Expanded newborn screening: social and ethical issues
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Conference Proceeding
Lessons from 30 years of selective screening for tetrahydrobiopterin deficiency
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Conference Proceeding
Implementation of the French Nationwide Cystic Fibrosis Newborn Screening Program
Munck, Anne, MD, Dhondt, Jean-Louis, MD, PhD, Sahler, Camille, Roussey, Michel, MD
Published in The Journal of pediatrics (01.08.2008)
Published in The Journal of pediatrics (01.08.2008)
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Phenylketonuria is still a major cause of mental retardation in Tunisia despite the possibility of treatment
Khemir, Sameh, El Asmi, Monia, Sanhaji, Haifa, Feki, Moncef, Jemaa, Riadh, Tebib, Neji, Dhondt, Jean Louis, Ben Dridi, Marie Françoise, Mebazaa, Abderraouf, Kaabachi, Naziha
Published in Clinical neurology and neurosurgery (01.11.2011)
Published in Clinical neurology and neurosurgery (01.11.2011)
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Tetrahydrobiopterin Deficiency: From Phenotype to Genotype
Blau, Nenad, Thöny, Beat, Heizmann, Claus W., Dhondt, Jean-Louis
Published in Pteridines (01.02.1993)
Published in Pteridines (01.02.1993)
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Clinical and EEG video‐polygraphic features of epileptic spasms in a child with dihydropteridine reductase deficiency. Efficiency of hydrocortisone
Mikaeloff, Yann, Plouin, Perrine, Dhondt, Jean‐Louis, Ponsot, Gérard, Dulac, Olivier
Published in Epileptic disorders (01.12.2000)
Published in Epileptic disorders (01.12.2000)
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Dihydropteridine Reductase Deficiency in a Large Consanguineous Tunisian Family: Clinical, Biochemical, and Neuropathologic Findings
Miladi, Najoua, Larnaout, Abdelmajid, Dhondt, Jean-Louis, Vincent, Marie-Françoise, Kaabachi, Naziha, Hentati, Fayçal
Published in Journal of child neurology (01.10.1998)
Published in Journal of child neurology (01.10.1998)
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Diagnosis of variants of hyperphenylalaninemia by determination of pterins in urine
Dhondt, Jean-Louis, Largilliere, Claude, Ardouin, Patrick, Farriaux, Jean-Pierre, Dautrevaux, Michel
Published in Clinica chimica acta (05.03.1981)
Published in Clinica chimica acta (05.03.1981)
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Neonatal hyperphenylalaninemia presumably caused by guanosine triphosphate-cyclohydrolase deficiency
Dhondt, Jean-Louis, Farriaux, Jean-Pierre, Boudha, Abdennacer, Largillière, Claude, Ringel, Jacques, Roger, Marie-Madeleine, Leeming, Robert J.
Published in The Journal of pediatrics (01.06.1985)
Published in The Journal of pediatrics (01.06.1985)
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Developmental aspects of pteridine metabolism and relationships with phenylalanine metabolism
Dhondt, Jean-Louis, Ardouin, Patrick, Hayte, Jean-Marie, Farriaux, Jean-Pierre
Published in Clinica chimica acta (26.10.1981)
Published in Clinica chimica acta (26.10.1981)
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Journal Article
Unconjugated pteridines in amniotic fluid during gestation
Dhondt, Jean-Louis, Hayte, Jean-Marie, Forzy, Gérard, Delcroix, Michel, Farriaux, Jean-Pierre
Published in Clinica chimica acta (30.12.1986)
Published in Clinica chimica acta (30.12.1986)
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