vigabatrin and Decreased Muscle Tone studies

vigabatrin and Decreased Muscle Tone

Research Excerpts

Excerpt	Relevance	Reference
"Angelman syndrome is a rare genetic disorder scarcely diagnosed before the age of two years."	1.37	Angelman syndrome and pseudo-hypsarrhythmia: a diagnostic pitfall. ( Convers, P; Darteyre, S; Lebrun, M; Mazzola, L; Ville, D, 2011)
"His younger brother had mild axial hypotonia when 5 months old."	1.36	[Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin]. ( Escalera, GI; Ferrer, I; Jakobs, C; Marina, LC; Pérez-Cerdá, C; Sala, PR; Salomons, GS, 2010)

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	1 (33.33)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Timeframe

Studies, this research(%)

All Research%

pre-1990

0 (0.00)

18.7374

1990's

0 (0.00)

18.2507

2000's

1 (33.33)

29.6817

2010's

2 (66.67)

24.3611

2020's

0 (0.00)

2.80

Authors

Authors	Studies
Escalera, GI	1
Ferrer, I	1
Marina, LC	1
Sala, PR	1
Salomons, GS	1
Jakobs, C	2
Pérez-Cerdá, C	1
Darteyre, S	1
Mazzola, L	1
Convers, P	1
Lebrun, M	1
Ville, D	1
Kölker, S	1
Hoffmann, GF	1
Schor, DS	1
Feyh, P	1
Wagner, L	1
Jeffrey, I	1
Pourfarzam, M	1
Okun, JG	1
Zschocke, J	1
Baric, I	1
Bain, MD	1
Chalmers, RA	1

Studies

Escalera, GI

Ferrer, I

Marina, LC

Sala, PR

Salomons, GS

Jakobs, C

Pérez-Cerdá, C

Darteyre, S

Mazzola, L

Convers, P

Lebrun, M

Ville, D

Kölker, S

Hoffmann, GF

Schor, DS

Feyh, P

Wagner, L

Jeffrey, I

Pourfarzam, M

Okun, JG

Zschocke, J

Baric, I

Bain, MD

Chalmers, RA

Other Studies

3 other studies available for vigabatrin and Decreased Muscle Tone

Article	Year
[Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin]. Anales de pediatria (Barcelona, Spain : 2003), 2010, Volume: 72, Issue:2 Topics: Adult; Dose-Response Relationship, Drug; Female; GABA Agents; gamma-Aminobutyric Acid; Humans; Infan	2010
Angelman syndrome and pseudo-hypsarrhythmia: a diagnostic pitfall. Epileptic disorders : international epilepsy journal with videotape, 2011, Volume: 13, Issue:3 Topics: Angelman Syndrome; Anticonvulsants; Chromosome Deletion; Chromosomes, Human, Pair 15; Diagnosis, Dif	2011
Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen. Neuropediatrics, 2003, Volume: 34, Issue:5 Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Anal	2003

Article

Year

[Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin].

Anales de pediatria (Barcelona, Spain : 2003), 2010, Volume: 72, Issue:2

Topics: Adult; Dose-Response Relationship, Drug; Female; GABA Agents; gamma-Aminobutyric Acid; Humans; Infan

2010

Angelman syndrome and pseudo-hypsarrhythmia: a diagnostic pitfall.

Epileptic disorders : international epilepsy journal with videotape, 2011, Volume: 13, Issue:3

Topics: Angelman Syndrome; Anticonvulsants; Chromosome Deletion; Chromosomes, Human, Pair 15; Diagnosis, Dif

2011

Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.

Neuropediatrics, 2003, Volume: 34, Issue:5

Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Anal

2003