glutamic acid and Polyneuropathy, Acquired

glutamic acid has been researched along with Polyneuropathy, Acquired in 3 studies

Research

Studies (3)

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

Authors

Authors	Studies
Delgado Rodrigues, RN; Goulart, LI; Prieto Peres, MF	1
Alvarado, MV; Busse, A; León, P; Monterroso, V; Sánchez, MA	1
Alevra, X; Christodoulou, K; Georgiou, DM; Hadjisavvas, A; Kleopa, KA; Kyriakides, T; Nicolaou, P; Zamba-Papanicolaou, E	1

Reviews

1 review(s) available for glutamic acid and Polyneuropathy, Acquired

Article	Year
Restless legs syndrome and pain disorders: what's in common? Current pain and headache reports, 2014, Volume: 18, Issue:11 Topics: Calcium Channel Blockers; Diagnosis, Differential; Dopamine Agonists; Fibromyalgia; gamma-Aminobutyric Acid; Glutamic Acid; Humans; Hypnotics and Sedatives; Iron; Melatonin; Migraine Disorders; Pain; Polyneuropathies; Restless Legs Syndrome; Serotonin; Sleep Deprivation; Vitamin D	2014

Article

Year

Restless legs syndrome and pain disorders: what's in common?

Current pain and headache reports, 2014, Volume: 18, Issue:11

Topics: Calcium Channel Blockers; Diagnosis, Differential; Dopamine Agonists; Fibromyalgia; gamma-Aminobutyric Acid; Glutamic Acid; Humans; Hypnotics and Sedatives; Iron; Melatonin; Migraine Disorders; Pain; Polyneuropathies; Restless Legs Syndrome; Serotonin; Sleep Deprivation; Vitamin D

2014

Other Studies

2 other study(ies) available for glutamic acid and Polyneuropathy, Acquired

Article	Year
A severe form of amyloidotic polyneuropathy in a Costa Rican family with a rare transthyretin mutation (Glu54Lys). American journal of medical genetics. Part A, 2004, Jul-15, Volume: 128A, Issue:2 Topics: Adult; Amyloidosis; Base Sequence; Blotting, Western; Coloring Agents; Congo Red; Costa Rica; DNA; DNA Mutational Analysis; Exons; Family Health; Female; Glutamic Acid; Humans; Immunohistochemistry; Lysine; Male; Molecular Sequence Data; Mouth Mucosa; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Polyneuropathies; Prealbumin	2004
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

A severe form of amyloidotic polyneuropathy in a Costa Rican family with a rare transthyretin mutation (Glu54Lys).

American journal of medical genetics. Part A, 2004, Jul-15, Volume: 128A, Issue:2

Topics: Adult; Amyloidosis; Base Sequence; Blotting, Western; Coloring Agents; Congo Red; Costa Rica; DNA; DNA Mutational Analysis; Exons; Family Health; Female; Glutamic Acid; Humans; Immunohistochemistry; Lysine; Male; Molecular Sequence Data; Mouth Mucosa; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Polyneuropathies; Prealbumin

2004

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