Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0003635 (apraxia)
 2,817 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds) .

Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .
Human Gene/Protein
aprataxin 0.013
senataxin 0.010
ALS4 0.006
APTX 0.004
SETX 0.003
FOXP2 0.002
PNKP 0.001
AOA 0.001
FAM149B1 0.000
C4orf21 0.000
ANKRD12 0.000
forkhead box P2 0.000
ZNF280D 0.000
NPHP1 0.000
MRI 0.000
NAGPA 0.000
MKS6 0.000
Rett syndrome 0.000
ATLD 0.000
PIK3R5 0.000
PAPOLG 0.000
KPTN 0.000
nephrocystin-4 0.000
EFCAB4B 0.000
NPHP4 0.000
PARP11 0.000
TSPAN9 0.000
IOSCA 0.000
SCAR1 0.000
Caytaxin 0.000
SANDO 0.000
glutaryl CoA dehydrogenase 0.000
nephrocystin 0.000
CDH18 0.000
FOXP2 protein 0.000
TMEM216 0.000
GLP2R 0.000
cerebellin 1 precursor 0.000
POLG protein 0.000
GATAD2B 0.000
RIMS1 0.000
CC2D2A 0.000
GNPTG 0.000
SACS 0.000
A-T 0.000
B3GALNT2 0.000
ATM protein 0.000
CNTNAP2 0.000
SLC30A9 0.000
galactose-1-phosphate uridyltransferase 0.000
NGL-1 0.000
IMP 0.000
ZFHX4 0.000
Abelson helper integration site 1 0.000
MYO10 0.000
She 0.000
INPP5E 0.000
STX6 0.000
COQ4 0.000
ADCK4 0.000
GRN 0.000
COQ6 0.000
PDE6D 0.000
frataxin 0.000
DNA ligase III 0.000
PSP 0.000
LBX1 0.000
Disrupted in schizophrenia 1 0.000
thioesterase superfamily member 2 0.000
SMCR8 0.000
XRCC1 protein 0.000
CBD 0.000
PDSS2 0.000
AHI1 0.000
TTRAP 0.000
NEK8 0.000
contactin 4 0.000
Synaptojanin 1 0.000
GNPTAB 0.000
forkhead box P1 0.000
FOXP1 0.000
SPTBN2 0.000
2E4 0.000
POMGnT1 0.000
TNRC6B 0.000
IMMP2L 0.000
SLC6A8 0.000
ADCK3 0.000
GRID2 0.000
meiotic recombination 11 0.000
X-ray repair cross-complementing protein 1 0.000
ELP4 0.000
asymmetrical 0.000
COQ9 0.000
nibrin 0.000
ZNF423 0.000
ATP8A2 0.000
tau protein 0.000
POMT2 0.000
BPP 0.000
CNTN4 0.000
DAG1 0.000
POMT1 0.000
ERC1 0.000
tyrosyl-DNA phosphodiesterase 1 0.000
NSA 0.000
MAP2 protein 0.000
PPP1R3 0.000
MECP2 0.000
TDP-43 0.000
NPHP2 0.000
TUSC3 0.000
KIAA0319 0.000
ATM 0.000
RNA helicase 0.000
SCA12 0.000
progranulin 0.000
MKL2 0.000
CMIP 0.000
NPHP3 0.000
XRCC1 0.000
NFBD1 0.000
ARL13B 0.000
MOBP 0.000
LBD 0.000
LAMA1 0.000
FTD 0.000
Succinic semialdehyde dehydrogenase 0.000
DARS2 0.000
HSL1 0.000
galactose-1-phosphate uridyl transferase 0.000
creatine transporter 0.000
AFG3L2 0.000
CHD3 0.000
TAU 0.000
MKS1 0.000
ALX4 0.000
ADSL 0.000
GALT 0.000
Hallervorden-Spatz syndrome 0.000
p101 0.000
WDR45 0.000
PSD 0.000
OFD 0.000
Aristaless-related homeobox 0.000
DISC1 protein 0.000
alpha-fetoprotein 0.000
MPV17 0.000
SPOCK1 0.000
KAT6A 0.000
fukutin 0.000
CACT 0.000
SCA8 0.000
