Neudle.com: hyperactive deep tendon reflexes

Differential
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abdominal distention

abdominal reflex, absent

achilles tendon, enlarged

acute respiratory distress syndrome

Addison's disease

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

Alexanders disease, adult onset

algorithm

alien hand syndrome

alopecia

altered states of consciousness

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amenorrhea

amphiphysin antibodies

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

ANA

anemia

anemia, megaloblastic

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

antibiotics, neurologic complications with

anticholinergic drugs

anticonvulsants

anticonvulsants, untoward effects of

apraxia of eye movements

areflexia

arm swing, reduced

arm weakness

Arnold Chiari malformation

arthralgia

arthritis

aspartate aminotransferase

atherosclerosis, premature

atlanto-axial subluxation

atrial fibrillation

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal dominant leukodystrophy

B 12 deficiency

Babinski sign

basal ganglia

basal ganglia, lesion of

Bickerstaff's brainstem encephalitis

BiPAP

bladder dysfunction

blindness

bone marrow transplantation

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brainstem

brainstem, atrophy

brainstem, dysfunction

bulbar palsy, acute-causes of

bulbar palsy, progressive

cachexia

CAG repeats

calcification, intracranial

camptocormia

campylobacter infection

cancer, unknown origin

cane

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carcinoma

carcinoma of breast

carcinoma of unknown origin

cardiomyopathy

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, spine

cataracts

caudate nucleus, atrophy

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar lesion

cerebellar plaques, amyloid

cerebral cortical atrophy

cerebral infarction

cerebral palsy

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cervical myelopathy

cervical spine

cervical spine abnormality

cervical spondylosis

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

chromosomal abnormality

chromosome 9

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clomipramine

clonazepam

clonus

clubfoot as related to neurologic disease

cobalamin C deficiency

congenital deformities

congenital malformation

congenital malformation, non CNS

congestive heart failure

corpus callosum, atrophy of

corpus callosum, lesion of

cortical-basal ganglionic degeneration

cough

COVID-19

cranial nerve palsies

cranial neuropathy

C-reactive protein, elevated

critical care unit

crossed adductor reflex

degenerative cervical myelopathy

degenerative diseases of CNS

dementia

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dental prostheses

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

denture cream

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diastematomyelia

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplopia

disability, neurological

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

drowsiness

drug induced neurologic disorders

drug interactions

drug overdose

drug overdose, management of

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, focal

dystonia, treatment of

eclampsia

eclampsia, postpartum

eczema

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electroretinograph

ELISA

emergencies, neurologic

emergency room

emotional lability

encephalitis

encephalitis, brainstem

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, progressive

endemic area

entrapment neuropathy

enzyme, defect

eosinophilia

ependymal

epileptic encephalopathy

Epstein-Barr virus

exome sequencing

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

fatty acid, elevated plasma content

fever

fibrillations

fine motor function, impaired

finger nose finger test

fundus, abnormality of

gadolinium

gag reflex, depressed

gait disorder

gait, spastic

gammaglobulin therapy, intravenous

gastric partitioning

Gaucher's disease

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

globus pallidus, lesion of

glucocerebrosidase

glutamic acid decarboxylase, antibody

glycoprotein

GM1 ganglioside antibodies

gout

granular osmiphilic material

granulomatous disease

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

hairline, abnormal

Hallervorden Spatz disease

hallucination

hallucination, auditory

hallucination, visual

head retraction reflex

helminthic infection of CNS

heralding manifestation

herniated disc

herniated disc, cervical

high arched feet

highly active antiretroviral therapy

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's disease, children

hyperpigmentation of skin

hypothalamus, disturbance of

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

inability to stand on tiptoes

inappropriate behavior

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

intellectual deterioration

internuclear ophthalmoplegia

intrauterine

intrinsic hand muscles, wasting of

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

laminectomy

laminectomy, cervical

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leprosy

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

liver function enzymes

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

Maghreb

malabsorption

malabsorption syndrome

malformation, CNS, congenital

mediastinum, lymph-node biopsy

mediastinum, mass of

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, CSF cell count-normal

meningitis, eosinophilic

meningoencephalitis

mental retardation

mental status, abnormal

metastasis to bone

methadone

methylmalonic acid, serum

methylmalonic acidemia

metrizamide

microangiopathy, brain

microcephaly

middle cerebellar peduncle, lesion, bilateral

Mills syndrome

Mini Mental Status Examination

miosis

misdiagnosis

mitochondrial disease

moclobemide

molecular genetics

mongolism

monoamine oxidase inhibitors

mortality

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, contrast enhanced, subependymal

