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  1. Book ; Online: Present possibilities in the prevention of cystic fibrosis in southern Europe / by Gianni Mastella

    Mastella, Gianni / World Health Organization. Hereditary Diseases Programme / Joint WHO/ICF(MA Task Force on Cystic Fibrosis (1990 : Leningrad/Moscow, USSR)

    1990  

    Abstract: ONLINE ... WHO/HDP/ICF(M)A/TF/90.4.WP.6. Unpublished ... English only ...

    Abstract ONLINE

    WHO/HDP/ICF(M)A/TF/90.4.WP.6. Unpublished

    English only

    10 p.
    Keywords Cystic fibrosis ; Genetic screening ; Europe ; prevention and control diagnosis
    Language English
    Publisher Geneva : World Health Organization
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Book ; Online: Present possibilities in the prevention of cystic fibrosis in southern Europe / by Gianni Mastella

    Mastella, Gianni / World Health Organization. Hereditary Diseases Programme / Joint WHO/ICF(MA Task Force on Cystic Fibrosis (1990 : Leningrad/Moscow, USSR)

    1990  

    Abstract: ONLINE ... WHO/HDP/ICF(M)A/TF/90.4.WP.6. Unpublished ... 10 p. ...

    Abstract ONLINE

    WHO/HDP/ICF(M)A/TF/90.4.WP.6. Unpublished

    10 p.
    Keywords Cystic Fibrosis ; Genetic Testing ; Europe ; prevention and control diagnosis
    Language English
    Publisher World Health Organization
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Book ; Conference proceedings: Cellular and molecular basis of cystic fibrosis

    Mastella, Gianni

    papers presented at a conference held in Verona, June 1987

    1988  

    Institution International Cystic Fibrosis (Mucoviscidosis) Association
    Author's details publ. under the auspices of the International Cystic Fibrosis (Mucovisidosis) Association. Gianni Mastella ..., ed
    Keywords Cystic Fibrosis / congresses
    Size XI, 487 S. : Ill., graph. Darst.
    Publisher San Francisco Pr
    Publishing place San Francisco, Calif
    Publishing country United States
    Document type Book ; Conference proceedings
    HBZ-ID HT003457852
    ISBN 0-911302-63-8 ; 978-0-911302-63-9
    Database Catalogue ZB MED Medicine, Health

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  4. Article ; Online: Sweat testing: can the conductivity analysis take the place of the classic Gibson and Cooke technique?

    Mastella, Gianni

    Jornal de pediatria

    2010  Volume 86, Issue 2, Page(s) 89–91

    MeSH term(s) Chlorides/analysis ; Cystic Fibrosis/diagnosis ; Electric Conductivity ; Electrodiagnosis/methods ; Filtration/methods ; Humans ; Infant ; Infant, Newborn ; Paper ; Sodium/analysis ; Sweat/chemistry
    Chemical Substances Chlorides ; Sodium (9NEZ333N27)
    Language English
    Publishing date 2010-03-25
    Publishing country Brazil
    Document type Comment ; Editorial
    ZDB-ID 731324-x
    ISSN 1678-4782 ; 0021-7557
    ISSN (online) 1678-4782
    ISSN 0021-7557
    DOI 10.2223/JPED.1997
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Teste do suor

    Gianni Mastella

    Jornal de Pediatria, Vol 86, Iss 2, Pp 89-

    a análise de condutividade pode tomar o lugar do método clássico de Gibson e Cooke? Sweat testing: can the conductivity analysis take the place of the classic Gibson and Cooke technique?

    2010  Volume 91

    Keywords Pediatrics ; RJ1-570 ; Medicine ; R ; DOAJ:Pediatrics ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language English
    Publishing date 2010-04-01T00:00:00Z
    Publisher Sociedade Brasileira de Pediatria
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Update of literature from cystic fibrosis registries 2012-2015. Part 6: Epidemiology, nutrition and complications.

    Salvatore, Donatello / Buzzetti, Roberto / Mastella, Gianni

    Pediatric pulmonology

    2017  Volume 52, Issue 3, Page(s) 390–398

    Abstract: Patient registries provide useful information to afford more knowledge on rare diseases like Cystic Fibrosis (CF). Twenty-two studies originating from national CF registries, focusing on demographics, survival, genetics, nutritional status, and non- ... ...

    Abstract Patient registries provide useful information to afford more knowledge on rare diseases like Cystic Fibrosis (CF). Twenty-two studies originating from national CF registries, focusing on demographics, survival, genetics, nutritional status, and non-pulmonary complications, were published between December 2011 and March 2015. The purpose of this review article is to examine these reports, aiming attention to the clinical characteristics of CF patients included in the registries, current, and estimated future epidemiological data, the role of gender gap, the increasing survival in different countries. Some studies offer insights into pubertal growth and non-pulmonary complications, such as liver disease, nephropathy, and cancer. Pediatr Pulmonol. 2017;52:390-398. © 2016 Wiley Periodicals, Inc.
    MeSH term(s) Cystic Fibrosis/complications ; Cystic Fibrosis/diagnosis ; Cystic Fibrosis/epidemiology ; Cystic Fibrosis/genetics ; Humans ; Lung Transplantation/adverse effects ; Nutritional Status ; Prognosis ; Puberty ; Registries ; Survival Analysis
    Language English
    Publishing date 2017-03
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 632784-9
    ISSN 1099-0496 ; 8755-6863
    ISSN (online) 1099-0496
    ISSN 8755-6863
    DOI 10.1002/ppul.23611
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: An overview of international literature from cystic fibrosis registries. Part 5: Update 2012-2015 on lung disease.

