-
1
-
-
84888394393
-
A solution pathway for preterm birth: accelerating a priority research agenda
-
Lackritz E.M., Wilson C.B., Guttmacher A.E., et al. A solution pathway for preterm birth: accelerating a priority research agenda. Lancet Glob Health 2013, 1(6):e328-e330.
-
(2013)
Lancet Glob Health
, vol.1
, Issue.6
, pp. e328-e330
-
-
Lackritz, E.M.1
Wilson, C.B.2
Guttmacher, A.E.3
-
2
-
-
84904200485
-
Newborn health research priorities beyond 2015
-
Yoshida S., Rudan I., Lawn J.E., et al. Newborn health research priorities beyond 2015. Lancet 2014, 384(1):e27-e29.
-
(2014)
Lancet
, vol.384
, Issue.1
, pp. e27-e29
-
-
Yoshida, S.1
Rudan, I.2
Lawn, J.E.3
-
3
-
-
33745964204
-
The genetics of bronchopulmonary dysplasia
-
Bhandari V., Gruen J.R. The genetics of bronchopulmonary dysplasia. Semin Perinatol 2006, 30(4):185-191.
-
(2006)
Semin Perinatol
, vol.30
, Issue.4
, pp. 185-191
-
-
Bhandari, V.1
Gruen, J.R.2
-
4
-
-
36048964461
-
Genetic approaches to complications of prematurity
-
Meng H., Gruen J.R. Genetic approaches to complications of prematurity. Front Biosci 2007, 12:2344-2351.
-
(2007)
Front Biosci
, vol.12
, pp. 2344-2351
-
-
Meng, H.1
Gruen, J.R.2
-
5
-
-
84946800671
-
Respiratory Distress Syndrome and Bronchopulmonary Dysplasia
-
American Lung Association (ALA). Respiratory Distress Syndrome and Bronchopulmonary Dysplasia. Lung Disease Data 2008. 2008.
-
(2008)
Lung Disease Data 2008
-
-
-
6
-
-
84886948089
-
Respiratory disorders in moderately preterm, late preterm, and early term infants
-
Mahoney A.D., Jain L. Respiratory disorders in moderately preterm, late preterm, and early term infants. Clin Perinatol 2013, 40(4):665-678.
-
(2013)
Clin Perinatol
, vol.40
, Issue.4
, pp. 665-678
-
-
Mahoney, A.D.1
Jain, L.2
-
7
-
-
7044238407
-
Respiratory complications of preterm birth
-
Fraser J., Walls M., McGuire W. Respiratory complications of preterm birth. Br Med J 2004, 329(4):962-965.
-
(2004)
Br Med J
, vol.329
, Issue.4
, pp. 962-965
-
-
Fraser, J.1
Walls, M.2
McGuire, W.3
-
8
-
-
84898638012
-
Genetic risk factors associated with respiratory distress syndrome
-
Jo H.S. Genetic risk factors associated with respiratory distress syndrome. Korean J Pediatr 2014, 57(4):157-163.
-
(2014)
Korean J Pediatr
, vol.57
, Issue.4
, pp. 157-163
-
-
Jo, H.S.1
-
9
-
-
73449095745
-
The genetic susceptibility to respiratory distress syndrome
-
Levit O., Jiang Y., Bizzarro M.J., et al. The genetic susceptibility to respiratory distress syndrome. Pediatr Res 2009, 66(6):693-697.
-
(2009)
Pediatr Res
, vol.66
, Issue.6
, pp. 693-697
-
-
Levit, O.1
Jiang, Y.2
Bizzarro, M.J.3
-
11
-
-
12244290316
-
Genetic influences in respiratory distress syndrome: a twin study
-
van Sonderen L., Halsema E.F., Spiering E.J., Koppe J.G. Genetic influences in respiratory distress syndrome: a twin study. Semin Perinatol 2002, 26(6):447-449.
-
(2002)
Semin Perinatol
, vol.26
, Issue.6
, pp. 447-449
-
-
van Sonderen, L.1
Halsema, E.F.2
Spiering, E.J.3
Koppe, J.G.4
-
12
-
-
0037208916
-
Surfactant protein B polymorphism and respiratory distress syndrome in premature twins
-
Marttila R., Haataja R., Ramet M., Lofgren J., Hallman M. Surfactant protein B polymorphism and respiratory distress syndrome in premature twins. Hum Genet 2003, 112(1):18-23.
