Page last updated: 2024-08-26

pyridinoline and Scoliosis

pyridinoline has been researched along with Scoliosis in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Ataman, E; Baumgartner, M; Chopra, M; Garcia, S; Giunta, C; Jones, K; Kariminejad, A; Kraenzlin, M; Marcelis, C; Rohrbach, M; Serdaroglu, G; Vandersteen, A; Yiş, U	1
Giunta, C; Jarisch, A; König, R; Steinmann, B; Zielen, S	1

Other Studies

2 other study(ies) available for pyridinoline and Scoliosis

Article	Year
Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation. Orphanet journal of rare diseases, 2011, Jun-23, Volume: 6 Topics: Adolescent; Adult; Amino Acids; Biopsy; Cells, Cultured; Child; Child, Preschool; Developmental Disabilities; DNA Mutational Analysis; Ehlers-Danlos Syndrome; Female; Fibroblasts; Genotype; Humans; Infant; Kyphosis; Male; Muscle Hypotonia; Phenotype; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Scoliosis; Skin	2011
Sibs affected with both Ehlers-Danlos syndrome type IV and cystic fibrosis. American journal of medical genetics, 1998, Aug-06, Volume: 78, Issue:5 Topics: Amino Acids; Collagen; Consanguinity; Cystic Fibrosis; Ehlers-Danlos Syndrome; Female; Genes, Recessive; Hand Deformities, Congenital; Humans; Hydroxylysine; Infant, Newborn; Nuclear Family; Pedigree; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Prognosis; Radiography; Scoliosis; Turkey	1998

Article

Year

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation.

Orphanet journal of rare diseases, 2011, Jun-23, Volume: 6

Topics: Adolescent; Adult; Amino Acids; Biopsy; Cells, Cultured; Child; Child, Preschool; Developmental Disabilities; DNA Mutational Analysis; Ehlers-Danlos Syndrome; Female; Fibroblasts; Genotype; Humans; Infant; Kyphosis; Male; Muscle Hypotonia; Phenotype; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Scoliosis; Skin

2011

Sibs affected with both Ehlers-Danlos syndrome type IV and cystic fibrosis.

American journal of medical genetics, 1998, Aug-06, Volume: 78, Issue:5

Topics: Amino Acids; Collagen; Consanguinity; Cystic Fibrosis; Ehlers-Danlos Syndrome; Female; Genes, Recessive; Hand Deformities, Congenital; Humans; Hydroxylysine; Infant, Newborn; Nuclear Family; Pedigree; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Prognosis; Radiography; Scoliosis; Turkey

1998