Zobrazeno 1 - 10
of 388
pro vyhledávání: '"M, Odievre"'
Publikováno v:
Archives de Pédiatrie. 10:689-693
Resume Objectifs. – Evaluer l’activite telephonique en pediatrie ambulatoire. Methodes. – Soixante dix-neuf pediatres appartenant a un organisme de formation medicale continue (l’Arepege) ont recueilli d’une facon prospective, les appels te
Autor:
C VANDERVEERE, M SINAASAPPEL, A MCDONAGH, P ROSENTHAL, P LABRUNE, M ODIEVRE, J FEVERY, J OTTE, P MCCLEAN, G BURK
Publikováno v:
Hepatology. 24:311-315
Publikováno v:
Journal de Chimie Physique. 92:1797-1800
We have developed a method for the evaluation of the muscle glycogen content by natural abundance C13 NMR and we here evaluate its diagnostic value on a large number of muscle diseases (20 glycogenoses and 42 other myopathies) and 8 normal subjects.
Autor:
M. Odievre
Publikováno v:
Journal of Inherited Metabolic Disease. 14:526-530
Some clinical clues should alert paediatricians to the possibility of metabolic liver diseases. They can be classified into three categories: (i) Manifestations due to hepatocellular necrosis, acute or subacute, which can reveal galactosaemia, heredi
Autor:
Shimon Moses, Gerrit Smit, M. Odievre, J. V. Leonard, Kurt Ullrich, J Fernandes, E. E. Matthews
Publikováno v:
Journal of Inherited Metabolic Disease. 13:411-418
In this retrospective study from five centres, 139 patients over 10 years of age with glycogen storage disease types I, III, VI and IX are described. Almost half of the patients with glycogen storage disease type Ia had retarded growth and most had h
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 10:316-321
Twenty-two full-term infants, nine asymptomatic and 13 symptomatic for chronic digestive problems, had long-term (mean = 21 h) esophageal pH monitoring. All children were observed in strictly standardized conditions including meals and body position.
Autor:
R. Gitzelmann, G. Mascali, Nicholas C.P. Cross, M. Vidailhet, Valentino Romano, C. Dazzo, M. Odievre, Gianfranco Sebastio, Beat Steinmann, R. de Franchis, Dean R. Tolan, Timothy M. Cox, Corrado Romano, Salvatore Musumeci, C. Grégori
Publikováno v:
The Lancet. 335:306-309
The molecular basis of hereditary fructose intolerance (HFI) was studied in 50 subjects (41 pedigrees, 82 apparently independent mutant alleles of aldolase B) by direct analysis of aldolase B genes amplified by means of the polymerase chain reaction.
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 10(8)
To assess the amount of telephone activity in outpatient pediatric practice.Seventy-nine pediatricians belonging to a continuing medical education group (Arepege) prospectively recorded data about all the telephone calls they took personally for 3 da
Publikováno v:
Acta Paediatrica. 79:707-709
A premature infant had three episodes of enterocolitis-like symptoms during the first three months of life. Brucella melitensis was isolated in a prolonged blood culture on day 85. The clinical manifestations disappeared under treatment and did not r
Publikováno v:
Annales de dermatologie et de venereologie. 120(11)