Publications by authors named "Francois Feillet"

95Publications

[Phenylketonuria, from diet to gene therapy].

Med Sci (Paris) 2020 Aug-Sep;36(8-9):725-734. Epub 2020 Aug 21.

Centre de référence des maladies métaboliques, Service de pédiatrie, CHRU de Nancy, 54000 Nancy, France - Inserm UMR_S 1256 (NGERE, Nutrition Génétique et Exposition aux Risques Environnementaux), Faculté de médecine de Nancy, Université de Lorraine, 54000 Nancy, France.

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http://dx.doi.org/10.1051/medsci/2020127DOI Listing
October 2020

Prolonged 25-OH Vitamin D Deficiency Does Not Impair Bone Mineral Density in Adult Patients With Vitamin D 25-Hydroxylase Deficiency (CYP2R1).

Calcif Tissue Int 2020 Aug 19;107(2):191-194. Epub 2020 May 19.

Reference Center for Inborn Errors of Metabolism, Pediatric Unit, University Hospital of Nancy, Nancy, France.

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http://dx.doi.org/10.1007/s00223-020-00704-4DOI Listing
August 2020

Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study.

EBioMedicine 2020 Jan 7;51:102623. Epub 2020 Jan 7.

University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, Nancy, France; Department of Molecular Medicine, Division of Biochemistry, Molecular Biology, Nutrition, and Metabolism, University Hospital of Nancy, Nancy, France; Reference Centre for Inborn Errors of Metabolism (ORPHA67872), University Hospital of Nancy, Nancy F-54000, France.

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http://dx.doi.org/10.1016/j.ebiom.2019.102623DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000351PMC
January 2020

Dietary practices in methylmalonic acidaemia: a European survey.

J Pediatr Endocrinol Metab 2020 Jan;33(1):147-155

Birmingham Women's and Children's Hospital, Birmingham, UK.

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http://dx.doi.org/10.1515/jpem-2019-0277DOI Listing
January 2020

Neurological manifestations in adults with phenylketonuria: new cases and review of the literature.

J Neurol 2020 Feb 7;267(2):531-542. Epub 2019 Nov 7.

Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Neurologie C, 69677, Bron Cedex, France.

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http://dx.doi.org/10.1007/s00415-019-09608-2DOI Listing
February 2020

SIRT1 activation rescues the mislocalization of RNA-binding proteins and cognitive defects induced by inherited cobalamin disorders.

Metabolism 2019 12 28;101:153992. Epub 2019 Oct 28.

Université de Lorraine, Inserm, UMRS 1256, NGERE - Nutrition, Genetics, and Environmental Risk Exposure, F-54000 Nancy, France; Université de Lorraine, CHRU-Nancy, National Center of Inborn Errors of Metabolism, F-54000 Nancy, France. Electronic address:

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http://dx.doi.org/10.1016/j.metabol.2019.153992DOI Listing
December 2019

Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis.

J Hum Genet 2020 Jan 23;65(2):91-98. Epub 2019 Oct 23.

INSERM UMR_S 1256, NGERE-Nutrition, Genetics, and Environmental Risk Exposure and Reference Centre for Inherited Metabolic Diseases (ORPHA67872), University Hospital of Nancy and Faculty of Medicine of Nancy, University of Lorraine, Nancy, France.

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http://dx.doi.org/10.1038/s10038-019-0689-yDOI Listing
January 2020

Mineral and vitamin intake of infants and young children: the Nutri-Bébé 2013 survey.

Eur J Nutr 2020 Sep 25;59(6):2463-2480. Epub 2019 Sep 25.

INSERM 1256, Lorraine University, 54000, Nancy, France.

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http://dx.doi.org/10.1007/s00394-019-02093-3DOI Listing
September 2020

Efficacy of low dose nitisinone in the management of alkaptonuria.

Mol Genet Metab 2019 07 19;127(3):184-190. Epub 2019 Jun 19.