MRI, disappearing lesion on

MRI, emergent

MRI, linear enhancement

MRI, negative

MRI, nodular enhancement

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis

mycobacterium kansasii

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelitis, transverse

myelogram

myelogram, complications of

myelogram, metrizamide

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myelopathy, tract-specific

myoclonus, stimulus sensitive

myopathy

myopathy, distal

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, thyroid disease causing

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal abstinence syndrome

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve root hypertrophy

neuritis, causes of

neuroaxonal dystrophy

neuroendocrinology

neurogenic bladder

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuropathology

neuropathology, peripheral nerves

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neuroprotective agents

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

ocular dysmetria

odontoid process

ophthalmoplegia

ophthalmoplegia, total

optic nerve, lesion of

optic neuropathy

optical coherence tomography

organ transplantation

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraparesis, spastic, tropical

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

paroxysmal neurologic disorder

pathology

periodic paralysis

periodic paralysis, thyrotoxic

perivascular enhancement

pernicious anemia

personality change

pes cavus

phenothiazine, dyskinesia associated with

phenylketonuria

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

POLR3B

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polypharmacy

polyradiculoneuropathy

pons, lesion of

position sensation

positive sharp waves

post transplant lymphoproliferative disease

posterior column disease

posterior leukoencephalopathy syndrome

postpartum

postural abnormality

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary lateral sclerosis

primitive neuroectodermal tumors

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

psychosis, acute

pulmonary embolism

pupil, dilated, bilateral

pupil, dilated, episodic

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

remote effect of cancer on the nervous system

renal failure

renal stones

renal transplantation

respirator

respiratory failure

respiratory tract infection

reticulum cell sarcoma

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

saccadic eye movements, abnormal

scoliosis, neurologic association with

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure

seizure, children

seizure, withdrawal

selective serotonin reuptake inhibitors

sensory loss

sensory loss, cortical

serotonin

serotonin agonist

serotonin syndrome

serum alanine aminotransferase

serum gamma glutamyl transferase

severe acute respiratory syndrome

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

slurred speech

snout reflex

sodium valproate

somatosensory evoked potentials

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, dorsal subpial enhancement

spinal cord, injury of

spinal cord, lesion of

spinal stenosis

spinal stenosis, familial

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 7

splenomegaly

spondylosis

spontaneous remission

stem cell transplantation

steppage gait

steroid therapy, CNS treatment and complications with

stiff legs

stiff man syndrome

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

superior cerebellar peduncle

teeth, number of in infants

temporal lobe, lesion

temporal lobe, lesion, bilateral

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic foot response

tonsillar herniation of cerebellum

trauma

trazodone

treatment of neurologic disorder

tremor

tremor, intention

tremulousness

tricyclic antidepressant

trigeminal nerve

trigeminal nerve, abnormality of

trinucleotide repeats

tripping

trismus

unconsciousness

unconsciousness, transient

venous thrombosis, non-cerebral

vertebral artery

vertebral artery occlusion

vertebral-basilar insufficiency

vertigo

vertigo, episodic

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual loss

visual loss, progressive

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

x-ray, cervical spine

x-ray, spine

zinc

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Unexplained Early Neurological Deterioration After Intravenous Thrombolysis
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Acute Carotid T Occlusion in a Young Patient
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Small Strokes Causing Severe Vertigo
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Controlled Trial of Transfusions for Silent Cerebral Infarcts in Sickle Cell Anemia
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Aspirin for Acute Stroke of Unknown Etiology in Resourse-Limited Settings
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Serial Magnetic Resonance Imaging Changes in Sporadic Creutzfeldt-Jakob Disease with Valine Homozygosity at Codon 129 of the Prion Protein Gene
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Alberta Stroke Program Early Computed Tomography Score to Select Patients for Endovascular Treatment
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The Acquired Metabolic Disorders of the Nervous System, Hepatic Stupor and Coma (Hepatic, or Portal-Systemic Encephalopathy)
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Opiates and Synthetic Analgesic Drugs
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Monoamine Oxidase Inhibitors
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Showing articles 1300 to 1350 of 6566 << Previous Next >>