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Pediatric Pulmonology
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April 3, 2008
Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene
Amy D McBee, Daniel J Wegner, Christopher S Carlson, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 15, 2014
An official American Thoracic Society statement: diagnosis and management of beryllium sensitivity and chronic beryllium disease
John R Balmes, Jerrold L Abraham, Raed A Dweik, et al.
Journal of Synchrotron Radiation
|
December 22, 2011
Assessing noise sources at synchrotron infrared ports
Ph Lerch, P Dumas, T Schilcher, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 8, 2022
Novel FOXF1-Stabilizing Compound TanFe Stimulates Lung Angiogenesis in Alveolar Capillary Dysplasia
Arun Pradhan, Lixiao Che, Vladimir Ustiyan, et al.
Plos One
|
March 27, 2019
CemOrange2 fusions facilitate multifluorophore subcellular imaging in C. elegans
Brian J Thomas, Ira E Wight, Wendy Y Y Chou, et al.
Pediatric Pulmonology
|
June 15, 2026
Respiratory Outcomes in Children With Neonatal Respiratory Distress Syndrome and Monoallelic ABCA3 Variants
Velda Ocasio Ramírez, Jennifer A Wambach, Rebekah J Nevel, et al.
Physical Review Letters
|
September 28, 2004
Fine structure in the energy region of the isoscalar giant quadrupole resonance: characteristic scales from a wavelet analysis
A Shevchenko, J Carter, R W Fearick, et al.
Psychotherapy and Psychosomatics
|
May 24, 2019
Two-Year Follow-Up after Treatment with the Cognitive Behavioral Analysis System of Psychotherapy versus Supportive Psychotherapy for Early-Onset Chronic Depression
Elisabeth Schramm, Levente Kriston, Moritz Elsaesser, et al.
Annals of the American Thoracic Society
|
February 29, 2020
Neuroendocrine Cell Hyperplasia of Infancy. Clinical Score and Comorbidities
Deborah R Liptzin, Kaci Pickett, John T Brinton, et al.
American Journal of Human Genetics
|
November 12, 2018
Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome
Jennifer A Wambach, Daniel J Wegner, Nivedita Patni, et al.
Page
of 29
Search research articles
Search
Showing results (251-260 of 285) with videos related to
Sort By:
Page
of 29
Pediatric Pulmonology
|
April 3, 2008
Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene
Amy D McBee, Daniel J Wegner, Christopher S Carlson, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 15, 2014
An official American Thoracic Society statement: diagnosis and management of beryllium sensitivity and chronic beryllium disease
John R Balmes, Jerrold L Abraham, Raed A Dweik, et al.
Journal of Synchrotron Radiation
|
December 22, 2011
Assessing noise sources at synchrotron infrared ports
Ph Lerch, P Dumas, T Schilcher, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 8, 2022
Novel FOXF1-Stabilizing Compound TanFe Stimulates Lung Angiogenesis in Alveolar Capillary Dysplasia
Arun Pradhan, Lixiao Che, Vladimir Ustiyan, et al.
Plos One
|
March 27, 2019
CemOrange2 fusions facilitate multifluorophore subcellular imaging in C. elegans
Brian J Thomas, Ira E Wight, Wendy Y Y Chou, et al.
Pediatric Pulmonology
|
June 15, 2026
Respiratory Outcomes in Children With Neonatal Respiratory Distress Syndrome and Monoallelic ABCA3 Variants
Velda Ocasio Ramírez, Jennifer A Wambach, Rebekah J Nevel, et al.
Physical Review Letters
|
September 28, 2004
Fine structure in the energy region of the isoscalar giant quadrupole resonance: characteristic scales from a wavelet analysis
A Shevchenko, J Carter, R W Fearick, et al.
Psychotherapy and Psychosomatics
|
May 24, 2019
Two-Year Follow-Up after Treatment with the Cognitive Behavioral Analysis System of Psychotherapy versus Supportive Psychotherapy for Early-Onset Chronic Depression
Elisabeth Schramm, Levente Kriston, Moritz Elsaesser, et al.
Annals of the American Thoracic Society
|
February 29, 2020
Neuroendocrine Cell Hyperplasia of Infancy. Clinical Score and Comorbidities
Deborah R Liptzin, Kaci Pickett, John T Brinton, et al.
American Journal of Human Genetics
|
November 12, 2018
Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome
Jennifer A Wambach, Daniel J Wegner, Nivedita Patni, et al.
Page
of 29