Pediatric Unit, Reference center for Inborn Errors of Metabolism of Nancy, University Children's Hospital, CHU Brabois, Vandoeuvre les Nancy, France; INSERM UMRS 1256 NGERE, Nutrition, Genetics, and Environmental Risk Exposure, National Center of Inborn Errors of Metabolism, Faculty of Medicine of Nancy, University of Lorraine and University Regional Hospital Center of Nancy, Vandoeuvre-les-Nancy F-54000, France. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2019.06.006DOI Listing
July 2019

Exome sequencing of cases with neural tube defects identifies candidate genes involved in one-carbon/vitamin B12 metabolisms and Sonic Hedgehog pathway.

Hum Genet 2019 Jul 28;138(7):703-713. Epub 2019 May 28.

INSERM U1256, NGERE-Nutrition, Genetics, and Environmental Risk Exposure, Faculty of Medicine of Nancy, University of Lorraine, 54000, Nancy, Vandoeuvre-lès-Nancy, France.

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http://dx.doi.org/10.1007/s00439-019-02015-7DOI Listing
July 2019

Neuropsychological Profile of Children with Early and Continuously Treated Phenylketonuria: Systematic Review and Future Approaches.

J Int Neuropsychol Soc 2019 07 29;25(6):624-643. Epub 2019 Apr 29.

Laboratory of Psychology, UBL, EA4638,University of Angers,49000 Angers,France.

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http://dx.doi.org/10.1017/S1355617719000146DOI Listing
July 2019

Annual Injection of Zoledronic Acid Improves Bone Status in Children with Cerebral Palsy and Rett Syndrome.

Calcif Tissue Int 2019 04 15;104(4):355-363. Epub 2018 Dec 15.

Centre de référence des erreurs innées du métabolisme, Hôpital d'Enfants, CHRU Nancy, Nancy, France.

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http://dx.doi.org/10.1007/s00223-018-0505-2DOI Listing
April 2019

Diagnostic and therapeutic recommendations for the treatment of hyperphenylalaninemia in patients 0-4 years of age.

Orphanet J Rare Dis 2018 09 29;13(1):173. Epub 2018 Sep 29.

Department of Pediatrics, Hôpital d'Enfants Brabois, CHU Nancy, Vandoeuvre les Nancy, France.

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http://dx.doi.org/10.1186/s13023-018-0911-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162894PMC
September 2018

[State of play of neonatal screening in France].

Med Sci (Paris) 2018 May 18;34 Hors série n°1:19-21. Epub 2018 Jun 18.

Chef de service, Professeur des Universités, Service de médecine infantile, CHU de Nancy - Hôpitaux de Brabois, Rue du Morvan, 54511 Vandoeuvre-lès- Nancy Cedex, France.

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http://dx.doi.org/10.1051/medsci/201834s110DOI Listing
May 2018

Vitamin D-Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?

J Bone Miner Res 2017 Sep 13;32(9):1893-1899. Epub 2017 Jul 13.

CHU de Nancy, Department of Pediatrics and Reference Center for Rare Hereditary Diseases of Metabolism, Vandoeuvre-lès-Nancy, France.

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http://dx.doi.org/10.1002/jbmr.3181DOI Listing
September 2017

Efficacy and safety of i.v. sodium benzoate in urea cycle disorders: a multicentre retrospective study.

Orphanet J Rare Dis 2016 Sep 23;11(1):127. Epub 2016 Sep 23.

Reference Centre for Inherited Metabolic Disorders (MaMEA), Hôpital Necker-Enfants Malades, Institut Imagine, Université Paris Descartes, 149 rue de Sèvres, 75743, Paris, Cedex 15, France.

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http://dx.doi.org/10.1186/s13023-016-0513-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034629PMC
September 2016

Effect of l-Arginine in One Patient with Peroxisome Biogenesis Disorder due to PEX12 Deficiency.

Neuropediatrics 2016 Jun 4;47(3):179-81. Epub 2016 Mar 4.

Reference Centre for Inborn Errors of Metabolism, University Hospital of Nancy, France.

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http://dx.doi.org/10.1055/s-0036-1578798DOI Listing
June 2016

A Phase 3 Trial of Sebelipase Alfa in Lysosomal Acid Lipase Deficiency.

