valine and Atrophy

valine has been researched along with Atrophy in 14 studies

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's9 (64.29)29.6817
2010's5 (35.71)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barker, RA; Bishop, S; Fallon, S; Hughes, L; Owen, AM; Rowe, JB; Williams-Gray, CH1
Bakker, SC; Hoogendoorn, ML; Hulshoff Pol, HE; Kahn, RS; Koolschijn, PC; van Haren, NE1
Erickson, KI; Miller, DL; Roecklein, KA1
Bouda, M; Hes, O; Hribova, P; Jindra, P; Reischig, T; Treska, V; Viklicky, O1
Demant, A; El Arbi, S; Horneff, G; Kohlschmidt, N1
Aronica, E; Poll-The, BT; Rozemuller-Kwakkel, JM; Troost, D; van der Heide, M; van Kempen, AA; van Slooten, HJ1
Kremer, BP; Rabelink, GM; Sinke, RJ; van de Warrenburg, BP; Vlak, MH1
Baghai, T; Bondy, B; Born, C; Bottlender, R; Frodl, T; Meisenzahl, EM; Möller, HJ; Reiser, M; Rupprecht, R; Schmitt, G; Schüle, C; Zill, P1
Horan, M; Jackson, A; Mayes, A; Miyajima, F; Ollier, W; Payton, A; Pendleton, N; Rabbitt, P; Thacker, N1
Andreasen, NC; Dawson, JD; Ho, BC; Wassink, TH1
Kawamura, Y; Kawasaki, Y; Kobayashi, S; Kurachi, M; Ozaki, N; Sasaoka, T; Seto, H; Suzuki, M; Takahashi, N; Takahashi, T; Tsuneki, H; Tsunoda, M; Zhou, SY1
Belet, U; Danaci, M; Incesu, L; Tasdemir, HA; Yazicioglu, AK1
Cooper, ME; Cox, AJ; Gilbert, RE; Kelly, DJ; Tolcos, M; Wilkinson-Berka, JL1
Abe, H; Doh-ura, K; Iida, T; Iwaki, T; Kawashima, T1

Reviews

1 review(s) available for valine and Atrophy

ArticleYear
The aging hippocampus: interactions between exercise, depression, and BDNF.
    The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry, 2012, Volume: 18, Issue:1

    Topics: Aging; Animals; Atrophy; Brain-Derived Neurotrophic Factor; Depression; Exercise; Genotype; Hippocampus; Humans; Memory; Methionine; Mice; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Rats; Valine

2012

Trials

1 trial(s) available for valine and Atrophy

ArticleYear
Long-term outcomes of pre-emptive valganciclovir compared with valacyclovir prophylaxis for prevention of cytomegalovirus in renal transplantation.
    Journal of the American Society of Nephrology : JASN, 2012, Volume: 23, Issue:9

    Topics: Acyclovir; Adult; Antiviral Agents; Atrophy; Biopsy; Cytomegalovirus; Cytomegalovirus Infections; Female; Fibrosis; Follow-Up Studies; Ganciclovir; Graft Survival; Humans; Kaplan-Meier Estimate; Kidney; Kidney Transplantation; Longitudinal Studies; Male; Middle Aged; Treatment Outcome; Valacyclovir; Valganciclovir; Valine

2012

Other Studies

12 other study(ies) available for valine and Atrophy

ArticleYear
The val158met COMT polymorphism's effect on atrophy in healthy aging and Parkinson's disease.
    Neurobiology of aging, 2010, Volume: 31, Issue:6

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Aging; Atrophy; Catechol O-Methyltransferase; Female; Genotype; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Genetic; Prefrontal Cortex; Regression Analysis; Valine; Young Adult

2010
Effects of brain-derived neurotrophic factor Val66Met polymorphism on hippocampal volume change in schizophrenia.
    Hippocampus, 2010, Volume: 20, Issue:9

    Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Atrophy; Brain-Derived Neurotrophic Factor; Female; Genetic Predisposition to Disease; Hippocampus; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Schizophrenia; Valine; Young Adult

2010
Infantile neuroaxonal dystrophy: a rare cause of early childhood ataxia with poor prognosis.
    Klinische Padiatrie, 2013, Volume: 225, Issue:1

    Topics: Atrophy; Base Pairing; Cerebellum; Child, Preschool; Chromosome Deletion; Diagnosis, Differential; Disease Progression; DNA Mutational Analysis; Exons; Frontal Lobe; Gait Ataxia; Group VI Phospholipases A2; Homozygote; Humans; Magnetic Resonance Imaging; Male; Neuroaxonal Dystrophies; Temporal Lobe; Valine