    Salvatore, Donatello / Buzzetti, Roberto / Mastella, Gianni

    Pediatric pulmonology

    2016  Volume 51, Issue 11, Page(s) 1251–1263

    Abstract: Patient registry data is a tool for defining the clinical course and risk factors in patients with less common diseases like Cystic Fibrosis. Forty-one registry-based reports on lung disease in Cystic Fibrosis were published between 2011 and 2015. The ... ...

    Abstract Patient registry data is a tool for defining the clinical course and risk factors in patients with less common diseases like Cystic Fibrosis. Forty-one registry-based reports on lung disease in Cystic Fibrosis were published between 2011 and 2015. The aim of this review is to describe and discuss the results of these reports, focusing on the risk factors for lung disease progression, specific microbiologic pathogens (e.g., non-tuberculous mycobacteria), disease complications, comparisons between registries of different countries, the impact of socio-economic status, and evaluation of benefits and costs of therapies. Techniques for improved clinical trial design were also studied. Pediatr Pulmonol. 2016;51:1251-1263. © 2016 Wiley Periodicals, Inc.
    MeSH term(s) Cystic Fibrosis ; Humans ; Periodicals as Topic ; Registries ; Risk Factors
    Language English
    Publishing date 2016-11
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 632784-9
    ISSN 1099-0496 ; 8755-6863
    ISSN (online) 1099-0496
    ISSN 8755-6863
    DOI 10.1002/ppul.23473
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Obituary: Gerd Döring.

    Quinton, Paul M / Mastella, Gianni / Worlitzsch, Dieter

    The international journal of biochemistry & cell biology

    2014  Volume 52, Page(s) 5–6

    MeSH term(s) Cystic Fibrosis/history ; History, 20th Century ; History, 21st Century
    Language English
    Publishing date 2014-06-20
    Publishing country Netherlands
    Document type Biography ; Historical Article ; Journal Article ; Portrait
    ZDB-ID 1228429-4
    ISSN 1878-5875 ; 1357-2725
    ISSN (online) 1878-5875
    ISSN 1357-2725
    DOI 10.1016/j.biocel.2013.12.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Book ; Conference proceedings: Cellular and molecular basis of cystic fibrosis

    Mastella, Gianni

    papers presented at a conference held in Verona, June 1987

    1988  

    Author's details Gianni Mastella, Paul M. Quinton, editors
    MeSH term(s) Cystic Fibrosis
    Language English
    Size xi, 487 p. :, ill.
    Publisher San Francisco Press
    Publishing place San Francisco
    Document type Book ; Conference proceedings
    ISBN 9780911302639 ; 0911302638
    Database Catalogue of the US National Library of Medicine (NLM)

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  10. Article ; Online: An overview of international literature from cystic fibrosis registries. Part 4: update 2011.

    Salvatore, Donatello / Buzzetti, Roberto / Baldo, Ermanno / Furnari, Maria Lucia / Lucidi, Vincenzina / Manunza, Daniela / Marinelli, Italo / Messore, Barbara / Neri, Anna Silvia / Raia, Valeria / Mastella, Gianni

    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

    2012  Volume 11, Issue 6, Page(s) 480–493

    Abstract: A total of 53 national cystic fibrosis (CF) patient registry studies published between July 2008 and November 2011 have been reviewed, focusing on the following topics: CF epidemiology, nutrition, microbiology, clinical complications, factors influencing ...

    Abstract A total of 53 national cystic fibrosis (CF) patient registry studies published between July 2008 and November 2011 have been reviewed, focusing on the following topics: CF epidemiology, nutrition, microbiology, clinical complications, factors influencing diagnosis and lung disease, effects of socioeconomic status, therapeutic strategy evaluation, clinical trial methodology. The studies describe the clinical characteristics of CF patients, the incidence and prevalence of disease and role of gender gap, as well as the influence of socioeconomic status and environmental factors on clinical outcomes, covering a variety of countries and ethnic groups. Original observations describe patients as they get older, with special reference to the adult presentation of CF and long-term survival. Methodological aspects are discussed, covering the design of clinical trials, survival analysis, auxometry, measures of quality of life, follow up of lung disease, predictability of disease progression and life expectancy. Microbiology studies have investigated the role of selected pathogens, such as Burkholderia species and MRSA. Pulmonary exacerbations are discussed both as a factor influencing morbidity and an endpoint in clinical trials. Finally, some studies give insights on complications, such as CF-related diabetes and hemoptysis, and emerging problems, such as chronic nephropathy.
    MeSH term(s) Cystic Fibrosis/epidemiology ; Cystic Fibrosis/therapy ; Humans ; Incidence ; Internationality ; Prevalence ; Registries/statistics & numerical data
    Language English
    Publishing date 2012-12
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2091075-7
    ISSN 1873-5010 ; 1569-1993
    ISSN (online) 1873-5010
    ISSN 1569-1993
    DOI 10.1016/j.jcf.2012.07.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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