LARGE 0.000
GRIN2A 0.000
C9orf72 0.000
RD3 0.000
SPCA2 0.000
boule 0.000
TUTase 0.000
TCF12 0.000
POLR2A 0.000
RHD 0.000
RAI1 0.000
DYX1C1 0.000
SCA17 0.000
fukutin-related protein 0.000
DPP6 0.000
COQ2 0.000
BCL11A 0.000
SLC22A3 0.000
glucocerebrosidase 0.000
TMEM106B 0.000
THAP1 0.000
galactose-1-phosphate uridylyltransferase 0.000
ELKS 0.000
TDP1 0.000
member 9 0.000
NARP 0.000
NCOR1 0.000
DNA helicase 0.000
CHMP2B 0.000
colony stimulating factor 1 receptor 0.000
SYNE1 0.000
PAO 0.000
ECD 0.000
MRE11 0.000
SLC22A2 0.000
ADORA2A 0.000
GalT 0.000
amyloid precursor protein 0.000
N33 0.000
KCNMA1 0.000
EN2 0.000
MIM 0.000
RNA polymerase II subunit 0.000
HEMO 0.000
EA1 0.000
jerky 0.000
EIF2AK3 0.000
Roy 0.000
CDKL5 0.000
CHD4 0.000
XRCC4 0.000
flap endonuclease 1 0.000
SCA2 0.000
CADASIL 0.000
SCA7 0.000
EPM1 0.000
MOCA 0.000
HINT 0.000
CPS1 0.000
Prion protein 0.000
MSD 0.000
inositol polyphosphate 5-phosphatase 0.000
ADL 0.000
presenilin 2 0.000
GPR56 0.000
McLeod syndrome 0.000
axonal 0.000
FDG 0.000
CAS 0.000
helicase 0.000
ROBO1 0.000
MEP 0.000
SCA1 0.000
SMD 0.000
PLA2G6 0.000
STN 0.000
NIPBL 0.000
14-3-3 0.000
PIQ 0.000
adenylosuccinate lyase 0.000
sepiapterin reductase 0.000
methyl-CpG binding protein 2 0.000
Cx46 0.000
SIII 0.000
ATPase 6 0.000
RARS 0.000
GDS 0.000
strabismus 0.000
GTX 0.000
Dopamine transporter 0.000
survival of motor neuron 0.000
EXT2 0.000
FRA3B 0.000
WDR5 0.000
MERRF 0.000
Frataxin 0.000
PSEN1 0.000
SATB2 0.000
CT1 0.000
imiglucerase 0.000
DNA repair protein 0.000
AHS 0.000
CMT2 0.000
PSE 0.000
CRHR1 0.000
TopBP1 0.000
DIVA 0.000
Glutamate receptor 0.000
DPS 0.000
CELF 0.000
PSEN2 0.000
dentatorubral-pallidoluysian atrophy 0.000
DVD 0.000
ARX 0.000
GTS 0.000
HIC 0.000
signal transduction protein 0.000
DCD 0.000
EMB 0.000
DNA ligase 0.000
RNase H1 0.000
PRNP 0.000
HLA-B51 0.000
alpha-tocopherol transfer protein 0.000
ataxia telangiectasia mutated 0.000
Sotos syndrome 0.000
histone deacetylase 4 0.000
activator 1 0.000
HDS 0.000
protein arginine methyltransferase 5 0.000
AIP 0.000
80 kDa) 0.000
KvLQT1 0.000
MELAS 0.000
CD87 0.000
presenilin 1 0.000
spinocerebellar ataxia type 2 0.000
MAP1B 0.000
CACNA1C 0.000
Sep 0.000
FUS 0.000
PGN 0.000
KAP 0.000
ADHD 0.000
forkhead transcription factor 0.000
IGF2R 0.000
NRF1 0.000
FIM 0.000
MDC1 0.000
Sta 0.000
classical) 0.000
TREM2 0.000
TARDBP 0.000
XPB 0.000
FAST 0.000
dopa-responsive dystonia 0.000
X-linked recessive 0.000
REL 0.000
CYP27A1 0.000
SDHA 0.000
SMN 0.000
ubiquitin 0.000
folliculin 0.000
GAA 0.000
NCS-1 0.000
SLI 0.000
MSS 0.000
more...
