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LAWRENCE MARK NOGEE M.D.
M.D.
Pediatrics Physician
NPI: 1972555076Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
D43577(MD)
Research & Publications (20)
Alterations in SP-B and SP-C expression in neonatal lung disease.
PMID 14977415·Annu Rev Physiol·2004
6-review
Mutations in the surfactant protein C gene associated with interstitial lung disease.
PMID 11893657·Chest·2002
8-other
Abnormal expression of surfactant protein C and lung disease.
PMID 12034561·Am J Respir Cell Mol Biol·2002
7-preclinical
A mutation in the surfactant protein C gene associated with familial interstitial lung disease.
PMID 11207353·N Engl J Med·2001
5-case
Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency.
PMID 10712351·Am J Respir Crit Care Med·2000
8-other
Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes.
PMID 19647838·J Pediatr·2009
5-case
Clinical, radiological and pathological features of ABCA3 mutations in children.
PMID 18024538·Thorax·2008
8-other
Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene.
PMID 18383112·Pediatr Pulmonol·2008
8-other
Population and disease-based prevalence of the common mutations associated with surfactant deficiency.
PMID 18317237·Pediatr Res·2008
4-observational
Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.
PMID 18955570·J Exp Med·2008
7-preclinical
A major deletion in the surfactant protein-B gene causing lethal respiratory distress.
PMID 17391469·Acta Paediatr·2007
5-case
Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease.
PMID 17429902·Acta Paediatr·2007
5-case
Unexplained neonatal respiratory distress due to congenital surfactant deficiency.
PMID 17517255·J Pediatr·2007
8-other
Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.
PMID 17597647·Pediatr Res·2007
8-other
ABCA3 deficiency presenting as persistent pulmonary hypertension of the newborn.
PMID 17719949·J Pediatr·2007
5-case
Diffuse lung disease in young children: application of a novel classification scheme.
PMID 17885266·Am J Respir Crit Care Med·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 600 N WOLFE ST, NELSON 2-133
BALTIMORE, MD 21287 - Phone
- (410) 955-5259
Quick Facts
- NPI
- 1972555076
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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