arginine and Acquired Neuromyotonia

arginine has been researched along with Acquired Neuromyotonia 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	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Damiani, E; Drögemüller, C; Drögemüller, M; Gentile, A; Leeb, T; Mascarello, F; Rossi, M; Sacchetto, R; Testoni, S	1
Eunson, LH; Hanna, MG; Jungbluth, H; Kinali, M; Manzur, AY; Mercuri, E; Muntoni, F; Sewry, CA	1

Other Studies

2 other study(ies) available for arginine and Acquired Neuromyotonia

Article	Year
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease. Genomics, 2008, Volume: 92, Issue:6 Topics: Amino Acid Sequence; Animals; Arginine; Cattle; Disease Models, Animal; DNA Mutational Analysis; Female; Humans; Isaacs Syndrome; Male; Molecular Sequence Data; Mutation, Missense; Myotonia Congenita; Pedigree; Physical Conditioning, Animal; Sarcoplasmic Reticulum Calcium-Transporting ATPases	2008
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia. Neuromuscular disorders : NMD, 2004, Volume: 14, Issue:10 Topics: Adult; Arginine; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Histological Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Muscle, Skeletal; Mutation; NAD; Phenotype; Potassium Channels, Voltage-Gated; Threonine	2004

Article

Year

Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.

Genomics, 2008, Volume: 92, Issue:6

Topics: Amino Acid Sequence; Animals; Arginine; Cattle; Disease Models, Animal; DNA Mutational Analysis; Female; Humans; Isaacs Syndrome; Male; Molecular Sequence Data; Mutation, Missense; Myotonia Congenita; Pedigree; Physical Conditioning, Animal; Sarcoplasmic Reticulum Calcium-Transporting ATPases

2008

Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia.

Neuromuscular disorders : NMD, 2004, Volume: 14, Issue:10

Topics: Adult; Arginine; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Histological Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Muscle, Skeletal; Mutation; NAD; Phenotype; Potassium Channels, Voltage-Gated; Threonine

2004