Related references
Note: Only part of the references are listed.Progressive Disease With Low Survival in Adult Patients With Pulmonary Fibrosis Carrying Surfactant-Related Gene Mutations An Observational Study
Dymph Klay et al.
CHEST (2023)
Identification of genetic susceptibility in preterm newborns with bronchopulmonary dysplasia by whole-exome sequencing: BIVM gene may play a role
Xi Luo et al.
EUROPEAN JOURNAL OF PEDIATRICS (2023)
Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms
Ayberk Akat et al.
PEDIATRIC RESEARCH (2022)
Verification of immunology-related genetic associations in BPD supports ABCA3 and five other genes
Felix Blume et al.
PEDIATRIC RESEARCH (2022)
Polymorphisms of fibronectin-1 (rs3796123; rs1968510; rs10202709; rs6725958; and rs35343655) are not associated with bronchopulmonary dysplasia in preterm infants
Katarzyna Kosik et al.
MOLECULAR AND CELLULAR BIOCHEMISTRY (2022)
Epigenome-wide association study of bronchopulmonary dysplasia in preterm infants: results from the discovery-BPD program
Xuting Wang et al.
CLINICAL EPIGENETICS (2022)
Interstitial lung disease in infancy and early childhood: a clinicopathological primer
Florian Peter Laenger et al.
EUROPEAN RESPIRATORY REVIEW (2022)
Pulmonary hypertension in the newborn- etiology and pathogenesis
Deepika Sankaran et al.
SEMINARS IN FETAL & NEONATAL MEDICINE (2022)
Heterogenous Disease Course and Long-Term Outcome of Children's Interstitial Lung Disease Related to Filamin A Gene Variants
Julia Carlens et al.
ANNALS OF THE AMERICAN THORACIC SOCIETY (2022)
Genetic and Biochemical Predictors of Neonatal Bronchopulmonary Dysplasia
May A. K. Abdellatif et al.
JOURNAL OF PEDIATRIC GENETICS (2022)
Diagnosis and management of bronchopulmonary dysplasia
Margaret Gilfillan et al.
BMJ-BRITISH MEDICAL JOURNAL (2021)
Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information
Dan Dai et al.
FRONTIERS IN GENETICS (2021)
Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review
Gloria Pelizzo et al.
BMC PEDIATRICS (2019)
Genetics of bronchopulmonary dysplasia: When things do not match up, it is only the beginning
Vineet Bhandari et al.
JOURNAL OF PEDIATRICS (2019)
The Diagnosis of Bronchopulmonary Dysplasia in Very Preterm Infants An Evidence-based Approach
Erik A. Jensen et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2019)
A review of filamin A mutations and associated interstitial lung disease
Erina Sasaki et al.
EUROPEAN JOURNAL OF PEDIATRICS (2019)
Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants
Dara G. Torgerson et al.
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY (2018)
Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth
Aaron Hamvas et al.
BMC GENETICS (2018)
Role of Genetic Susceptibility in the Development o Bronchopulmonary Dysplasia
Richard B. Parad et al.
JOURNAL OF PEDIATRICS (2018)
Chronic interstitial lung disease in children
Matthias Griese
EUROPEAN RESPIRATORY REVIEW (2018)
Exosomal microRNA predicts and protects against severe bronchopulmonary dysplasia in extremely premature infants
Charitharth Vivek Lal et al.
JCI INSIGHT (2018)
Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene
Mari Mahlman et al.
SCIENTIFIC REPORTS (2017)
The genetic predisposition to bronchopulmonary dysplasia
Kun-Hsing Yu et al.
CURRENT OPINION IN PEDIATRICS (2016)
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study
Paola Carrera et al.
CLINICA CHIMICA ACTA (2015)
Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations
Donatella Peca et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2015)
Association of vitamin D binding protein polymorphisms with bronchopulmonary dysplasia: a case-control study of gc globulin and bronchopulmonary dysplasia
O. Serce Pehlevan et al.
JOURNAL OF PERINATOLOGY (2015)
Genes Encoding Vascular Endothelial Growth Factor A (VEGF-A) and VEGF Receptor 2 (VEGFR-2) and Risk for Bronchopulmonary Dysplasia
Mari Mahlman et al.
NEONATOLOGY (2015)
Antioxidant response genes sequence variants and BPD susceptibility in VLBW infants
Venkatesh Sampath et al.
