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Wim Wuyts

Showing results (121-130 of 135) with videos related to

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American Journal of Human Genetics|August 25, 2015
Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver SyndromeJosephina A N Meester, Laura Southgate, Anna-Barbara Stittrich, et al.
Frontiers in Medicine|October 14, 2021
Management of Acute Exacerbation of Idiopathic Pulmonary Fibrosis in Specialised and Non-specialised ILD Centres Around the WorldMarkus Polke, Yasuhiro Kondoh, Marlies Wijsenbeek, et al.
The European Respiratory Journal|February 16, 2020
Acute exacerbation of idiopathic pulmonary fibrosis: international survey and call for harmonisationMichael Kreuter, Markus Polke, Simon L F Walsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 5, 2022
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defectsAuriane Cospain, Ana Rivera-Barahona, Erwan Dumontet, et al.
Plos Genetics|May 3, 2011
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndromeMargot E Bowen, Eric D Boyden, Ingrid A Holm, et al.
American Journal of Human Genetics|October 23, 2003
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studyIgnacio Del Castillo, Miguel A Moreno-Pelayo, Francisco J Del Castillo, et al.
Biorxiv : the Preprint Server for Biology|July 2, 2026
Alveolar niche disruption and aberrant epithelial reprogramming are early hallmarks of idiopathic pulmonary fibrosisAurelien Justet, Venerino Poletti, Cristian Coarfa, et al.
ERJ Open Research|April 3, 2023
Delineating associations of progressive pleuroparenchymal fibroelastosis in patients with pulmonary fibrosisEyjolfur Gudmundsson, An Zhao, Nesrin Mogulkoc, et al.
Human Mutation|June 21, 2018
Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohortJosephina A N Meester, Maja Sukalo, Kim C Schröder, et al.
The European Respiratory Journal|September 2, 2017
Diagnostic accuracy of a clinical diagnosis of idiopathic pulmonary fibrosis: an international case-cohort studySimon L F Walsh, Toby M Maher, Martin Kolb, et al.
Pageof 14

Showing results (121-130 of 135) with videos related to

Sort By:
Pageof 14
American Journal of Human Genetics|August 25, 2015
Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver SyndromeJosephina A N Meester, Laura Southgate, Anna-Barbara Stittrich, et al.
Frontiers in Medicine|October 14, 2021
Management of Acute Exacerbation of Idiopathic Pulmonary Fibrosis in Specialised and Non-specialised ILD Centres Around the WorldMarkus Polke, Yasuhiro Kondoh, Marlies Wijsenbeek, et al.
The European Respiratory Journal|February 16, 2020
Acute exacerbation of idiopathic pulmonary fibrosis: international survey and call for harmonisationMichael Kreuter, Markus Polke, Simon L F Walsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 5, 2022
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defectsAuriane Cospain, Ana Rivera-Barahona, Erwan Dumontet, et al.
Plos Genetics|May 3, 2011
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndromeMargot E Bowen, Eric D Boyden, Ingrid A Holm, et al.
American Journal of Human Genetics|October 23, 2003
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studyIgnacio Del Castillo, Miguel A Moreno-Pelayo, Francisco J Del Castillo, et al.
Biorxiv : the Preprint Server for Biology|July 2, 2026
Alveolar niche disruption and aberrant epithelial reprogramming are early hallmarks of idiopathic pulmonary fibrosisAurelien Justet, Venerino Poletti, Cristian Coarfa, et al.
ERJ Open Research|April 3, 2023
Delineating associations of progressive pleuroparenchymal fibroelastosis in patients with pulmonary fibrosisEyjolfur Gudmundsson, An Zhao, Nesrin Mogulkoc, et al.
Human Mutation|June 21, 2018
Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohortJosephina A N Meester, Maja Sukalo, Kim C Schröder, et al.
The European Respiratory Journal|September 2, 2017
Diagnostic accuracy of a clinical diagnosis of idiopathic pulmonary fibrosis: an international case-cohort studySimon L F Walsh, Toby M Maher, Martin Kolb, et al.
Pageof 14