Results
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112.
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113.
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Sequential genotyping of Pseudomonas aeruginosa from upper and lower airways of cystic fibrosis patients. [electronic resource] by
- Jung, A
- Kleinau, I
- Schönian, G
- Bauernfeind, A
- Chen, C
- Griese, M
- Döring, G
- Göbel, U
- Wahn, U
- Paul, K
Producer: 20030402
In:
The European respiratory journal vol. 20
Availability: No items available.
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114.
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Anti-GM-CSF antibodies in paediatric pulmonary alveolar proteinosis. [electronic resource] by
- Latzin, P
- Tredano, M
- Wüst, Y
- de Blic, J
- Nicolai, T
- Bewig, B
- Stanzel, F
- Köhler, D
- Bahuau, M
- Griese, M
Producer: 20050201
In:
Thorax vol. 60
Availability: No items available.
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115.
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Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene. [electronic resource] by
- Brasch, F
- Griese, M
- Tredano, M
- Johnen, G
- Ochs, M
- Rieger, C
- Mulugeta, S
- Müller, K M
- Bahuau, M
- Beers, M F
Producer: 20050310
In:
The European respiratory journal vol. 24
Availability: No items available.
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116.
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Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonate. [electronic resource] by
- Parappil, Hussain
- Al Baridi, Ahmad
- ur Rahman, Sajjad
- Kitchi, Mahmood H
- Ruef, P
- Griese, M
- Lohse, P
- Aslanidis, C
- Schmitz, G
- Koch, L
- Poeschl, J
Producer: 20130729
In:
BMJ case reports vol. 2011
Availability: No items available.
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117.
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Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency. [electronic resource] by
- Tredano, M
- van Elburg, R M
- Kaspers, A G
- Zimmermann, L J
- Houdayer, C
- Aymard, P
- Hull, W M
- Whitsett, J A
- Elion, J
- Griese, M
- Bahuau, M
Producer: 20000124
In:
Human mutation vol. 14
Availability: No items available.
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118.
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Inhaled glutathione decreases PGE2 and increases lymphocytes in cystic fibrosis lungs. [electronic resource] by
- Hartl, D
- Starosta, V
- Maier, K
- Beck-Speier, I
- Rebhan, C
- Becker, B F
- Latzin, P
- Fischer, R
- Ratjen, F
- Huber, R M
- Rietschel, E
- Krauss-Etschmann, S
- Griese, M
Producer: 20051205
In:
Free radical biology & medicine vol. 39
Availability: No items available.
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119.
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Diversity of the basic defect of homozygous CFTR mutation genotypes in humans. [electronic resource] by
- Stanke, F
- Ballmann, M
- Bronsveld, I
- Dörk, T
- Gallati, S
- Laabs, U
- Derichs, N
- Ritzka, M
- Posselt, H-G
- Harms, H K
- Griese, M
- Blau, H
- Mastella, G
- Bijman, J
- Veeze, H
- Tümmler, B
Producer: 20080122
In:
Journal of medical genetics vol. 45
Availability: No items available.
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120.
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Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis. [electronic resource] by
- Griese, M
- Brasch, F
- Aldana, V R
- Cabrera, M M
- Goelnitz, U
- Ikonen, E
- Karam, B J
- Liebisch, G
- Linder, M D
- Lohse, P
- Meyer, W
- Schmitz, G
- Pamir, A
- Ripper, J
- Rolfs, A
- Schams, A
- Lezana, F J
Producer: 20100416
In:
Clinical genetics vol. 77
Availability: No items available.
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