The European Reference Network on Rare Lung Diseases (ERN-LUNG) ambition to offer better lung health for all
Presse Med. 2023 Sep 10:104172. doi: 10.1016/j.lpm.2023.104172. Online ahead of print.NO ABSTRACTPMID:37699508 | DOI:10.1016/j.lpm.2023.104172 (Source: Presse Medicale)
Source: Presse Medicale - September 12, 2023 Category: General Medicine Authors: Marc Humbert Thomas Wagner Source Type: research
The European Reference Network on Rare Lung Diseases (ERN-LUNG) ambition to offer better lung health for all
Presse Med. 2023 Sep 10:104172. doi: 10.1016/j.lpm.2023.104172. Online ahead of print.NO ABSTRACTPMID:37699508 | DOI:10.1016/j.lpm.2023.104172 (Source: Presse Medicale)
Source: Presse Medicale - September 12, 2023 Category: General Medicine Authors: Marc Humbert Thomas Wagner Source Type: research
The European Reference Network on Rare Lung Diseases (ERN-LUNG) ambition to offer better lung health for all
Presse Med. 2023 Sep 10:104172. doi: 10.1016/j.lpm.2023.104172. Online ahead of print.NO ABSTRACTPMID:37699508 | DOI:10.1016/j.lpm.2023.104172 (Source: Presse Medicale)
Source: Presse Medicale - September 12, 2023 Category: General Medicine Authors: Marc Humbert Thomas Wagner Source Type: research
The European Reference Network on Rare Lung Diseases (ERN-LUNG) ambition to offer better lung health for all
Presse Med. 2023 Sep 10:104172. doi: 10.1016/j.lpm.2023.104172. Online ahead of print.NO ABSTRACTPMID:37699508 | DOI:10.1016/j.lpm.2023.104172 (Source: Presse Medicale)
Source: Presse Medicale - September 12, 2023 Category: General Medicine Authors: Marc Humbert Thomas Wagner Source Type: research
The European Reference Network on Rare Lung Diseases (ERN-LUNG) ambition to offer better lung health for all
Presse Med. 2023 Sep 10:104172. doi: 10.1016/j.lpm.2023.104172. Online ahead of print.NO ABSTRACTPMID:37699508 | DOI:10.1016/j.lpm.2023.104172 (Source: Presse Medicale)
Source: Presse Medicale - September 12, 2023 Category: General Medicine Authors: Marc Humbert Thomas Wagner Source Type: research
Lymphangioleiomyomatosis
Presse Med. 2023 Sep 9:104173. doi: 10.1016/j.lpm.2023.104173. Online ahead of print.ABSTRACTLymphangioleiomyomatosis (LAM) is an ultra-rare, slowly progressive neoplastic cystic disease, belonging to the group of PEComas. It can occur sporadically or associated to tuberous sclerosis complex disease and affects mainly women in child-birth age. Dyspnoea is the most frequent symptom referred to the time of diagnosis, however spontaneous pneumothorax may be a typical presentation associated to extrathoracic manifestations, such as renal angiomyolipomas. In the last decade, important advances in understanding molecular mechani...
Source: Presse Medicale - September 11, 2023 Category: General Medicine Authors: Davide Elia Roberto Cassandro Antonella Caminati Francesca Luisi Sergio Harari Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 29;52(3):104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research
Alpha1-antitrypsin deficiency: An updated review
Presse Med. 2023 Jul 28:104170. doi: 10.1016/j.lpm.2023.104170. Online ahead of print.ABSTRACTAlpha1-antitrypsin deficiency (AATD) is a rare autosomal recessive disease associated with the homozygous Z variant of the SERPINA1 gene. Clinical expression of AATD, reported 60 years ago associate a severe deficiency, pulmonary emphysema and/or liver fibrosis. Pulmonary emphysema is due to the severe alpha1-antitrypsin deficiency of the ZZ homozygous status and is favored by smoking. Liver fibrosis is due to the ZZ homozygous status and is favored by obesity and excessive chronic alcohol intake, with a risk of liver cancer. Diag...
Source: Presse Medicale - July 30, 2023 Category: General Medicine Authors: Jean-Fran çois Mornex Julie Traclet Olivier Guillaud Magali Dechomet Christine Lombard Mathias Ruiz Didier Revel Philippe Reix Vincent Cottin Source Type: research