Physician

Pediatric Pulmonology

Dr. Thomas W. Ferkol Jr., MD

Thomas W. Ferkol Jr., MD practices Pediatric Pulmonology. He researched medicine at The Ohio State University College of Medicine. Thomas Ferkol is also published. He has 32 publications published. The lastest publication: "Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review.'

Publications

Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review.
Ventilatory control and supplemental oxygen in premature infants with apparent chronic lung disease.
Clinical Features of Childhood Primary Ciliary Dyskinesia By Genotype and Ultrastructural Phenotype.
Picking up speed: advances in the genetics of primary ciliary dyskinesia.
Sources of Methodological Variability in Phase Angles from Respiratory Inductance Plethysmography in Preterm Infants.
The global burden of respiratory disease.
Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype.
FDG PET imaging in cystic fibrosis.
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.
Standardizing Nasal Nitric Oxide Measurement as a Test for Primary Ciliary Dyskinesia.
Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms.
ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6.
LRRC6 Mutation Causes Primary Ciliary Dyskinesia with Dynein Arm Defects.
Primary Ciliary Dyskinesia-Causing Mutations in Amish and Mennonite Communities.
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia.
Ciliopathies: The Central Role of Cilia in a Spectrum of Pediatric Disorders.
The emerging genetics of primary ciliary dyskinesia.
Hitting the target: new treatments for cystic fibrosis.
The Effect of Polarized Release of CXC-chemokines from Wild-type and Cystic Fibrosis Murine Airway Epithelial Cells.
Primary ciliary dyskinesia in Amish communities.
Aquagenic wrinkling of the palms in cystic fibrosis: comparison with controls and genotype-phenotype correlations.
[18F]fluorodeoxyglucose positron emission tomography for lung antiinflammatory response evaluation.
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.
Airway inflammation in cystic fibrosis.
Transmission of Panton-Valentine leukocidin-positive Staphylococcus aureus between patients with cystic fibrosis.
Panton-Valentine Leukocidin-positive methicillin-resistant Staphylococcus aureus lung infection in patients with cystic fibrosis.
Regulation of systemic and local neutrophil responses by G-CSF during pulmonary Pseudomonas aeruginosa infection.
Quantifying pulmonary inflammation in cystic fibrosis with positron emission tomography.
Delivery of CFTR by adenoviral vector to cystic fibrosis mouse lung in a model of chronic Pseudomonas aeruginosa lung infection.
Inflammatory response in airway epithelial cells isolated from patients with cystic fibrosis.
CCDC65 Mutation Causes Primary Ciliary Dyskinesia with Normal Ultrastructure and Hyperkinetic Cilia.

Schools

Ohio State University College of Medicine
University Of Nc
Case Western Reserve University

Doctors Specialties

Pediatric Pulmonology

Accepted Insurances

Education

Case Western Reserve University - University Hospitals
University of North Carolina Hospitals
The Ohio State University College of Medicine

Hospital

St. Louis Children's Hospital
Barnes-Jewish Hospital

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