valine and Demyelinating Diseases

valine has been researched along with Demyelinating Diseases 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
SCOTT, EB	1
Alevra, X; Christodoulou, K; Georgiou, DM; Hadjisavvas, A; Kleopa, KA; Kyriakides, T; Nicolaou, P; Zamba-Papanicolaou, E	1

Other Studies

2 other study(ies) available for valine and Demyelinating Diseases

Article	Year
HISTOPATHOLOGY OF AMINO ACID DEFICIENCIES. VII. VALINE. Experimental and molecular pathology, 1964, Volume: 3 Topics: Brain; Deficiency Diseases; Demyelinating Diseases; Facial Nerve; Myocardium; Neurologic Manifestations; Pathology; Research; Thymus Gland; Valine; Vestibular Nerve	1964
Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X. Neurology, 2006, Feb-14, Volume: 66, Issue:3 Topics: Aged; Amino Acid Substitution; Central Nervous System Diseases; Charcot-Marie-Tooth Disease; Connexins; Demyelinating Diseases; Electromyography; Female; Gap Junction beta-1 Protein; Glutamic Acid; HeLa Cells; Humans; Leucine; Male; Middle Aged; Mutation, Missense; Neural Conduction; Pedigree; Phenotype; Polyneuropathies; Proline; Sural Nerve; Valine	2006

Article

Year

HISTOPATHOLOGY OF AMINO ACID DEFICIENCIES. VII. VALINE.

Experimental and molecular pathology, 1964, Volume: 3

Topics: Brain; Deficiency Diseases; Demyelinating Diseases; Facial Nerve; Myocardium; Neurologic Manifestations; Pathology; Research; Thymus Gland; Valine; Vestibular Nerve

1964

Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.

Neurology, 2006, Feb-14, Volume: 66, Issue:3

Topics: Aged; Amino Acid Substitution; Central Nervous System Diseases; Charcot-Marie-Tooth Disease; Connexins; Demyelinating Diseases; Electromyography; Female; Gap Junction beta-1 Protein; Glutamic Acid; HeLa Cells; Humans; Leucine; Male; Middle Aged; Mutation, Missense; Neural Conduction; Pedigree; Phenotype; Polyneuropathies; Proline; Sural Nerve; Valine

2006