Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Enrique Fernández Bustillo"'
Autor:
Luis Rodrigo, Nuria Álvarez, Enrique Fernández-Bustillo, Javier Salas-Puig, Marcos Huerta, Carlos Hernández-Lahoz
Publikováno v:
Nutrients, Vol 10, Iss 5, p 573 (2018)
The Gilles de la Tourette syndrome (GTS) and Non-Coeliac Gluten Sensitivity (NCGS) may be associated. We analyse the efficacy of a gluten-free diet (GFD) in 29 patients with GTS (23 children; six adults) in a prospective pilot study. All of them foll
Externí odkaz:
https://doaj.org/article/c205c01efb11427f82ada48206e4dcef
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 4 (2010)
Background: Our earlier publications have demonstrated that alpha-1 antitrypsin (AAT) deficiency is not a rare disorder in the United States with at least 33,728 PI*ZZ homozygote individuals at risk. Method: Using data on the prevalences of the two m
Externí odkaz:
https://doaj.org/article/7b4a0d4b7f604a1c98642b2d2d86e249
Autor:
Nuria Álvarez, Enrique Fernández-Bustillo, Luis Rodrigo, Carlos Hernández-Lahoz, Marcos Huerta, Javier Salas-Puig
Publikováno v:
Nutrients
Nutrients, Vol 10, Iss 5, p 573 (2018)
Nutrients; Volume 10; Issue 5; Pages: 573
Nutrients, Vol 10, Iss 5, p 573 (2018)
Nutrients; Volume 10; Issue 5; Pages: 573
The Gilles de la Tourette syndrome (GTS) and Non-Coeliac Gluten Sensitivity (NCGS) may be associated. We analyse the efficacy of a gluten-free diet (GFD) in 29 patients with GTS (23 children; six adults) in a prospective pilot study. All of them foll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3366d63b47b32ce0b736f34c5e6c7fea
https://doi.org/10.20944/preprints201804.0332.v1
https://doi.org/10.20944/preprints201804.0332.v1
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
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
Autor:
Enrique Fernández-Bustillo, Brigita Sitkauskiene, Ignacio Blanco, Raimundas Sakalauskas, Sabina Janciauskiene, Danielius Serapinas
Publikováno v:
Respiratory Medicine. 102:1654-1658
Background: Alphal-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients with chronic obstructive pulmonary disease (COPD). The objective of the present screening was to estimate the AAT gene frequency and prevalence and to identif
Autor:
Izabela Nita, Sabina Janciauskiene, Enrique Fernández-Bustillo, Ignacio Blanco, Daniel Arbesú, Frederick J. de Serres, Aurora Astudillo, Victoriano Cárcaba
Publikováno v:
Journal of Musculoskeletal Pain. 15:9-23
Objectives: During the last few years, clinical, epidemiological, and pathological evidence has suggested that inherited alpha-1 antitrypsin [AAT] deficiency might play a role in the development of the fibromyalgia syndrome [FMS], probably because of
Publikováno v:
COPD: Journal of Chronic Obstructive Pulmonary Disease. 3:133-139
Alpha-1 antitrypsin deficiency is known as a significant genetic risk factor for COPD for carriers of phenotype PIMZ, and for phenotypes PIZZ and PISZ. Genetic epidemiological studies for alpha-1 antitrypsin deficiency conducted by others on both COP
Autor:
Daniel Arbesú, Ignacio Blanco, Enrique Fernández-Bustillo, Daniel Al Kassam, Frederick J. de Serres, Carmen Rodríguez
Publikováno v:
Journal of Musculoskeletal Pain. 14:5-12
Background: Recent evidence suggests that the alpha1-antitrypsin [AT] gene may play a role in the pathogenesis of the fibromyalgia syndrome [FMS]. The objective of the present study is to compare the AT gene frequency between FMS patients and the gen
Publikováno v:
Genetics in Medicine. 7:175-184
Purpose: To determine the frequencies of the protease inhibitor (PI) deficiency alleles of α1-antitrypsin deficiency (AAT Deficiency) in indigenous populations in 12 countries in Sub-Sahara Africa because of their potential impact on the health in t