Neudle.com: tongue atrophy

Differential
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abdominal muscle paralysis

abducens nerve paralysis

abducens nerve paralysis, bilateral

abortion, spontaneous

acanthocytosis

acid maltase deficiency

acid maltase deficiency, adult

acromicria

agenesis of aqueduct of Sylvius

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

anemia

anemia, megaloblastic

Angelman syndrome

angiography, posterior fossa

anorexia

anterior horn cell disease

aphonia

apraxia

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arterial dissection, carotid

arthralgia

arthritis

arylsulfatase B

aspartate aminotransferase

Babinski-Nageotte syndrome

basal ganglia

basal ganglia, degeneration

brachial plexus injury

brachial plexus, lesion of

brainstem, infarction of

brainstem, lesion of

brainstem, metastasis to

bright tongue sign

bulbar palsy

bulbar palsy, progressive

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

CAT scan, base of skull

CAT scan, false negative

caudate nucleus, atrophy

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar atrophy, primary

cerebellar lesion

cerebral cortical atrophy

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cervical osteophyte

cervical spine

cervical spine abnormality

cervical spine disease

chromosomal abnormality

chromosome 15

chromosome 5

Clinical Pathologic Conference(C.P.C.)

cognition

conduction block

congenital bilateral perisylvian syndrome

congenital heart disease

congestive heart failure

cornea, opacity of

corpus callosum, lesion of

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial nerve palsies, unilateral

cranial nerve tumor

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

crying, pathologic

cultured skin fibroblasts

cyst, porencephalic

deafness

degenerative diseases of CNS

dementia

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dermatitis herpetiformis

developmental retardation

dexterity, impaired

diarrhea

differential diagnosis

diplegia, brachial

diplopia

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drooling

dysarthria

dyskinesia, buccal lingual facial

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

entrapment neuropathy

enzyme treatment

enzyme, defect

epidemiology of neurology

face, inexpressive

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

fluorescene in situ hybridization

foot drop

foramen magnum, lesion of

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gadolinium

gag reflex, depressed

gait disorder

gait, spastic

gait, waddling

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

glomus jugulare tumor

gluten ataxia

gluten sensitivity

gluten-free diet

glycogen storage disease

GM1 ganglioside antibodies

grasp reflex

growth hormone deficiency

growth retardation

Guillain Barre syndrome

headache, intermittent

hypoglossal nerve paralysis

hypogonadism

hypopigmentation of skin

infectious mononucleosis, neurologic findings with

influenza A virus

insular cortex

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

jaundice

jaw closure weakness

jaw jerk, abnormal

jugular foramen syndrome

lactic dehydrogenase(LDH)

language disorders in children

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macrognathia

malabsorption

malformation, CNS, congenital

masseter muscle wasting

masseter muscle weakness

mastectomy, radical

medial medullary syndrome

medulla oblongata, infarction of

medulla oblongata, lesion of

medulla oblongata, neoplasm of

meningioma

mental retardation

mental status, abnormal

methylmalonic acid, serum

monoclonal gammopathy

MRI, contrast enhanced

MRI, skull bone changes

MRI, spinal cord

mucopolysaccharidoses

multiple sclerosis

mumps virus

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

nasopharyngeal carcinoma

neck pain

neck weakness

neonatal infection, viral

nerve conduction studies

nerve conduction studies, motor

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuroma

neuromuscular disease, electrodiagnosis of

neuropathy, motor, multifocal

neuropathy, multifocal

occipital condyle fracture

occipital condyle syndrome

occipital pain

opened mouth

operculum syndrome

operculum syndrome, bilateral

palate, paralysis-unilateral

paraspinal muscle weakness

peripheral blood smear, abnormal

peripheral nerve, lesion of

pernicious anemia

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

posterior inferior cerebellar artery syndrome

postural abnormality

Prader-Labhart-Willi syndrome

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prognathism

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

pseudomyotonia

psychiatric problems in neurologic disorders

puberty

puberty, delayed

quadriparesis

radiation therapy, CNS treatment and complications with

recurrent laryngeal nerve paralysis

renal stones

repetitive nerve stimulation

respiratory failure

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rheumatoid pachymeningitis

scoliosis, neurologic association with

sensory loss, cortical

sensory nerve action potentials

sensory symptoms

serologic testing

short stature

Sicard-Collet syndrome

skin, biopsy

skin, lesions in neurologic disorders

skull fracture, basal

speech disorder, childhood

speech, delayed development of

spinal cord, compression of

spinal muscular atrophy

spinal muscular atrophy, classification

standing difficulty

sternocleidomastoid wasting

sternocleidomastoid weakness

strabismus

suck, poor

symmetric brain lesions

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tongue, fasciculations of

tongue, hemiatrophy of

tongue, impaired movements of

tongue, protrusion of

transient ischemic attack

trapezius weakness

trauma

treatment of neurologic disorder

vagus nerve, lesion of

vasculitides

viral infection

viral infection, CNS

visual acuity, decreased

visual field defect

vocal cord paralysis

vocalizations

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

word-finding difficulty

writing

X-linked bulbospinal neuronopathy

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Dysthyroid Orbitopathy
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Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
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Hydrocephalus Is a Determinant of Early Mortality in Putaminal Hemorrhage
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Neuroimaging in Deteriorating Patients with Cerebellar Infarcts and Mass Effect
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Toxoplasmosis Manifesting as Hydroephalus on Computed Tomography
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The Split Hand in ALS has a Cortical Basis
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Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
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Glatiramer Acetate (Copaxone) Treatment in Relapsing-Remitting MS
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Language Disturbances in Corticobasal Degeneration
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Progressive Necrotic Myelopathy
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Blindness in a Strict Vegan
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