PEDIATRIC RESEARCH (2015)
Copy Number Variation in Bronchopulmonary Dysplasia
Thomas J. Hoffmann et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2014)
Single Mutations in ABCA3 Increase the Risk for Neonatal Respiratory Distress Syndrome in Late Preterm Infants (Gestational Age 34-36 weeks)
Hodad M. Naderi et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2014)
Genotype-Phenotype Correlations for Infants and Children with ABCA3 Deficiency
Jennifer A. Wambach et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2014)
Altered Lung Development in Bronchopulmonary Dysplasia
Alice Hadchouel et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2014)
Postnatal Inflammation in the Pathogenesis of Bronchopulmonary Dysplasia
Vineet Bhandari
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2014)
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia
Johanna M. Huusko et al.
BMC MEDICAL GENETICS (2014)
Novel ABCA3 mutations as a cause of respiratory distress in a term newborn
Jean-Pierre Goncalves et al.
GENE (2014)
GSTM1 and GSTT1 gene polymorphisms as major risk factors for bronchopulmonary dysplasia in a Chinese Han population
Xijuan Wang et al.
GENE (2014)
Detecting epistasis in human complex traits
Wen-Hua Wei et al.
NATURE REVIEWS GENETICS (2014)
Respiratory Insufficiency in a Newborn With Congenital Hypothyroidism Due To a New Mutation of TTF-1/NKX2.1 Gene
Teresa Salerno et al.
PEDIATRIC PULMONOLOGY (2014)
Null ABCA3 in Humans: Large Homozygous ABCA3 Deletion, Correlation to Clinical-Pathological Findings
Paola Carrera et al.
PEDIATRIC PULMONOLOGY (2014)
Association of vitamin D receptor gene polymorphisms and bronchopulmonary dysplasia
Ozge Altun Koroglu et al.
PEDIATRIC RESEARCH (2014)
Filamin A Mutation May Be Associated With Diffuse Lung Disease Mimicking Bronchopulmonary Dysplasia in Premature Newborns
Amanda Lord et al.
RESPIRATORY CARE (2014)
Association of a vascular endothelial growth factor polymorphism with the development of bronchopulmonary dysplasia in Japanese premature newborns
Kazumichi Fujioka et al.
SCIENTIFIC REPORTS (2014)
An Official American Thoracic Society Clinical Practice Guideline: Classification, Evaluation, and Management of Childhood Interstitial Lung Disease in Infancy
Geoffrey Kurland et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2013)
Genetic testing in children with surfactant dysfunction
Simona Turcu et al.
ARCHIVES OF DISEASE IN CHILDHOOD (2013)
Candidate gene association studies: a comprehensive guide to useful in silico tools
Radhika Patnala et al.
BMC GENETICS (2013)
Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1
Aaron Hamvas et al.
CHEST (2013)
Genetic and Epidemiological Risk Factors in the Development of Bronchopulmonary Dysplasia
Beena Mailaparambil et al.
DISEASE MARKERS (2013)
Association of a FGFR-4 Gene Polymorphism with Bronchopulmonary Dysplasia and Neonatal Respiratory Distress
Milad Rezvani et al.
DISEASE MARKERS (2013)
Association of surfactant protein B gene polymorphisms (C/A-18, C/T1580, intron 4 and A/G9306) and haplotypes with bronchopulmonary dysplasia in chinese han population
Bao-huan Cai et al.
JOURNAL OF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY-MEDICAL SCIENCES (2013)
Functional Genetic Variation in NFKBIA and Susceptibility to Childhood Asthma, Bronchiolitis, and Bronchopulmonary Dysplasia
Salman Ali et al.
JOURNAL OF IMMUNOLOGY (2013)
Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine
N. Hepping et al.
JOURNAL OF PERINATOLOGY (2013)
Single Nucleotide Polymorphism in Toll-like Receptor 6 Is Associated With a Decreased Risk for Ureaplasma Respiratory Tract Colonization and Bronchopulmonary Dysplasia in Preterm Infants
Alexandra H. Winters et al.
PEDIATRIC INFECTIOUS DISEASE JOURNAL (2013)
TNF-238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population
Nasser A. Elhawary et al.
PEDIATRIC PULMONOLOGY (2013)
Allele-specific N-glycosylation delays human surfactant protein B secretion in vitro and associates with decreased protein levels in vivo
Saija Taponen et al.
