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Matthias Griese

Showing results (201-210 of 280) with videos related to

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Orphanet Journal of Rare Diseases|July 23, 2022
Randomized controlled phase 2 trial of hydroxychloroquine in childhood interstitial lung diseaseMatthias Griese, Matthias Kappler, Florian Stehling, et al.
ERJ Open Research|December 17, 2025
Persistent tachypnoea of infancy and neuroendocrine cell hyperplasia of infancy: from systematic review to future directionsNadia Nathan, Magdalena Grochowska, Katarzyna Krenke, et al.
The European Respiratory Journal|November 18, 2011
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung diseaseMichael S D Kormann, Andreas Hector, Veronica Marcos, et al.
Allergy|February 23, 2019
Lung disease in STAT3 hyper-IgE syndrome requires intense therapyCarolin Kröner, Jens Neumann, Julia Ley-Zaporozhan, et al.
BMC Pulmonary Medicine|November 18, 2024
Protocol and research program of the European registry and biobank for interstitial lung diseases (eurILDreg)Ekaterina Krauss, Silke Tello, Jennifer Naumann, et al.
The European Respiratory Journal|June 6, 2024
ERS statement on transition of care in childhood interstitial lung diseasesPetr Pohunek, Effrosyni Manali, Susanne Vijverberg, et al.
Clinical Genetics|June 24, 2021
Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancyChristina K Rapp, Ine Van Dijck, Lucia Laugwitz, et al.
Orphanet Journal of Rare Diseases|June 15, 2014
Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?Laurent Enaud, Alice Hadchouel, Aurore Coulomb, et al.
Pediatric Research|September 17, 2015
Surfactant proteins in pediatric interstitial lung diseaseMatthias Griese, Elke Lorenz, Meike Hengst, et al.
Frontiers in Medicine|May 21, 2025
Respiratory and other organ manifestations in <i>NKX2-1</i>-related disorders: a systematic reviewKatarzyna Michel, Alba Ruiz-Ramos, Laia Nou-Fontanet, et al.
Pageof 28

Showing results (201-210 of 280) with videos related to

Sort By:
Pageof 28
Orphanet Journal of Rare Diseases|July 23, 2022
Randomized controlled phase 2 trial of hydroxychloroquine in childhood interstitial lung diseaseMatthias Griese, Matthias Kappler, Florian Stehling, et al.
ERJ Open Research|December 17, 2025
Persistent tachypnoea of infancy and neuroendocrine cell hyperplasia of infancy: from systematic review to future directionsNadia Nathan, Magdalena Grochowska, Katarzyna Krenke, et al.
The European Respiratory Journal|November 18, 2011
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung diseaseMichael S D Kormann, Andreas Hector, Veronica Marcos, et al.
Allergy|February 23, 2019
Lung disease in STAT3 hyper-IgE syndrome requires intense therapyCarolin Kröner, Jens Neumann, Julia Ley-Zaporozhan, et al.
BMC Pulmonary Medicine|November 18, 2024
Protocol and research program of the European registry and biobank for interstitial lung diseases (eurILDreg)Ekaterina Krauss, Silke Tello, Jennifer Naumann, et al.
The European Respiratory Journal|June 6, 2024
ERS statement on transition of care in childhood interstitial lung diseasesPetr Pohunek, Effrosyni Manali, Susanne Vijverberg, et al.
Clinical Genetics|June 24, 2021
Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancyChristina K Rapp, Ine Van Dijck, Lucia Laugwitz, et al.
Orphanet Journal of Rare Diseases|June 15, 2014
Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?Laurent Enaud, Alice Hadchouel, Aurore Coulomb, et al.
Pediatric Research|September 17, 2015
Surfactant proteins in pediatric interstitial lung diseaseMatthias Griese, Elke Lorenz, Meike Hengst, et al.
Frontiers in Medicine|May 21, 2025
Respiratory and other organ manifestations in <i>NKX2-1</i>-related disorders: a systematic reviewKatarzyna Michel, Alba Ruiz-Ramos, Laia Nou-Fontanet, et al.
Pageof 28