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François Feillet

Research Profile

Disorders

Phenylketonurias

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Celine Chery; Jean Devignes; François Feillet; Jean-Noel Freund; Philippe Gérard; Isabelle Gross; Rosa-Maria Guéant-Rodriguez; Alain Hehn; Elise Jeannesson; Thomas Josse; Nadir Mrabet; OUSSALAH Abderrahim; Laurent Peyrin-Biroulet; Jean-Marc Alberto; Cyril Besseau; Frédéric Bourgaud; Jean-Louis Guéant
Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant.
Stephanie Bourion-Bedes; François Feillet; Francis Guillemin; Cedric Baumann; Chrystele Bonnemains; Solenn Kermarrec; Fabienne Ligier; Bernard Kabuth
Prognostic value of early therapeutic alliance in weight recovery: a prospective cohort of 108 adolescents with anorexia nervosa.
Raphaël Teissier; Murielle Assoun; Aline Cano; Loïc de Parscau; François Feillet; Alain Fouilhoux; Karine Mention; Emmanuel Nowak; Emmanuel Oger; Hélène Ogier
Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation.

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All Publications

2013: Celine Chery; Jean Devignes; François Feillet; Jean-Noel Freund; Philippe Gérard; Isabelle Gross; Rosa-Maria Guéant-Rodriguez; Alain Hehn; Elise Jeannesson; Thomas Josse; Nadir Mrabet; OUSSALAH Abderrahim; Laurent Peyrin-Biroulet; Jean-Marc Alberto; Cyril Besseau; Frédéric Bourgaud; Jean-Louis Guéant
Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant.
Biochimie 2013;95(5):995-1001.
2013: Stephanie Bourion-Bedes; François Feillet; Francis Guillemin; Cedric Baumann; Chrystele Bonnemains; Solenn Kermarrec; Fabienne Ligier; Bernard Kabuth
Prognostic value of early therapeutic alliance in weight recovery: a prospective cohort of 108 adolescents with anorexia nervosa.
The Journal of adolescent health : official publication of the Society for Adolescent Medicine 2013;52(3):344-50.
2012: Raphaël Teissier; Murielle Assoun; Aline Cano; Loïc de Parscau; François Feillet; Alain Fouilhoux; Karine Mention; Emmanuel Nowak; Emmanuel Oger; Hélène Ogier
Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation.
Journal of inherited metabolic disease 2012;35(6):993-9.
2012: Oriane Leuret; Sylvie Odent; Magalie Barth; Loïc de Parscau; Didier Eyer; François Feillet; Brigitte Gilbert-Dussardier; Alice Kuster; F Labarthe
Efficacy and safety of BH4 before the age of 4 years in patients with mild phenylketonuria.
Journal of inherited metabolic disease 2012;35(6):975-81.
2012: François Feillet; R Garnotel; E Jeannesson; F Labarthe; H Ogier; V Valayanopoulos; A Vassault; Christine Vianey-Saban; C Aquaviva; J Baruteau; G Briand; B Chabrol; David Cheillan; P de Lonlay; D Dobbelaere
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2012;19(2):184-93.
2011: Farès Namour; Wolfgang Sperl; Sandra Audonnet; Celine Chery; Gabriele Dobrovoljski; François Feillet; JL Gueant
Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7.
Haematologica 2011;96(11):1715-9.
2011: Antoine Kimmoun; Nicolas Dessalles; François Feillet; Alain Gerard; Gaittha Munagamage; Bruno Levy
Unexpected awakening from comatose thyroid storm after a single intravenous injection of L-carnitine.
Intensive care medicine 2011;37(10):1716-7.
2011: Thierry Forges; Patricia Monnier; Bruno Leheup; David Cheillan; Michèle Brivet; Aurelio Barbarino; Jean-Louis Guéant; François Feillet
Ovarian tissue cryopreservation and subsequent spontaneous pregnancies in a patient with classic galactosemia.
Fertility and sterility 2011;95(1):290.e1-3.
2010: D Brajon; P Carassou; L Pruna; François Feillet; P Kaminsky
[Ornithine transcarbamylase deficiency in adult].
La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne 2010;31(10):709-11.