-
(2003)
Hum Genet
, vol.112
, Issue.1
, pp. 18-23
-
-
Marttila, R.1
Haataja, R.2
Ramet, M.3
Lofgren, J.4
Hallman, M.5
-
13
-
-
4043070735
-
Respiratory distress syndrome in twin infants compared with singletons
-
Marttila R., Kaprio J., Hallman M. Respiratory distress syndrome in twin infants compared with singletons. Am J Obstet Gynecol 2004, 191(1):271-276.
-
(2004)
Am J Obstet Gynecol
, vol.191
, Issue.1
, pp. 271-276
-
-
Marttila, R.1
Kaprio, J.2
Hallman, M.3
-
14
-
-
84882773609
-
The genetics of disorders affecting the premature newborn
-
Elsevier, D.L. Rimoin, J.M. Connor, P.R.E. KBR (Eds.)
-
Prosnitz A., Gruen J.R., Bhandari V. The genetics of disorders affecting the premature newborn. Emery and Rimoin's Principles and Practice of Medical Genetics 2013, 1-22. Elsevier. 6th ed. D.L. Rimoin, J.M. Connor, P.R.E. KBR (Eds.).
-
(2013)
Emery and Rimoin's Principles and Practice of Medical Genetics
, pp. 1-22
-
-
Prosnitz, A.1
Gruen, J.R.2
Bhandari, V.3
-
15
-
-
84896459977
-
Predictors of bronchopulmonary dysplasia or death in premature infants with a patent ductus arteriosus
-
Chock V.Y., Punn R., Oza A., et al. Predictors of bronchopulmonary dysplasia or death in premature infants with a patent ductus arteriosus. Pediatr Res 2014, 75(4):570-575.
-
(2014)
Pediatr Res
, vol.75
, Issue.4
, pp. 570-575
-
-
Chock, V.Y.1
Punn, R.2
Oza, A.3
-
16
-
-
84886062104
-
Morbidity and mortality in preterm neonates with patent ductus arteriosus on day 3
-
Sellmer A., Bjerre J.V., Schmidt M.R., et al. Morbidity and mortality in preterm neonates with patent ductus arteriosus on day 3. Arch Dis Child Fetal Neonatal Ed 2013, 98(6):F505-F510.
-
(2013)
Arch Dis Child Fetal Neonatal Ed
, vol.98
, Issue.6
, pp. F505-F510
-
-
Sellmer, A.1
Bjerre, J.V.2
Schmidt, M.R.3
-
17
-
-
61549132605
-
Genetic contribution to patent ductus arteriosus in the premature newborn
-
Bhandari V., Zhou G., Bizzarro M.J., et al. Genetic contribution to patent ductus arteriosus in the premature newborn. Pediatrics 2009, 123(2):669-673.
-
(2009)
Pediatrics
, vol.123
, Issue.2
, pp. 669-673
-
-
Bhandari, V.1
Zhou, G.2
Bizzarro, M.J.3
-
18
-
-
84884353023
-
Increased prevalence of congenital heart defects in monozygotic and dizygotic twins
-
Herskind A.M., Almind Pedersen D., Christensen K. Increased prevalence of congenital heart defects in monozygotic and dizygotic twins. Circulation 2013, 128(11):1182-1188.
-
(2013)
Circulation
, vol.128
, Issue.11
, pp. 1182-1188
-
-
Herskind, A.M.1
Almind Pedersen, D.2
Christensen, K.3
-
19
-
-
65349163518
-
Determination of genetic predisposition to patent ductus arteriosus in preterm infants
-
Dagle J.M., Lepp N.T., Cooper M.E., et al. Determination of genetic predisposition to patent ductus arteriosus in preterm infants. Pediatrics 2009, 123(4):1116-1123.
-
(2009)
Pediatrics
, vol.123
, Issue.4
, pp. 1116-1123
-
-
Dagle, J.M.1
Lepp, N.T.2
Cooper, M.E.3
-
20
-
-
56249148193
-
The diagnosis, management, and postnatal prevention of intraventricular hemorrhage in the preterm neonate
-
[vii]
-
McCrea H.J., Ment L.R. The diagnosis, management, and postnatal prevention of intraventricular hemorrhage in the preterm neonate. Clin Perinatol 2008, 35(4):777-792. [vii].