N Engl J Med 2015 Sep;373(11):1010-20

From the Northwestern University Feinberg School of Medicine and the Ann and Robert H. Lurie Children's Hospital, Chicago (B.K.B.); Icahn School of Medicine, Mount Sinai, New York (M.B.), and Women and Children's Hospital of Buffalo, Buffalo (R.E.) - both in New York; Centre Hospitalier Universitaire Brabois-Hôpital d'Enfants, Vandoeuvre-lès-Nancy (F.F.), and University Hospital Necker-Enfants Malades and Imagine Institute, Paris (V.V.) - both in France; University Hospital Center Zagreb and University of Zagreb, School of Medicine, Zagreb, Croatia (I.B.); Cincinnati Children's Hospital Medical Center, Cincinnati (T.A.B.); Hospital Universitario La Paz, Madrid (C.C.G.); Ege University Medical Faculty, Izmir (M.C.), and Gazi University Medical Faculty, Ankara (F.E.) - both in Turkey; Hospital Infantil de México Federico Gómez, Mexico City (A.C.-S.); Cambridge University Hospitals, Cambridge, United Kingdom (P.D.); Unit of Rare Diseases, Department of Pediatrics, Gaslini Institute, Genoa (M.D.R.), and University of Padua, Padua (M.S.) - both in Italy; Stanford University, Palo Alto (G.M.E.), and University of California, San Francisco, San Francisco ( J.K.) - both in California; Children's Hospital of Philadelphia, Philadelphia (C.F.); Alfred I. duPont Hospital for Children, Wilmington, DE (K.N.F.); University of Arizona Cancer Center, Tucson (C.L.); Villa Metabolica, Center of Pediatric and Adolescent Medicine, University of Mainz, Mainz (E.M.), and University Hospital Freiburg, Freiburg (K.O.S.) - both in Germany; Boston Children's Hospital, Boston (E.G.N.), and Synageva BioPharma, Lexington (Y.Y., S.E., S.R.-C., A.G.Q.) - both in Massachusetts; John Hunter Children's Hospital, and Discipline of Paediatrics and Child Health, University of Newcastle, Newcastle, NSW (S.N.), Royal Children's Hospital, Parkville, VIC (H.P.), and Royal Brisbane and Women's Hospital, Brisbane, QLD (M.W.) - all in Australia; Faculty Hospital, Palacky University, Olomouc, Czech Republic

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http://dx.doi.org/10.1056/NEJMoa1501365DOI Listing
September 2015

Diagnosis, quality of life, and treatment of patients with Hunter syndrome in the French healthcare system: a retrospective observational study.

Orphanet J Rare Dis 2015 Apr 12;10:43. Epub 2015 Apr 12.

Centre de Référence Maladies Métaboliques de l'enfant et de l'adulte, Hôpital Universitaire Necker-Enfants Malades et Institut IMAGINE, Paris, France.

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http://www.ojrd.com/content/10/1/43
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http://dx.doi.org/10.1186/s13023-015-0259-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407793PMC
April 2015

Tetrahydrobiopterin (BH4) responsiveness in neonates with hyperphenylalaninemia: a semi-mechanistically-based, nonlinear mixed-effect modeling.

Mol Genet Metab 2015 Apr 7;114(4):564-9. Epub 2015 Feb 7.

Merck Institute for Pharmacometrics, Merck Serono S.A., EPFL Innovation Park - Building I, CH-1015 Lausanne, Switzerland. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2015.01.013DOI Listing
April 2015

Fructose 1,6-bisphosphatase deficiency: clinical, biochemical and genetic features in French patients.

J Inherit Metab Dis 2015 Sep 20;38(5):881-7. Epub 2015 Jan 20.

Service de Biochimie, CHU Bicêtre, AP-HP, Le Kremlin-Bicêtre, France.

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http://dx.doi.org/10.1007/s10545-014-9804-6DOI Listing
September 2015

Mapping the functional landscape of frequent phenylalanine hydroxylase (PAH) genotypes promotes personalised medicine in phenylketonuria.

J Med Genet 2015 Mar 16;52(3):175-85. Epub 2015 Jan 16.

Department of Molecular Pediatrics, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany.

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http://dx.doi.org/10.1136/jmedgenet-2014-102621DOI Listing
March 2015

Management of adult patients with phenylketonuria: survey results from 24 countries.