2010: François Feillet; Francjan J van Spronsen; Anita MacDonald; Friedrich K Trefz; Mübeccel Demirkol; Marcello Giovannini; Amaya Bélanger-Quintana; Nenad Blau
Challenges and pitfalls in the management of phenylketonuria.
Pediatrics 2010;126(2):333-41.
2010: Philippa B Mills; Emma J Footitt; Kevin A Mills; Karin Tuschl; Sarah Aylett; Sophia Varadkar; Cheryl Hemingway; Neil Marlow; Janet Rennie; Peter Baxter; Olivier Dulac; Rima Nabbout; William J Craigen; Bernhard Schmitt; François Feillet; Ernst Christensen; Pascale de Lonlay; Mike G Pike; M Imelda Hughes; Eduard A Struys; Cornelis Jakobs; Sameer M Zuberi; Peter T Clayton
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency).
Brain : a journal of neurology 2010;133(Pt 7):2148-59.
2010: Thierry Forges; Céline Chery; Sandra Audonnet; François Feillet; Jean-Louis Gueant
Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients.
Molecular genetics and metabolism 2010;100(2):143-8.
2010: Carole Giraud; Jeanne Dussau; Emilie Azouguene; François Feillet; Jean Philippe Puech; Catherine Caillaud
Rapid identification of HEXA mutations in Tay-Sachs patients.
Biochemical and biophysical research communications 2010;392(4):599-602.
2010: Nenad Blau; Amaya Bélanger-Quintana; Mübeccel Demirkol; François Feillet; Marcello Giovannini; Anita MacDonald; Friedrich K Trefz; Francjan J van Spronsen
Management of phenylketonuria in Europe: survey results from 19 countries.
Molecular genetics and metabolism 2010;99(2):109-15.
2010: François Feillet; Anita MacDonald; Danielle Hartung Perron; Barbara Burton
Outcomes beyond phenylalanine: an international perspective.
Molecular genetics and metabolism 2010;99 Suppl 1():S79-85.
2009: Anh T Nguyen; Aude Bressenot; Simona Manolé; Marie A Galloy; Jean P Bronowicki; Michel Vidailhet; François Feillet; Michel Claudon
Contrast-enhanced ultrasonography in patients with glycogen storage disease type Ia and adenomas.
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine 2009;28(4):497-505.
2009: Nenad Blau; Amaya Bélanger-Quintana; Mübeccel Demirkol; François Feillet; Marcello Giovannini; Anita MacDonald; Friedrich K Trefz; Francjan J van Spronsen
Optimizing the use of sapropterin (BH(4)) in the management of phenylketonuria.
Molecular genetics and metabolism 2009;96(4):158-63.
2009: Damien Galanaud; Ayman Tourbah; Stéphane Lehéricy; Nathalie Leveque; Bénédicte Heron; Thierry Billette de Villemeur; Nathalie Guffon; François Feillet; Nicole Baumann; marie T vanier; Frédéric Sedel
24 month-treatment with miglustat of three patients with Niemann-Pick disease type C: follow up using brain spectroscopy.
Molecular genetics and metabolism 2009;96(2):55-8.
2008: Cyril Gitiaux; Emmanuel Roze; Kiyoka Kinugawa; Constance Flamand-Rouvière; Nathalie Boddaert; Emmanuelle Apartis; Vassili Valayannopoulos; Guy Touati; Jacques Motte; David Devos; Karine Mention; Dries Dobbelaere; Diana Rodriguez; Agathe Roubertie; Brigitte Chabrol; François Feillet; Marie Vidailhet; Nadia Bahi-Buisson
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients.
Movement disorders : official journal of the Movement Disorder Society 2008;23(16):2392-7.
2008: Nadia Bahi-Buisson; Emmanuel Roze; Carlo Dionisi; Fabienne Escande; Vassili Valayannopoulos; François Feillet; Claudine Heinrichs; Bernadette Chadefaux-Vekemans; Bernard Dan; Pascale de Lonlay
Neurological aspects of hyperinsulinism-hyperammonaemia syndrome.
Developmental medicine and child neurology 2008;50(12):945-9.
2008: Antoine Kimmoun; Georges Abboud; Jean Strazeck; Marc Merten; Jean-Louis Guéant; François Feillet
Acute decompensation of isovaleric acidemia induced by Graves' disease.
Intensive care medicine 2008;34(12):2315-6.
