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philippe labrune
philippe labrune
professeur de pédiatrie
在 aphp.fr 的电子邮件经过验证
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引用次数
引用次数
年份
Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I)
J Rake, G Visser, P Labrune, JV Leonard, K Ullrich, PG Smit
European journal of pediatrics 161, S20-S34, 2002
4662002
Molecular classification of hepatocellular adenoma associates with risk factors, bleeding, and malignant transformation
JC Nault, G Couchy, C Balabaud, G Morcrette, S Caruso, JF Blanc, ...
Gastroenterology 152 (4), 880-894. e6, 2017
3842017
Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literature
P Labrune, P Trioche, I Duvaltier, P Chevalier, M Odièvre
Journal of pediatric gastroenterology and nutrition 24 (3), 276-279, 1997
3791997
No perinatal HIV-1 transmission from women with effective antiretroviral therapy starting before conception
L Mandelbrot, R Tubiana, J Le Chenadec, C Dollfus, A Faye, E Pannier, ...
Clinical Infectious Diseases 61 (11), 1715-1725, 2015
3602015
CHARGE syndrome: report of 47 cases and review
AL Tellier, V Cormier‐Daire, V Abadie, J Amiel, S Sigaudy, D Bonnet, ...
American journal of medical genetics 76 (5), 402-409, 1998
3141998
Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies
A Fischer, J Provot, JP Jais, A Alcais, N Mahlaoui, D Adoue, N Aladjidi, ...
Journal of Allergy and Clinical Immunology 140 (5), 1388-1393. e8, 2017
3122017
Glucose-6-phosphatase deficiency
R Froissart, M Piraud, AM Boudjemline, C Vianey-Saban, F Petit, ...
Orphanet journal of rare diseases 6, 1-12, 2011
2802011
Guidelines for management of glycogen storage disease type I–European Study on Glycogen Storage Disease Type I (ESGSD I)
J Rake, G Visser, P Labrune, JV Leonard, K Ullrich, PG Smit
European journal of pediatrics 161, S112-S119, 2002
2652002
Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type Ib: results of the European Study on Glycogen Storage Disease type I
G Visser, JP Rake, J Fernandes, P Labrune, JV Leonard, S Moses, ...
The Journal of pediatrics 137 (2), 187-191, 2000
2592000
Neonatal characteristics in rapidly progressive perinatally acquired HIV-1 disease
MJ Mayaux, M Burgard, JP Teglas, J Cottalorda, A Krivine, F Simon, ...
Jama 275 (8), 606-610, 1996
2151996
International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up
L Welling, LE Bernstein, GT Berry, AB Burlina, F Eyskens, M Gautschi, ...
Journal of inherited metabolic disease 40, 171-176, 2017
2072017
Current therapy for Crigler–Najjar syndrome type 1: report of a world registry
CN Van der Veere, M Sinaasappel, AF McDonagh, P Rosenthal, ...
Hepatology 24 (2), 311-315, 1996
1951996
Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome
CP Sentner, IJ Hoogeveen, DA Weinstein, R Santer, E Murphy, ...
Journal of inherited metabolic disease 39, 697-704, 2016
1652016
Effectiveness of chest physiotherapy in infants hospitalized with acute bronchiolitis: a multicenter, randomized, controlled trial
V Gajdos, S Katsahian, N Beydon, V Abadie, L De Pontual, S Larrar, ...
PLoS medicine 7 (9), e1000345, 2010
1552010
Molecular characterization of hepatocellular adenomas developed in patients with glycogen storage disease type I
J Calderaro, P Labrune, G Morcrette, S Rebouissou, D Franco, S Prévot, ...
Journal of Hepatology 58 (2), 350-357, 2013
1542013
Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy
P Labrune, C Lacroix, F Goutieres, J De Laveaucoupet, P Chevalier, ...
Neurology 46 (5), 1297-1297, 1996
1471996
GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation
JC Nault, M Fabre, G Couchy, C Pilati, E Jeannot, JT Van Nhieu, ...
Journal of hepatology 56 (1), 184-191, 2012
1412012
Consensus guidelines for management of glycogen storage disease type 1b—European Study on Glycogen Storage Disease Type 1
G Visser, JP Rake, P Labrune, JV Leonard, S Moses, K Ullrich, U Wendel, ...
European journal of pediatrics 161, S120-S123, 2002
1402002
The natural history of classic galactosemia: lessons from the GalNet registry
ME Rubio-Gozalbo, M Haskovic, AM Bosch, B Burnyte, AI Coelho, ...
Orphanet journal of rare diseases 14, 1-11, 2019
1322019
Successful treatment of severe cardiomyopathy in glycogen storage disease type III With D, L-3-hydroxybutyrate, ketogenic and high-protein diet
V Valayannopoulos, F Bajolle, JB Arnoux, S Dubois, N Sannier, ...
Pediatric Research 70 (6), 638-641, 2011
1322011
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