F. Brasch

发表

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation.

R. Hennekam, J. Tolmie, G. Mortier, 2007, American Journal of Human Genetics.

HNPCC: Six new pathogenic mutations

K. Schulmann, W. Schmiegel, S. Hahn, 2004, BMC Medical Genetics.

Decrease of the surface fraction of surfactant proteins containing clara cells and type II pneumocytes in a rat asthma model.

R. Pabst, A. Schmiedl, F. Brasch, 2005, Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie.

Hyperventilation induces release of cytokines from perfused mouse lung.

K. Müller, H. Volk, S. Uhlig, 1998, American journal of respiratory and critical care medicine.

Incidence and classification of pediatric diffuse parenchymal lung diseases in Germany

M. Griese, R. von Kries, D. Hartl, 2009, Orphanet journal of rare diseases.

Surfactant protein B in type II pneumocytes and intra-alveolar surfactant forms of human lungs.

K. Müller, M. Ochs, S. Guttentag, 2004, American journal of respiratory cell and molecular biology.

Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency.

T. Langmann, M. Ochs, G. Schmitz, 2006, American journal of respiratory and critical care medicine.

Viral and Clinical Oncology of Head and Neck Cancers

H. Sudhoff, I. Todt, F. Brasch, 2022, Current Oncology Reports.

Categorizing diffuse parenchymal lung disease in children

M. Griese, M. Kappler, P. Lohse, 2015, Orphanet Journal of Rare Diseases.

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

K. Müller, M. Ochs, G. Johnen, 2004, European Respiratory Journal.

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

U. Holmskov, K. Skjødt, N. Palaniyar, 2006, Scandinavian journal of immunology.

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

S. Uhlig, L. Wollin, F. Brasch, 1995, The American journal of pathology.

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

K. Müller, W. Schmiegel, A. Tromm, 2003, European journal of gastroenterology & hepatology.

Pulmonary hypertension presenting with apnea, cyanosis, and failure to thrive in a young child.

M. Griese, N. Regamey, F. Brasch, 2011, Chest.

Effect of surfactant on ventilation-induced mediator release in isolated perfused mouse lungs.

S. Uhlig, C. Stamme, F. Brasch, 2002, Pulmonary pharmacology & therapeutics.

Tools to explore ABCA3 mutations causing interstitial lung disease

S. Reu, G. Liebisch, M. Griese, 2016, Pediatric pulmonology.

Nonspecific Interstitial Pneumonia, Alveolar Proteinosis, and Abnormal Proprotein Trafficking Resulting from a Spontaneous Mutation in the Surfactant Protein C Gene

S. Russo, M. Ochs, A. Pettenazzo, 2005, Pediatric Research.

Early alterations in intracellular and alveolar surfactant of the rat lung in response to endotoxin.

S. Uhlig, C. Stamme, F. Brasch, 1998, American journal of respiratory and critical care medicine.

HNPCC-associated small bowel cancer: clinical and molecular characteristics.

K. Schulmann, W. Schmiegel, C. Engel, 2005, Gastroenterology.

Cyclooxygenase-2-Dependent Bronchoconstriction in Perfused Rat Lungs Exposed to Endotoxin

K. Müller, S. Uhlig, A. Wendel, 1996, Molecular medicine.

Cysteine protease activity is required for surfactant protein B processing and lamellar body genesis.

S. Guttentag, Lauren Robinson, F. Bühling, 2003, American journal of respiratory cell and molecular biology.

Involvement of cathepsin H in the processing of the hydrophobic surfactant-associated protein C in type II pneumocytes.

K. Müller, A. ten Brinke, M. Ochs, 2002, American journal of respiratory cell and molecular biology.

mouse lungs: its acceleration by reduction Removal of a dimeric form of surfactant protein C from

M. Ochs, G. Johnen, M. Griese, 2015 .

Surfactant proteins in pulmonary alveolar proteinosis in adults

K. Müller, M. Ochs, S. Guttentag, 2004, European Respiratory Journal.

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

K. Müller, M. Ochs, V. Schauer-Vukašinović, 2003, Journal of Biological Chemistry.

Mapping of capillary flow, cellular redox state, and resting membrane potential in hypoperfused rat myocardium.

G. Hellige, F. Brasch, F. Vetterlein, 1999, American journal of physiology. Heart and circulatory physiology.

AHEART November 46/5

G. Hellige, F. Brasch, F. Vetterlein, 1999 .

Evaluation of lanthanide tracer methods in the study of mammalian pulmonary parenchyma and cardiac muscle by electron energy‐loss spectroscopy

A. Schmiedl, F. Brasch, H. Fehrenbach, 1994, Journal of microscopy.

Adult polyglucosan body disease

K. Müller, J. Malin, T. Ziemssen, 2003, Neurology.

Long-term follow-up and treatment of congenital alveolar proteinosis

T. Nicolai, O. Muensterer, M. Griese, 2011, BMC pediatrics.

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

F. Brasch, B. May, T. Griga, 1999, Hepato-gastroenterology.

Primary head and neck cancer cell cultures are susceptible to proliferation of Epstein-Barr virus infected lymphocytes

H. Sudhoff, J. Florido, G. Escames, 2023, BMC Cancer.

Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood

S. Reu, A. Guenther, J. Ley-Zaporozhan, 2018, Orphanet Journal of Rare Diseases.

[Poorly differentiated neuroendocrine small-cell carcinoma of the gallbladder].