2008: François Feillet; Céline Chery; Fares Namour; Antoine Kimmoun; Elisabeth Favre; Elisabeth Lorentz; Shyue-Fang Battaglia-Hsu; Jean-Louis Guéant
Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemia.
Early human development 2008;84(9):561-7.
2008: Anne Davit-Spraul; Catherine Costa; Mokhtar Zater; Dalila Habes; Jacques Berthelot; Pierre Broué; François Feillet; Olivier Bernard; Philippe Labrune; Christiane Baussan
Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutations.
Molecular genetics and metabolism 2008;94(4):443-7.
2008: François Feillet; Marc Merten; Shyue-Fang Battaglia-Hsu; Daniel Rabier; Keiko Kobayashi; Jean Straczek; Michèle Brivet; Elisabeth Favre; Jean-Louis Guéant
Evidence of cataplerosis in a patient with neonatal classical galactosemia presenting as citrin deficiency.
Journal of hepatology 2008;48(3):517-22.
2008: François Feillet; Lorne Clarke; Concetta Meli; Mark Lipson; Andrew A Morris; Paul Harmatz; Diane R Mould; Bruce Green; Alex Dorenbaum; Marcello Giovannini; Erik Foehr
Pharmacokinetics of sapropterin in patients with phenylketonuria.
Clinical pharmacokinetics 2008;47(12):817-25.
2008: Marcel R Zurflüh; Johannes Zschocke; Martin Lindner; François Feillet; Céline Chery; Alberto Burlina; Raymond C Stevens; Beat Thöny; Nenad Blau
Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
Human mutation 2008;29(1):167-75.
2007: B K Burton; D K Grange; A Milanowski; G Vockley; François Feillet; Eric A Crombez; Véronique Abadie; Cary O Harding; Stephen D Cederbaum; D Dobbelaere; A Smith; Alejandro Dorenbaum
The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.
Journal of inherited metabolic disease 2007;30(5):700-7.
2007: Harvey L Levy; Andrzej Milanowski; Anupam Chakrapani; Maureen Cleary; Philip Lee; Friedrich K Trefz; Chester Whitley; François Feillet; Annette S Feigenbaum; Judith D Bebchuk; Heidi Christ-Schmidt; Alejandro Dorenbaum
Efficacy of sapropterin dihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III randomised placebo-controlled study.
Lancet 2007;370(9586):504-10.
2007: Hélène Ogier de Baulny; Véronique Abadie; François Feillet; Loïc de Parscau
Management of phenylketonuria and hyperphenylalaninemia.
The Journal of nutrition 2007;137(6 Suppl 1):1561S-1563S; discussion 1573S-1575S.
2006: MA Cleary; François Feillet; Fiona J White; Michel Vidailhet; A MacDonald; A Grimsley; Nicole Maurin; Hélène Ogier de Baulny; P J Rutherford
Randomised controlled trial of essential fatty acid supplementation in phenylketonuria.
European journal of clinical nutrition 2006;60(7):915-20.
2006: François Feillet
[Phenylketonuria].
Presse médicale (Paris, France : 1983) 2006;35(3 Pt 2):502-8.
2005: François Feillet
[Height and weight growth delay].
La Revue du praticien 2005;55(20):2285-90.
2005: Hugues Lucron; M Chipaux; Gilles Bosser; S Le Tacon; Jean-Paul Lethor; François Feillet; Guillaume Burger; Pierre Monin; François Marçon
[Complications of prostaglandin E1 treatment of congenital heart disease in paediatric medical intensive care].
Archives des maladies du coeur et des vaisseaux 2005;98(5):524-30.
2005: Véronique Abadie; Jacques Berthelot; François Feillet; Nicole Maurin; A Mercier; H Ogier de Baulny; Loïc de Parscau
[Management of phenylketonuria and hyperphenylalaninemia: the French guidelines].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2005;12(5):594-601.
2004: François Feillet; Véronique Abadie; Jacques Berthelot; Nicole Maurin; Hélène Ogier; Michel Vidailhet; Jean-Pierre Farriaux; Loïc de Parscau
Maternal phenylketonuria: the French survey.
European journal of pediatrics 2004;163(9):540-6.
2004: Hugues Lucron; Gilles Bosser; Jean-Paul Lethor; Danièle Sommelet; François Feillet; Guillaume Burger; Pierre Monin; François Marçon
[Kawasaki disease in newborns and infants: refractory forms to immunoglobulin therapy].