Disease
apraxia 0.999
aphasia 0.014
agnosia 0.012
agraphia 0.010
Corticobasal degeneration 0.006
Ideomotor apraxia 0.006
acalculia 0.005
AOA2 0.003
aphemia 0.003
Ideational apraxia 0.003
speech disorder 0.002
anomia 0.002
Constructional apraxia 0.002
alexia 0.002
Apraxia of speech 0.002
ALS4 0.002
progressive supranuclear palsy 0.001
Balint's syndrome 0.001
Joubert syndrome 0.001
Verbal dyspraxia 0.001
anarthria 0.001
anosognosia 0.001
motor aphasia 0.001
dementia 0.001
astereognosis 0.001
Cogan 0.001
disorientation 0.001
agrammatism 0.001
mutism 0.001
AOA 0.001
Pick's disease 0.001
dyscalculia 0.001
dysgraphia 0.001
Oral apraxia 0.001
transcortical aphasia 0.001
language disorder 0.001
dysphasia 0.001
Handwringing 0.000
Gestural apraxia 0.000
Motor speech disorder 0.000
cortex; degeneration 0.000
pathological emotionality 0.000
Presenile and senile dementia 0.000
Pallidonigral degeneration 0.000
Dysprosody 0.000
Wernicke's aphasia 0.000
parkinsonism 0.000
conduction aphasia 0.000
Gerstmann 0.000
GD III 0.000
Progressive Nonfluent Aphasia 0.000
cerebellotrigeminal and focal dermal dysplasia 0.000
Musical alexia 0.000
Transcortical motor aphasia 0.000
autotopagnosia 0.000
hemiparesis 0.000
cognitive motor disorder 0.000
CMT2B2 0.000
Logorrhea 0.000
developmental coordination disorder 0.000
articulation disorder 0.000
Finger agnosia 0.000
SCAE 0.000
Apraxia of gait 0.000
ATLD 0.000
AOS 0.000
dyslexia 0.000
Alzheimer's disease 0.000
Marchiafava-Bignami disease 0.000
word deafness 0.000
Rett syndrome 0.000
Delayed visual maturation 0.000
Spastic ataxia 0.000
delayed speech 0.000
brain atrophy 0.000
camptocormia 0.000
global aphasia 0.000
developmental delay 0.000
moria 0.000
Early Onset Cerebellar Ataxia 0.000
Friedreich's ataxia 0.000
stroke 0.000
NPHP1 0.000
echolalia 0.000
IOSCA 0.000
XLAG 0.000
NPHP4 0.000
ATM 0.000
writing disorder 0.000
Landau-Kleffner syndrome 0.000
choreoathetosis 0.000
disturbed concentration 0.000
Cogan's syndrome 0.000
Cranial nerves 0.000
Cranial nerves 0.000
amnesia 0.000
SANDO 0.000
perseveration 0.000
cognitive impairment 0.000
galactosemia 0.000
Auditory agnosia 0.000
Dementia with Lewy bodies 0.000
pseudobulbar palsy 0.000
communication disorder 0.000
memory impairment 0.000
mild memory disturbance 0.000
ATP synthase deficiency 0.000
Pick's disease with Pick bodies 0.000
frontal lobe syndrome 0.000
SCAN1 0.000
amusia 0.000
stuttering 0.000
abulia 0.000
akinesia 0.000
Adenylosuccinate lyase deficiency 0.000
movement disorder 0.000
Parkinson's disease 0.000
eye movement disorder 0.000
Idiopathic thrombocytopenia 0.000
hereditary ataxia 0.000
MILS 0.000
Visual agnosia 0.000
Worster-Drought syndrome 0.000
Speech impairment 0.000
cerebral degeneration 0.000
WWS 0.000
basal ganglia disease 0.000
cognitive disorder 0.000
Primary Progressive Aphasia 0.000
Gillespie syndrome 0.000
Parietal lobe 0.000
nystagmus 0.000
Gaucher disease 0.000
specific language impairment 0.000
Porencephaly 0.000
Cerebellum 0.000
PSP 0.000
GALK 0.000
Frontal lobe 0.000
specific developmental disorders 0.000
Prosopagnosia 0.000
GALT 0.000
stereotypies 0.000
hallucinations 0.000
Akinetic mutism 0.000
hereditary chorea 0.000
autism 0.000
Progressive dementia 0.000
Cerebellar atrophy 0.000
atonic seizure 0.000
FTLD 0.000
telangiectasia 0.000
Pisa syndrome 0.000
NPHP2 0.000
sensory disturbance 0.000
intellectual impairment 0.000
Dystonia 0.000
deaf mutism 0.000
dysphagia 0.000
mental retardation 0.000
cross-dependence 0.000
vitamin E deficiency 0.000
presenile dementia 0.000
