Geralyn LaVecchia
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Geralyn LaVecchia has a total of 34 co-authors. Here are the top co-authors by number of shared publications:
- Janice Wang
Division of Pulmonary, Critical Care and Sleep Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, New Hyde Park, New York, NY 11042, USA
2 shared publications - Theresa Frantzen
Division of Pulmonary, Critical Care and Sleep Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, New Hyde Park, New York, NY 11042, USA
2 shared publications - Aileen Espinal
Division of Pulmonary, Critical Care and Sleep Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, New Hyde Park, NY 11042, United States
1 shared publication - Alison T. Lennox
Division of Pediatric Pulmonology, Allergy, Immunology, and Sleep Medicine, New York Medical College, Valhalla, NY 10595, United States
1 shared publication - Amy Plachta
Division of Pediatric Pulmonology, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York, NY 10003, United States
1 shared publication - Andrei Constantinescu
Division of Pediatric Pulmonology, Department of Pediatrics, Columbia University Irving Medical Center, NewYork-Presbyterian Morgan Stanley Children's Hospital, New York, NY
1 shared publication
Latest Publications
- Open Access
Evolving Nutritional Needs in Cystic Fibrosis
The course of cystic fibrosis (CF) as a nutritional illness is diverging since the introduction of highly effective modulator therapy, leading to more heterogeneous phenotypes of the disease despite CF genetic mutations that portend worse prognosis. This may become more evident as we follow the pediatric CF population into adulthood as some highly effective modulator therapies (HEMT) are approved for those as young as 1 year old. This review will outline the current research and knowledge available in the evolving nutritional health of people with CF as it relates to the impact of HEMT on anthropometrics, body composition, and energy expenditure, exocrine and endocrine pancreatic insufficiencies (the latter resulting in CF-related diabetes), vitamin and mineral deficiencies, and nutritional health in CF as it relates to pregnancy and lung transplantation.
Open AccessEvolving Nutritional Needs in Cystic Fibrosis
The course of cystic fibrosis (CF) as a nutritional illness is diverging since the introduction of highly effective modulator therapy, leading to more heterogeneous phenotypes of the disease despite CF genetic mutations that portend worse prognosis. This may become more evident as we follow the pediatric CF population into adulthood as some highly effective modulator therapies (HEMT) are approved for those as young as 1 year old. This review will outline the current research and knowledge available in the evolving nutritional health of people with CF as it relates to the impact of HEMT on anthropometrics, body composition, and energy expenditure, exocrine and endocrine pancreatic insufficiencies (the latter resulting in CF-related diabetes), vitamin and mineral deficiencies, and nutritional health in CF as it relates to pregnancy and lung transplantation.
- 21 February 2022
- Published by Elsevier in Journal of Cystic Fibrosis
- Vol. 21 (3) , e176-e183
The clinical impact of the Covid-19 pandemic first wave on patients with cystic fibrosis in New York
- 21 February 2022
- Published by Elsevier in Journal of Cystic Fibrosis
- Vol. 21 (3) , e176-e183
The clinical impact of the Covid-19 pandemic first wave on patients with cystic fibrosis in New York