Archives des maladies du coeur et des vaisseaux 2004;97(5):522-8.
2004: Emile K Amouzou; Nicodème W Chabi; Charles E Adjalla; Rosa-Maria Rodriguez-Guéant; François Feillet; Christian Villaume; Ambaliou Sanni; Jean-Louis Guéant
High prevalence of hyperhomocysteinemia related to folate deficiency and the 677C-->T mutation of the gene encoding methylenetetrahydrofolate reductase in coastal West Africa.
The American journal of clinical nutrition 2004;79(4):619-24.
2003: François Feillet; G Steinmann; C Vianey-Saban; Christian de Chillou; Nicolas Sadoul; E Lefebvre; Michel Vidailhet; Pierre-Edouard Bollaert
Adult presentation of MCAD deficiency revealed by coma and severe arrythmias.
Intensive care medicine 2003;29(9):1594-7.
2003: François Feillet
[Metabolic emergencies: main visceral features excluding neurologic features].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2003;10 Suppl 1():49s-51s.
2003: Nicolas Sirvent; Etienne Bérard; Pascal Chastagner; François Feillet; Karin Wagner; Danièle Sommelet
Hypothalamic dysfunction associated with neuroblastoma: evidence for a new Paraneoplastic syndrome?
Medical and pediatric oncology 2003;40(5):326-8.
2001: Véronique Abadie; Jacques Berthelot; François Feillet; Nicole Maurin; A Mercier; Hélène Ogier de Baulny; Loïc de Parscau
Neonatal screening and long-term follow-up of phenylketonuria: the French database.
Early human development 2001;65(2):149-58.
2000: CD Capo-chichi; François Feillet; Jean-Louis Guéant; K Amouzou; N Zonon; Ambaliou Sanni; E Lefebvre; K Assimadi; Michel Vidailhet
Concentrations of riboflavin and related organic acids in children with protein-energy malnutrition.
The American journal of clinical nutrition 2000;71(4):978-86.
2000: CD Capo-chichi; Jean-Louis Guéant; François Feillet; Farès Namour; Michel Vidailhet
Analysis of riboflavin and riboflavin cofactor levels in plasma by high-performance liquid chromatography.
Journal of chromatography. B, Biomedical sciences and applications 2000;739(1):219-24.
1999: François Feillet; A Borsa; Pierre Monin
[Intraosseous approach, yes but...].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1999;6(12):1349-50.
1999: V Procaccio; B Mousson; Réjane Beugnot; Hervé Duborjal; François Feillet; G Putet; I Pignot-Paintrand; A Lombès; R De Coo; H Smeets; Joël Lunardi; Jean-Paul Issartel
Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.
The Journal of clinical investigation 1999;104(1):83-92.
1999: François Feillet; B Mousson; Y Grignon; J V Leonard; Michel Vidailhet
Necrotizing encephalopathy and macrocephaly with mitochondrial complex I deficiency.
Pediatric neurology 1999;20(4):305-8.
1998: François Feillet; B Levy; Gilles Bosser; J Derelle; Pierre-Edouard Bollaert; Pierre Monin
Severe hypoxaemia induced by an intrapulmonary arterio-venous fistula: indication for nitric oxide.
European journal of pediatrics 1998;157(12):1036.
1998: R Gauthier; CA Beyaert; François Feillet; R Peslin; Pierre Monin; François Marchal
Respiratory oscillation mechanics in infants with bronchiolitis during mechanical ventilation.
Pediatric pulmonology 1998;25(1):18-31.
1993: François Feillet; H J Parra; K Kamian; J M Bard; J C Fruchart; M Vidailhet
Lipoprotein metabolism in marasmic children of northern Mauritania.
The American journal of clinical nutrition 1993;58(4):484-8.
1993: François Feillet; C Karcher; M Vidailhet; Pierre Monin
[Treatment of a respiratory form of myasthenia with venoglobulins combined with anticholinesterase agents and corticoids].
Archives françaises de pédiatrie 1993;50(2):174-5.
1990: Pierre Monin; François Feillet; J M Hascoet; P Vert
Effect of sympathetic nervous system on cerebral blood flow in the newborn piglet.
Biology of the neonate 1990;58(4):192-9.