Page last updated: 2024-08-23

heme and Rachitis

heme has been researched along with Rachitis in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Grenier, A; Meister, A; New, MI; Rifkind, AB; Sassa, S; Starkman, H; Steinherz, PG; Stoner, E; Wellner, D; Wellner, VP	1
Berry, JL; Davies, M; Heath, DA; Mawer, EB; Mee, AP; Mylchreest, S; Paterson, CR; Read, AP; Rucka, AK; Smith, SJ; Tassabehji, M	1

Other Studies

2 other study(ies) available for heme and Rachitis

Article	Year
Biochemical studies of a patient with hereditary hepatorenal tyrosinemia: evidence of glutathione deficiency. Pediatric research, 1984, Volume: 18, Issue:12 Topics: Erythrocytes; Fanconi Syndrome; Female; Glutathione; Heme; Humans; Infant; Liver; Liver Diseases; Mass Spectrometry; Mixed Function Oxygenases; Phosphates; Pyrroles; Rickets; Syndrome; Tyrosine	1984
Novel mutations in the 1alpha-hydroxylase (P450c1) gene in three families with pseudovitamin D-deficiency rickets resulting in loss of functional enzyme activity in blood-derived macrophages. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 1999, Volume: 14, Issue:5 Topics: 24,25-Dihydroxyvitamin D 3; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase; Base Sequence; Cells, Cultured; Child; Child, Preschool; Cholestanetriol 26-Monooxygenase; Chromosomes, Human, Pair 12; Cloning, Molecular; Cytochrome P-450 Enzyme System; DNA; Female; Ferredoxins; Heme; Humans; Infant; Introns; Macrophages; Male; Molecular Sequence Data; Mutation; Pedigree; Polymorphism, Genetic; Rickets; Steroid Hydroxylases	1999

Article

Year

Biochemical studies of a patient with hereditary hepatorenal tyrosinemia: evidence of glutathione deficiency.

Pediatric research, 1984, Volume: 18, Issue:12

Topics: Erythrocytes; Fanconi Syndrome; Female; Glutathione; Heme; Humans; Infant; Liver; Liver Diseases; Mass Spectrometry; Mixed Function Oxygenases; Phosphates; Pyrroles; Rickets; Syndrome; Tyrosine

1984

Novel mutations in the 1alpha-hydroxylase (P450c1) gene in three families with pseudovitamin D-deficiency rickets resulting in loss of functional enzyme activity in blood-derived macrophages.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 1999, Volume: 14, Issue:5

Topics: 24,25-Dihydroxyvitamin D 3; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase; Base Sequence; Cells, Cultured; Child; Child, Preschool; Cholestanetriol 26-Monooxygenase; Chromosomes, Human, Pair 12; Cloning, Molecular; Cytochrome P-450 Enzyme System; DNA; Female; Ferredoxins; Heme; Humans; Infant; Introns; Macrophages; Male; Molecular Sequence Data; Mutation; Pedigree; Polymorphism, Genetic; Rickets; Steroid Hydroxylases

1999