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1. Full Text Teste do suor e fibrose cística: Panorama da realização do teste em centros públicos e privados do estado de São Paulo
by Servidoni, Maria Fátima and Gomez, Carla Cristina Souza and Marson, Fernando Augusto Lima and Toro, Adyléia Aparecida Dalbo Contrera and Ribeiro, Maria Ângela Gonçalves de Oliveira and Ribeiro, José Dirceu and Ribeiro, Antônio Fernando and Vieira Junior, Francisco Ubaldo and Amaral, Margarida Duarte and Damaceno, Neiva and Rodrigues, Joaquim Carlos and Ferrari, Giesela Fleischer and Sdepanian, Vera Lucia and Salomão Junior, João Batista and Chiba, Sônia Mayumi and Lorena, Sônia Letícia Silva and Fernandes, Maria Inêz Machado
Jornal Brasileiro de Pneumologia, ISSN 1806-3713, 2017, Volume 43, Issue 2, pp. 121 - 128
Cystic fibrosis/prevention & control | Sweat | Cystic fibrosis/diagnosis
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2. Full Text Infecção por pseudomonas aeruginosa em pacientes com fibrose cística: Evidências científicas sobre o impacto clínico, diagnóstico e tratamento
by Da Silva Filho, Luiz Vicente Ribeiro Ferreira and Ferreira, Flavia de Aguiar and Reis, Francisco José Caldeira and De Britto, Murilo Carlos Amorim and Levy, Carlos Emilio and Clark, Otavio and Ribeiro, José Dirceu
Jornal Brasileiro de Pneumologia, ISSN 1806-3713, 07/2013, Volume 39, Issue 4, pp. 495 - 512
Cystic fibrosis/drug therapy | Pseudomonas aeruginosa | Evidence-based medicine | Cystic fibrosis/diagnosis
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3. Cystic fibrosis: fifty years of progress. And now what?
by Nau, Jean-Yves
Revue medicale suisse, ISSN 1660-9379, 01/2015, Volume 11, Issue 459, p. 326
Cystic Fibrosis - therapy | Pregnancy | Humans | Preimplantation Diagnosis | Cystic Fibrosis - diagnosis | Female | Cystic Fibrosis - epidemiology | Child
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4. Full Text Contribuição da análise molecular do gene regulador da condutância transmembrana na fibrose cística na investigação diagnóstica de pacientes com suspeita de fibrose cística leve ou doença atípica
by Dal'Maso, Vinícius Buaes and Mallmann, Lucas and Siebert, Marina and Simon, Laura and Saraiva-Pereira, Maria Luiza and Dalcin, Paulo de Tarso Roth
Jornal Brasileiro de Pneumologia, ISSN 1806-3713, 03/2013, Volume 39, Issue 2, pp. 181 - 189
Cystic fibrosis/genetics | Cystic fibrosis transmembrane conductance regulator | Cystic fibrosis/diagnosis
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5. Full Text Cystic fibrosis: course of management in Algeria
by Boukari, R and Groupe d'étude sur mucoviscidose
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 05/2015, Volume 22, Issue 5 Suppl 1, p. 5
Cystic Fibrosis - therapy | Program Development | Algeria - epidemiology | Humans | Cystic Fibrosis - diagnosis | Consanguinity | Delayed Diagnosis | Cystic Fibrosis - epidemiology | Health Priorities
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6. Cystic fibrosis in the adult patient
by Nemitz, I and Nicod, L
Revue medicale suisse, ISSN 1660-9379, 08/2013, Volume 9, Issue 395, p. 1549
Cystic Fibrosis - therapy | Prognosis | Cystic Fibrosis - genetics | Humans | Middle Aged | Quality of Life | Cystic Fibrosis - diagnosis | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Female | Mutation
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7. Cystic Fibrosis: toward a genetic treatment; Clostridium difficile versus Clostridium difficile
by Nau, Jean-Yves
Revue medicale suisse, ISSN 1660-9379, 05/2015, Volume 11, Issue 476, p. 1210
Cystic Fibrosis - therapy | Cystic Fibrosis - blood | Humans | Cystic Fibrosis Transmembrane Conductance Regulator - agonists | Spores, Bacterial | Treatment Outcome | Aminophenols - therapeutic use | Biomarkers - blood | Clostridium difficile - pathogenicity | Clostridium Infections - microbiology | Aminopyridines - therapeutic use | Cystic Fibrosis - genetics | Quinolones - therapeutic use | Cystic Fibrosis - diagnosis | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Benzodioxoles - therapeutic use | Clostridium Infections - therapy | Mutation | Drug Therapy, Combination
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8. Cystic fibrosis: despite progress, still a serious illness
by Bellon, Gabriel and Reix, Philippe
La Revue du praticien, ISSN 0035-2640, 01/2011, Volume 61, Issue 1, p. 91
Age Factors | Cystic Fibrosis - genetics | Humans | Survival Analysis | Cystic Fibrosis - diagnosis | Cystic Fibrosis - mortality | Early Diagnosis
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9. Full Text First diagnosis of cystic fibrosis in Afghanistan and description of a new mutation
by Vic, P and Manalai, GG and Labat, F and Sabet, W and Leis, A and Ferec, C
ARCHIVES DE PEDIATRIE, ISSN 0929-693X, 02/2010, Volume 17, Issue 2, pp. 180 - 181
IDENTIFICATION | PEDIATRICS | Afghanistan | Genetic Testing | Humans | Child, Preschool | Cooperative Behavior | Male | Mutation - genetics | Interdisciplinary Communication | DNA Mutational Analysis | Health Services Accessibility | Cystic Fibrosis - genetics | Cystic Fibrosis - diagnosis | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Consanguinity | Developing Countries
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10. Rare diseases:"a matter for specialists?"
