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Annales De Biologie Clinique
|
November 26, 2004
[Influence of pyridoxal phosphate in measuring aminotransferases activities in patients with viral hepatitis]
G Férard, F Imbert-Bismut, D Messous, et al.
Archives Francaises De Pediatrie
|
June 1, 1987
[Double-blind study of the efficacy of an antiserotoninergic drug, pizotifen, in Duchenne's muscular dystrophy]
D Steru, J P Paclet, G Barthelet, et al.
Journal of Clinical Pathology
|
May 1, 1997
In situ detection of lipid peroxidation in chronic hepatitis C: correlation with pathological features
V Paradis, P Mathurin, M Kollinger, et al.
Annales De Biologie Clinique
|
June 7, 2002
[Enzyme calibrators: principle and practical use]
J M Lessinger, F Schiele, A Vialle, et al.
Journal of Clinical Pathology
|
November 24, 1999
Low hepatic iron concentration: evaluation of two complementary methods, colorimetric assay and iron histological scoring
F Imbert-Bismut, F Charlotte, B Turlin, et al.
Annales De Biologie Clinique
|
June 14, 2005
[Results transferability on RXL, ARX, X-Pand, BN2 (Dade Behring) and modular DP (Roche Diagnostics) analysers: application to component assays of fibrotest and Actitest]
F Imbert-Bismut, D Messous, A Raoult, et al.
European Journal of Human Genetics : EJHG
|
November 30, 2017
Points to consider for laboratories reporting results from diagnostic genomic sequencing
D F Vears, K Sénécal, A J Clarke, et al.
Journal of Viral Hepatitis
|
January 13, 2001
Hepatic porphyrin concentration and uroporphyrinogen decarboxylase activity in hepatitis C virus infection
E Brudieux, V de Lédinghen, M J Moran, et al.
Clinical Genetics
|
March 4, 2016
The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome
B Schönewolf-Greulich, M-I Tejada, K Stephens, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2023
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome
E Viora-Dupont, A Denommé-Pichon, M Chevarin, et al.
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of 3
Search research articles
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Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Annales De Biologie Clinique
|
November 26, 2004
[Influence of pyridoxal phosphate in measuring aminotransferases activities in patients with viral hepatitis]
G Férard, F Imbert-Bismut, D Messous, et al.
Archives Francaises De Pediatrie
|
June 1, 1987
[Double-blind study of the efficacy of an antiserotoninergic drug, pizotifen, in Duchenne's muscular dystrophy]
D Steru, J P Paclet, G Barthelet, et al.
Journal of Clinical Pathology
|
May 1, 1997
In situ detection of lipid peroxidation in chronic hepatitis C: correlation with pathological features
V Paradis, P Mathurin, M Kollinger, et al.
Annales De Biologie Clinique
|
June 7, 2002
[Enzyme calibrators: principle and practical use]
J M Lessinger, F Schiele, A Vialle, et al.
Journal of Clinical Pathology
|
November 24, 1999
Low hepatic iron concentration: evaluation of two complementary methods, colorimetric assay and iron histological scoring
F Imbert-Bismut, F Charlotte, B Turlin, et al.
Annales De Biologie Clinique
|
June 14, 2005
[Results transferability on RXL, ARX, X-Pand, BN2 (Dade Behring) and modular DP (Roche Diagnostics) analysers: application to component assays of fibrotest and Actitest]
F Imbert-Bismut, D Messous, A Raoult, et al.
European Journal of Human Genetics : EJHG
|
November 30, 2017
Points to consider for laboratories reporting results from diagnostic genomic sequencing
D F Vears, K Sénécal, A J Clarke, et al.
Journal of Viral Hepatitis
|
January 13, 2001
Hepatic porphyrin concentration and uroporphyrinogen decarboxylase activity in hepatitis C virus infection
E Brudieux, V de Lédinghen, M J Moran, et al.
Clinical Genetics
|
March 4, 2016
The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome
B Schönewolf-Greulich, M-I Tejada, K Stephens, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2023
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome
E Viora-Dupont, A Denommé-Pichon, M Chevarin, et al.
Page
of 3