J. Chazalette

发表

Production of elastase, exotoxin A, and alkaline protease in sputa during pulmonary exacerbation of cystic fibrosis in patients chronically infected by Pseudomonas aeruginosa

M. Bally, M. Jaffar-Bandjee, A. Lazdunski, 1995, Journal of clinical microbiology.

Imaging changes in the pancreas in cystic fibrosis: a retrospective evaluation of 55 cases seen over a period of 9 years.

C. Férec, J. Carrère, J. Chazalette, 2000, Journal of pediatric gastroenterology and nutrition.

Complex allele [-102T>A+S549R(T>G)] is associated with milder forms of cystic fibrosis than allele S549R(T>G) alone

M. Patton, M. Claustres, D. Bozon, 1999, Human Genetics.

Lung Transplantation

B. Kreitmann, J. Camboulives, J. Chazalette, 2003, Steinkopff.

Behaviour of serum immunoreactive trypsin after serum activation by enterokinase in normal and cystic fibrosis patients. Evidence of a trypsin-alpha 1-proteinase inhibitor complex in some cystic fibrosis patients.

C. Figarella, J. Carrère, J. Chazalette, 1989, Biochimica et biophysica acta.

[Benign intracranial hypertension in children].

J. Chazalette, 1971, Pediatrie.

A Double-Blind Comparison of RU-41740 (‘Biostim’) and Placebo in Recurrent Upper Respiratory Tract Infections in Children with Cystic Fibrosis

G. Lenoir, J. Derelle, D. Olive, 1991 .

[Abdominal aorta aneurysm during Bourneville's tuberous sclerosis].

P. Mollard, F. Freycon, P. Guibaud, 1971, Pediatrie.

Chronic airway colonization by Penicillium emersonii in a patient with cystic fibrosis.

J. Bouchara, J. Carrère, D. Chabasse, 1999, Medical mycology.

FATTY-ACID COMPOSITION OF SERUM-LECITHINS IN CYSTIC-FIBROSIS PATIENTS WITHOUT STEATORRHŒA

C. Galabert, J. Chazalette, M. Filliat, 1978, The Lancet.

Fatty-acid composition of serum-lecithins in cystic-fibrosis patients without steatorrhoea.

C. Galabert, J. Chazalette, M. Filliat, 1978, Lancet.

[Proteins of bronchial secretions in mucoviscidosis. Role of infection].

J. Tournier, P. Sadoul, J. Jacquot, 1983, Bulletin europeen de physiopathologie respiratoire.

Bronchopulmonary mycoses in cystic fibrosis: results of a five-year longitudinal study.

J. Bouchara, J. Carrère, D. Chabasse, 2000 .

Clinical Significance of Scedosporium apiospermum in Patients with Cystic Fibrosis

J. Bouchara, J. Carrère, D. Chabasse, 2000, European Journal of Clinical Microbiology and Infectious Diseases.

Fungal colonization and immune response to fungi in cystic fibrosis

J. Bouchara, J. Carrère, D. Chabasse, 1995 .

Effects of ursodeoxycholic acid on liver function in patients with cystic fibrosis and chronic cholestasis.

C. Figarella, C. Galabert, J. Montet, 1992, The Journal of pediatrics.

Pharmacokinetics of cyclosporine A in bilateral lung transplantation candidates with cystic fibrosis.

P. Bertault-peres, A. Durand, M. Noirclerc, 1990, Transplantation proceedings.

Partial splenectomy—worth the risk

J. Chazalette, J. Feigelson, D. Louis, 2003, Archives of disease in childhood.

40 kilobase deletion (CF 40 kb del 4–10) removes exons 4 to 10 of the cystic fibrosis transmembrane conductance regulator gene

D. Bozon, J. Chazalette, M. Mathieu, 1998, Human mutation.

Cystic Fibrosis and Portal Hypertension Interest of Partial Splenectomy

J. Chazalette, D. Louis, Chazalette Jp, 1993, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Partial splenectomy for portal hypertension in cystic fibrosis related liver disease

P. Reix, I. Durieu, G. Bellon, 2007, Pediatric pulmonology.

Mutation analysis in 600 French cystic fibrosis patients.

D. Bozon, R. Gilly, M. Mathieu, 1994, Journal of medical genetics.

Lung transplantation in cystic fibrosis

A. Ribéri, D. Métras, B. Kreitmann, 2003 .

Improvement of cystic fibrosis airway mucus transportability by recombinant human DNase is related to changes in phospholipid profile.

J. Zahm, C. Galabert, C. Großkopf, 1998, American journal of respiratory and critical care medicine.

Lysinuric protein intolerance. Urinary amino acid excretion at 2 and 9 days of age

M. Candito, F. Sebag, M. Mathieu, 1994, Journal of Inherited Metabolic Disease.

[Double lung transplantation. Report of the 1st French case and comments on the 5 subsequent cases].

J. Dumon, D. Métras, J. Camboulives, 1989, Annales de Chirurgie.