amnesic syndrome 0.000
multi-infarct dementia 0.000
49,XXXXY syndrome 0.000
Creutzfeldt-Jakob disease 0.000
encephalopathy 0.000
Prosody 0.000
mental retardation 0.000
Molybdenum cofactor deficiency 0.000
Benson 0.000
neuropathy 0.000
SCA12 0.000
cognitive deficit 0.000
Binswanger 0.000
CND 0.000
DVD 0.000
Kluver-Bucy syndrome 0.000
motor neuron disease 0.000
progressive chorea 0.000
incontinence 0.000
peripheral neuropathy 0.000
memory disorder 0.000
oxyuriasis 0.000
Refsum disease 0.000
confusion 0.000
brain dysfunction 0.000
Oppenheim 0.000
disinhibition 0.000
Ohtahara syndrome 0.000
Pontocerebellar hypoplasia 0.000
cerebral artery aneurysm 0.000
pineal region tumor 0.000
epidemic encephalitis 0.000
epilepsy 0.000
behavior disorder 0.000
cerebral infarction 0.000
SCA8 0.000
Hallervorden-Spatz disease 0.000
Tapia 0.000
Congenital hepatic fibrosis 0.000
psycho-organic syndrome 0.000
Meige syndrome 0.000
developmental language disorder 0.000
amyotrophic lateral sclerosis 0.000
moderate mental retardation 0.000
idiopathic disorder 0.000
Capgras syndrome 0.000
NPHP3 0.000
Neonatal diabetes mellitus 0.000
Posterior 0.000
Oropharyngeal dysphagia 0.000
delusions 0.000
senile dementia 0.000
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 0.000
degenerative disease 0.000
SCA17 0.000
Upper limb 0.000
perception disorder 0.000
mild mental retardation 0.000
monosomy 18p 0.000
neurobehavioral problems 0.000
LBD 0.000
learning disorder 0.000
delirium 0.000
primary lateral sclerosis 0.000
MELAS 0.000
Vascular dementia 0.000
cri-du-chat syndrome 0.000
hydrocephalus 0.000
flat affect 0.000
Semantic dementia 0.000
delayed language 0.000
developmental disabilities 0.000
sphingolipidosis 0.000
blunted affect 0.000
McLeod syndrome 0.000
IgG2 deficiency 0.000
ventricular dilatation 0.000
vestibular nystagmus 0.000
hallucinosis 0.000
anterograde amnesia 0.000
Huntington's disease 0.000
pinealoma 0.000
aspiration pneumonia 0.000
pinealoma 0.000
severe mental retardation 0.000
Chronic progressive external ophthalmoplegia 0.000
catatonic schizophrenia 0.000
CADASIL 0.000
olivopontocerebellar atrophy 0.000
TSH deficiency 0.000
Goldstein 0.000
neurological disease 0.000
Immune reconstitution inflammatory syndrome 0.000
IRD 0.000
SCA2 0.000
macrocephaly 0.000
hemichorea 0.000
SCA7 0.000
Syndrome 0.000
FHA 0.000
cerebellar syndrome 0.000
Demented 0.000
blindness 0.000
incontinence 0.000
NPH 0.000
amphetamine abuse 0.000
MSD 0.000
optic atrophy 0.000
lipoproteinemia 0.000
SSD 0.000
hypernasality 0.000
Asperger syndrome 0.000
leukoencephalopathy 0.000
HDL1 0.000
dysautonomia 0.000
hyperornithinemia 0.000
Minamata disease 0.000
abnormal involuntary movements 0.000
prolapse 0.000
Rasmussen encephalitis 0.000
cerebral thrombosis 0.000
organic brain syndrome 0.000
SCA1 0.000
SMD 0.000
radioulnar synostosis 0.000
Down syndrome 0.000
dyskinesia 0.000
hemiparkinsonism 0.000
retrobulbar neuritis 0.000
entropion 0.000
Lennox-Gastaut syndrome 0.000
insane 0.000
Disorder 0.000
Fahr's disease 0.000
cerebral palsy 0.000
Spinocerebellar ataxia 0.000
facial palsy 0.000
Globus 0.000
Wilson's disease 0.000
EXT2 0.000
DWI 0.000
leptomeningitis 0.000
retrograde amnesia 0.000
MELAS 0.000
MERRF 0.000
Frontotemporal dementia 0.000
torsion dystonia 0.000
Arachnoid cysts 0.000
psychomotor impairment 0.000
Lennox-Gastaut syndrome 0.000
transient global amnesia 0.000
hypoadrenocorticism 0.000
polyneuropathy 0.000
minimal brain dysfunction 0.000
strabismus 0.000
psychosis 0.000
diplegia 0.000
more...
