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Ugeskrift for Laeger
|
April 8, 2021
[Genetic screening of adopted individuals]
Tanja Røhmer Wriedt, Anne-Marie Axø Gerdes, Laura Kristine Roos, et al.
American Journal of Medical Genetics. Part A
|
November 3, 2023
Aortic dissection in a young male with persistent ductus arteriosus and a novel variant in MYLK
Maria Bejerholm Boelman, Thomas van Overeem Hansen, Matthias Nybro Smith, et al.
Ugeskrift for Laeger
|
January 25, 2021
[The Danish screening programme for haemoglobinopathies]
Andreas Glenthøj, Mie Samson, Nina Toft, et al.
Ugeskrift for Laeger
|
November 15, 2014
[The genome and cardiology]
Henning Bundgaard, Birgitte Rode Diness, Jacob Tfelt-Hansen, et al.
Journal of the Neurological Sciences
|
May 29, 2020
Expanding the cerebrovascular phenotype of the p.R258H variant in ACTA2 related hereditary thoracic aortic disease (HTAD)
Birgitte Rode Diness, Rachel Nina Palmquist, Rikke Norling, et al.
BMJ (Clinical Research Ed.)
|
June 19, 2008
Effect of 50,000 IU vitamin A given with BCG vaccine on mortality in infants in Guinea-Bissau: randomised placebo controlled trial
Christine Stabell Benn, Birgitte Rode Diness, Adam Roth, et al.
American Journal of Medical Genetics. Part A
|
October 12, 2024
Reclassification of an FBN1 variant emphasizes the importance of segregation analysis, information sharing, and multidisciplinary teamwork in understanding genetic variants in health and disease
Dorte L Lildballe, Sara Markholt, Christina Daugaard Lyngholm, et al.
The Journal of Infectious Diseases
|
August 6, 2010
The effect of high-dose vitamin A supplementation given with bacille Calmette-Guérin vaccine at birth on infant rotavirus infection and diarrhea: a randomized prospective study from Guinea-Bissau
Birgitte Rode Diness, Dorthe Christoffersen, Ulla Britt Pedersen, et al.
Clinical Genetics
|
April 18, 2021
Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families
Fiona McKenzie, Kym Mina, Bert Callewaert, et al.
BMJ (Clinical Research Ed.)
|
March 11, 2010
Vitamin A supplementation and BCG vaccination at birth in low birthweight neonates: two by two factorial randomised controlled trial
Christine Stabell Benn, Ane Baerent Fisker, Bitiguida Mutna Napirna, et al.
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Search research articles
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Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Ugeskrift for Laeger
|
April 8, 2021
[Genetic screening of adopted individuals]
Tanja Røhmer Wriedt, Anne-Marie Axø Gerdes, Laura Kristine Roos, et al.
American Journal of Medical Genetics. Part A
|
November 3, 2023
Aortic dissection in a young male with persistent ductus arteriosus and a novel variant in MYLK
Maria Bejerholm Boelman, Thomas van Overeem Hansen, Matthias Nybro Smith, et al.
Ugeskrift for Laeger
|
January 25, 2021
[The Danish screening programme for haemoglobinopathies]
Andreas Glenthøj, Mie Samson, Nina Toft, et al.
Ugeskrift for Laeger
|
November 15, 2014
[The genome and cardiology]
Henning Bundgaard, Birgitte Rode Diness, Jacob Tfelt-Hansen, et al.
Journal of the Neurological Sciences
|
May 29, 2020
Expanding the cerebrovascular phenotype of the p.R258H variant in ACTA2 related hereditary thoracic aortic disease (HTAD)
Birgitte Rode Diness, Rachel Nina Palmquist, Rikke Norling, et al.
BMJ (Clinical Research Ed.)
|
June 19, 2008
Effect of 50,000 IU vitamin A given with BCG vaccine on mortality in infants in Guinea-Bissau: randomised placebo controlled trial
Christine Stabell Benn, Birgitte Rode Diness, Adam Roth, et al.
American Journal of Medical Genetics. Part A
|
October 12, 2024
Reclassification of an FBN1 variant emphasizes the importance of segregation analysis, information sharing, and multidisciplinary teamwork in understanding genetic variants in health and disease
Dorte L Lildballe, Sara Markholt, Christina Daugaard Lyngholm, et al.
The Journal of Infectious Diseases
|
August 6, 2010
The effect of high-dose vitamin A supplementation given with bacille Calmette-Guérin vaccine at birth on infant rotavirus infection and diarrhea: a randomized prospective study from Guinea-Bissau
Birgitte Rode Diness, Dorthe Christoffersen, Ulla Britt Pedersen, et al.
Clinical Genetics
|
April 18, 2021
Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families
Fiona McKenzie, Kym Mina, Bert Callewaert, et al.
BMJ (Clinical Research Ed.)
|
March 11, 2010
Vitamin A supplementation and BCG vaccination at birth in low birthweight neonates: two by two factorial randomised controlled trial
Christine Stabell Benn, Ane Baerent Fisker, Bitiguida Mutna Napirna, et al.
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of 3