Page last updated: 2024-08-17

nad and Amyoplasia Congenita

nad has been researched along with Amyoplasia Congenita in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Barone, R; Borrelli, L; Costanzo, P; Esposito, G; Izzo, P; Pavone, L; Salvatore, F; Vitagliano, L; Zagari, A	1
Bharucha, EP; Dastur, DK; Razzak, ZA	1

Other Studies

2 other study(ies) available for nad and Amyoplasia Congenita

Article	Year
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function. The Biochemical journal, 2004, May-15, Volume: 380, Issue:Pt 1 Topics: Amino Acid Substitution; Anemia, Hemolytic, Congenital; Arthrogryposis; Circular Dichroism; Codon; Fructose-Bisphosphate Aldolase; Glycine; Heterozygote; Humans; Infant; Kinetics; Male; Models, Molecular; Molecular Weight; Muscle Weakness; Mutagenesis, Site-Directed; Mutation, Missense; NAD; Point Mutation; Protein Conformation; Protein Denaturation; Protein Structure, Tertiary; Recombinant Fusion Proteins; Structure-Activity Relationship	2004
Arthrogryposis multiplex congenita. 2. Muscle pathology and pathogenesis. Journal of neurology, neurosurgery, and psychiatry, 1972, Volume: 35, Issue:4 Topics: Adenosine Triphosphatases; Arthrogryposis; Child; Creatine Kinase; Denervation; Electromyography; Glucosyltransferases; Histocytochemistry; Humans; Muscle Development; Muscle Spindles; Muscles; Muscular Atrophy; NAD; Staining and Labeling; Succinate Dehydrogenase	1972

Article

Year

Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.

The Biochemical journal, 2004, May-15, Volume: 380, Issue:Pt 1

Topics: Amino Acid Substitution; Anemia, Hemolytic, Congenital; Arthrogryposis; Circular Dichroism; Codon; Fructose-Bisphosphate Aldolase; Glycine; Heterozygote; Humans; Infant; Kinetics; Male; Models, Molecular; Molecular Weight; Muscle Weakness; Mutagenesis, Site-Directed; Mutation, Missense; NAD; Point Mutation; Protein Conformation; Protein Denaturation; Protein Structure, Tertiary; Recombinant Fusion Proteins; Structure-Activity Relationship

2004

Arthrogryposis multiplex congenita. 2. Muscle pathology and pathogenesis.

Journal of neurology, neurosurgery, and psychiatry, 1972, Volume: 35, Issue:4

Topics: Adenosine Triphosphatases; Arthrogryposis; Child; Creatine Kinase; Denervation; Electromyography; Glucosyltransferases; Histocytochemistry; Humans; Muscle Development; Muscle Spindles; Muscles; Muscular Atrophy; NAD; Staining and Labeling; Succinate Dehydrogenase

1972