Neudle.com: cranial nerve palsies familial

Differential
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abdominal muscle paralysis

abducens nerve paralysis

abiotrophy

acetazolamide

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve

acoustic nerve, vestibular division of

adverse drug reaction

ageusia

alcohol intolerance

alkylating agents

altered states of consciousness

alveolar hypoventilation

anterior spinal artery

anterior tibial muscle weakness

atlanto-axial subluxation

atonic bladder

atrioventricular block

autonomic dysfunction

baldness

basal ganglia, calcification of

benign essential tremor

benign essential tremor, refractory

blepharospasm

blind spot, enlarged

blindness

blindness, congenital

blood dyscrasias, neurologic findings with

bone density

bone density, increased

botulinum toxin

bradycardia

brainstem, dysfunction

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

cachexia

calcification, intracranial

calf atrophy

calf hypertrophy

carbonic anhydrase II deficiency

CAT scan, base of skull

cataracts

cauda equina

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

central core disease

cerebral edema

cerebritis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrovascular accident

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

children

cholesterol, HDL

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Coats syndrome

compression fracture

compression neuropathy

congenital heart disease

congenital malformation

congenital myasthenic syndromes

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, familial

cranial nerve palsies, recurrent

cranial nerve tumor

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying

crying, pathologic

cryopyrin-associated periodic syndrome

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

Dejerine-Sottas syndrome

dementia

denervation of muscle

descending paralysis

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

differential diagnosis

diplopia

dislocated hip, congenital

dissociated sensory loss

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

drug induced neurologic disorders

Duane syndrome

dural sinus thrombosis

dystonia musculorum deformens

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, treatment of

DYT1 mutation

electrocardiogram, abnormal

electromyogram

ELISA

Emery-Dreifuss muscular dystrophy

endarterectomy, carotid

endovascular therapy

entrapment neuropathy

enzyme, defect

ependymoma

epidemiology of neurology

episodic disorders

erythema migrans

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, familial

facial nerve palsy, recurrent

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

fine motor function, impaired

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

gests antagoniste

globoid cells

granulomatosis with polyangiitis

granulomatous disease

heart block, complete

hematuria, microscopic

hemianopia

hemiparesis

hemiplegia

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

high arched palate

Hirschprung's disease

histochemistry

histochemistry of muscle

hyperostosis corticalis generalisata familiaris

hyperostosis cranialis interna

hyperreflexia

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hypofibrinogenemia

hypoglossal nerve paralysis

iatrogenic neurologic disorders

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

intellectual deficit

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrinsic hand muscles, wasting of

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

laughing, pathologic

leg weakness, bilateral

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukopenia

lid closure, weakness of

life expectancy

light-near dissociation, causes of

lumbar puncture

Lyme disease

lymphadenopathy

lymphoma involving CNS

lymphomatoid granulomatosis

malignant hyperpyrexia

medulla oblongata, lesion of

meningoencephalopathy

methylhydrazine derivatives

microcephaly

misdiagnosis

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

mononeuropathy multiplex

mortality

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, treatment of

MRI

MRI, abnormal

MRI, contrast enhanced

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myopathy, distal Laing

myopathy, mitochondrial

myopathy, vacuolar

myotonia

myotonia dystrophica

myotonia dystrophica, classification

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, sensory

nerve hypertrophy

nerve root hypertrophy

neurofibroma

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuromuscular junction

neuropathology

neuropathy

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, vasculitic, systemic

nystagmus, dissociated

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

ophthalmoplegia, recurrent

opisthotonus

optic atrophy

optic atrophy, bilateral

optic disc cup

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

orchitis

orthostatic hypotension

osteoporosis

osteosclerosis, autosomal dominant

paraspinal muscle weakness

paratrigeminal syndrome

paresthesias

Parkinson disease

Parkinsonism syndrome

percussion induced muscle contraction

pericarditis

pleocytosis of cerebrospinal fluid

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

postural abnormality

pregnancy, neurologic complications in

primary lateral sclerosis

procarbazine

prognathism

prognosis

progressive neurologic disorder

propranolol

proptosis

proteinuria

proximal muscle atrophy

pseudobulbar palsy

pseudomyotonia

psychomotor retardation

ptosis

ptosis, bilateral

ptosis, unilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pyramidal tract dysfunction

