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Items: 1 to 20 of 85

1.

Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutation.

Dunbar AE 3rd, Wert SE, Ikegami M, Whitsett JA, Hamvas A, White FV, Piedboeuf B, Jobin C, Guttentag S, Nogee LM.

Pediatr Res. 2000 Sep;48(3):275-82.

PMID:
10960490
2.

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
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.
5.

Aberrant SP-B mRNA in lung tissue of patients with congenital alveolar proteinosis (CAP).

Lin Z, deMello DE, Batanian JR, Khammash HM, DiAngelo S, Luo J, Floros J.

Clin Genet. 2000 May;57(5):359-69. Erratum in: Clin Genet 2000 Aug;58(2):156.

PMID:
10852370
6.

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
7.

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
8.

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
9.

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.

10.

cDNA sequence and alternative mRNA splicing of surfactant-associated protein C (SP-C) in rabbit lung.

Connelly I, Possmayer F.

Biochim Biophys Acta. 1992 Jul 29;1127(2):199-207.

PMID:
1643107
11.

Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency.

Nogee LM, Wert SE, Proffit SA, Hull WM, Whitsett JA.

Am J Respir Crit Care Med. 2000 Mar;161(3 Pt 1):973-81.

PMID:
10712351
12.

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
13.

Inherited disorders of neonatal lung diseases.

Yurdakök M.

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

14.

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
15.
16.
17.

Congenital alveolar proteinosis caused by a novel mutation of the surfactant protein B gene and misalignment of lung vessels in consanguineous kindred infants.

Wallot M, Wagenvoort C, deMello D, Müller KM, Floros J, Roll C.

Eur J Pediatr. 1999 Jun;158(6):513-8.

PMID:
10378403
18.

Surfactant protein B deficiency caused by a novel mutation involving multiple exons of the SP-B gene.

Schuerman FA, Griese M, Gille JP, Brasch F, Noorduyn LA, van Kaam AH.

Eur J Med Res. 2008 Jun 24;13(6):281-6.

PMID:
18558554
19.

[Clinical, biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolism: SP-B deficiency and alveolar proteinosis].

Tredano M, Blic JD, Griese M, Fournet JC, Elion J, Bahuau M.

Ann Biol Clin (Paris). 2001 Mar-Apr;59(2):131-48. Review. French.

PMID:
11282516
20.

Absence of lamellar bodies with accumulation of dense bodies characterizes a novel form of congenital surfactant defect.

Tryka AF, Wert SE, Mazursky JE, Arrington RW, Nogee LM.

Pediatr Dev Pathol. 2000 Jul-Aug;3(4):335-45.

PMID:
10890249
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