PEDIATRIC RESEARCH (2013)
A Genome-Wide Association Study (GWAS) for Bronchopulmonary Dysplasia
Hui Wang et al.
PEDIATRICS (2013)
Ultrastructural Characterization of Genetic Diffuse Lung Diseases in Infants and Children: A Cohort Study and Review
Arianna Citti et al.
ULTRASTRUCTURAL PATHOLOGY (2013)
ATP-binding cassette member A3 (E292V) gene mutation and pulmonary morbidity in very-low-birth-weight infants
Christoph Haertel et al.
ACTA PAEDIATRICA (2012)
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants
Betti Giusti et al.
FREE RADICAL RESEARCH (2012)
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children
Florence Flamein et al.
HUMAN MOLECULAR GENETICS (2012)
Serum mannose-binding lectin (MBL) gene polymorphism and low MBL levels are associated with neonatal sepsis and pneumonia
H. Ozkan et al.
JOURNAL OF PERINATOLOGY (2012)
Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates
K. K. Ryckman et al.
JOURNAL OF PERINATOLOGY (2012)
Influence of Common Non-Synonymous Toll-like Receptor 4 Polymorphisms on Bronchopulmonary Dysplasia and Prematurity in Human Infants
Pascal M. Lavoie et al.
PLOS ONE (2012)
A TLR5 (g.1174C>T) variant that encodes a stop codon (R392X) is associated with bronchopulmonary dysplasia
Venkatesh Sampath et al.
PEDIATRIC PULMONOLOGY (2012)
IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants
Joanna Floros et al.
PEDIATRIC RESEARCH (2012)
Single ABCA3 Mutations Increase Risk for Neonatal Respiratory Distress Syndrome
Jennifer A. Wambach et al.
PEDIATRICS (2012)
Association between bronchopulmonary dysplasia and MBL2 and IL1-RN polymorphisms
Bilin Cetinkaya Cakmak et al.
PEDIATRICS INTERNATIONAL (2012)
Interleukin-6 polymorphism and bronchopulmonary dysplasia risk in very low-birthweight infants
Touhei Usuda et al.
PEDIATRICS INTERNATIONAL (2012)
Identification of SPOCK2 As a Susceptibility Gene for Bronchopulmonary Dysplasia
Alice Hadchouel et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2011)
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis
Barbara Kleinlein et al.
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION (2011)
HLA and bronchopulmonary dysplasia susceptibility: A pilot study
Gustavo Rocha et al.
DISEASE MARKERS (2011)
A Polymorphism in the Macrophage Migration Inhibitory Factor Promoter Is Associated With Bronchopulmonary Dysplasia
Giusi Prencipe et al.
PEDIATRIC RESEARCH (2011)
Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect
Donatella Peca et al.
RESPIRATORY RESEARCH (2011)
Conditional deletion of Abca3 in alveolar type II cells alters surfactant homeostasis in newborn and adult mice
Valerie Besnard et al.
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY (2010)
Genetics of bronchopulmonary dysplasia in the age of genomics
Pascal M. Lavoie et al.
CURRENT OPINION IN PEDIATRICS (2010)
Surfactant Protein-C Promoter Variants Associated With Neonatal Respiratory Distress Syndrome Reduce Transcription
Jennifer A. Wambach et al.
PEDIATRIC RESEARCH (2010)
Tumour necrosis factor (-308A) polymorphism in very preterm infants with bronchopulmonary dysplasia: a meta-analysis
M. Chauhan et al.
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION (2009)
Genomic copy number variation, human health, and disease
Louise V. Wain et al.
LANCET (2009)
Developmental and Genetic Regulation of Human Surfactant Protein B in vivo
Aaron Hamvas et al.
NEONATOLOGY (2009)
Haplotype analysis of ABCA3: association with respiratory distress in very premature infants
Minna K. Karjalainen et al.
ANNALS OF MEDICINE (2008)
Matrix Metalloproteinase Gene Polymorphisms and Bronchopulmonary Dysplasia: Identification of MMP16 as a New Player in Lung Development
Alice Hadchouel et al.
PLOS ONE (2008)
Wilson-Mikity syndrome: Updated diagnostic criteria based on nine cases and a review of the literature
Amy Hoepker et al.