Symptom
Apraxic 0.004
ataxia 0.003
dysarthria 0.002
clumsiness 0.001
blepharospasm 0.001
dystonia 0.001
cerebellar ataxia 0.001
myoclonus 0.001
Poverty of facial expression 0.000
bradykinesia 0.000
Extrapyramidal rigidity 0.000
Frozen gait 0.000
Pyramidal signs 0.000
hypotonia 0.000
amimia 0.000
chorea 0.000
Respiratory abnormalities 0.000
aprosodia 0.000
tremor 0.000
hemihypesthesia 0.000
personality change 0.000
Retropulsion 0.000
apathy 0.000
hemiplegia 0.000
forgetfulness 0.000
paresis 0.000
Bell's phenomenon 0.000
memory loss 0.000
visual hallucination 0.000
delayed language development 0.000
mirror writing 0.000
weakness 0.000
seizures 0.000
Aphasic 0.000
spasticity 0.000
astasia 0.000
incoordination 0.000
abnormal gait 0.000
Motor dysfunction 0.000
ataxic gait 0.000
Swallowing problems 0.000
Kernig's sign 0.000
Plantar flexion 0.000
Opposition 0.000
ophthalmoplegia 0.000
asterixis 0.000
muscle rigidity 0.000
drooling 0.000
General symptoms 0.000
aphonia 0.000
athetosis 0.000
abiotrophy 0.000
Behavioral symptoms 0.000
prominent nose 0.000
Parkinsonian tremor 0.000
Extrapyramidal symptoms 0.000
monoplegia 0.000
Visual disturbances 0.000
hypertonia 0.000
tonic-clonic seizure 0.000
agitation 0.000
Neurologic symptoms 0.000
arm weakness 0.000
metamorphopsia 0.000
headache 0.000
paraparesis 0.000
Psychiatric symptoms 0.000
clonus 0.000
hepatosplenomegaly 0.000
prostration 0.000
loss of taste 0.000
Involuntary Movement 0.000
motor symptom 0.000
paresthesia 0.000
hyperemesis gravidarum 0.000
ketonuria 0.000
breath holding 0.000
spasm 0.000
pallor 0.000
limb pain 0.000
leg edema 0.000
anosmia 0.000
physical appearance 0.000
partial seizure 0.000
CSR 0.000
photophobia 0.000
torticollis 0.000
bloating 0.000
general problem 0.000
thinning 0.000
blurred vision 0.000
dysesthesia 0.000
tense 0.000
hypersomnia 0.000
dizziness 0.000
catatonia 0.000
urinary frequency 0.000
productive cough 0.000
tachypnea 0.000
constipation 0.000
muscle stiffness 0.000
Mills 0.000
tingling 0.000
numbness 0.000
lethargy 0.000
anorexia 0.000
vomiting 0.000
pain 0.000
alexithymia 0.000
vertigo 0.000
cough 0.000
Depressive symptoms 0.000
chronic cough 0.000
hopelessness 0.000
stridor 0.000
hepatomegaly 0.000
dry eye 0.000
asthenia 0.000
snoring 0.000
hoarseness 0.000
polyuria 0.000
acute abdomen 0.000
bone pain 0.000
sleepiness 0.000
functional recovery 0.000
exertional dyspnea 0.000
acute pain 0.000
fatigue 0.000
cachexia 0.000
erythema 0.000
nausea 0.000
myalgia 0.000
tinnitus 0.000
acidity 0.000
arthralgia 0.000
hypothermia 0.000
distraction 0.000
insomnia 0.000
back pain 0.000
anesthesia 0.000
collapse 0.000
discomfort 0.000
