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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 8, 2012
[Diagnosis of hypochromic microcytic anemia in children]
M de Montalembert, J-L Bresson, C Brouzes, et al.
Human Genetics
|
December 22, 1998
Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyria
H Puy, U Gross, J C Deybach, et al.
Journal of Hepatology
|
July 18, 2000
Hepatocellular carcinoma in patients with acute hepatic porphyria: frequency of occurrence and related factors
C Andant, H Puy, C Bogard, et al.
Blood
|
March 9, 1999
Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestation
L Gouya, H Puy, J Lamoril, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1992
Thyroid hormone extraction by plasma exchange: a study of extraction rate
H Puy, J Lamoril, J M Marcelli, et al.
Diabete & Metabolisme
|
March 1, 1993
Metformin effects on peripheral sensitivity to insulin in non diabetic obese subjects
S Fendri, X Debussche, H Puy, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
August 7, 2009
The molecular genetics of erythropoietic protoporphyria
G H Elder, L Gouya, S D Whatley, et al.
Molecular and Cellular Probes
|
February 5, 2000
New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyria
U Gross, H Puy, M Doss, et al.
Human Heredity
|
April 27, 2000
Identification of a prevalent nonsense mutation (W283X) and two novel mutations in the porphobilinogen deaminase gene of Swiss patients with acute intermittent porphyria
X Schneider-Yin, C Bogard, U B Rüfenacht, et al.
Annales De Biologie Clinique
|
February 4, 2005
[Non-radioimmunometric NT-ProBNP and BNP assays: impact of diluent, age, gender, BMI]
Y Alibay, C Schmitt, A Beauchet, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 68) with videos related to
Sort By:
Page
of 7
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 8, 2012
[Diagnosis of hypochromic microcytic anemia in children]
M de Montalembert, J-L Bresson, C Brouzes, et al.
Human Genetics
|
December 22, 1998
Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyria
H Puy, U Gross, J C Deybach, et al.
Journal of Hepatology
|
July 18, 2000
Hepatocellular carcinoma in patients with acute hepatic porphyria: frequency of occurrence and related factors
C Andant, H Puy, C Bogard, et al.
Blood
|
March 9, 1999
Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestation
L Gouya, H Puy, J Lamoril, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1992
Thyroid hormone extraction by plasma exchange: a study of extraction rate
H Puy, J Lamoril, J M Marcelli, et al.
Diabete & Metabolisme
|
March 1, 1993
Metformin effects on peripheral sensitivity to insulin in non diabetic obese subjects
S Fendri, X Debussche, H Puy, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
August 7, 2009
The molecular genetics of erythropoietic protoporphyria
G H Elder, L Gouya, S D Whatley, et al.
Molecular and Cellular Probes
|
February 5, 2000
New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyria
U Gross, H Puy, M Doss, et al.
Human Heredity
|
April 27, 2000
Identification of a prevalent nonsense mutation (W283X) and two novel mutations in the porphobilinogen deaminase gene of Swiss patients with acute intermittent porphyria
X Schneider-Yin, C Bogard, U B Rüfenacht, et al.
Annales De Biologie Clinique
|
February 4, 2005
[Non-radioimmunometric NT-ProBNP and BNP assays: impact of diluent, age, gender, BMI]
Y Alibay, C Schmitt, A Beauchet, et al.
Page
of 7