-
(2008)
Clin Perinatol
, vol.35
, Issue.4
, pp. 777-792
-
-
McCrea, H.J.1
Ment, L.R.2
-
21
-
-
33745302079
-
Familial and genetic susceptibility to major neonatal morbidities in preterm twins
-
Bhandari V., Bizzarro M.J., Shetty A., et al. Familial and genetic susceptibility to major neonatal morbidities in preterm twins. Pediatrics 2006, 117(6):1901-1906.
-
(2006)
Pediatrics
, vol.117
, Issue.6
, pp. 1901-1906
-
-
Bhandari, V.1
Bizzarro, M.J.2
Shetty, A.3
-
22
-
-
84899102316
-
Maternal race, demography, and health care disparities impact risk for intraventricular hemorrhage in preterm neonates
-
Shankaran S., Lin A., Maller-Kesselman J., et al. Maternal race, demography, and health care disparities impact risk for intraventricular hemorrhage in preterm neonates. J Pediatr 2014, 164(5):1005-1011.e3.
-
(2014)
J Pediatr
, vol.164
, Issue.5
, pp. 1005-1011.e3
-
-
Shankaran, S.1
Lin, A.2
Maller-Kesselman, J.3
-
23
-
-
0023980160
-
Intraventricular hemorrhage in preterm twin gestation infants
-
Viscardi R.M., Donn S.M., Rayburn W.F., Schork M.A. Intraventricular hemorrhage in preterm twin gestation infants. J Perinatol 1988, 8(2):114-117.
-
(1988)
J Perinatol
, vol.8
, Issue.2
, pp. 114-117
-
-
Viscardi, R.M.1
Donn, S.M.2
Rayburn, W.F.3
Schork, M.A.4
-
24
-
-
0031474807
-
Neonatal neurologic characteristics of preterm twin infants <1,250 gm birth weight
-
Perlman J.M., Broyles R.S., Rogers C.G. Neonatal neurologic characteristics of preterm twin infants <1,250 gm birth weight. Pediatr Neurol 1997, 17(4):322-326.
-
(1997)
Pediatr Neurol
, vol.17
, Issue.4
, pp. 322-326
-
-
Perlman, J.M.1
Broyles, R.S.2
Rogers, C.G.3
-
25
-
-
79960244410
-
Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates
-
Ryckman K.K., Dagle J.M., Kelsey K., Momany A.M., Murray J.C. Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates. Pediatr Res 2011, 70(1):90-95.
-
(2011)
Pediatr Res
, vol.70
, Issue.1
, pp. 90-95
-
-
Ryckman, K.K.1
Dagle, J.M.2
Kelsey, K.3
Momany, A.M.4
Murray, J.C.5
-
26
-
-
84866078413
-
Genetic polymorphisms of antioxidant enzymes in preterm infants
-
Poggi C., Giusti B., Vestri A., Pasquini E., Abbate R., Dani C. Genetic polymorphisms of antioxidant enzymes in preterm infants. J Matern Fetal Neonatal Med 2012, 25(Suppl. 4):131-134.
-
(2012)
J Matern Fetal Neonatal Med
, vol.25
, pp. 131-134
-
-
Poggi, C.1
Giusti, B.2
Vestri, A.3
Pasquini, E.4
Abbate, R.5
Dani, C.6
-
27
-
-
84900451853
-
Gene-environment interactions in severe intraventricular hemorrhage of preterm neonates
-
Ment L.R., Aden U., Lin A., et al. Gene-environment interactions in severe intraventricular hemorrhage of preterm neonates. Pediatr Res 2014, 75(1-2):241-250.
-
(2014)
Pediatr Res
, vol.75
, Issue.1-2
, pp. 241-250
-
-
Ment, L.R.1
Aden, U.2
Lin, A.3
-
28
-
-
77957693638
-
Heritability of apnea of prematurity: a retrospective twin study
-
Bloch-Salisbury E., Hall M.H., Sharma P., Boyd T., Bednarek F., Paydarfar D. Heritability of apnea of prematurity: a retrospective twin study. Pediatrics 2010, 126(4):e779-e787.
-
(2010)
Pediatrics
, vol.126
, Issue.4
, pp. e779-e787
-
-
Bloch-Salisbury, E.1
Hall, M.H.2
Sharma, P.3
Boyd, T.4
Bednarek, F.5
Paydarfar, D.6
-
29
-
-
84883827892
-
Current definitions for neonatal apnoea: are they evidence based?