Eur J Pediatr 2015 Jan 6;174(1):119-27. Epub 2014 Dec 6.

Kreiskliniken Reutlingen GmbH, School of Medicine, Outpatient Medical Centre, University of Tuebingen, Gammertingen, Germany,

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http://dx.doi.org/10.1007/s00431-014-2458-4DOI Listing
January 2015

Mutations in SLC13A5 cause autosomal-recessive epileptic encephalopathy with seizure onset in the first days of life.

Am J Hum Genet 2014 Jul;95(1):113-20

Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Centre Hospitalier Universitaire Dijon, 21079 Dijon, France; Equipe d'Accueil 4271, Génétique des Anomalies du Développement, Université de Bourgogne, 21079 Dijon, France; Laboratoire de Génétique Moléculaire, Plateau Technique de Biologie, Centre Hospitalier Universitaire Dijon, 21079 Dijon, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.06.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085634PMC
July 2014

Use of sapropterin dihydrochloride in maternal phenylketonuria. A European experience of eight cases.

J Inherit Metab Dis 2014 Sep 1;37(5):753-62. Epub 2014 May 1.

Department of Pediatrics, Hôpital d'Enfants Brabois, CHU Nancy, Vandoeuvre les Nancy, France,

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http://dx.doi.org/10.1007/s10545-014-9716-5DOI Listing
September 2014

Extensive striatal, cortical, and white matter brain MRI abnormalities in Wilson disease.

Neurology 2013 Oct;81(17):1557

From the French National Reference Centre for Wilson's Disease (J.-M.T., F.W.), Biological Toxicology Laboratory (S.E.B., J.P.), Neuroradiology (J.-P.G.), and Laboratoire de Biochimie et Biologie Moléculaire (P.C.), AP-HP, Hôpital Lariboisière, Paris; and National Reference Centre for Inborn Errors of Metabolism (F.F.), INSERM U954, Nancy, France.

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http://dx.doi.org/10.1212/WNL.0b013e3182a95883DOI Listing
October 2013

Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia.

Hum Mol Genet 2013 Nov 3;22(22):4591-601. Epub 2013 Jul 3.

Inserm U954 Nutrition-Genetics-Environmental Risk Exposure and Reference Centre of Inborn Metabolism Diseases, Medical Faculty of Nancy University and University Hospital Centre, Nancy, France.

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http://dx.doi.org/10.1093/hmg/ddt308DOI Listing
November 2013

Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation.

J Inherit Metab Dis 2012 Nov 5;35(6):993-9. Epub 2012 Jun 5.

Department of Pediatrics, Brest University Hospital, CHRU Morvan, 2 avenue Foch, 29200, Brest, France.

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http://dx.doi.org/10.1007/s10545-012-9491-0DOI Listing
November 2012

Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7.

Haematologica 2011 Nov 12;96(11):1715-9. Epub 2011 Jul 12.

Faculté de Médecine, INSERM U954 Nutrition, Genetics, and Environmental Risk Exposure, Vandoeuvre Les Nancy, France.

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http://dx.doi.org/10.3324/haematol.2011.043984DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3208692PMC
November 2011

Acute metabolic encephalopathy in two patients treated with asparaginase and ondasetron.

Am J Hematol 2011 Mar;86(3):323-5

Department of Pediatric Oncology, Centre Oscar Lambret, Lille, France. h.sudour@o-lambret

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http://dx.doi.org/10.1002/ajh.21964DOI Listing
March 2011

Ovarian tissue cryopreservation and subsequent spontaneous pregnancies in a patient with classic galactosemia.

Fertil Steril 2011 Jan;95(1):290.e1-3

INSERM U954, Nutrition, Genetics, and Environmental Risk Exposure, Nancy University Medical School, and Department of Pediatrics and Clinical Genetics, University Hospital of Nancy, Vandoeuvre lès Nancy, France.

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http://dx.doi.org/10.1016/j.fertnstert.2010.06.014DOI Listing
January 2011

Challenges and pitfalls in the management of phenylketonuria.

Pediatrics 2010 Aug 12;126(2):333-41. Epub 2010 Jul 12.

