Jean‐Louis Dhondt - Concepedia

Author

Jean‐Louis Dhondt

Hôpital Saint-Philibert

Also Known As

Dhondt, J Dhondt, J L Dhondt, J-L Dhondt, J. -L. Dhondt, J. D'HONDT, J. D'Hondt, J. D'hondt, J. Dhondt, J. D’Hondt

181

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Hôpital Saint-Philibert Centre Hospitalier Universitaire de Lille Association Française pour le Dépistage et la Prévention des Handicaps de l’Enfant University of Zurich Centre de Biologie Structurale

About

Jean‐Louis Dhondt is an author at Hôpital Saint-Philibert specializing in medicine, pharmacology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	23	553
2	Health Sciences	4	4	124
3	Natural Sciences	2	2	29
4	Public Health	2	2	47
5	Education	1	1	67

Jean‐Louis Dhondt

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
International database of tetrahydrobiopterin deficiencies Nenad Blau, Isobel Barnes, Jean‐Louis Dhondt Journal of Inherited Metabolic Disease	1995	137
Implementation of the French Nationwide Cystic Fibrosis Newborn Screening Program À. Munck, Jean‐Louis Dhondt, Camille Sahler, The Journal of Pediatrics Early DiagnosisNewborn ScreeningNeonatologyEarly ScreeningDiagnosis	2008	67
Tetrahydrobiopterin Deficiency: From Phenotype to Genotype Nenad Blau, Beat Thöny, Claus W. Heizmann, Pteridines Human GrowthGeneticsDefective GeneDisease Gene IdentificationGenetic Medicine	1993	65
Primapterin, anapterin, and 6-oxo-primapterin, three new 7-substituted pterins identified in a patient with hyperphenylalaninemia H.‐Ch. Curtius, Th. Kuster, A. Matasović, Biochemical and Biophysical Research Communications PharmacologyUrologyMedicineNew 7-Substituted Pterins	1988	50
Economic evaluation of cost‐benefit ratio of neonatal screening procedure for phenylketonuria and hypothyroidism Jean‐Louis Dhondt, J. P. Farriaux, Jean-Claude Sailly, Journal of Inherited Metabolic Disease	1991	44
Neonatal screening: from the ‘Guthrie age’ to the ‘genetic age’ Jean‐Louis Dhondt Journal of Inherited Metabolic Disease	2007	43
Diagnosis of variants of hyperphenylalaninemia by determination of pterins in urine Jean‐Louis Dhondt, C Largillière, Patrick Ardouin, Clinica Chimica Acta UrologyMedicineRenal PathologyChronic Kidney DiseaseNephrology	1981	42
Developmental aspects of pteridine metabolism and relationships with phenylalanine metabolism Jean‐Louis Dhondt, Patrick Ardouin, J.M. Hayte, Clinica Chimica Acta BiochemistryPhysiologyThyroid HormoneMetabolismHuman Metabolism	1981	39
Changes of Cerebral Biopterin and Biogenic Amine Metabolism in Leukemic Children Receiving 5 g/m2 Intravenous Methotrexate Frédéric Millot, Jean‐Louis Dhondt, Françoise Mazingue, Pediatric Research Biogenic Amine MetabolismBiochemistryMedicineInherited Metabolic DiseaseHematology	1995	38
Physical growth in patients with phenylketonuria Jean‐Louis Dhondt, C Largillière, L. Moreno, Journal of Inherited Metabolic Disease Renal FunctionBody CompositionPhysiologyClinical NutritionPhysical Growth	1995	37

Page 1