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La Revue Du Praticien
|
October 22, 1998
[Monofactorial heredity]
P de Lonlay
Biochimica Et Biophysica Acta
|
December 23, 2008
The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib
P de Lonlay, N Seta
Diabetes & Metabolism
|
February 14, 2007
Diabetes and hypoglycaemia in young children and mutations in the Kir6.2 subunit of the potassium channel: therapeutic consequences
I Flechtner, P de Lonlay, M Polak
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 27, 2003
[Molecular tests and metabolic diseases]
P de Lonlay, I Giurgea, J M Saudubray
Pharmaceutical Development and Technology
|
January 14, 2015
Pediatric drug formulation of sodium benzoate extended-release granules
E Combescot, G Morat, P de Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 21, 2020
Clinical phenotype associated with TANGO2 gene mutation
C Hoebeke, A Cano, P De Lonlay, et al.
International Journal of Cardiology
|
September 18, 1998
Fatty acid beta-oxidation deficiency masquerading as fulminant myocarditis
P de Lonlay-Debeney, J C Fournet, D Bonnet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 1, 1996
[Remission of severe hypoglycemic incidents in young diabetic children treated with subcutaneous infusion]
N Tubiana-Rufi, P de Lonlay, J Bloch, et al.
Annales D'Endocrinologie
|
August 29, 2000
[Molecular basis of hyperinsulinisms]
P de Lonlay-Debeney, J J Robert, J M Saudubray
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 23, 2009
[Metabolic emergencies: diagnostic algorithm of lactic acidosis]
V Valayannopoulos, J-B Arnoux, M Rio, et al.
Page
of 14
Search research articles
Search
Showing results (1-10 of 131) with videos related to
Sort By:
Page
of 14
La Revue Du Praticien
|
October 22, 1998
[Monofactorial heredity]
P de Lonlay
Biochimica Et Biophysica Acta
|
December 23, 2008
The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib
P de Lonlay, N Seta
Diabetes & Metabolism
|
February 14, 2007
Diabetes and hypoglycaemia in young children and mutations in the Kir6.2 subunit of the potassium channel: therapeutic consequences
I Flechtner, P de Lonlay, M Polak
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 27, 2003
[Molecular tests and metabolic diseases]
P de Lonlay, I Giurgea, J M Saudubray
Pharmaceutical Development and Technology
|
January 14, 2015
Pediatric drug formulation of sodium benzoate extended-release granules
E Combescot, G Morat, P de Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 21, 2020
Clinical phenotype associated with TANGO2 gene mutation
C Hoebeke, A Cano, P De Lonlay, et al.
International Journal of Cardiology
|
September 18, 1998
Fatty acid beta-oxidation deficiency masquerading as fulminant myocarditis
P de Lonlay-Debeney, J C Fournet, D Bonnet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 1, 1996
[Remission of severe hypoglycemic incidents in young diabetic children treated with subcutaneous infusion]
N Tubiana-Rufi, P de Lonlay, J Bloch, et al.
Annales D'Endocrinologie
|
August 29, 2000
[Molecular basis of hyperinsulinisms]
P de Lonlay-Debeney, J J Robert, J M Saudubray
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 23, 2009
[Metabolic emergencies: diagnostic algorithm of lactic acidosis]
V Valayannopoulos, J-B Arnoux, M Rio, et al.
Page
of 14