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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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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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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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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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Adult polyglucosan body disease: a postmortem correlation study

Neurology, 2003-07, Vol.61 (2), p.263-265

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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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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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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Cysteine Protease Activity Is Required for Surfactant Protein B Processing and Lamellar Body Genesis

American journal of respiratory cell and molecular biology, 2003-01, Vol.28 (1), p.69-79

2003

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Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease

American journal of medical genetics. Part A, 2004-04, Vol.126A (1), p.18-26

2004

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Pulmonary megakaryocyte-embolism in contact with osteomyelofibrosis

Pneumologie (Stuttgart, Germany), 2005-06, Vol.59 (6), p.376-377

2005

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Involvement of Cathepsin H in the Processing of the Hydrophobic Surfactant-Associated Protein C in Type II Pneumocytes

American journal of respiratory cell and molecular biology, 2002-06, Vol.26 (6), p.659-670

2002

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Collagenous colitis: implications for the role of vascular endothelial growth factor in repair mechanisms

European journal of gastroenterology & hepatology, 2004-04, Vol.16 (4), p.397-402

2004

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No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

European journal of human genetics : EJHG, 2008-05, Vol.16 (5), p.587-592

2008

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Immunohistochemical localization of vascular endothelial growth factor in colonic mucosa of patients with inflammatory bowel disease

Hepato-gastroenterology, 2002-01, Vol.49 (43), p.116

2002

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Increased production of vascular endothelial growth factor by intestinal mucosa of patients with inflammatory bowel disease

Hepato-gastroenterology, 1999-03, Vol.46 (26), p.920

1999

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Pulmonary interstitial glycogenosis – A systematic analysis of new cases

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

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

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

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

Pivotal Role of Cathepsin K in Lung Fibrosis

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

Cysteine Protease Activity Is Required for Surfactant Protein B Processing and Lamellar Body Genesis

Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease

Pulmonary megakaryocyte-embolism in contact with osteomyelofibrosis

Involvement of Cathepsin H in the Processing of the Hydrophobic Surfactant-Associated Protein C in Type II Pneumocytes

Collagenous colitis: implications for the role of vascular endothelial growth factor in repair mechanisms

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

Immunohistochemical localization of vascular endothelial growth factor in colonic mucosa of patients with inflammatory bowel disease

Increased production of vascular endothelial growth factor by intestinal mucosa of patients with inflammatory bowel disease

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