Research map: Comment on “Early Life Food Desert Status Is Associated With Alpha and Gamma Tocopherol Levels and Infant Lung Function”
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The vitamin E isoforms α-tocopherol and γ-tocopherol have opposite associations with spirometric parameters: the CARDIA study
· Michelle E. Marchese · 2014 · 50 citations · Cited by this paper
TAP1 Deficiency Mimicking Primary Ciliary Dyskinesia in a Child With Recurrent Sinopulmonary Infections: A Case Report
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New reference ranges for interpreting forced expiratory manoeuvres in infants and implications for clinical interpretation: a multicentre collaboration
· Sooky Lum · 2015 · 38 citations · Cited by this paper
Volumetric Capnography for Assessing Pre‐ and Post‐Operative Intrapulmonary Shunt in Congenital Pulmonary Lymphangiectasia: A Case Report
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Fat-soluble vitamins A and E and health disparities in a cohort of pregnant women at delivery
· Corrine Hanson · 2018 · 18 citations · Cited by this paper
Agreement of Diaphragmatic Excursion Between Anterior Subcostal and Posterior Subcostal Ultrasonography in Premature Neonates
· 2026 · Related
Early Life Food Desert Status Is Associated With Alpha and Gamma‐Tocopherol Levels and Infant Lung Function
· Garen S. Wolff · 2026 · 2 citations · Cited by this paper
Cystic Fibrosis Newborn Screening: Cost Trajectory as a Marker to Improve Health Outcomes
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Bronchodilator Responsiveness in Preterm‐Born Children With Chronic Lung Disease: Importance of Individualized Testing
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Performance Evaluation of a Novel Cystic Fibrosis Caregiver Burden Measure Demonstrates Significant Challenges for Parents of Children With CF During the Early Years: The Irish Comparative Outcomes Study (ICOS)
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Administrative Prevalence and Healthcare Utilization of Pediatric Cystic Fibrosis in a Middle‐Income Country: A 10‐Year Analysis of National Administrative Data
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Respiratory Outcomes in Children With Neonatal Respiratory Distress Syndrome and Monoallelic ABCA3 Variants
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Real‐World Clinical Outcomes of Lumacaftor‐Ivacaftor or Tezacaftor‐Ivacaftor Therapy in Children With Cystic Fibrosis Homozygous for Phe508del
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