Zobrazeno 1 - 10
of 296
pro vyhledávání: '"F.J. de Serres"'
Publikováno v:
Monaldi Archives for Chest Disease, Vol 67, Iss 4 (2016)
Background. AAT deficiency is not a rare disease, but one of the most common congenital disorders increasing susceptibility of deficiency individuals to both lung and liver disease as well as other several adverse health effects. Therefore, informati
Externí odkaz:
https://doaj.org/article/8b415713d13449cbb60b3bc1949ae58b
Publikováno v:
Monaldi Archives for Chest Disease, Vol 71, Iss 3 (2016)
Background. AAT deficiency is not a rare disease, but one of the most common congenital disorders increasing susceptibility of individuals with this deficiency to both lung and liver disease as well as other several adverse health effects. Studies to
Externí odkaz:
https://doaj.org/article/ddd3c7eebcf14ffabb688522e3746923
Autor:
I. Blanco, H. Canto, J. Flóres, C. Camblor, V. Cárcaba, F.J. de Serres, S. Janciauskiene, E.F. Bustillo
Publikováno v:
Monaldi Archives for Chest Disease, Vol 69, Iss 4 (2016)
A young Caucasian female with severe bronchial asthma and Alpha1-antitrypsin (AAT) deficiency, MZ phenotype, experienced a quick and severe limitation of her physical capacity, which negatively affected her psychological state and social life, though
Externí odkaz:
https://doaj.org/article/e1c801b1b63f4dd99e8487aad99205d5
Publikováno v:
Monaldi Archives for Chest Disease, Vol 63, Iss 3 (2005)
Background. Critical to the effective diagnosis and management of disease is information on its prevalence in a particular geographic area such as Italy. Alpha-1- antitrypsin deficiency (AAT Deficiency) is one of the most common serious hereditary di
Externí odkaz:
https://doaj.org/article/448719ae1e5946a29bf01ffc04b90300
Autor:
Ignacio Blanco, F.J. de Serres
Publikováno v:
Journal of Internal Medicine. 276:311-335
Alpha-1 antitrypsin (AAT) deficiency is an under-recognized hereditary disorder associated with the premature onset of chronic obstructive pulmonary disease, liver cirrhosis in children and adults, and less frequently, relapsing panniculitis, systemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::163a4a3e546561b963243ffcc452aa45
https://doi.org/10.1111/joim.12239
https://doi.org/10.1111/joim.12239
Publikováno v:
Monaldi Archives for Chest Disease, Vol 67, Iss 4 (2016)
Background. AAT deficiency is not a rare disease, but one of the most common congenital disorders increasing susceptibility of deficiency individuals to both lung and liver disease as well as other several adverse health effects. Therefore, informati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b12ac065a6607d79c9e996c1f20c095
https://doi.org/10.4081/monaldi.2007.476
https://doi.org/10.4081/monaldi.2007.476
Autor:
C Camblor, Ignacio Blanco, Victoriano Cárcaba, Juana M. Flores, Enrique Fernandez Bustillo, H Canto, Sabina Janciauskiene, F.J. de Serres
Publikováno v:
Monaldi Archives for Chest Disease, Vol 69, Iss 4 (2016)
A young Caucasian female with severe bronchial asthma and Alpha1-antitrypsin (AAT) deficiency, MZ phenotype, experienced a quick and severe limitation of her physical capacity, which negatively affected her psychological state and social life, though
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::332f58f1c00003f9ef03111b5bb0b58e
https://www.monaldi-archives.org/index.php/macd/article/view/380
https://www.monaldi-archives.org/index.php/macd/article/view/380
Publikováno v:
Monaldi Archives for Chest Disease, Vol 71, Iss 3 (2016)
Background. AAT deficiency is not a rare disease, but one of the most common congenital disorders increasing susceptibility of individuals with this deficiency to both lung and liver disease as well as other several adverse health effects. Studies to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32723b815fc0bd18a383b36ca95aa282
https://www.monaldi-archives.org/index.php/macd/article/view/354
https://www.monaldi-archives.org/index.php/macd/article/view/354
Publikováno v:
Clinical Genetics. 64:382-397
Alpha-1-antitrypsin deficiency (AAT deficiency) is one of the most common serious hereditary disorders in the world, as its affects all major racial subgroups worldwide, and there are an estimated 120.5 million carriers and deficient subjects worldwi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b10f0de682efdbc59fbe6f6ab070bfd7
https://doi.org/10.1034/j.1399-0004.2003.00143.x
https://doi.org/10.1034/j.1399-0004.2003.00143.x
Publikováno v:
Clinical Genetics. 63:490-509
Alpha-1-antitrypsin deficiency (AAT deficiency) is one of the most common serious hereditary disorders in the world because it affects all major racial subgroups worldwide and there are at least 120.5 million carriers and deficient subjects worldwide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d2c1907ad5a43da31b9777cc3b0dc31
https://doi.org/10.1034/j.1399-0004.2003.00078.x
https://doi.org/10.1034/j.1399-0004.2003.00078.x