Search Results - "Labarthe F"

HIGHLY RESPONSIVE AND ACCURATE TEMPERATURE MEASUREMENTS IN ORTHOGONAL CUTTING THROUGH INNOVATIVE SINGLE LEG THERMOCOUPLE.

Authors: Hamm, I. Rossi, F. Poulachon, G. et al.

Source: MM Science Journal; Jul2021, p4660-4666, 7p

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Signes néonatals des maladies héréditaires du métabolisme

Alternate Title: Clinical presentation of inborn metabolic diseases in the neonatal period

Authors: Labarthe, F. Tardieu, M. de Parscau, L. et al.

Source: Archives de Pédiatrie. Sep2012, Vol. 19 Issue 9, p953-958. 6p.

Enzymothérapie substitutive chez un nourrisson atteint de maladie de Pompe : évolution cardiologique

Alternate Title: Enzyme replacement therapy in a boy with infantile Pompe disease: Cardiac follow-up

Authors: Bonnefoy, R. Labarthe, F. Paoli, F. et al.

Source: Archives de Pédiatrie. Dec2008, Vol. 15 Issue 12, p1760-1764. 5p.

Fish-oil supplementation reduces stimulation of plasma glucose fluxes during exercise in untrained males.

Authors: Delarue J Labarthe F Cohen R

Source: British Journal of Nutrition. Oct2003, Vol. 90 Issue 4, p777-786. 10p.

Conduite à tenir devant une cardiomyopathie ou un trouble du rythme

Alternate Title: Management of metabolic cardiomyopathy and conduction defects in children

Authors: Labarthe, F. Paoli, F. Chantepie, A.

Source: Archives de Pédiatrie. Jun2009, Vol. 16 Issue 6, p643-645. 3p.

Nouvelles approches thérapeutiques des anomalies de la β-oxydation mitochondriale

Alternate Title: New therapeutic approaches in mitochondrial fatty acid oxidation disorders

Authors: Labarthe, F.¹ labarthe@med.univ-tours.fr

Source: Archives de Pédiatrie. May2008, Vol. 15 Issue 5, p608-610. 3p.

767 Octanoate, a medium-chain fatty acid, improves the response to stress in spontaneously hypertensive rat hearts

Authors: Labarthe, F. Bouchard, B. Khairallah, M. et al.

Source: European Journal of Heart Failure. Supplements. Jun2004, Vol. 2 Issue 1, p166. 1p.

Encéphalopathie néonatale: quand évoquer une maladie métabolique héréditaire ?

Alternate Title: Neonatal encephalopathy: when to suspect an inborn error of metabolism?

Authors: Tardieu, M. Favrais, G. Labarthe, F.

Source: Revue de Médecine Périnatale. Jun2013, Vol. 5 Issue 2, p99-105. 7p.

Quand penser à une maladie métabolique devant une hypoglycémie en maternité ?

Authors: Labarthe, F.¹ labarthe@med.univ-tours.fr

Source: Archives de Pédiatrie. May2014 Supplement 1, Vol. 21 Issue 5, p200-201. 2p.

Troubles du comportement : les maladies métaboliques par intoxication

Alternate Title: Behavior and psychiatric symptoms: intoxication diseases in inborn errors of metabolism

Authors: Labarthe, F. Blasco, H. Maillot, F.

Source: Archives de Pédiatrie. Jun2010, Vol. 17 Issue 6, p800-801. 2p.

Maladies métaboliques en période néonatale : comment traiter durant les 48 premières heures ?

Authors: Labarthe, F. Tardieu, M. Benoist, J.-F. et al.

Source: Archives de Pédiatrie. Jun2012 Supplement, Vol. 19 Issue 6s1, pH161-H162. 0p.

Le priapisme : une complication pédiatrique grave de la maladie de Fabry

Alternate Title: Priapism: a severe paediatric complication of Fabry disease

Authors: Labarthe, F. de Bodman, C. Maruani, A. et al.

Source: Revue de Médecine Interne. Dec2010 Supplement 2, Vol. 31, pS217-S219. 0p.

400 Decreased bone mineral density in adolescents and young adults with cystic fibrosis: prevalence and risk factors

Authors: Jourdain, A. Labarthe, F. Willot, S. et al.

Source: Journal of Cystic Fibrosis. Jul2007, Vol. 6, pS98-S98. 1p.

Coqueluche maligne et exsanguino-transfusion.

Authors: Chantreuil, J. Fakhri, N. Labarthe, F. et al.

Source: Archives de Pédiatrie. Jan2015, Vol. 22 Issue 1, p84-87. 4p.

Variabilité clinique et conduite diagnostique des cytopathies mitochondriales : à propos d’une série de 18 cas pédiatriques

Alternate Title: Clinical variability and diagnosis steps in childhood mitochondrial disease

Authors: Mercier, S. Josselin de Wasch, M. Labarthe, F. et al.

Source: Archives de Pédiatrie. Apr2009, Vol. 16 Issue 4, p322-330. 9p.

Successful treatment with fumagillin of the first pediatric case of digestive microsporidiosis in a liver-kidney transplant.

Authors: Desoubeaux, G. Maakaroun‐Vermesse, Z. Lier, C. et al.

Source: Transplant Infectious Disease. Dec2013, Vol. 15 Issue 6, pE250-E259. 10p.

Validation of plasma amino acid profile using UHPLC-mass spectrometer (QDa) as a screening method in a metabolic disorders reference centre: Performance and accreditation concerns.

Authors: Bruno, C. Veyrat-Durebex, C. Lumbu Lukuntonda, C.H. et al.

Source: Clinical Biochemistry. Jun2021, Vol. 92, p34-45. 12p.

SFP-P126 – Sport et exercice physique – Place de l’activité physique dans la vie quotidienne des adolescents

Authors: Bodet, E. Willot, S. Labarthe, F. et al.

Source: Archives de Pédiatrie. May2008, Vol. 15 Issue 5, p980-981. 2p.

Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M).

Authors: Chabrol, B. Jacquin, P. Francois, L. et al.

Source: Archives de Pédiatrie. Jul2018, Vol. 25 Issue 5, p344-349. 6p.