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Journal of Neurochemistry
|
August 1, 1986
Enhancement of gamma-aminobutyric acid binding by quazepam, a benzodiazepine derivative with preferential affinity for type I benzodiazepine receptors
M G Corda, E Sanna, A Concas, et al.
Journal of Hepatology
|
March 1, 1995
Uneven hepatic copper distribution in Wilson's disease
G Faa, V Nurchi, L Demelia, et al.
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)
|
January 15, 2002
Brain copper, iron, magnesium, zinc, calcium, sulfur and phosphorus storage in Wilson's disease
G Faa, M Lisci, M P Caria, et al.
Journal of Medical Genetics
|
February 1, 1997
Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I
M C Rosatelli, A Meloni, V Faa, et al.
Journal of Hepatology
|
November 1, 1995
Uneven hepatic iron and phosphorus distribution in beta-thalassemia
R Ambu, G Crisponi, R Sciot, et al.
Biological Trace Element Research
|
December 15, 2020
The Role of Magnesium in Pregnancy and in Fetal Programming of Adult Diseases
Daniela Fanni, C Gerosa, V M Nurchi, et al.
Journal of Medical Genetics
|
September 21, 2011
Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease
J Uusimaa, H Jungbluth, C Fratter, et al.
Journal of Inorganic Biochemistry
|
July 18, 2024
Solution studies, synthesis and antibacterial activity of Ga(III) complexes with bis-kojate derivatives
L More O'Ferrall, A Fantasia, K Chan, et al.
Dalton Transactions (Cambridge, England : 2003)
|
March 10, 2016
Hydroxypyridinones with enhanced iron chelating properties. Synthesis, characterization and in vivo tests of 5-hydroxy-2-(hydroxymethyl)pyridine-4(1H)-one
J I Lachowicz, V M Nurchi, G Crisponi, et al.
American Journal of Human Genetics
|
July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation
H van Bokhoven, B C Hamel, M Bamshad, et al.
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of 3
Search research articles
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Showing results (21-30 of 30) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 30 results.
Journal of Neurochemistry
|
August 1, 1986
Enhancement of gamma-aminobutyric acid binding by quazepam, a benzodiazepine derivative with preferential affinity for type I benzodiazepine receptors
M G Corda, E Sanna, A Concas, et al.
Journal of Hepatology
|
March 1, 1995
Uneven hepatic copper distribution in Wilson's disease
G Faa, V Nurchi, L Demelia, et al.
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)
|
January 15, 2002
Brain copper, iron, magnesium, zinc, calcium, sulfur and phosphorus storage in Wilson's disease
G Faa, M Lisci, M P Caria, et al.
Journal of Medical Genetics
|
February 1, 1997
Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I
M C Rosatelli, A Meloni, V Faa, et al.
Journal of Hepatology
|
November 1, 1995
Uneven hepatic iron and phosphorus distribution in beta-thalassemia
R Ambu, G Crisponi, R Sciot, et al.
Biological Trace Element Research
|
December 15, 2020
The Role of Magnesium in Pregnancy and in Fetal Programming of Adult Diseases
Daniela Fanni, C Gerosa, V M Nurchi, et al.
Journal of Medical Genetics
|
September 21, 2011
Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease
J Uusimaa, H Jungbluth, C Fratter, et al.
Journal of Inorganic Biochemistry
|
July 18, 2024
Solution studies, synthesis and antibacterial activity of Ga(III) complexes with bis-kojate derivatives
L More O'Ferrall, A Fantasia, K Chan, et al.
Dalton Transactions (Cambridge, England : 2003)
|
March 10, 2016
Hydroxypyridinones with enhanced iron chelating properties. Synthesis, characterization and in vivo tests of 5-hydroxy-2-(hydroxymethyl)pyridine-4(1H)-one
J I Lachowicz, V M Nurchi, G Crisponi, et al.
American Journal of Human Genetics
|
July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation
H van Bokhoven, B C Hamel, M Bamshad, et al.
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of 3