Margaret Rosenfeld

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Audio-based cough detection has become more pervasive in recent years because of its utility in evaluating treatments and the potential to impact the quality of life for individuals with chronic cough. We critically examine the current state of the art in cough detection, concluding that existing approaches expose private audio recordings of users and(More)
Home spirometry is gaining acceptance in the medical community because of its ability to detect pulmonary exacerbations and improve outcomes of chronic lung ailments. However, cost and usability are significant barriers to its widespread adoption. To this end, we present SpiroSmart, a low-cost mobile phone application that performs spirometry sensing using(More)
The motive forces for ciliary movement are generated by large multiprotein complexes referred to as outer dynein arms (ODAs), which are preassembled in the cytoplasm prior to transport to the ciliary axonemal compartment. In humans, defects in structural components, docking complexes, or cytoplasmic assembly factors can cause primary ciliary dyskinesia(More)
  • Adam J. Shapiro, Maimoona A. Zariwala, Thomas Ferkol, Stephanie D. Davis, Scott D. Sagel, Sharon D. Dell +8 others
  • 2016
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, rare lung disease resulting in chronic oto-sino-pulmonary disease in both children and adults. Many physicians incorrectly diagnose PCD or eliminate PCD from their differential diagnosis due to inexperience with diagnostic testing methods. Thus far, all therapies used for PCD are unproven(More)
RATIONALE Yoga has been shown to improve outcomes in patients with asthma but has not been investigated in cystic fibrosis (CF) patients. METHODS This was a prospective pilot study to evaluate the safety of a standardized yoga program among CF patients aged 12 to 25 years. Participants engaged in a 50-minute yoga session twice weekly for 8 weeks conducted(More)
BACKGROUND Cerebrospinal fluid shunt infection can be recalcitrant. Recurrence is common despite appropriate therapy for the pathogens identified by culture. Improved diagnostic and therapeutic approaches are required, and culture-independent molecular approaches to cerebrospinal fluid shunt infections have not been described. OBJECTIVES To identify the(More)
Spirometry is the most widely employed objective measure of lung function. It is central to the diagnosis and management of lung ailments like asthma, chronic obstructive pulmonary disease, and cystic fibrosis. Spirometry is generally performed in medical clinics using clinical spirometers---devices that measure the instantaneous exhaled flow (liters/sec.).(More)
  • Catherine Ann Byrnes, Suzanna Vidmar, Joyce L Cheney, John B Carlin, David S Armstrong, Peter J Cooper +22 others
  • 2013
BACKGROUND Newborn screening allows novel treatments for cystic fibrosis (CF) to be trialled in early childhood before irreversible lung injury occurs. As respiratory exacerbations are a potential trial outcome variable, we determined their rate, duration and clinical features in preschool children with CF; and whether they were associated with growth, lung(More)
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