Page last updated: 2024-08-26

pyridinoline and Hyperkyphosis

pyridinoline has been researched along with Hyperkyphosis 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	1 (50.00)	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
Al-Gazali, LI; Brunner, HG; Giunta, C; Kraenzlin, ME; Randolph, A; Steinmann, B	1

Reviews

1 review(s) available for pyridinoline and Hyperkyphosis

Article	Year
Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers-Danlos syndrome (EDS VIA). American journal of medical genetics. Part A, 2005, Mar-01, Volume: 133A, Issue:2 Topics: Abnormalities, Multiple; Amino Acids; Collagen Type III; Collagen Type V; Consanguinity; Diagnosis, Differential; Edema; Ehlers-Danlos Syndrome; Electrophoresis, Polyacrylamide Gel; Female; Growth Disorders; Humans; Infant; Kyphosis; Muscle Hypotonia; Mutation; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Syndrome	2005

Article

Year

Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers-Danlos syndrome (EDS VIA).

American journal of medical genetics. Part A, 2005, Mar-01, Volume: 133A, Issue:2

Topics: Abnormalities, Multiple; Amino Acids; Collagen Type III; Collagen Type V; Consanguinity; Diagnosis, Differential; Edema; Ehlers-Danlos Syndrome; Electrophoresis, Polyacrylamide Gel; Female; Growth Disorders; Humans; Infant; Kyphosis; Muscle Hypotonia; Mutation; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Syndrome

2005

Other Studies

1 other study(ies) available for pyridinoline and Hyperkyphosis

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

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