Page last updated: 2024-08-17

aspartic acid and Albers-Schoenberg Disease

aspartic acid has been researched along with Albers-Schoenberg Disease in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Albagha, OM; Caliumi, C; D'Erasmo, E; Delfini, E; Diacinti, D; Iacobini, M; Letizia, C; Migliaccio, S; Ralston, SH; Roggini, M; Taranta, A; Teti, A	1
Buzzi, D; Castellano Chiodo, D; DiRocco, M; Gandolfo, C; Morana, G; Rossi, A	1

Other Studies

2 other study(ies) available for aspartic acid and Albers-Schoenberg Disease

Article	Year
Type II benign osteopetrosis (Albers-Schönberg disease) caused by a novel mutation in CLCN7 presenting with unusual clinical manifestations. Calcified tissue international, 2004, Volume: 74, Issue:1 Topics: Adolescent; Amino Acid Substitution; Aspartic Acid; Biomarkers; Cells, Cultured; Chloride Channels; DNA Mutational Analysis; Exons; Genes, Dominant; Heterozygote; Humans; Male; Mutation; Osteoclasts; Osteopetrosis; Pedigree; Radiography; RNA, Messenger; Sequence Analysis, DNA	2004
Neuroimaging findings in malignant infantile osteopetrosis due to OSTM1 mutations. Neuropediatrics, 2007, Volume: 38, Issue:3 Topics: Aspartic Acid; Choline; Creatine; DNA Mutational Analysis; Female; Heredodegenerative Disorders, Nervous System; Humans; Infant; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Membrane Proteins; Mutation; Osteopetrosis; Ubiquitin-Protein Ligases	2007

Article

Year

Type II benign osteopetrosis (Albers-Schönberg disease) caused by a novel mutation in CLCN7 presenting with unusual clinical manifestations.

Calcified tissue international, 2004, Volume: 74, Issue:1

Topics: Adolescent; Amino Acid Substitution; Aspartic Acid; Biomarkers; Cells, Cultured; Chloride Channels; DNA Mutational Analysis; Exons; Genes, Dominant; Heterozygote; Humans; Male; Mutation; Osteoclasts; Osteopetrosis; Pedigree; Radiography; RNA, Messenger; Sequence Analysis, DNA

2004

Neuroimaging findings in malignant infantile osteopetrosis due to OSTM1 mutations.

Neuropediatrics, 2007, Volume: 38, Issue:3

Topics: Aspartic Acid; Choline; Creatine; DNA Mutational Analysis; Female; Heredodegenerative Disorders, Nervous System; Humans; Infant; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Membrane Proteins; Mutation; Osteopetrosis; Ubiquitin-Protein Ligases

2007