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Pediatric Nephrology (Berlin, Germany)
|
February 21, 2007
Nephrocystin and ciliary defects not only in the kidney?
Christian von Schnakenburg, Manfred Fliegauf, Heymut Omran
Cardiology in the Young
|
July 28, 2022
Amiodarone-sirolimus interaction in a neonate with tuberous sclerosis complex
Daniel Ebrahimi-Fakhari, Hans G Kehl, Heymut Omran
Annual Review of Physiology
|
October 25, 2006
Genetic defects in ciliary structure and function
Maimoona A Zariwala, Michael R Knowles, Heymut Omran
Current Opinion in Pulmonary Medicine
|
September 15, 2025
Primary ciliary dyskinesia phenotypes and correlation with genotype
Amjad Horani, Wallace Wee, Heymut Omran, et al.
Proceedings of the American Thoracic Society
|
September 20, 2011
The emerging genetics of primary ciliary dyskinesia
Maimoona A Zariwala, Heymut Omran, Thomas W Ferkol
Genes & Development
|
June 18, 2014
Multicilin drives centriole biogenesis via E2f proteins
Lina Ma, Ian Quigley, Heymut Omran, et al.
Annals of Neurology
|
January 26, 2005
Autosomal recessive rippling muscle disease with homozygous CAV3 mutations
Christian Kubisch, Uwe-Peter Ketelsen, Ingrid Goebel, et al.
Journal of Pediatric Hematology/Oncology
|
August 18, 2017
Successful Extracorporeal Life Support in a Pediatric Hematopoietic Stem Cell Transplant Recipient With Periengraftment Respiratory Failure
Jenny Potratz, Martina Ahlmann, Claudia Rössig, et al.
The Clinical Respiratory Journal
|
March 4, 2017
DYNC2H1 mutation causes Jeune syndrome and recurrent lung infections associated with ciliopathy
Nagehan Emiralioglu, Julia Wallmeier, Heike Olbrich, et al.
International Journal of Molecular Sciences
|
September 28, 2021
Current and Future Treatments in Primary Ciliary Dyskinesia
Tamara Paff, Heymut Omran, Kim G Nielsen, et al.
Page
of 21
Search research articles
Search
Showing results (11-20 of 208) with videos related to
Sort By:
Page
of 21
Pediatric Nephrology (Berlin, Germany)
|
February 21, 2007
Nephrocystin and ciliary defects not only in the kidney?
Christian von Schnakenburg, Manfred Fliegauf, Heymut Omran
Cardiology in the Young
|
July 28, 2022
Amiodarone-sirolimus interaction in a neonate with tuberous sclerosis complex
Daniel Ebrahimi-Fakhari, Hans G Kehl, Heymut Omran
Annual Review of Physiology
|
October 25, 2006
Genetic defects in ciliary structure and function
Maimoona A Zariwala, Michael R Knowles, Heymut Omran
Current Opinion in Pulmonary Medicine
|
September 15, 2025
Primary ciliary dyskinesia phenotypes and correlation with genotype
Amjad Horani, Wallace Wee, Heymut Omran, et al.
Proceedings of the American Thoracic Society
|
September 20, 2011
The emerging genetics of primary ciliary dyskinesia
Maimoona A Zariwala, Heymut Omran, Thomas W Ferkol
Genes & Development
|
June 18, 2014
Multicilin drives centriole biogenesis via E2f proteins
Lina Ma, Ian Quigley, Heymut Omran, et al.
Annals of Neurology
|
January 26, 2005
Autosomal recessive rippling muscle disease with homozygous CAV3 mutations
Christian Kubisch, Uwe-Peter Ketelsen, Ingrid Goebel, et al.
Journal of Pediatric Hematology/Oncology
|
August 18, 2017
Successful Extracorporeal Life Support in a Pediatric Hematopoietic Stem Cell Transplant Recipient With Periengraftment Respiratory Failure
Jenny Potratz, Martina Ahlmann, Claudia Rössig, et al.
The Clinical Respiratory Journal
|
March 4, 2017
DYNC2H1 mutation causes Jeune syndrome and recurrent lung infections associated with ciliopathy
Nagehan Emiralioglu, Julia Wallmeier, Heike Olbrich, et al.
International Journal of Molecular Sciences
|
September 28, 2021
Current and Future Treatments in Primary Ciliary Dyskinesia
Tamara Paff, Heymut Omran, Kim G Nielsen, et al.
Page
of 21