discomfort 0.000
overweight 0.000
abdominal pain 0.000
diarrhea 0.000
Drug
Benserazide 0.000
PPA 0.000
Frontal 0.000
CVA 0.000
Sinemet 0.000
Sinemet 0.000
EMB 0.000
Ritalin 0.000
Spectrum 0.000
DBS 0.000
Botox 0.000
Pregabalin 0.000
Leucovorin 0.000
Adalimumab 0.000
Sinemet 0.000
Vitamin B 0.000
Urokinase 0.000
Triad 0.000
CSF 0.000
Spectrum 0.000
Phosphatidylserine 0.000
Triad 0.000
uPA 0.000
MDS 0.000
Galactose 0.000
Acyclovir 0.000
Vitamin B12 0.000
Rituximab 0.000
Vitamin K 0.000
CTA 0.000
BH4 0.000
AZT 0.000
Fluorescein 0.000
Ringer's solution 0.000
AZT 0.000
EPA 0.000
Fluorescein 0.000
lactose 0.000
Albumin 0.000
Mutagen 0.000
vitamin E 0.000
ROS 0.000
lysine 0.000
Monit 0.000
ampicillin 0.000
caffeine 0.000
Leaf 0.000
Dial 0.000
Dermatol 0.000
Enzyme
polynucleotide kinase 0.000
m-AAA protease 0.000
TUT 0.000
3'-phosphatase 0.000
galactose-1-phosphate uridylyltransferase 0.000
glucocerebrosidase 0.000
GalT 0.000
sepiapterin reductase 0.000
adenylosuccinate lyase 0.000
Lod 0.000
uridyltransferase 0.000
FAST 0.000
DNA ligase 0.000
DNA ligase 0.000
CYP27A1 0.000
galactokinase 0.000
GTP cyclohydrolase I 0.000
NAT 0.000
RNA ligase 0.000
GCA 0.000
acyl-CoA dehydrogenase 0.000
GABA transaminase 0.000
botulinum neurotoxin 0.000
LasR 0.000
SCS 0.000
cholinesterase 0.000
phenylalanine hydroxylase 0.000
acyl-CoA dehydrogenase 0.000
DAT 0.000
TOR 0.000
choline acetyltransferase 0.000
ornithine transcarbamylase 0.000
acetylcholinesterase 0.000
DNA polymerase 0.000
NADH dehydrogenase 0.000
PARP 0.000
RNA polymerase 0.000
phosphatidylinositol 3-kinase 0.000
STR 0.000
enolase 0.000
citrate synthase 0.000
creatine kinase 0.000
urokinase-type plasminogen activator 0.000
MIP 0.000
ceruloplasmin 0.000
phosphorylase 0.000
diaphorase 0.000
catalase 0.000
aldehyde dehydrogenase 0.000
GSK 0.000
phosphodiesterase 0.000
cytochrome oxidase 0.000
complex I 0.000
protein kinase 0.000
topoisomerase 0.000
topoisomerase 0.000
tissue plasminogen activator 0.000
thromboplastin 0.000
tyrosine hydroxylase 0.000
RNase 0.000
luciferase 0.000
RNase 0.000
proteasome 0.000
lactate dehydrogenase 0.000
thrombin 0.000
alkaline phosphatase 0.000
mitogen-activated protein kinase 0.000
Compound
Carbidopa-levodopa 0.000
IMP 0.000
3 PS 0.000
PSP 0.000
His 0.000
TDP 0.000
RD4 0.000
PPA 0.000
MOCA 0.000
coenzyme Q10 0.000
Clin 0.000
Pergolide 0.000
MEP 0.000
DNA 0.000
Pyridoxine 0.000
MEP 0.000
SSD 0.000
Amytal 0.000
PPA 0.000
Xenon 0.000
Dec 0.000
Amitriptyline 0.000
Ritalin 0.000
adenylate 0.000
CoQ 0.000
Corticosterone 0.000
A 71 0.000
L-DOPA 0.000
methyl methanesulfonate 0.000
DBS 0.000
tetraphosphate 0.000
EMC 0.000
TBS 0.000
