proline and Brown Tendon Sheath Syndrome

proline has been researched along with Brown Tendon Sheath Syndrome 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	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Camaño, P; DiMauro, S; Emmanuele, V; Hirano, M; Otaegui, D; Oz, O; Paradas, C	1
Beemer, FA; de Sain, MG; Dorland, B; Emanuel, BS; Kahn, RS; Kemner, C; Rappaport, EF; Sijmens-Morcus, ME; Sprong, M; Turetsky, BI; van Engeland, H; Vorstman, JA	1

Other Studies

2 other study(ies) available for proline and Brown Tendon Sheath Syndrome

Article	Year
Longitudinal clinical follow-up of a large family with the R357P Twinkle mutation. JAMA neurology, 2013, Volume: 70, Issue:11 Topics: Arginine; Blepharoptosis; DNA Helicases; Family Health; Female; Humans; Longitudinal Studies; Middle Aged; Mitochondrial Proteins; Mutation; Ocular Motility Disorders; Proline	2013
Proline affects brain function in 22q11DS children with the low activity COMT 158 allele. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Volume: 34, Issue:3 Topics: Adolescent; Alleles; Catechol O-Methyltransferase; Child; DiGeorge Syndrome; Dopamine; Electroencephalography; Female; Genotype; Humans; Male; Ocular Motility Disorders; Prefrontal Cortex; Proline; Proline Oxidase; Reflex, Startle; Sensory Gating	2009

Article

Year

Longitudinal clinical follow-up of a large family with the R357P Twinkle mutation.

JAMA neurology, 2013, Volume: 70, Issue:11

Topics: Arginine; Blepharoptosis; DNA Helicases; Family Health; Female; Humans; Longitudinal Studies; Middle Aged; Mitochondrial Proteins; Mutation; Ocular Motility Disorders; Proline

2013

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Volume: 34, Issue:3

Topics: Adolescent; Alleles; Catechol O-Methyltransferase; Child; DiGeorge Syndrome; Dopamine; Electroencephalography; Female; Genotype; Humans; Male; Ocular Motility Disorders; Prefrontal Cortex; Proline; Proline Oxidase; Reflex, Startle; Sensory Gating

2009