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Items: 1 to 20 of 130

1.

Pathophysiology and treatment of surfactant protein-B deficiency.

Hamvas A, Nogee LM, deMello DE, Cole FS.

Biol Neonate. 1995;67 Suppl 1:18-31. Review.

PMID:
7647155
2.

Inherited disorders of neonatal lung diseases.

Yurdakök M.

Turk J Pediatr. 2004 Apr-Jun;46(2):105-14. Review.

3.

Hereditary surfactant protein B deficiency resulting from a novel mutation.

Somaschini M, Wert S, Mangili G, Colombo A, Nogee L.

Intensive Care Med. 2000 Jan;26(1):97-100.

PMID:
10663288
4.

Transient surfactant protein B deficiency in a term infant with severe respiratory failure.

Klein JM, Thompson MW, Snyder JM, George TN, Whitsett JA, Bell EF, McCray PB Jr, Nogee LM.

J Pediatr. 1998 Feb;132(2):244-8.

PMID:
9506635
5.

Targeted disruption of the surfactant protein B gene disrupts surfactant homeostasis, causing respiratory failure in newborn mice.

Clark JC, Wert SE, Bachurski CJ, Stahlman MT, Stripp BR, Weaver TE, Whitsett JA.

Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7794-8.

6.

A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds.

Nogee LM, Garnier G, Dietz HC, Singer L, Murphy AM, deMello DE, Colten HR.

J Clin Invest. 1994 Apr;93(4):1860-3.

7.

[Clinical thinking and decision making in practice: a full-term neonate with misunderstood respiratory insufficiency].

van Heijst AF, Semmekrot BA, Kollée LA, van de Bor M.

Ned Tijdschr Geneeskd. 1999 Jun 12;143(24):1256-60. Dutch.

PMID:
10396336
8.

Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency.

Tredano M, van Elburg RM, Kaspers AG, Zimmermann LJ, Houdayer C, Aymard P, Hull WM, Whitsett JA, Elion J, Griese M, Bahuau M.

Hum Mutat. 1999;14(6):502-9.

PMID:
10571948
9.

Partial deficiency of surfactant protein B in an infant with chronic lung disease.

Ballard PL, Nogee LM, Beers MF, Ballard RA, Planer BC, Polk L, deMello DE, Moxley MA, Longmore WJ.

Pediatrics. 1995 Dec;96(6):1046-52.

PMID:
7491219
10.

Human surfactant protein B: structure, function, regulation, and genetic disease.

Whitsett JA, Nogee LM, Weaver TE, Horowitz AD.

Physiol Rev. 1995 Oct;75(4):749-57. Review.

PMID:
7480161
11.
12.

Molecular and phenotypic variability in the congenital alveolar proteinosis syndrome associated with inherited surfactant protein B deficiency.

deMello DE, Nogee LM, Heyman S, Krous HF, Hussain M, Merritt TA, Hsueh W, Haas JE, Heidelberger K, Schumacher R, et al.

J Pediatr. 1994 Jul;125(1):43-50.

PMID:
8021783
13.

Surfactant protein B deficiency in infants with respiratory failure.

Wilder MA.

J Perinat Neonatal Nurs. 2004 Jan-Mar;18(1):61-7. Review.

PMID:
15027668
14.

Pulmonary surfactant metabolism in infants lacking surfactant protein B.

Beers MF, Hamvas A, Moxley MA, Gonzales LW, Guttentag SH, Solarin KO, Longmore WJ, Nogee LM, Ballard PL.

Am J Respir Cell Mol Biol. 2000 Mar;22(3):380-91.

PMID:
10696076
15.

Lung transplantation for treatment of infants with surfactant protein B deficiency.

Hamvas A, Nogee LM, Mallory GB Jr, Spray TL, Huddleston CB, August A, Dehner LP, deMello DE, Moxley M, Nelson R, Cole FS, Colten HR.

J Pediatr. 1997 Feb;130(2):231-9.

PMID:
9042125
16.

Regulation and function of pulmonary surfactant protein B.

Pryhuber GS.

Mol Genet Metab. 1998 Aug;64(4):217-28. Review.

PMID:
9758711
17.

Aberrant processing of surfactant protein C in hereditary SP-B deficiency.

Vorbroker DK, Profitt SA, Nogee LM, Whitsett JA.

Am J Physiol. 1995 Apr;268(4 Pt 1):L647-56.

PMID:
7537464
18.

Neonatal respiratory disease due to surfactant protein B deficiency.

Ballard PL.

J Perinatol. 1996 Mar-Apr;16(2 Pt 2 Su):S28-34. Review. No abstract available.

PMID:
8732546
19.

Surfactant protein B deficiency: clinical, histological and molecular evaluation.

Williams GD, Christodoulou J, Stack J, Symons P, Wert SE, Murrell MJ, Nogee LM.

J Paediatr Child Health. 1999 Apr;35(2):214-20.

PMID:
10365365
20.

Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population.

Rämet M, Haataja R, Marttila R, Floros J, Hallman M.

Am J Hum Genet. 2000 May;66(5):1569-79. Epub 2000 Apr 4.

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