PEDIATRIC PULMONOLOGY (2008)
Genetic Risk Factors of Bronchopulmonary Dysplasia
Przemko Kwinta et al.
PEDIATRIC RESEARCH (2008)
Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the National Institutes of Health
Pascal M. Lavoie et al.
PEDIATRICS (2008)
Association of polymorphisms in the mannose-binding lectin gene and pulmonary morbidity in preterm infants
A. Hilgendorff et al.
GENES AND IMMUNITY (2007)
Ultrastructural and molecular analysis in fatal neonatal interstitial pneumonia caused by a novel ABCA3 mutation
Elisabeth Bruder et al.
MODERN PATHOLOGY (2007)
Unexplained neonatal respiratory distress due to congenital surfactant deficiency
Marco Somaschini et al.
JOURNAL OF PEDIATRICS (2007)
ABCA3 inactivation in mice causes respiratory failure, loss of pulmonary surfactant, and depletion of lung phosphatidylglycerol
Michael L. Fitzgerald et al.
JOURNAL OF LIPID RESEARCH (2007)
Genetic analysis of the dystroglycan gene in bronchopulmonary dysplasia affected premature newborns
Paola Concolino et al.
CLINICA CHIMICA ACTA (2007)
Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease
Ola D. Saugstad et al.
ACTA PAEDIATRICA (2007)
Association of interferon γ T+874A and interleukin 12 p40 promoter CTCTAA/GC polymorphism with the need for respiratory support and perinatal complications in low birthweight neonates
G. Bokodi et al.
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION (2007)
Single nucleotide polymorphisms of tumor necrosis factor-alpha and the susceptibility to bronchopulmonary dysplasia
Sonya S. Strassberg et al.
PEDIATRIC PULMONOLOGY (2007)
Selectin polymorphisms and perinatal morbidity in low-birthweight infants
Laszlo Derzbach et al.
ACTA PAEDIATRICA (2006)
Genetic polymorphisms of hemostasis genes and primary outcome of very low birth weight infants
Christoph Haertel et al.
PEDIATRICS (2006)
Familial and genetic susceptibility to major neonatal morbidities in preterm twins
Vineet Bhandari et al.
PEDIATRICS (2006)
Genetic variants of surfactant proteins A, B, C, and D in bronchopulmonary dysplasia
J. Pavlovic et al.
DISEASE MARKERS (2006)
Deletion allele of angiotensin-converting enzyme is associated with increased risk and severity of bronchopulmonary dysplasia
SNJ Kazzi et al.
JOURNAL OF PEDIATRICS (2005)
Ultrastructure of lamellar bodies in congenital surfactant deficiency
V Edwards et al.
ULTRASTRUCTURAL PATHOLOGY (2005)
ABCA3 mutations associated with pediatric interstitial lung disease
JE Bullard et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2005)
Interleukin-10-1082 G/A polymorphism and risk of death or bronchopulmonary dysplasia in ventilated very low birth weight infants
K Yanamandra et al.
PEDIATRIC PULMONOLOGY (2005)
Hydroxychloroquine and surfactant protein C deficiency
DM Rosen et al.
NEW ENGLAND JOURNAL OF MEDICINE (2005)
ABCA3 gene mutations in newborns with fatal surfactant deficiency
S Shulenin et al.
NEW ENGLAND JOURNAL OF MEDICINE (2004)
Tumor necrosis factor-α allele lymphotoxin-α+250 is associated with the presence and severity of placental inflammation among preterm births
S Nadya et al.
PEDIATRIC RESEARCH (2004)
Data mining and multiparameter analysis of lung surfactant protein genes in bronchopulmonary dysplasia
M Rova et al.
HUMAN MOLECULAR GENETICS (2004)
Genetic mechanisms of surfactant deficiency
LM Nogee
BIOLOGY OF THE NEONATE (2004)
Surfactant protein A and B genetic variants in respiratory distress syndrome in singletons and twins
R Marttila et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2003)
Surfactant protein B polymorphism and respiratory distress syndrome in premature twins
R Marttila et al.
HUMAN GENETICS (2003)
Polymorphisms of surfactant protein B encoding gene: modifiers of the course of neonatal respiratory distress syndrome?
V Makri et al.
EUROPEAN JOURNAL OF PEDIATRICS (2002)
A mutation in the surfactant protein C gene associated with familial interstitial lung disease.
LM Nogee et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
Share Paper
