tryptophan and Chondrodystrophic Myotonia

tryptophan has been researched along with Chondrodystrophic Myotonia in 3 studies

Research

Studies (3)

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

Authors

Authors	Studies
Ballhausen, D; Bellus, G; Bonafé, L; Classen, M; Cohn, DH; Cole, WG; Hamel, BC; Hecht, JT; Spranger, J; Superti-Furga, A; Terhal, P; Unger, SL; Zabel, B	1
Matsui, Y	1
Bona, C; Ionescu, V; Stánescu, V	1

Reviews

1 review(s) available for tryptophan and Chondrodystrophic Myotonia

Article	Year
[Type IX collagen diseases]. Clinical calcium, 2006, Volume: 16, Issue:11 Topics: Animals; Collagen Diseases; Collagen Type IX; Humans; Lumbar Vertebrae; Mice; Mice, Transgenic; Musculoskeletal Diseases; Mutation; Osteochondrodysplasias; Polymorphism, Genetic; Spinal Diseases; Tryptophan	2006

Other Studies

2 other study(ies) available for tryptophan and Chondrodystrophic Myotonia

Article	Year
Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279W. Journal of medical genetics, 2003, Volume: 40, Issue:1 Topics: Adolescent; Adult; Amino Acid Substitution; Anion Transport Proteins; Arginine; Biological Transport; Carrier Proteins; Child; Chromosome Mapping; Female; Genes, Recessive; Homozygote; Humans; Male; Membrane Transport Proteins; Middle Aged; Mutation; Osteochondrodysplasias; Phenotype; Sulfate Transporters; Sulfates; Tryptophan	2003
Histochemical studies on tibial growing cartilage in polyepiphysial dysplasia (Feirbank disease, Müller-Ribbing-Krankheit). Acta histochemica, 1965, Aug-14, Volume: 21, Issue:5 Topics: Adolescent; Cartilage; Child; DNA; Epiphyses; Female; Glycoproteins; Glycosaminoglycans; Histidine; Histocytochemistry; Histones; Humans; In Vitro Techniques; Male; Osteochondrodysplasias; Proteins; RNA; Staining and Labeling; Tibia; Tryptophan	1965

Article

Year

Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279W.

Journal of medical genetics, 2003, Volume: 40, Issue:1

Topics: Adolescent; Adult; Amino Acid Substitution; Anion Transport Proteins; Arginine; Biological Transport; Carrier Proteins; Child; Chromosome Mapping; Female; Genes, Recessive; Homozygote; Humans; Male; Membrane Transport Proteins; Middle Aged; Mutation; Osteochondrodysplasias; Phenotype; Sulfate Transporters; Sulfates; Tryptophan

2003

Histochemical studies on tibial growing cartilage in polyepiphysial dysplasia (Feirbank disease, Müller-Ribbing-Krankheit).

Acta histochemica, 1965, Aug-14, Volume: 21, Issue:5

Topics: Adolescent; Cartilage; Child; DNA; Epiphyses; Female; Glycoproteins; Glycosaminoglycans; Histidine; Histocytochemistry; Histones; Humans; In Vitro Techniques; Male; Osteochondrodysplasias; Proteins; RNA; Staining and Labeling; Tibia; Tryptophan

1965