Coenzyme Q10 0.000
Sudan I 0.000
Neuronal 0.000
Cereb 0.000
Etanercept 0.000
Memantine 0.000
TBI 0.000
GD3 0.000
gamma-hydroxybutyric acid 0.000
Phosphatidylserine 0.000
DSM 0.000
AMP 0.000
Lamotrigine 0.000
MIT 0.000
MIT 0.000
Hearts 0.000
INT 0.000
pyridazine 0.000
pyridazine 0.000
Olanzapine 0.000
MSG 0.000
TAR 0.000
T 1 0.000
Acyclovir 0.000
Creatine 0.000
Galactose 0.000
Bromocriptine 0.000
Coronal 0.000
DIC 0.000
Glycogen synthase 0.000
Vitamin K 0.000
CIT 0.000
Formal 0.000
Argentine 0.000
CAT 0.000
CAT 0.000
Maps 0.000
N-acetylaspartate 0.000
Histidine 0.000
DAT 0.000
CAT 0.000
A 1 0.000
valine 0.000
Clozapine 0.000
L-carnitine 0.000
folinic acid 0.000
HVA 0.000
Dopa 0.000
galactose 0.000
C2H2 0.000
THE 0.000
glucose 0.000
TMP 0.000
Lithium 0.000
TMP 0.000
TMP 0.000
Wellcome 0.000
GAL 0.000
Haloperidol 0.000
APS 0.000
T10 0.000
Haloperidol 0.000
Parenteral 0.000
isoleucine 0.000
FK506 0.000
isoleucine 0.000
ADP-ribose 0.000
Phosphatidylinositol 0.000
Austin 0.000
CIT 0.000
TMP 0.000
A 42 0.000
AAA 0.000
DHA 0.000
PAC 0.000
DTPA 0.000
phosphate 0.000
Guo 0.000
EPA 0.000
6-12 0.000
AZT 0.000
A 3 0.000
iron 0.000
PAM 0.000
PAM 0.000
glutamine 0.000
DHA 0.000
fluorine 0.000
glutamate 0.000
DHA 0.000
aldehyde 0.000
Guo 0.000
silver 0.000
Ile 0.000
GABA 0.000
piperazine 0.000
GABA 0.000
oxygen 0.000
butyric acid 0.000
ubiquinone 0.000
aldehyde 0.000
butyric acid 0.000
methionine 0.000
creatinine 0.000
ornithine 0.000
ornithine 0.000
ornithine 0.000
ornithine 0.000
ornithine 0.000
Isoproterenol 0.000
Lactate 0.000
butyric acid 0.000
Letter 0.000
CO2 0.000
Neurotol 0.000
H2O2 0.000
dUTP 0.000
arginine 0.000
H2S 0.000
Dopamine 0.000
TCA 0.000
lysine 0.000
guanidine 0.000
GMP 0.000
ADP 0.000
ADP 0.000
molybdenum 0.000
leucine 0.000
AMPA 0.000
zinc 0.000
Lead 0.000
aspartic acid 0.000
aspartic acid 0.000
ADP 0.000
aspartic acid 0.000
aluminum 0.000
aspartic acid 0.000
Off 0.000
proline 0.000
noradrenaline 0.000
potassium 0.000
Thyroid 0.000
Asp 0.000
gamma-aminobutyric acid 0.000
serine 0.000
glutamic acid 0.000
cyanide 0.000
bromide 0.000
water 0.000
ACTH 0.000
pyrimidine 0.000
pyrimidine 0.000
caffeine 0.000
iodine 0.000
Phe 0.000
SDS 0.000
tyrosine 0.000
retinoic acid 0.000
hydroxide 0.000
phenol 0.000
methane 0.000
HCl 0.000
pyridine 0.000
GTP 0.000
carbonate 0.000
sodium 0.000
Dial 0.000
alanine 0.000
hydrogen 0.000
Pac 0.000
Gly 0.000
tryptophan 0.000
tryptophan 0.000
tryptophan 0.000
calcium 0.000
tryptophan 0.000
threonine 0.000
ammonia 0.000
NH2 0.000
PEG 0.000
ATP 0.000
urea 0.000
nitrogen 0.000
cysteine 0.000
copper 0.000
nitric oxide 0.000
Cardiol 0.000
sulfate 0.000
salt 0.000