2013
Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology.
    Acta neuropathologica, 2005, Volume: 109, Issue:4

    Topics: Arginine; Atrophy; Calbindins; Cerebellum; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Humans; Immunohistochemistry; Infant, Newborn; Male; Methionine; Microscopy, Electron, Transmission; Muscle, Skeletal; Mutation; Neuroglia; Neurons; Phosphotransferases (Phosphomutases); S100 Calcium Binding Protein G; Threonine; Valine; Vimentin

2005
Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype.
    Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:7

    Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Atrophy; Basal Ganglia Diseases; Cerebellum; DNA Mutational Analysis; Exons; Female; Glutamic Acid; Humans; Isoenzymes; Magnetic Resonance Imaging; Male; Middle Aged; Mutation, Missense; Myoclonus; Netherlands; Pedigree; Phenotype; Protein Kinase C; Spinocerebellar Ataxias; Tremor; Valine

2006
Association of the brain-derived neurotrophic factor Val66Met polymorphism with reduced hippocampal volumes in major depression.
    Archives of general psychiatry, 2007, Volume: 64, Issue:4

    Topics: Adult; Amygdala; Atrophy; Brain-Derived Neurotrophic Factor; Cross-Sectional Studies; Depressive Disorder, Major; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Methionine; Neuronal Plasticity; Polymorphism, Genetic; Valine

2007
Brain-derived neurotrophic factor polymorphism Val66Met influences cognitive abilities in the elderly.
    Genes, brain, and behavior, 2008, Volume: 7, Issue:4

    Topics: Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Atrophy; Brain-Derived Neurotrophic Factor; Cognition Disorders; Cohort Studies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Memory; Memory Disorders; Methionine; Middle Aged; Mutation; Neuropsychological Tests; Polymorphism, Genetic; Valine

2008
Association between brain-derived neurotrophic factor Val66Met gene polymorphism and progressive brain volume changes in schizophrenia.
    The American journal of psychiatry, 2007, Volume: 164, Issue:12

    Topics: Adult; Antipsychotic Agents; Atrophy; Brain; Brain-Derived Neurotrophic Factor; Cognition Disorders; Female; Frontal Lobe; Genetic Variation; Genotype; Humans; Longitudinal Studies; Magnetic Resonance Imaging; Male; Methionine; Neuronal Plasticity; Neuropsychological Tests; Polymorphism, Genetic; Schizophrenia; Schizophrenic Psychology; Severity of Illness Index; Valine

2007
Association between the brain-derived neurotrophic factor Val66Met polymorphism and brain morphology in a Japanese sample of schizophrenia and healthy comparisons.
    Neuroscience letters, 2008, Apr-11, Volume: 435, Issue:1

    Topics: Adult; Amino Acid Substitution; Atrophy; Brain; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Female; Functional Laterality; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Japan; Magnetic Resonance Imaging; Male; Methionine; Parahippocampal Gyrus; Polymorphism, Genetic; Schizophrenia; Valine

2008
[Maple syrup urine disease].
    La Radiologia medica, 2001, Volume: 102, Issue:3

    Topics: Atrophy; Brain; Cerebellum; Chromatography, Paper; Female; Humans; Infant; Isoleucine; Leucine; Magnetic Resonance Imaging; Maple Syrup Urine Disease; Mesencephalon; Valine

2001
Attenuation of tubular apoptosis by blockade of the renin-angiotensin system in diabetic Ren-2 rats.
    Kidney international, 2002, Volume: 61, Issue:1

    Topics: Angiotensin-Converting Enzyme Inhibitors; Animals; Animals, Genetically Modified; Antihypertensive Agents; Apoptosis; Atrophy; Autoradiography; Diabetes Mellitus, Experimental; Diabetic Nephropathies; Epidermal Growth Factor; Female; Fibrosis; Gene Expression; In Situ Hybridization; In Situ Nick-End Labeling; Kidney Tubules; Nephritis, Interstitial; Perindopril; Rats; Renin-Angiotensin System; RNA, Messenger; Tetrazoles; Transforming Growth Factor beta; Valine; Valsartan

2002
An atypical case of sporadic Creutzfeldt-Jakob disease with Parkinson's disease.
    Neuropathology : official journal of the Japanese Society of Neuropathology, 2001, Volume: 21, Issue:4

    Topics: Aged; Atrophy; Cerebral Cortex; Creutzfeldt-Jakob Syndrome; Fatal Outcome; Female; Genetic Carrier Screening; Humans; Middle Aged; Parkinson Disease; Prions; Valine

2001