-
Elder D.E., Campbell A.J., Galletly D. Current definitions for neonatal apnoea: are they evidence based?. J Paediatr Child Health 2013, 49(9):E388-E396.
-
(2013)
J Paediatr Child Health
, vol.49
, Issue.9
, pp. E388-E396
-
-
Elder, D.E.1
Campbell, A.J.2
Galletly, D.3
-
31
-
-
0242611416
-
Consanguinity and apnea of prematurity
-
Tamim H., Khogali M., Beydoun H., Melki I., Yunis K., National Collaborative Perinatal Neonatal Network Consanguinity and apnea of prematurity. Am J Epidemiol 2003, 158(10):942-946.
-
(2003)
Am J Epidemiol
, vol.158
, Issue.10
, pp. 942-946
-
-
Tamim, H.1
Khogali, M.2
Beydoun, H.3
Melki, I.4
Yunis, K.5
National Collaborative Perinatal Neonatal, Network6
-
32
-
-
84893128450
-
Pathogenesis implication for necrotizing enterocolitis prevention in preterm very-low-birth-weight infants
-
Chen A.C., Chung M.Y., Chang J.H., Lin H.C. Pathogenesis implication for necrotizing enterocolitis prevention in preterm very-low-birth-weight infants. J Pediatr Gastroenterol Nutr 2014, 58(1):7-11.
-
(2014)
J Pediatr Gastroenterol Nutr
, vol.58
, Issue.1
, pp. 7-11
-
-
Chen, A.C.1
Chung, M.Y.2
Chang, J.H.3
Lin, H.C.4
-
33
-
-
79958215232
-
The NFKB1 (g.-24519delATTG) variant is associated with necrotizing enterocolitis (NEC) in premature infants
-
Sampath V., Le M., Lane L., et al. The NFKB1 (g.-24519delATTG) variant is associated with necrotizing enterocolitis (NEC) in premature infants. J Surg Res 2011, 169(1):e51-e57.
-
(2011)
J Surg Res
, vol.169
, Issue.1
, pp. e51-e57
-
-
Sampath, V.1
Le, M.2
Lane, L.3
-
34
-
-
84863842621
-
Association between mannose-binding lectin gene polymorphisms and necrotizing enterocolitis in preterm infants
-
Prencipe G., Azzari C., Moriondo M., et al. Association between mannose-binding lectin gene polymorphisms and necrotizing enterocolitis in preterm infants. J Pediatr Gastroenterol Nutr 2012, 55(2):160-165.
-
(2012)
J Pediatr Gastroenterol Nutr
, vol.55
, Issue.2
, pp. 160-165
-
-
Prencipe, G.1
Azzari, C.2
Moriondo, M.3
-
35
-
-
84922281882
-
Genome-wide expression profiles of necrotizing enterocolitis versus spontaneous intestinal perforation in human intestinal tissues: dysregulation of functional pathways
-
Chan K.Y., Leung K.T., Tam Y.H., et al. Genome-wide expression profiles of necrotizing enterocolitis versus spontaneous intestinal perforation in human intestinal tissues: dysregulation of functional pathways. Ann Surg 2014, 260(6):1128-1137.
-
(2014)
Ann Surg
, vol.260
, Issue.6
, pp. 1128-1137
-
-
Chan, K.Y.1
Leung, K.T.2
Tam, Y.H.3
-
36
-
-
84901774414
-
Retinopathy of prematurity
-
Asano M.K., Dray P.B. Retinopathy of prematurity. Dis Mon 2014, 60(6):282-291.
-
(2014)
Dis Mon
, vol.60
, Issue.6
, pp. 282-291
-
-
Asano, M.K.1
Dray, P.B.2
-
37
-
-
84886246337
-
Retinopathy of prematurity
-
Hellstrom A., Smith L.E., Dammann O. Retinopathy of prematurity. Lancet 2013, 382(9902):1445-1457.
-
(2013)
Lancet
, vol.382
, Issue.9902
, pp. 1445-1457
-
-
Hellstrom, A.1
Smith, L.E.2
Dammann, O.3
-
38
-
-
84878171739
-
Retinopathy of prematurity-incidence today
-
Zin A., Gole G.A. Retinopathy of prematurity-incidence today. Clin Perinatol 2013, 40(2):185-200.