A. Altendorf-Hofmann, F. Brasch, W. Sendt, 2012, Zentralblatt fur Chirurgie.

Quinolines attenuate PAF-induced pulmonary pressor responses and edema formation.

K. Müller, S. Falk, S. Uhlig, 1999, American journal of respiratory and critical care medicine.

Pulmonary interstitial glycogenosis - A systematic analysis of new cases.

S. Reu, J. Ley-Zaporozhan, M. Griese, 2018, Respiratory medicine.

Persistent Tachypnea of Infancy. Usual and Aberrant.

S. Reu, E. Kerem, J. Ley-Zaporozhan, 2016, American journal of respiratory and critical care medicine.

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

E. Ikonen, G. Schmitz, A. Rolfs, 2010, Clinical genetics.

G. Mortier, D. Fitzpatrick, R. Hennekam, 2007, American journal of human genetics.

M. Sattler, F. Delhommel, N. Kiper, 2021, Clinical genetics.

Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients

S. Lau, M. Gappa, J. Seidenberg, 2015, European Respiratory Journal.

Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function

Robert W. Taylor, W. Chung, A. Borczuk, 2018, American journal of human genetics.

Intracellular and intraalveolar localization of surfactant protein A (SP-A) in the parenchymal region of the human lung.

K. Müller, M. Ochs, G. Johnen, 2002, American journal of respiratory cell and molecular biology.

Hypersensitivity pneumonitis: lessons for diagnosis and treatment of a rare entity in children

M. Griese, D. Hartl, F. Brasch, 2013, Orphanet Journal of Rare Diseases.

Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry‐based case series

S. Reu, K. Poplawska, J. Ley-Zaporozhan, 2020, Pediatric pulmonology.

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

H. Sudhoff, M. Görner, F. Brasch, 2013, European journal of cancer care.

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

H. Sudhoff, R. Riemann, I. Todt, 2019, HNO.

Morphometric characterisation of the fine structure of human type II pneumocytes

A. Schmiedl, F. Brasch, T. Wahlers, 1995, The Anatomical record.

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

C. Houdayer, J. Elion, M. Griese, 2004, American journal of medical genetics. Part A.

SURFACTANTPROTEINB DEFICIENCYCAUSEDBYANOVELMUTATION INVOLVINGMULTIPLEEXONSOFTHESP-B GENE*

M. Griese, F. Brasch, A. V. Kaam, 2008 .

Lung disease caused by ABCA3 mutations

J. Seidenberg, S. Reu, M. Proesmans, 2016, Thorax.

[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)].

M. Kloor, D. Aust, C. Poremba, 2004, Der Pathologe.

Distribution of surfactant proteins in type II pneumocytes of newborn, 14-day old, and adult rats: an immunoelectron microscopic and stereological study

M. Ochs, G. Johnen, A. Schmiedl, 2005, Histochemistry and Cell Biology.

Prognostic Factors for Long-Term Survival after Surgical Resection of Primary Cardiac Sarcoma

J. Gummert, F. Brasch, W. Hsieh, 2019, The Thoracic and Cardiovascular Surgeon.

Prevalence of the mismatch-repair-deficient phenotype in colonic adenomas arising in HNPCC patients: results of a 5-year follow-up study

M. Kloor, D. Aust, C. Poremba, 2006, International Journal of Colorectal Disease.

Pivotal role of cathepsin K in lung fibrosis.

T. Welte, P. Saftig, R. Hartig, 2004, The American journal of pathology.

Ultrastructural pathology of the alveolar type II pneumocytes of human donor lungs

M. Ochs, A. Haverich, A. Schmiedl, 1998, Virchows Archiv.

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

K. Müller, F. Brasch, B. May, 2002, Hepato-gastroenterology.

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

A. V. van Kaam, M. Griese, F. Brasch, 2008, European Journal of Medical Research.

Head and neck cancer cells terminally differentiate reflecting their tissue of origin: a rationale for differentiation therapies

H. Sudhoff, K. Niehaus, J. Florido, 2023, bioRxiv.

Computed chest tomography in an animal model for decompression sickness: radiologic, physiologic, and pathologic findings

K. Müller, M. Heller, K. Tetzlaff, 2000, European Radiology.

Genetic alterations affecting the C‐terminus of cyclin D1 are recurrent events in mantle cell lymphoma

W. Klapper, M. Tiemann, I. Iaccarino, 2022, Histopathology.

Can airways close completely?

S. Uhlig, F. Brasch, A. Wohlsen, 2000, Journal of applied physiology.

Mapping of capillary flow, cellular redox state, and resting membrane potential in hypoperfused rat myocardium.

G. Hellige, F. Brasch, F. Vetterlein, 1999, American journal of physiology. Heart and circulatory physiology.