Professor of Pediatrics, Johns Hopkins University School of Medicine
Neonat/Perinatology
Dr. Lawrence M. Nogee, MD
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Lawrence Nogee is an expert in the field of Neonat/Perinatology. He went to medical school at Johns Hopkins University School of Medicine. Johns Hopkins University School of Medicine is a top medical college. Johns Hopkins University School of Medicine has a rank of 3 in research and a 29 in primary care He over the years received 4 awards: "America's Top Doctors", "Top Doctors:Baltimore Area", "Top Doctors:Washington-Baltimore" and "Super Doctor". Lawrence M. Nogee, MD is also published. He has 86 publications published. The lastest publication: "Genetics of the hydrophobic surfactant proteins.'
Publications
- Genotype-phenotype correlations for infants and children with ABCA3 deficiency.
- Large ABCA3 and SFTPC Deletions Resulting in Lung Disease.
- Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.
- Frontiers in pulmonary hypertension in infants and children with bronchopulmonary dysplasia.
- An intronic ABCA3 mutation that is responsible for respiratory disease.
- Molecular and Cellular Characteristics of ABCA3 Mutations Associated with Diffuse Parenchymal Lung Diseases in Children.
- Pulmonary Nodules in a Newborn With ATP-Binding Cassette Transporter A3 (ABCA3) Mutations.
- Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy.
- Fatal familial lung disease caused by ABCA3 deficiency without identified ABCA3 mutations.
- Genetic Basis of Children's Interstitial Lung Disease.
- Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes.
- Genetic disorders of surfactant dysfunction.
- Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.
- Usual interstitial pneumonia in an adolescent with ABCA3 mutations.
- Population and disease-based prevalence of the common mutations associated with surfactant deficiency.
- Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene.
- ABCA3 deficiency presenting as persistent pulmonary hypertension of the newborn.
- Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.
- Unexplained neonatal respiratory distress due to congenital surfactant deficiency.
- Genetically engineered mice in understanding the basis of neonatal lung disease.
- ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease.
- Defects in surfactant synthesis: clinical implications.
- Long-term outcomes after infant lung transplantation for surfactant protein B deficiency related to other causes of respiratory failure.
- Surfactant composition and function in patients with ABCA3 mutations.
- Genetics of pediatric interstitial lung disease.
- ABCA3 mutations associated with pediatric interstitial lung disease.
- A common mutation in the surfactant protein C gene associated with lung disease.
- Progressive lung disease and surfactant dysfunction with a deletion in surfactant protein C gene.
- Informed consent for genetic research.
- N-terminally extended surfactant protein (SP) C isolated from SP-B-deficient children has reduced surface activity and inhibited lipopolysaccharide binding.
- ABCA3 gene mutations in newborns with fatal surfactant deficiency.
- Alterations in SP-B and SP-C expression in neonatal lung disease.
- Expression of a human surfactant protein C mutation associated with interstitial lung disease disrupts lung development in transgenic mice.
- Abnormal expression of surfactant protein C and lung disease.
- Mutations in the surfactant protein C gene associated with interstitial lung disease.
- Persistent tachypnea and hypoxia in a 3-month-old term infant.
- Genetic mechanisms of surfactant deficiency.
- Diffuse lung disease in young children: application of a novel classification scheme.
- Genetic disorders of surfactant proteins.
- A major deletion in the surfactant protein-B gene causing lethal respiratory distress.
- Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease.
- Surfactant dysfunction.
- Familial neuroendocrine cell hyperplasia of infancy.
- Variable phenotype associated with SP-C gene mutations: fatal case with the I73T mutation.
- Clinical, radiological and pathological features of ABCA3 mutations in children.
- Neonatal respiratory failure due to a novel mutation in the surfactant protein C gene.
- Ultrastructure of lamellar bodies in congenital surfactant deficiency.
- More reasons to hold on additional doses of antenatal steroids.
- Increased expression of pulmonary surfactant proteins in oxygen-exposed rats.
- Relationships among surfactant fraction lipids, proteins and biophysical properties in the developing rat lung.
- Isolation and characterization of a small intestinal surfactant-like particle containing alkaline phosphatase and other digestive enzymes.
- Increased synthesis and mRNA of surfactant protein A in oxygen-exposed rats.
- Hyaline membrane disease and surfactant protein, SAP-35, in diabetes in pregnancy.
- Effects of pulmonary oxygen injury on airway content of surfactant-associated protein A.
- Requirement of the collagenous domain for carbohydrate processing and secretion of a surfactant protein, SP-A.
- Organization of repeated regions within the Epstein-Barr virus DNA molecule.
- Human surfactant protein B: structure, function, regulation, and genetic disease.
- Partial deficiency of surfactant protein B in an infant with chronic lung disease.
- Aberrant processing of surfactant protein C in hereditary SP-B deficiency.
- Pathophysiology and treatment of surfactant protein-B deficiency.
- Molecular and phenotypic variability in the congenital alveolar proteinosis syndrome associated with inherited surfactant protein B deficiency.
- Ultrastructure of lung in surfactant protein B deficiency.
- Surfactant protein B deficiency: antenatal diagnosis and prospective treatment with surfactant replacement.
- A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds.
- Surfactant protein B deficiency: radiographic manifestations.
- Brief report: deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis.
- Lung transplantation for treatment of infants with surfactant protein B deficiency.
- Surfactant protein-B deficiency.
- Human pulmonary alveolar proteinosis associated with a defect in GM-CSF/IL-3/IL-5 receptor common beta chain expression.
- Transient surfactant protein B deficiency in a term infant with severe respiratory failure.
- Genetics of the hydrophobic surfactant proteins.
- Surfactant protein B deficiency: clinical, histological and molecular evaluation.
- Hereditary surfactant protein B deficiency resulting from a novel mutation.
- Deficiency of lamellar bodies in alveolar type II cells associated with fatal respiratory disease in a full-term infant.
- Pulmonary surfactant metabolism in infants lacking surfactant protein B.
- Population-based estimates of surfactant protein B deficiency.
- Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency.
- Absence of lamellar bodies with accumulation of dense bodies characterizes a novel form of congenital surfactant defect.
- Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutation.
- Recurrent familial neonatal deaths: hereditary surfactant protein B deficiency.
- A mutation in the surfactant protein C gene associated with familial interstitial lung disease.
- Surfactant protein deficiency in familial interstitial lung disease.
- Genetic disorders of neonatal respiratory function.
- Use of capnography in the delivery room for assessment of endotracheal tube placement.
- Population-based screening for rare mutations: high-throughput DNA extraction and molecular amplification from Guthrie cards.
Schools
Johns Hopkins University School of Medicine
Johns Hopkins Hospital
Chldns Hospital Med Center
Doctors Specialties
- Neonatal Medicine
- Neonat/Perinatology
Accepted Insurances
Awards
- America's Top Doctors
- Top Doctors:Baltimore Area
- Top Doctors:Washington-Baltimore
- Super Doctor
Education
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Cincinnati Children's Hospital Medical Center -
Johns Hopkins University -
Johns Hopkins University School of Medicine
Hospital
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Johns Hopkins Hospital
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