by Holué, C
La Revue du praticien, ISSN 0035-2640, 01/2012, Volume 62, Issue 1, p. 81
Cystic Fibrosis - therapy | Exercise Therapy - methods | France - epidemiology | Prevalence | Delivery of Health Care - organization & administration | Humans | Treatment Outcome | Cystic Fibrosis - diet therapy | Rare Diseases | Cystic Fibrosis - epidemiology | Medicine | Interdisciplinary Communication | Specialization | Cystic Fibrosis - diagnosis | Cystic Fibrosis - rehabilitation | Infant, Newborn | Neonatal Screening - organization & administration
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11. Full Text A cystic fibrosis center in a general hospital: the Versailles experience
by Foucaud, P and Bonnel, A and Ajzenman, C and Le Monnier, A and Le Jalle, S and Borel, B
ARCHIVES DE PEDIATRIE, ISSN 0929-693X, 06/2010, Volume 17, Issue 6, pp. 727 - 728
PEDIATRICS | Cystic Fibrosis - therapy | Quality Assurance, Health Care - organization & administration | Cross-Sectional Studies | Humans | Child, Preschool | Cooperative Behavior | Infant | Cystic Fibrosis - epidemiology | Pregnancy | Interdisciplinary Communication | Referral and Consultation - organization & administration | Patient Care Team - organization & administration | Adolescent | Hospitals, Special - organization & administration | Cystic Fibrosis - diagnosis | Female | Hospitals, Pediatric - organization & administration | Hospitals, Public - organization & administration | France | Child | Infant, Newborn
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12. Cystic fibrosis
: diagnosis and protocols
by Amaral, Margarida D and Kunzelmann, Karl
2011, Methods in molecular biology, ISBN 1617791164, Volume 741-742., 2 v.
Cystic fibrosis | Diagnosis
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13. Young children with serious disorders as a result of late diagnosis of cystic fibrosis
by Merkus, P J F M and Tiddens, H A W N and Pijnenburg, M W H and Boehmer, A L M and de Jongste, J C
Nederlands tijdschrift voor geneeskunde, ISSN 0028-2162, 06/2006, Volume 150, Issue 24, p. 1362
Diagnosis, Differential | Mass Screening | Prognosis | Time Factors | Humans | Child, Preschool | Cystic Fibrosis - diagnosis | Cystic Fibrosis - complications | Child
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14. Full Text Neonatal screening of cystic fibrosis: which benefits?
by Brouard, J and Laurans, M and Arion, A and Kauffmann, D and Sevin, I and Laroche, D and Travert, G and Duhamel, JF
ARCHIVES DE PEDIATRIE, ISSN 0929-693X, 06/2005, Volume 12, Issue 6, pp. 643 - 645
SURVIVAL | PEDIATRICS | neonatal screening | clinical outcome | cystic fibrosis | Cystic Fibrosis - diagnosis | Neonatal Screening | Humans | Infant, Newborn
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15. Full Text Neonatal screening for cystic fibrosis
by Esperon, Luiz Carlos
Jornal de pediatria, ISSN 0021-7557, 03/2003, Volume 79, Issue 2, p. 193
Humans | Cystic Fibrosis - diagnosis | Neonatal Screening | Infant, Newborn
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16. Full Text Cystic fibrosis in Brazil: the pediatrician's turn
by Camargos, Paulo A M
Jornal de pediatria, ISSN 0021-7557, 09/2004, Volume 80, Issue 5, p. 344
Pediatrics | Humans | Age of Onset | Survival Analysis | Brazil | Child, Preschool | Cystic Fibrosis - diagnosis | Infant | Child
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17. Mucoviscidosis: France is heading towards biological rather than genetic screening
by Nau, Jean-Yves
Revue medicale suisse, ISSN 1660-9379, 11/2005, Volume 1, Issue 41, p. 2700
Cystic Fibrosis - blood | Cystic Fibrosis - genetics | Humans | Cystic Fibrosis - diagnosis | Neonatal Screening - methods | France | Infant, Newborn
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18. Problems posed by genetic diseases: cystic fibrosis
by Bellon, Gabriel and Reix, Philippe
La Revue du praticien, ISSN 0035-2640, 04/2006, Volume 56, Issue 8, p. 883
Cystic Fibrosis - therapy | Cystic Fibrosis - genetics | Humans | Cystic Fibrosis - diagnosis | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Mutation
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19. Full Text Cystic fibrosis: the French neonatal screening organization, preliminary results
by Munck, A and Sahler, C and Briard, M and Vidailhet, M and Farriaux, JP
ARCHIVES DE PEDIATRIE, ISSN 0929-693X, 06/2005, Volume 12, Issue 6, pp. 646 - 649
PEDIATRICS | neonatal screening | meconium ileus | CFFR analysis | immunoreactive trypsin | Mass Screening - organization & administration | Cystic Fibrosis - diagnosis | Decision Trees | France | Humans | Infant, Newborn
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20. Cystic fibrosis and neonatal screening
by Nau, Jean-Yves
Revue medicale suisse, ISSN 1660-9379, 05/2007, Volume 3, Issue 110, p. 1212
Ethics, Medical | Cystic Fibrosis - genetics | Humans | Neonatal Screening - ethics | Cystic Fibrosis - diagnosis | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Mutation | France | Infant, Newborn
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