Service de Médecine Infantile 1, Centre de Référence des Maladies Héréditaires du Métabolisme, INSERM U 954, CHU Brabois Enfants, Vandoeuvre les Nancy, France.

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http://dx.doi.org/10.1542/peds.2009-3584DOI Listing
August 2010

Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients.

Mol Genet Metab 2010 Jun 6;100(2):143-8. Epub 2010 Mar 6.

INSERM U954 Nutrition, Genetics, and Environmental Risk Exposure, Faculté de Médecine, 9 avenue de la Forêt de Haye, Vandoeuvre les Nancy, France.

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http://dx.doi.org/10.1016/j.ymgme.2010.03.002DOI Listing
June 2010

Outcomes beyond phenylalanine: an international perspective.

Mol Genet Metab 2010 ;99 Suppl 1:S79-85

Reference Centre for Inborn Errors of Metabolism, INSERM U954, Department of Pediatrics, Children's Hospital of Nancy, Allée du Morvan, Vandoeuvre les Nancy 54500, France.

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http://dx.doi.org/10.1016/j.ymgme.2009.09.015DOI Listing
June 2010

Nutritional issues in treating phenylketonuria.

J Inherit Metab Dis 2010 Dec 12;33(6):659-64. Epub 2010 Feb 12.

Centre de référence des maladies héréditaires du métabolisme de Nancy, INSERM U 954, Hôpital d'Enfants, CHU Brabois, Allée du Morvan, Vandoeuvre les Nancy 54500, France.

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http://dx.doi.org/10.1007/s10545-010-9043-4DOI Listing
December 2010

Rapid identification of HEXA mutations in Tay-Sachs patients.

Biochem Biophys Res Commun 2010 Feb 25;392(4):599-602. Epub 2010 Jan 25.

Service de Biochimie et Génétique Moléculaire, Groupe Hospitalier Cochin-Saint-Vincent-de Paul, Assistance Publique-Hôpitaux de Paris, EA3620, Université Paris Descartes, Paris, France.

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http://dx.doi.org/10.1016/j.bbrc.2010.01.088DOI Listing
February 2010

Management of phenylketonuria in Europe: survey results from 19 countries.

Mol Genet Metab 2010 Feb 13;99(2):109-15. Epub 2009 Sep 13.

University Children's Hospital, Zürich, Switzerland.

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http://dx.doi.org/10.1016/j.ymgme.2009.09.005DOI Listing
February 2010

Contrast-enhanced ultrasonography in patients with glycogen storage disease type Ia and adenomas.

J Ultrasound Med 2009 Apr;28(4):497-505

Department of Pediatric Radiology, Children's Hospital, Institut National de la Santé et de la Recherche Médicale, Vandoeuvre, France.

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http://dx.doi.org/10.7863/jum.2009.28.4.497DOI Listing
April 2009

Optimizing the use of sapropterin (BH(4)) in the management of phenylketonuria.

Mol Genet Metab 2009 Apr 8;96(4):158-63. Epub 2009 Feb 8.

Division of Clinical Chemistry and Biochemistry, University Children's Hospital, Steinwiesstrasse 75, CH-8032 Zürich, Switzerland.

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http://dx.doi.org/10.1016/j.ymgme.2009.01.002DOI Listing
April 2009

Neurological aspects of hyperinsulinism-hyperammonaemia syndrome.

Dev Med Child Neurol 2008 Dec;50(12):945-9

Department of Paediatric Neurology and Metabolic Diseases, Necker Children's Hospital, Paris V University, Paris, France.

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http://dx.doi.org/10.1111/j.1469-8749.2008.03114.xDOI Listing
December 2008

Pharmacokinetics of sapropterin in patients with phenylketonuria.

Clin Pharmacokinet 2008 ;47(12):817-25

Centre de Référence des Maladies Héréditaires du Métabolisme, Hôpital d'Enfants, CHU Brabois, Vandoeuvre les Nancy, France.

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http://dx.doi.org/10.2165/0003088-200847120-00006DOI Listing
March 2009

24 month-treatment with miglustat of three patients with Niemann-Pick disease type C: follow up using brain spectroscopy.

