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Pulmonary interstitial glycogenosis – A systematic analysis of new cases

Respiratory medicine, 2018-07, Vol.140, p.11-20

2018

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Malignant Transformation of Temporal Bone Schneiderian Papilloma Associated with HPV-6

Case reports in otolaryngology, 2021, Vol.2021, p.6684254-5

2021

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A rare pathology of the petrous part of the temporal bone: adenoma of the middle ear

HNO, 2020-01, Vol.68 (1), p.55

2020

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Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene

The European respiratory journal, 2004-07, Vol.24 (1), p.30-39

2004

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Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis

Clinical genetics, 2010-02, Vol.77 (2), p.119-130

2010

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Surfactant proteins in pulmonary alveolar proteinosis in adults

The European respiratory journal, 2004-09, Vol.24 (3), p.426-435

2004

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Eine seltene Pathologie des Felsenbeins: Das Adenom des Mittelohres

HNO, 2020, Vol.68 (1), p.55-58

2020

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Microfibril‐associated Protein 4 Binds to Surfactant Protein A (SP‐A) and Colocalizes with SP‐A in the Extracellular Matrix of the Lung

Scandinavian journal of immunology, 2006-08, Vol.64 (2), p.104-116

2006

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The pulmonary surfactant system of the human lung — aetiology and pathogenesis of pulmonary alveolar proteinosis

Pathology, research and practice, 2004, Vol.200 (4), p.263-263

Brasch, F.

2004

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Multimodality treatment for poorly differentiated neuroendocrine head and neck carcinomas - a single institution experience

European journal of cancer care, 2013-09, Vol.22 (5), p.648-652

2013

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Intracellular and Intraalveolar Localization of Surfactant Protein A (SP-A) in the Parenchymal Region of the Human Lung

American journal of respiratory cell and molecular biology, 2002-01, Vol.26 (1), p.91-98

2002

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P35 Spatial proteomics and metabolomics investigations in head & neck cancers

Oral oncology, 2022-11, Vol.134, p.106164, Article 106164

2022

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A rare pathology of the petrous part of the temporal bone: adenoma of the middle ear

HNO, 2020-01, Vol.68 (1), p.55-58

2020

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Adult polyglucosan body disease: a postmortem correlation study

Neurology, 2003-07, Vol.61 (2), p.263

2003

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

European journal of medical research, 2008-06, Vol.13 (6), p.281-286

2008

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P28 Head and neck cancer cells differentiate resembling their tissue of origin

Oral oncology, 2022-11, Vol.134, p.106159, Article 106159

2022

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Pivotal Role of Cathepsin K in Lung Fibrosis

The American journal of pathology, 2004-06, Vol.164 (6), p.2203-2216

2004

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C50 CYSTIC FIBROSIS AND UNCOMMON PEDIATRIC DISEASES: Chronic Tachypnoe Of Infancy - Diagnostic Assessment With And Without Biopsy

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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Functional and fine structural changes in isolated rat lungs challenged with endotoxin ex vivo and in vitro

The American journal of pathology, 1995-05, Vol.146 (5), p.1235-1247

1995

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Surfactant Protein B in Type II Pneumocytes and Intra-Alveolar Surfactant Forms of Human Lungs

American journal of respiratory cell and molecular biology, 2004-04, Vol.30 (4), p.449-458

2004

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CR3/108--Congenital alveolar capillary dysplasia with familiary microphthalmia

Paediatric respiratory reviews, 2006, Vol.7 Suppl 1, p.S326-S326

2006

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CR10/80--Lymphoid interstitial pneumonia and Kabuki-Syndrome in a young man

Paediatric respiratory reviews, 2006, Vol.7 Suppl 1, p.S329-S329

2006

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Involvement of Napsin A in the C- and N-terminal Processing of Surfactant Protein B in Type-II Pneumocytes of the Human Lung

The Journal of biological chemistry, 2003-12, Vol.278 (49), p.49006-49014

2003

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Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene

Pediatric research, 2005, Vol.57 (1), p.89-98

2005

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Pulmonary interstitial glycogenosis – A systematic analysis of new cases

Malignant Transformation of Temporal Bone Schneiderian Papilloma Associated with HPV-6

A rare pathology of the petrous part of the temporal bone: adenoma of the middle ear

Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene

Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis

Surfactant proteins in pulmonary alveolar proteinosis in adults

Eine seltene Pathologie des Felsenbeins: Das Adenom des Mittelohres

Microfibril‐associated Protein 4 Binds to Surfactant Protein A (SP‐A) and Colocalizes with SP‐A in the Extracellular Matrix of the Lung

The pulmonary surfactant system of the human lung — aetiology and pathogenesis of pulmonary alveolar proteinosis

Multimodality treatment for poorly differentiated neuroendocrine head and neck carcinomas - a single institution experience

Intracellular and Intraalveolar Localization of Surfactant Protein A (SP-A) in the Parenchymal Region of the Human Lung

P35 Spatial proteomics and metabolomics investigations in head & neck cancers

A rare pathology of the petrous part of the temporal bone: adenoma of the middle ear

International management platform for children's interstitial lung disease (chILD-EU)

Adult polyglucosan body disease: a postmortem correlation study

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

P28 Head and neck cancer cells differentiate resembling their tissue of origin

Pivotal Role of Cathepsin K in Lung Fibrosis

C50 CYSTIC FIBROSIS AND UNCOMMON PEDIATRIC DISEASES: Chronic Tachypnoe Of Infancy - Diagnostic Assessment With And Without Biopsy

Functional and fine structural changes in isolated rat lungs challenged with endotoxin ex vivo and in vitro

Surfactant Protein B in Type II Pneumocytes and Intra-Alveolar Surfactant Forms of Human Lungs

CR3/108--Congenital alveolar capillary dysplasia with familiary microphthalmia

CR10/80--Lymphoid interstitial pneumonia and Kabuki-Syndrome in a young man

Involvement of Napsin A in the C- and N-terminal Processing of Surfactant Protein B in Type-II Pneumocytes of the Human Lung

Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene

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