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G Crisponi

Showing results (21-30 of 30) with videos related to

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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 receptorsM G Corda, E Sanna, A Concas, et al.
Journal of Hepatology|March 1, 1995
Uneven hepatic copper distribution in Wilson's diseaseG 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 diseaseG 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 IM C Rosatelli, A Meloni, V Faa, et al.
Journal of Hepatology|November 1, 1995
Uneven hepatic iron and phosphorus distribution in beta-thalassemiaR 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 DiseasesDaniela 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 diseaseJ 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 derivativesL 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)-oneJ 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 correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
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 receptorsM G Corda, E Sanna, A Concas, et al.
Journal of Hepatology|March 1, 1995
Uneven hepatic copper distribution in Wilson's diseaseG 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 diseaseG 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 IM C Rosatelli, A Meloni, V Faa, et al.
Journal of Hepatology|November 1, 1995
Uneven hepatic iron and phosphorus distribution in beta-thalassemiaR 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 DiseasesDaniela 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 diseaseJ 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 derivativesL 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)-oneJ 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 correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Pageof 3