/78d6f8f7-25f3-461b-a859-80b543e47898
https://vbn.aau.dk/da/publications/78d6f8f7-25f3-461b-a859-80b543e47898
Publikováno v:
Herlin, M, Højland, A T & Petersen, M B 2014, ' Familial occurrence of Mayer-Rokitansky-Küster-Hauser syndrome : A case report and review of the literature ', American Journal of Medical Genetics. Part A, vol. 164, no. 9, pp. 2276-2286 . https://doi.org/10.1002/ajmg.a.36652
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital disorder of still unknown etiology, characterized by uterovaginal agenesis and can be associated with renal, skeletal and cardiac malformations. Most cases are sporadic. We report on a f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5b2a73e6a775902d3f2b4d67cbad2b4
https://pure.au.dk/portal/da/publications/familial-occurrence-of-mayerrokitanskykusterhauser-syndrome(0384cca2-4c70-4e48-b2ad-f0b0e81f1ec8).html
https://pure.au.dk/portal/da/publications/familial-occurrence-of-mayerrokitanskykusterhauser-syndrome(0384cca2-4c70-4e48-b2ad-f0b0e81f1ec8).html
Publikováno v:
Bjørsum-Meyer, T, Herlin, M, Qvist, N & Petersen, M B 2016, ' Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence : two case reports and a review of the literature ', Journal of Medical Case Reports, vol. 10, no. 1, 374 . https://doi.org/10.1186/s13256-016-1127-9
Bjørsum-Meyer, T, Herlin, M, Qvist, N & Petersen, M B 2016, ' Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence : two case reports and a review of the literature ', Journal of Medical Case Reports, vol. 10, 374 . https://doi.org/10.1186/s13256-016-1127-9
Journal of Medical Case Reports
Bjørsum-Meyer, T, Herlin, M, Qvist, N & Petersen, M B 2016, ' Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence : two case reports and a review of the literature ', Journal of Medical Case Reports, vol. 10, 374 . https://doi.org/10.1186/s13256-016-1127-9
Journal of Medical Case Reports
BACKGROUND: The vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association and Mayer-Rokitansky-Küster-Hauser syndrome are rare conditions. We aimed to present two cases wi
Autor:
Morten Herlin, Søren Peter Jonstrup, Allan Thomas Højland, Inge Søkilde Pedersen, Poul Henning Madsen, Anja Ernst, Henrik Okkels, Vang Le-Quy, Henrik Krarup, Michael Bjørn Petersen
Publikováno v:
Aarhus University
Herlin, M, Jonstrup, S P, Højland, A T, Pedersen, I S, Madsen, P H, Ernst, A, Okkels, H, Le, V, Krarup, H & Petersen, M B 2013, ' Investigations on the Molecular Genetic Etiology of Mayer-Rokitansky-Kuster-Hauser Syndrome in two Cousins using Exome Sequencing ', ASHG, American Society of Human Genetics, Boston, United States, 22/10/2013-26/10/2013 . < http://abstracts.ashg.org/cgi-bin/2013/ashg13s.pl >
Aalborg University
Herlin, M, Jonstrup, S P, Højland, A T, Pedersen, I S, Madsen, P H, Ernst, A, Okkels, H, Le, V Q, Krarup, H & Petersen, M B 2013, ' Investigations on the Molecular Genetic Etiology of Mayer-Rokitansky-Kuster-Hauser Syndrome in two Cousins using Exome Sequencing ', ASHG, annual meeting, Boston, USA, 22/10/2013-26/10/2013 .
Herlin, M, Jonstrup, S P, Højland, A T, Pedersen, I S, Madsen, P H, Ernst, A, Okkels, H, Le, V, Krarup, H & Petersen, M B 2013, ' Investigations on the Molecular Genetic Etiology of Mayer-Rokitansky-Kuster-Hauser Syndrome in two Cousins using Exome Sequencing. ', Annual Meeting of the American Society of Human Genetics, Boston, MA, United States, 22/10/2013-26/10/2013 .
Herlin, M, Jonstrup, S P, Højland, A T, Pedersen, I S, Madsen, P H, Ernst, A, Okkels, H, Le, V, Krarup, H & Petersen, M B 2013, ' Investigations on the Molecular Genetic Etiology of Mayer-Rokitansky-Kuster-Hauser Syndrome in two Cousins using Exome Sequencing ', ASHG, American Society of Human Genetics, Boston, United States, 22/10/2013-26/10/2013 . < http://abstracts.ashg.org/cgi-bin/2013/ashg13s.pl >
Aalborg University
Herlin, M, Jonstrup, S P, Højland, A T, Pedersen, I S, Madsen, P H, Ernst, A, Okkels, H, Le, V Q, Krarup, H & Petersen, M B 2013, ' Investigations on the Molecular Genetic Etiology of Mayer-Rokitansky-Kuster-Hauser Syndrome in two Cousins using Exome Sequencing ', ASHG, annual meeting, Boston, USA, 22/10/2013-26/10/2013 .
Herlin, M, Jonstrup, S P, Højland, A T, Pedersen, I S, Madsen, P H, Ernst, A, Okkels, H, Le, V, Krarup, H & Petersen, M B 2013, ' Investigations on the Molecular Genetic Etiology of Mayer-Rokitansky-Kuster-Hauser Syndrome in two Cousins using Exome Sequencing. ', Annual Meeting of the American Society of Human Genetics, Boston, MA, United States, 22/10/2013-26/10/2013 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1aae8a9d7be1a35344e6cf9a4ec845d2
https://pure.au.dk/portal/en/publications/investigations-on-the-molecular-genetic-etiology-of-mayerrokitanskykusterhauser-syndrome-in-two-cousins-using-exome-sequencing(64441b7a-f7ce-4750-88c6-6453798c07f2).html
https://pure.au.dk/portal/en/publications/investigations-on-the-molecular-genetic-etiology-of-mayerrokitanskykusterhauser-syndrome-in-two-cousins-using-exome-sequencing(64441b7a-f7ce-4750-88c6-6453798c07f2).html