-
(2013)
Clin Perinatol
, vol.40
, Issue.2
, pp. 185-200
-
-
Zin, A.1
Gole, G.A.2
-
39
-
-
36749026344
-
Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies
-
Holmstrom G., van Wijngaarden P., Coster D.J., Williams K.A. Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies. Br J Ophthalmol 2007, 91(12):1704-1708.
-
(2007)
Br J Ophthalmol
, vol.91
, Issue.12
, pp. 1704-1708
-
-
Holmstrom, G.1
van Wijngaarden, P.2
Coster, D.J.3
Williams, K.A.4
-
40
-
-
77954752428
-
Profile of asymmetrical retinopathy of prematurity in twins
-
Azad R., Chandra P., Patwardhan S.D., Gupta A. Profile of asymmetrical retinopathy of prematurity in twins. Indian J Ophthalmol 2010, 58(3):209-211.
-
(2010)
Indian J Ophthalmol
, vol.58
, Issue.3
, pp. 209-211
-
-
Azad, R.1
Chandra, P.2
Patwardhan, S.D.3
Gupta, A.4
-
41
-
-
33750958906
-
Genetic susceptibility to retinopathy of prematurity
-
Bizzarro M.J., Hussain N., Jonsson B., et al. Genetic susceptibility to retinopathy of prematurity. Pediatrics 2006, 118(5):1858-1863.
-
(2006)
Pediatrics
, vol.118
, Issue.5
, pp. 1858-1863
-
-
Bizzarro, M.J.1
Hussain, N.2
Jonsson, B.3
-
42
-
-
66249126322
-
Pitfalls, problems, and progress in bronchopulmonary dysplasia
-
Bhandari A., Bhandari V. Pitfalls, problems, and progress in bronchopulmonary dysplasia. Pediatrics 2009, 123(6):1562-1573.
-
(2009)
Pediatrics
, vol.123
, Issue.6
, pp. 1562-1573
-
-
Bhandari, A.1
Bhandari, V.2
-
44
-
-
79955819610
-
New Bronchopulmonary Dysplasia: a clinical review
-
Bhandari A., Bhandari V. New Bronchopulmonary Dysplasia: a clinical review. Clin Pulm Med 2011, 18(3):137-143.
-
(2011)
Clin Pulm Med
, vol.18
, Issue.3
, pp. 137-143
-
-
Bhandari, A.1
Bhandari, V.2
-
45
-
-
0029809766
-
Evidence from twin study implies possible genetic susceptibility to bronchopulmonary dysplasia
-
Parker R.A., Lindstrom D.P., Cotton R.B. Evidence from twin study implies possible genetic susceptibility to bronchopulmonary dysplasia. Semin Perinatol 1996, 20(3):206-209.
-
(1996)
Semin Perinatol
, vol.20
, Issue.3
, pp. 206-209
-
-
Parker, R.A.1
Lindstrom, D.P.2
Cotton, R.B.3
-
46
-
-
51649115601
-
Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health
-
Lavoie P.M., Pham C., Jang K.L. Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health. Pediatrics 2008, 122(3):479-485.
-
(2008)
Pediatrics
, vol.122
, Issue.3
, pp. 479-485
-
-
Lavoie, P.M.1
Pham, C.2
Jang, K.L.3
-
47
-
-
84882257642
-
A genome-wide association study (GWAS) for bronchopulmonary dysplasia
-
Wang H., Julien K.R., Stevenson D.K., et al. A genome-wide association study (GWAS) for bronchopulmonary dysplasia. Pediatrics 2013, 132(2):290-297.
-
(2013)
Pediatrics
, vol.132
, Issue.2
, pp. 290-297
-
-
Wang, H.1
Julien, K.R.2
Stevenson, D.K.3
-
48
-
-
84908230456
-
Copy number variation in bronchopulmonary dysplasia
-
Hoffmann T.J., Shaw G.M., Stevenson D.K., et al. Copy number variation in bronchopulmonary dysplasia. Am J Med Genet A 2014, 164A(10):2672-2675.
-
(2014)
Am J Med Genet A
, vol.164A
, Issue.10
, pp. 2672-2675
-
-
Hoffmann, T.J.1
Shaw, G.M.2
Stevenson, D.K.3
-
49
-
-
84876106293
-
Progress in understanding the genetics of bronchopulmonary dysplasia
-
Shaw G.M., O'Brodovich H.M. Progress in understanding the genetics of bronchopulmonary dysplasia. Semin Perinatol 2013, 37(2):85-93.