Mol Genet Metab 2009 Feb 13;96(2):55-8. Epub 2008 Nov 13.

Department of Neuroradiology and Center for NeuroImaging Research-CENIR , Pitié-Salpêtrière Hospital, Assistance Publique Hôpitaux de Paris, France.

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http://dx.doi.org/10.1016/j.ymgme.2008.10.002DOI Listing
February 2009

Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutations.

Mol Genet Metab 2008 Aug 9;94(4):443-7. Epub 2008 Jun 9.

Laboratoire de Biochimie, CHU de Bicêtre, Assistance Publique-Hôpitaux de Paris, 78, rue du Général Leclerc, 94275 Le Kremlin Bicêtre Cedex, France et Université Paris XI, IFR Bicêtre, France.

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http://dx.doi.org/10.1016/j.ymgme.2008.05.003DOI Listing
August 2008

Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemia.

Early Hum Dev 2008 Sep 5;84(9):561-7. Epub 2008 Mar 5.

Reference Centre for Inborn Errors of Metabolism, Department of Pediatry, CHU of Nancy, Allée du Morvan, Vandoeuvre les Nancy, 54500, France.

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http://dx.doi.org/10.1016/j.earlhumdev.2008.01.003DOI Listing
September 2008

Evidence of cataplerosis in a patient with neonatal classical galactosemia presenting as citrin deficiency.

J Hepatol 2008 Mar 31;48(3):517-22. Epub 2007 Dec 31.

Centre de Référence des Maladies Héréditaires du Métabolisme et Inserm U724, CHU et Faculté de Médecine de Nancy, France.

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http://dx.doi.org/10.1016/j.jhep.2007.11.016DOI Listing
March 2008

Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.

Hum Mutat 2008 Jan;29(1):167-75

Division of Clinical Chemistry and Biochemistry, University Children's Hospital, Zürich, Switzerland.

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http://dx.doi.org/10.1002/humu.20637DOI Listing
January 2008

Management of phenylketonuria and hyperphenylalaninemia.

J Nutr 2007 06;137(6 Suppl 1):1561S-1563S; discussion 1573S-1575S

Service de Neurologie et Maladies Métaboliques, Hôpital R. Debré, Assistance Publique des Hôpitaux de Paris, 75019 Paris, France.

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http://dx.doi.org/10.1093/jn/137.6.1561SDOI Listing
June 2007

[Phenylketonuria].

Presse Med 2006 Mar;35(3 Pt 2):502-8

Service de Médecine Infantile III, Hôpital d'Enfants, CHU Brabois, Vandoeuvre les Nancy.

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http://dx.doi.org/10.1016/s0755-4982(06)74625-5DOI Listing
March 2006

[Height and weight growth delay].

Rev Prat 2005 Dec;55(20):2285-90

Service de médecine infantile I, hôpital d'Enfants, CHU Brabois, 54500 Vandoeuvre-lès-Nancy.

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December 2005

Maternal phenylketonuria: the French survey.

Eur J Pediatr 2004 Sep 6;163(9):540-6. Epub 2004 Jul 6.

Department of Paediatrics, CHU Brabois, Allée du morvan, 54500, Vandoeuvre les Nancy, France,

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http://dx.doi.org/10.1007/s00431-004-1482-1DOI Listing
September 2004

Hypothalamic dysfunction associated with neuroblastoma: evidence for a new Paraneoplastic syndrome?

Med Pediatr Oncol 2003 May;40(5):326-8

Service de Pédiatrie, Unité d'Oncologie et Hématologie Pédiatrique, CHU de Nice, France.

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http://dx.doi.org/10.1002/mpo.10157DOI Listing
May 2003

Utilization of cornstarch in glycogen storage disease type Ia.

Eur J Gastroenterol Hepatol 2002 Nov;14(11):1251-6

Biochemistry, Metabolism, Endocrinology Unit, Institute of Child Health, Great Ormond Street Hospital for Children, NHS Trust, London, UK.

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http://pdfs.journals.lww.com/eurojgh/2002/11000/Utilization_
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http://dx.doi.org/10.1097/00042737-200211000-00014DOI Listing
November 2002