recurrent laryngeal nerve paralysis

red eye

renal tubular acidosis

rheumatoid arthritis, neurologic complications of

riboflavin transporter deficiency

scoliosis, neurologic association with

seizure

sensorineural hearing loss

sensory loss, truncal

shoulder-girdle wasting

shunt procedure, lumboperitoneal

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

sleep

slit lamp examination

spinal cord, compression of

spinal cord, ischemic lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spirochete infection

splenomegaly

spontaneous muscle activity

stent, venous sinus

steroid therapy, CNS treatment and complications with

stimulation, deep brain

subarachnoid hemorrhage

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tetanus

thalamotomy

thalamus, focused ultrasound ablation

third nerve palsy

third nerve palsy, pupil sparing in

thrombocytopenia

tick bite

tinnitus

tomaculous neuropathy

tongue, enlarged

tongue, impaired movements of

treatment of neurologic disorder

tremor

tremor, intention

tremor, postural

tremor, surgical treatment of

tremor, treatment of

trigeminal nerve

trigeminal nerve, hypertrophy

trigeminal nerve, lesion of

trigeminal neuralgia

trigeminal neuropathy

trinucleotide repeats

trochlear nerve

trochlear nerve palsy

vincristine neurotoxicity

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

wheelchair

whistle, inability to

white matter disease

wide based gait

Wildervanck's syndrome

winging of scapula

Wolfram syndrome

wrist drop

Showing articles 550 to 600 of 5671 << Previous Next >>

Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
Neurol 46:1133-1137, Pareyson,D.,et al, 1996

Adult-Onset MELAS
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Neurogenic Muscle Hypertrophy
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Delayed Radiation-Induced Bulbar Palsy
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Cytomegalovirus Infection and Guillain-Barre Syndrome:The Clinical, Electrophysiologic, and Prognostic Features
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MR Findings in Listerial Rhombencephalitis
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Pseudotumor Associated with CNS Lymphoma
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Blepharospasm:Report of a Workshop
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The Long-Term Outcome of Microvascular Decompression for Trigeminal Neuralgia
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Treatment of Trigeminal Neuralgia (Editorial)
NEJM 334:1125-1126, Fields,H.L., 1996

Recurrent Bell's Palsy
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Cranial Nerve Palsy in Spontaneous Dissection of the Extracranial Internal Carotid Artery
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Deep Brain Stimulation for Essential Tremor
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Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
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Bell Palsy and Herpes Simplex Virus:Identification of Viral DNA in Endoneurial Fluid and Muscle
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Meningitis, Vasculitis, and Cerebritis Caused by CNS Histoplasmosis:Radiologic-Pathologic Correlation
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Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
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Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
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Congenital Unilateral Facial Paralysis
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Intermittent Diplopia and Strabismus Caused by Ocular Neuromyotonia
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Reversible Blindness Secondary to Acute Sphenoid Sinusitis
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VIIIth Cranial Nerve Involvement in Sarcoidosis
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Management of Acoustic Neuroma
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Progressive Blurring of Vision in Both Eyes
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Neurologic Manifestations in Children with Lyme Disease
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Clinical Correlates of Secondary Meningitis in HIV-Infected Adults
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Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
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Chronic Hypertrophic Cranial Pachymeningitis Associated with HTLV-I Infection
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Eye Movement Abnormalities in Systemic Lupus Erythematosus
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Simultaneous, Multiple Cranial Neuropathies in Diabetes Mellitus
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Polyneuritis Cranialis Due to Varicell-Zoster Virus in the Absence of Rash
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Painful Oculomotor Palsy Caused by Posterior-Draining Dural Carotid Cavernous Fistulas
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Oculomotor Nerve Invasion by Lymphoma Demonstrated by MRI
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MR of Oculomotor Nerve Plasy
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Prolonged Paralysis After Neuromuscular Blockage
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Clinical and Public Health Aspects of Tuberculous Meningitis in Children
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Showing articles 550 to 600 of 5671 << Previous Next >>