arginine and Hypophosphatemia, Familial

arginine has been researched along with Hypophosphatemia, Familial in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (66.67)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baum, M; Seikaly, MG	1
Borelli, A; Frazzatto, ES; Latronico, AC; Leite, MO; Mechica, JB; Mendonca, BB	1
Feldman, D; Gardezi, SA; Malloy, PJ; Nguyen, C; Peleg, S; Posner, GH	1

Trials

1 trial(s) available for arginine and Hypophosphatemia, Familial

Article	Year
Stimulation of growth hormone secretion in children with X-linked hypophosphatemia. Pediatric nephrology (Berlin, Germany), 1995, Volume: 9, Issue:6 Topics: Adolescent; Arginine; Body Height; Child; Child, Preschool; Female; Growth Disorders; Growth Hormone; Humans; Hypophosphatemia, Familial; Infant; Insulin-Like Growth Factor I; Levodopa; Male; Stimulation, Chemical	1995

Other Studies

2 other study(ies) available for arginine and Hypophosphatemia, Familial

Article	Year
A novel nonsense mutation in the first zinc finger of the vitamin D receptor causing hereditary 1,25-dihydroxyvitamin D3-resistant rickets. The Journal of clinical endocrinology and metabolism, 1997, Volume: 82, Issue:11 Topics: Arginine; Base Sequence; Calcitriol; Child; Codon; DNA, Complementary; Humans; Hypophosphatemia, Familial; Male; Pedigree; Point Mutation; Polymerase Chain Reaction; Receptors, Calcitriol; Zinc Fingers	1997
A rationale for treatment of hereditary vitamin D-resistant rickets with analogs of 1 alpha,25-dihydroxyvitamin D(3). The Journal of biological chemistry, 2001, Aug-03, Volume: 276, Issue:31 Topics: Amino Acid Substitution; Animals; Arginine; Binding, Competitive; Calcitriol; Cell Line; Cells, Cultured; Chlorocebus aethiops; COS Cells; Cysteine; Fibroblasts; Genes, Reporter; Humans; Hypophosphatemia, Familial; Kinetics; Leucine; Mutagenesis, Site-Directed; Phenylalanine; Receptors, Calcitriol; Recombinant Proteins; Skin; Structure-Activity Relationship; Transcription, Genetic; Transcriptional Activation; Transfection	2001

Article

Year

A novel nonsense mutation in the first zinc finger of the vitamin D receptor causing hereditary 1,25-dihydroxyvitamin D3-resistant rickets.

The Journal of clinical endocrinology and metabolism, 1997, Volume: 82, Issue:11

Topics: Arginine; Base Sequence; Calcitriol; Child; Codon; DNA, Complementary; Humans; Hypophosphatemia, Familial; Male; Pedigree; Point Mutation; Polymerase Chain Reaction; Receptors, Calcitriol; Zinc Fingers

1997

A rationale for treatment of hereditary vitamin D-resistant rickets with analogs of 1 alpha,25-dihydroxyvitamin D(3).

The Journal of biological chemistry, 2001, Aug-03, Volume: 276, Issue:31

Topics: Amino Acid Substitution; Animals; Arginine; Binding, Competitive; Calcitriol; Cell Line; Cells, Cultured; Chlorocebus aethiops; COS Cells; Cysteine; Fibroblasts; Genes, Reporter; Humans; Hypophosphatemia, Familial; Kinetics; Leucine; Mutagenesis, Site-Directed; Phenylalanine; Receptors, Calcitriol; Recombinant Proteins; Skin; Structure-Activity Relationship; Transcription, Genetic; Transcriptional Activation; Transfection

2001