Zobrazeno 1 - 10
of 685
pro vyhledávání: '"J, Kachaner"'
Autor:
Gianfranco Butera, J Kachaner, Damien Bonnet, Arnold Munnich, Sidi D, Massimo Chessa, Bonhoeffer P, Stanislas Lyonnet, Laurence Iserin
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Objective—To compare the morphology of the pulmonary vessels in tetralogy of Fallot or pulmonary atresia-ventricular septal defect (PA-VSD) with (del22q) and without 22q11 deletion (non-del22q). Patients—94 consecutive infants (54 with tetralogy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44189abe382ed91d1f05357439bf90cd
https://doi.org/10.1136/hrt.79.2.186
https://doi.org/10.1136/hrt.79.2.186
Publikováno v:
European Radiology. 7:S127-S130
Iopentol (Imagopaque, Nycomed Imaging AS, Oslo, Norway) 300 mg.l/ml was compared with iopromide (Ultravist, Schering AG. Berlin, Germany) 300 mg I/ml in pediatric angiocardiography in 97 children (48 and 49 patients, mean age 2.8 and 4.1 years in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a518bfeaa6cf3bc0ed62e58be8fd541b
https://doi.org/10.1007/pl00006878
https://doi.org/10.1007/pl00006878
Autor:
P, Le Coz, J, Kachaner
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 17
Every medical decision-making is to do justice to the one who suffers and who considers his pain as nonsensical. This requirement falls into 3 universal ethical principles, governing the patient-doctor relationship: the autonomy of the person even if
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a493deb3aeb74f788dcd2eefb6090e3
https://pubmed.ncbi.nlm.nih.gov/20172455
https://pubmed.ncbi.nlm.nih.gov/20172455
Autor:
Claude Planché, J. Kachaner, Alain Serraf, Chambran P, G. Blaysat, Jacqueline Bruniaux, Jérôme Petit, François Lacour-Gayet, Jean Losay
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 100:808-816
From Jan. 1, 1983, to Jan. 1, 1988, 66 consecutive neonates with coarctation and severe hypoplasia of the transverse arch underwent coarctation repair by resection of the coarctation and reconstruction of the aortic arch. Mean age at operation was 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15a31ee10f12b12b1502a29595dc1f15
https://doi.org/10.1016/s0022-5223(19)36822-9
https://doi.org/10.1016/s0022-5223(19)36822-9
Publikováno v:
Journal de Pédiatrie et de Puériculture. 3:258-266
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a94b3896259e093ef9a8b115a5b2ae8c
https://doi.org/10.1016/s0987-7983(05)80060-x
https://doi.org/10.1016/s0987-7983(05)80060-x
Autor:
J, Kachaner
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 98(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::484290959e8bffa01a6fa76e4e002f9d
https://pubmed.ncbi.nlm.nih.gov/15966590
https://pubmed.ncbi.nlm.nih.gov/15966590
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::337f11ef890254f06a274481a97703e7
https://pubmed.ncbi.nlm.nih.gov/14509803
https://pubmed.ncbi.nlm.nih.gov/14509803
Publikováno v:
Heart (British Cardiac Society). 89(2)
Hypertrophic cardiomyopathy (HCM) carries an increased risk of sudden death, especially in children and young adults. We investigated heart rate variability (HRV) in children with HCM, in order to evaluate its prognostic value. Seventeen patients (9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bdf9dedac64482a6a05850fbee0871f
https://pubmed.ncbi.nlm.nih.gov/12527679
https://pubmed.ncbi.nlm.nih.gov/12527679
Autor:
J, Kachaner
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 9
A congenital heart disease is said intractable when the only options are either heart transplantation or a complex palliative programme including several interventions leading to a mid-term Fontan-type circulation. The latter uses the single ventricl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bbec53a60e68bf1d8c302f042d406ce5
https://pubmed.ncbi.nlm.nih.gov/11998413
https://pubmed.ncbi.nlm.nih.gov/11998413
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 94(5)
Dilated cardiomyopathy is a rare and unrecognised complication of propionic acidosis. It usually progresses to chronic cardiac failure with a poor prognosis. The authors report three cases of cardiomyopathy due to this condition. One of the children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a73005b821a2f3dd0a7a5c7947e2b57
https://pubmed.ncbi.nlm.nih.gov/11434026
https://pubmed.ncbi.nlm.nih.gov/11434026