Neudle.com: face inexpressive

Differential
(Click to cross reference)

abdominal distention

abducens nerve paralysis

abducens nerve paralysis, bilateral

abiotrophy

acoustic nerve

acute intermittant porphyria

airway obstruction

alcoholism

alveolar hypoventilation

aminoacidopathies

aminoacidurias

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, sensory symptoms in

anal wink response

anesthesia, general

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

arterial dissection, bilateral

arterial dissection, carotid

autonomic dysfunction

autonomic dysfunction, acute

Bickerstaff's brainstem encephalitis

brain biopsy, false negative

brainstem

brainstem, hypoplasia

bulbar palsy, juvenile

bulbar palsy, progressive

cachexia

calcification, intracranial

calf atrophy

campylobacter infection

carcinoembryonic antigen

carcinoembryonic antigen, cerebrospinal fluid

cauda equina, enhancement

central nervous system, infection of

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

chest pain

chest x-ray, abnormal

Clinical Pathologic Conference(C.P.C.)

congenital bilateral perisylvian syndrome

congenital heart disease

congenital malformation

congenital myopathy

congestive heart failure

constipation

corneal dystrophy

corneal reflex, abnormal

corneal reflex, absent

corneal transplant

corpus callosum

corpus callosum, thinning

cough

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, recurrent

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

denervation of muscle

denervation potentials

depression

descending paralysis

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus, chemical

diarrhea

differential diagnosis

difficulty climbing stairs

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, brachial

diplopia

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drooling

drowsiness

dysarthria

dyskinesia, buccal lingual facial

dysphagia

dysphonia

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electromyogram, decremental response

emotional lability

encephalitis

encephalitis, brainstem

encephalopathy

enteritis

epidemiology of neurology

erythema migrans

face, inexpressive

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, congenital

facial nerve palsy, recurrent

facial swelling

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fourth ventricle, floor

F-wave response

gag reflex, depressed

gait disorder

gastrointestinal perforation

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gender

gene mutation

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, neuropathology of inflammatory lesion of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

hallucination, auditory

hearing loss, unilateral

heart block

herpes simplex encephalitis

hydrocephalus, communicating

hypokalemic periodic paralysis

hyponatremia

hypoosmolality of serum

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

infection

insular cortex

intellectual deficit

intracranial hypertension, benign

intracranial pressure, increased

intrinsic hand muscles, wasting of

language disorders in children

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

leukopenia

level of consciousness, decreased

lid closure, weakness of

life expectancy

low back pain

lumbosacral radiculopathy

Lyme disease

lymphadenopathy

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

macrocephaly

malformation, CNS, congenital

maple syrup urine disease

masked facies

masseter muscle wasting

Meckel's cave

meningeal biopsy

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

meningitis, lymphomatous

meningitis, monocytic

meningitis, plasma cell

monoclonal gammopathy

mononeuritis multiplex

MRI, contrast enhanced

MRI, cranial nerves

MRI, spinal cord

MRI, spine

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle biopsy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, infantile and juvenile

myopathy, mitochondrial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

nerve root enhancement

neuritis

neurogenic vs.myopathic atrophy

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neurological intensive care

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronopathy

neuronopathy, sensory and motor

neuropathology

neuropathy

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, neonatal

ophthalmoplegia, total

opsoclonus

optic neuritis

optic neuropathy

optic neuropathy, bilateral

paralysis, acute areflexic

percussion induced muscle contraction

periodic paralysis

perioral numbness

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polymicrogyria

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, lymphomatous

polyradiculoneuropathy

potassium

pregnancy, neurologic complications in

primary CNS histiocytic sarcoma

primary lateral sclerosis

prognosis

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, light reflex, abnormal

pyramidal tract dysfunction

quadriparesis

quadriparesis, progressive

quadriplegia

rabies, nervous system involvement with

repetitive nerve stimulation

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

scoliosis, neurologic association with

screening

sedimentation rate, elevated

seizure

seizure, recurrent

sensorineural hearing loss

sensory loss

sensory loss, truncal

sensory symptoms

serologic testing

shoulder, numbness

shoulder-girdle wasting

skin, biopsy

skin, lesions in neurologic disorders

slit lamp examination

spinal muscular atrophy

spinal muscular atrophy, classification

spontaneous muscle activity

steppage gait

steroid

steroid therapy, CNS treatment and complications with

stool culture

symmetric brain lesions

Tangier's disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tongue, fasciculations of

tongue, impaired movements of

tongue, pain

tongue, weakness

transient neurologic deficit

transposition of the great vessels

transverse smile

treatment of neurologic disorder

tremor

tremor, intention

trigeminal nerve, abnormality of

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

unconsciousness

urine osmolality, elevated

Waldenstrom's macroglobulinemia

walking, difficulty with

Watson-Schwartz reaction

weakness

weakness, generalized

weakness, progressive

weight loss

wheelchair

whistle, inability to

Showing articles 50 to 100 of 647 << Previous Next >>

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Human-To-Human Transmission of Rabies Virus by Corneal Transplant
NEJM 300:603-604, Houff,S.A.,et al, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Criteria for Diagnosis of Guillain-Barre Syndrome
Ann Neurol 3:565, , 1978

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Neurological Manifestations of Sarcoidosis
Neurol 15:1147, Wiederholt,W.,et al, 1965

Clinical and Imaging Features of Cobb Syndrome
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Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Eagle Syndrome
Stat Pearls NBK 430789, Bokhari,M.R.,et al, 2024

Visualising Facial Distortions in Prosopometamorphopsia
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

Bilateral Hemifacial Spasm and Left Glossopharyngeal Neuralgia Caused by Bilateral Vertebral Artery Displacement
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IgG4-Related Orbital Inflammation
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Progressive Cranial Neuropathy
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Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
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Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
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A 62-Year-Old Woman with Transient Vision Loss
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Manganese Accumulation in the Brain
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Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
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A Teenager With Right-Sides Headache and Periorbital Changes
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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A 25-Year-Old Woman With Eye Swelling and HEadache
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Cavernous Sinus Thrombosis
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Bilateral Trigeminal Neuralgia - A Condition of the Upper Neck
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Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
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A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
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Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Recent Advances in the Diagnosis and Management of Cluster Headache
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Sweet Syndrome
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Sturge-Weber Syndrome
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Levetiracetam in Management of Bilateral Trigeminal Neuralgia Due to Large Glomus Tumor Case Report
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Cervical Discopathy in Idiopathic Trigeminal Neuralgia:More than a Coincidence?
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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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The Tolosa-Hunt Syndrome
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Ocular Findings in the Sturge-Weber Syndrome
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Multiple Facial Ulcers Following a Stroke
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Rapidly Progressive Thalamic Dementia
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Clinicopathologic Conference, Normal Pressure Hydrocephalus
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A 64-Year-Old Man with Multiple Cranial Neuropathies
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A Rare Presentation of Whipple Disease
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Cavernous Sinus Thrombosis
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Showing articles 50 to 100 of 647 << Previous Next >>