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The Journal of Experimental Medicine
|
October 29, 2008
Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA
Takuji Suzuki, Takuro Sakagami, Bruce K Rubin, et al.
Nature Communications
|
August 9, 2020
A lung tropic AAV vector improves survival in a mouse model of surfactant B deficiency
Martin H Kang, Laura P van Lieshout, Liqun Xu, et al.
Chest
|
February 23, 2013
Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1
Aaron Hamvas, Robin R Deterding, Susan E Wert, et al.
Human Molecular Genetics
|
November 10, 2011
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children
Florence Flamein, Laure Riffault, Céline Muselet-Charlier, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 15, 2019
Current Status and Future Opportunities in Lung Precision Medicine Research with a Focus on Biomarkers. An American Thoracic Society/National Heart, Lung, and Blood Institute Research Statement
Ann Chen Wu, James P Kiley, Patricia J Noel, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 22, 2007
Diffuse lung disease in young children: application of a novel classification scheme
Gail H Deutsch, Lisa R Young, Robin R Deterding, et al.
Pediatric Pulmonology
|
April 1, 2025
Genetic Testing Utilization in the U.S. Registry for Childhood Interstitial and Diffuse Lung Diseases
Laura A Voss, Rebekah J Nevel, Jennifer A Wambach, et al.
Obstetrics and Gynecology
|
December 8, 2017
Ethical Considerations Concerning Amnioinfusions for Treating Fetal Bilateral Renal Agenesis
Jeremy Sugarman, Jean Anderson, Ahmet A Baschat, et al.
Acta Neuropathologica
|
February 10, 2018
NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease
Johanna Uusimaa, Riitta Kaarteenaho, Teija Paakkola, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 16, 2018
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline
Adam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 83) with videos related to
Sort By:
Page
of 9
The Journal of Experimental Medicine
|
October 29, 2008
Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA
Takuji Suzuki, Takuro Sakagami, Bruce K Rubin, et al.
Nature Communications
|
August 9, 2020
A lung tropic AAV vector improves survival in a mouse model of surfactant B deficiency
Martin H Kang, Laura P van Lieshout, Liqun Xu, et al.
Chest
|
February 23, 2013
Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1
Aaron Hamvas, Robin R Deterding, Susan E Wert, et al.
Human Molecular Genetics
|
November 10, 2011
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children
Florence Flamein, Laure Riffault, Céline Muselet-Charlier, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 15, 2019
Current Status and Future Opportunities in Lung Precision Medicine Research with a Focus on Biomarkers. An American Thoracic Society/National Heart, Lung, and Blood Institute Research Statement
Ann Chen Wu, James P Kiley, Patricia J Noel, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 22, 2007
Diffuse lung disease in young children: application of a novel classification scheme
Gail H Deutsch, Lisa R Young, Robin R Deterding, et al.
Pediatric Pulmonology
|
April 1, 2025
Genetic Testing Utilization in the U.S. Registry for Childhood Interstitial and Diffuse Lung Diseases
Laura A Voss, Rebekah J Nevel, Jennifer A Wambach, et al.
Obstetrics and Gynecology
|
December 8, 2017
Ethical Considerations Concerning Amnioinfusions for Treating Fetal Bilateral Renal Agenesis
Jeremy Sugarman, Jean Anderson, Ahmet A Baschat, et al.
Acta Neuropathologica
|
February 10, 2018
NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease
Johanna Uusimaa, Riitta Kaarteenaho, Teija Paakkola, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 16, 2018
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline
Adam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
Page
of 9