User:Shatha Tailakh
Appearance
NEUROLOGY
المقالة الإنجليزية | طول المقالة الإنجليزية | الأهمية | الجودة | طول المقالة العربية |
---|---|---|---|---|
Electrodiagnostic medicine | 930 | Low | Start | Missing |
Adipsia | 1542 | Low | Stub | Missing |
Allen Brain Atlas | 1939 | Low | C | Missing |
Alzheimer's disease organizations | 205 | Mid | Start | Missing |
Autoscopy | 710 | Mid | Start | Missing |
Beevor's axiom | 713 | Low | Stub | 133 |
Behavioral neurology | 440 | Mid | Start | 430 |
Beta-2 transferrin | 178 | Low | Stub | 194 |
Neuroscience of multilingualism | 7534 | Low | B | Missing |
Biochemistry of Alzheimer's disease | 4172 | Mid | C | Missing |
Blindsight | 6345 | Low | Start | Missing |
BonnetΓÇôDechaumeΓÇôBlanc syndrome | 1530 | Mid | B | Missing |
Brain healing | 411 | Low | Start | 305 |
Cerebral shunt | 3074 | Mid | C | Missing |
Cerebrospinal fluid penetration | 41 | Low | Stub | 47 |
Cognitive reserve | 2718 | Low | B | Missing |
Cranial ultrasound | 767 | Mid | Start | Missing |
CSF/serum albumin ratio | 185 | Low | Stub | 123 |
CSF/serum glucose ratio | 150 | Low | Stub | 95 |
Dehydroascorbic acid | 1329 | Low | Start | Missing |
Direct pathway of movement | 598 | Low | Start | Missing |
Discoid meniscus | 710 | Low | Start | Missing |
Dual brain theory | 1232 | Low | Start | Missing |
Engel classification | 1059 | Low | Start | Missing |
Epileptogenesis | 1358 | Mid | C | Missing |
Erythropoietin in neuroprotection | 4164 | Low | C | Missing |
Expanded Disability Status Scale | 464 | Low | Start | Missing |
Field of view | 1408 | Low | Start | Missing |
Giant depolarizing potentials | 254 | Low | Start | Missing |
History of neurology | 1824 | Low | Start | Missing |
Holonomic brain theory | 3452 | Low | Start | Missing |
IKK2 | 2953 | Low | Start | Missing |
Indirect pathway of movement | 643 | Low | Start | Missing |
Inhibitory postsynaptic potential | 2371 | Low | Start | Missing |
Intermittent rhythmic delta activity | 68 | Low | Stub | Missing |
Kernohan's notch | 3032 | Low | C | Missing |
Kindling | 1943 | Low | Start | Missing |
Kindling model | 726 | Low | Start | Missing |
Long-term depression | 5990 | Mid | Start | Missing |
Effects of long-term benzodiazepine use | 10088 | Mid | C | Missing |
McDonald criteria | 2492 | Mid | Start | Missing |
Memory erasure | 2579 | Low | Start | Missing |
Microstimulation | 235 | Mid | Start | Missing |
Midline shift | 820 | Low | Start | Missing |
Modified Ashworth scale | 159 | Low | Stub | Missing |
Monitoring | 2308 | Low | Start | Missing |
Motor unit number estimation | 570 | Low | Start | Missing |
Multisensory integration | 10782 | Mid | B | Missing |
Nerve guidance conduit | 15694 | Low | B | Missing |
Nerve tissue protein | 1026 | Low | C | 42 |
Neural clique | 236 | Low | Start | 237 |
Neural ensemble | 1794 | Low | C | Missing |
Neural tissue engineering | 2967 | Low | C | 120 |
Neuro-ophthalmology | 1028 | Low | Start | Missing |
Neuroanthropology | 1060 | Low | Start | Missing |
Neuroeffector junction | 3104 | Low | Start | Missing |
Neurofibrillary tangle | 2969 | Mid | C | Missing |
Neurohospitalist | 94 | Low | Stub | Missing |
Neuroimmunology | 2941 | Mid | Start | 141 |
Neuroinflammation | 1975 | Low | C | Missing |
Neurologic music therapy | 2883 | Low | Start | Missing |
Neurological research into dyslexia | 2934 | Low | C | Missing |
Neuromodulation | 1667 | Low | Start | Missing |
Neuronal tuning | 936 | Low | Start | Missing |
Neurooncology | 3212 | Mid | Start | Missing |
Neuroprotection | 4395 | Low | Start | Missing |
Neuropsychiatry | 2384 | Mid | B | 476 |
Neuroradiology | 323 | Low | Start | 285 |
Neurotmesis | 1257 | Mid | C | Missing |
New daily persistent headache | 2564 | Mid | Start | Missing |