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Ida Vogel

Showing results (41-50 of 147) with videos related to

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Fetal Diagnosis and Therapy|September 11, 2018
Population-Based Screening for Trisomies and Atypical Chromosomal Abnormalities: Improving Efficacy using the Combined First Trimester Screening Algorithm as well as Individual Risk ParametersIda Vogel, Ann Tabor, Charlotte Ekelund, et al.
Placenta|October 18, 2025
Placental mosaicism for structural chromosomal variants: follow-up of 251 Danish cases (1983-2021)Simon Horsholt Thomsen, Ida Charlotte Bay Lund, Iben Bache, et al.
Case Reports in Gastrointestinal Medicine|January 11, 2013
Goblet cell carcinoid in a patient with neurofibromatosis type 1: a rare combinationTine Gregersen, Nanna Holt, Henning Gronbaek, et al.
Clinical Case Reports|July 7, 2017
Isolated congenital hepatic fibrosis associated with <i>TMEM67</i> mutations: report of a new genotype-phenotype relationshipIda Vogel, Peter Ott, Dorte Lildballe, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|March 5, 2024
Encounters with public and professional understandings of Down syndrome: A qualitative study of parents' experiencesEllen H Steffensen, Stephanie L Santoro, Lars H Pedersen, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|June 1, 2005
Preterm delivery predicted by soluble CD163 and CRP in women with symptoms of preterm deliveryIda Vogel, Jakob Grove, Poul Thorsen, et al.
In Vivo (Athens, Greece)|November 5, 2004
Biphasic effect of relaxin, inhibitable by a collagenase inhibitor, on the strength of human fetal membranesIda Vogel, Astrid Petersen, Lone Kjeld Petersen, et al.
World Journal of Gastroenterology|February 25, 2020
New tight junction protein 2 variant causing progressive familial intrahepatic cholestasis type 4 in adults: A case reportChun-Shan Wei, Naja Becher, Jenny Blechingberg Friis, et al.
Research in Developmental Disabilities|June 21, 2016
Epilepsy and cataplexy in Angelman syndrome. Genotype-phenotype correlationsLine Granild Bie Mertz, Rikke Christensen, Ida Vogel, et al.
Clinical Case Reports|May 5, 2017
First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarrayHeidi Kristine Støve, Naja Becher, Vibike Gjørup, et al.
Pageof 15

Showing results (41-50 of 147) with videos related to

Sort By:
Pageof 15
Fetal Diagnosis and Therapy|September 11, 2018
Population-Based Screening for Trisomies and Atypical Chromosomal Abnormalities: Improving Efficacy using the Combined First Trimester Screening Algorithm as well as Individual Risk ParametersIda Vogel, Ann Tabor, Charlotte Ekelund, et al.
Placenta|October 18, 2025
Placental mosaicism for structural chromosomal variants: follow-up of 251 Danish cases (1983-2021)Simon Horsholt Thomsen, Ida Charlotte Bay Lund, Iben Bache, et al.
Case Reports in Gastrointestinal Medicine|January 11, 2013
Goblet cell carcinoid in a patient with neurofibromatosis type 1: a rare combinationTine Gregersen, Nanna Holt, Henning Gronbaek, et al.
Clinical Case Reports|July 7, 2017
Isolated congenital hepatic fibrosis associated with <i>TMEM67</i> mutations: report of a new genotype-phenotype relationshipIda Vogel, Peter Ott, Dorte Lildballe, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|March 5, 2024
Encounters with public and professional understandings of Down syndrome: A qualitative study of parents' experiencesEllen H Steffensen, Stephanie L Santoro, Lars H Pedersen, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|June 1, 2005
Preterm delivery predicted by soluble CD163 and CRP in women with symptoms of preterm deliveryIda Vogel, Jakob Grove, Poul Thorsen, et al.
In Vivo (Athens, Greece)|November 5, 2004
Biphasic effect of relaxin, inhibitable by a collagenase inhibitor, on the strength of human fetal membranesIda Vogel, Astrid Petersen, Lone Kjeld Petersen, et al.
World Journal of Gastroenterology|February 25, 2020
New tight junction protein 2 variant causing progressive familial intrahepatic cholestasis type 4 in adults: A case reportChun-Shan Wei, Naja Becher, Jenny Blechingberg Friis, et al.
Research in Developmental Disabilities|June 21, 2016
Epilepsy and cataplexy in Angelman syndrome. Genotype-phenotype correlationsLine Granild Bie Mertz, Rikke Christensen, Ida Vogel, et al.
Clinical Case Reports|May 5, 2017
First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarrayHeidi Kristine Støve, Naja Becher, Vibike Gjørup, et al.
Pageof 15