-
(2013)
Semin Perinatol
, vol.37
, Issue.2
, pp. 85-93
-
-
Shaw, G.M.1
O'Brodovich, H.M.2
-
50
-
-
84897038691
-
Association of a vascular endothelial growth factor polymorphism with the development of bronchopulmonary dysplasia in Japanese premature newborns
-
Fujioka K., Shibata A., Yokota T., et al. Association of a vascular endothelial growth factor polymorphism with the development of bronchopulmonary dysplasia in Japanese premature newborns. Sci Rep 2014, 4:4459.
-
(2014)
Sci Rep
, vol.4
, pp. 4459
-
-
Fujioka, K.1
Shibata, A.2
Yokota, T.3
-
51
-
-
84945473845
-
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study
-
[Epub ahead of print]
-
Carrera P., Di Resta C., Volonteri C., et al. Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study. Clin Chim Acta 2015, http://dx.doi.org/10.1016/j.cca.2015.01.001. [Epub ahead of print].
-
(2015)
Clin Chim Acta
-
-
Carrera, P.1
Di Resta, C.2
Volonteri, C.3
-
52
-
-
78651483900
-
The impact of environmental and genetic factors on neonatal late-onset sepsis
-
Bizzarro M.J., Jiang Y., Hussain N., Gruen J.R., Bhandari V., Zhang H. The impact of environmental and genetic factors on neonatal late-onset sepsis. J Pediatr 2011, 158(2):234-238.e1.
-
(2011)
J Pediatr
, vol.158
, Issue.2
, pp. 234-238.e1
-
-
Bizzarro, M.J.1
Jiang, Y.2
Hussain, N.3
Gruen, J.R.4
Bhandari, V.5
Zhang, H.6
-
53
-
-
38049036445
-
Mannose-binding lectin (MBL) genotype in relation to risk of nosocomial infection in pre-term neonates in the neonatal intensive care unit
-
van der Zwet W.C., Catsburg A., van Elburg R.M., Savelkoul P.H., Vandenbroucke-Grauls C.M. Mannose-binding lectin (MBL) genotype in relation to risk of nosocomial infection in pre-term neonates in the neonatal intensive care unit. Clin Microbiol Infect 2008, 14(2):130-135.
-
(2008)
Clin Microbiol Infect
, vol.14
, Issue.2
, pp. 130-135
-
-
van der Zwet, W.C.1
Catsburg, A.2
van Elburg, R.M.3
Savelkoul, P.H.4
Vandenbroucke-Grauls, C.M.5
-
54
-
-
77957255529
-
Role of polymorphic variants as genetic modulators of infection in neonatal sepsis
-
Abu-Maziad A., Schaa K., Bell E.F., et al. Role of polymorphic variants as genetic modulators of infection in neonatal sepsis. Pediatr Res 2010, 68(4):323-329.
-
(2010)
Pediatr Res
, vol.68
, Issue.4
, pp. 323-329
-
-
Abu-Maziad, A.1
Schaa, K.2
Bell, E.F.3
-
55
-
-
84904396536
-
Genetic polymorphisms and sepsis in premature neonates
-
Esposito S., Zampiero A., Pugni L., et al. Genetic polymorphisms and sepsis in premature neonates. PLoS One 2014, 9(7):e101248.
-
(2014)
PLoS One
, vol.9
, Issue.7
, pp. e101248
-
-
Esposito, S.1
Zampiero, A.2
Pugni, L.3
-
56
-
-
84924539126
-
Integrated genomic analyses in bronchopulmonary dysplasia
-
Ambalavanan N., Cotten C.M., Page G.P., et al. Integrated genomic analyses in bronchopulmonary dysplasia. J Pediatr 2015, 166(3):531-537.e13.
-
(2015)
J Pediatr
, vol.166
, Issue.3
, pp. 531-537.e13
-
-
Ambalavanan, N.1
Cotten, C.M.2
Page, G.P.3
-
57
-
-
81455155717
-
Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia
-
Hadchouel A., Durrmeyer X., Bouzigon E., et al. Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia. Am J Respir Crit Care Med 2011, 184(10):1164-1170.
-
(2011)
Am J Respir Crit Care Med
, vol.184
, Issue.10
, pp. 1164-1170
-
-
Hadchouel, A.1
Durrmeyer, X.2
Bouzigon, E.3
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