galactose has been researched along with Nephrocalcinosis in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Milla, PJ; Pahari, A; van't Hoff, WG | 1 |
| Balfe, JW; Barbar, M; El-Naggar, W; Taha, D | 1 |
| Altinöz, S; Ecevit, C; Kasahara, M; Maeda, M; Oztürk, AA; Soylu, OB; Temizkan, AK | 1 |
3 other study(ies) available for galactose and Nephrocalcinosis
| Article | Year |
|---|---|
Neonatal nephrocalcinosis in association with glucose-galactose malabsorption.
Topics: Calcium; Diarrhea; Galactose; Glucose; Growth Disorders; Humans; Hypercalcemia; Infant, Newborn; Karyotyping; Kidney; Malabsorption Syndromes; Male; Nephrocalcinosis; Oxalates; Polyuria; Ultrasonography | 2003 |
Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis.
Topics: Acidosis, Renal Tubular; Female; Galactose; Glucose; Glucose Metabolism Disorders; Humans; Infant; Infant, Newborn; Malabsorption Syndromes; Male; Nephrocalcinosis | 2005 |
Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.
Topics: Fanconi Syndrome; Female; Galactose; Glucose; Glucose Metabolism Disorders; Humans; Infant; Malabsorption Syndromes; Mutation, Missense; Nephrocalcinosis; Sodium-Glucose Transporter 1 | 2008 |