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 700 to 750 of 5743 << Previous Next >>

Clinical Outcome in Aggressively Treated Meningeal Gliomatosis
Neurol 42:252-254, Grant,R.,et al, 1992

Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
Arch Neurol 49:170-173, Malik,S.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Spinal Accesory (11th) Nerve Palsy Following Carotid Endarterectomy
Neurol 42:674-675, Sweeney,P.J.&Wilbourn,A.J., 1992

Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
Ann Neurol 31:299-304, Danek,A.,et al, 1992

Nervous System Lyme Borreliosis-Revisited
Arch Neurol 49:102-107, Finkel,M.J.&Halperin,J.J., 1992

Invasion of the Central Nervous System by Borrelia Burgdorferi in Acute Disseminated Infection
JAMA 267:1364-1367, Luft,B.J.,et al, 1992

Cranial Nerve Involvement with Lyme Borreliosis Demonstrated by Magnetic Resonance Imaging
Neurol 42:671-673, Nelson,J.A.,et al, 1992

MRI of Intracranial Neurovascular Compression
J Comput Assist Tomogr 16:503-505, Furuya,Y.,et al, 1992

Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992

Endovascular Treatment of Vertebral Arteriovenous Fistula
Radiology 183:361-367, Beaujeux,R.L.,et al, 1992

Enhancement Along the Normal Facial Nerve in the Facial Canal:MR Imaging and Anatomic Correlation
Radiology 183:391-394, Gebarski,S.S.,et al, 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Numb Chin Syndrome in Cancer Patients:Etiology, Response to Treatment, and Prognostic Significance
Neurol 42:1181-1184, Lossos,A.&Seigal,T., 1992

Intracerebral Haemorrhage After Dermal Nitrate Application
BMJ 305:1000, Boggild,M., 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
NEJM 327:1069-1074, Bilous,R.W.,et al, 1992

Hemifacial Spasm:Evaluation of Magnetic Resonance Imaging & Magnetic Resonance Tomographic Angiography
Ann Neurol 32:502-506, Adler,C.H.,et al, 1992

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Lyme Borreliosis in Bell's Palsy
Neurol 42:1268-1270, Halperin,J.J.,et al, 1992

Absence of Cyme Borreliosis Among Patients with Presumed Bell's Palsy
Arch Neurol 49:940-943, Kuiper,H.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Twelve Cases of Pituitary Apoplexy
Arch Int Med 152:1893-1899, Vidal,E.,et al, 1992

Spontaneous Remission of a Third-Nerve Palsy in Meningeal Lymphoma
Ann Neurol 32:100-102, Galetta,S.L.,et al, 1992

Cavernous Sinus Syndrome and Systemic Lupus Erythematosus
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Paramedian Thalamopeduncular Infarction:Clinical Syndromes and Magnetic REsonance Imaging
Ann Neurol 32:162-171, Tatemichi,T.K.,et al, 1992

Midbrain Syndromes of Benedikt, Claude, and Nothnagel:Setting the Record Straight
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Haemorrhage in the Inferior Colliculus
Neuroradiology 34:347, Nagao,M.,et al, 1992

Neuro-Ophthalmic Features of Carotid Cavernous Fistulas and Their Treatment by Endoarterial Balloon Embolisation
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Centrofacial Malignant Granulomas, Clinicopath Study of 40 Cases and Review of the Literature
Medicine 71:179-195, Grange,C.,et al, 1992

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

Post-Irradation Neuromyotona Affecting Trigeminal Nerve Distribution:An Unusual Presentation
Neurol 42:1102-1104, Diaz,J.M.,et al, 1992

Idiopathic Intracranial Hypertension:Report of Seven Cases
Am J Med 93:391-395, Jain,N.&Rosner,F., 1992

Treatment of Lyme Disease
The Medical Letter 34:95-97, , 1992

Treatment of Hemifacial Spasm with Botulinum Toxin
Muscle & Nerve 15:1045-1049992., Yoshimura,D.M.,et al, 1992

Spontaneous Rupture of the Common Carotid Artery:A Case Report
Head & Neck 14:496-501992., Kim,K.H.,et al, 1992

Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
Brain 115:979-989, Harding,A.E.,et al, 1992

Fracture of the Occipital Condyle:Case Report
Spine 17:1119-1121, Bozboga,M.,et al, 1992

Evolution of Oculomotor Nerve palsies
J Clin Neuro-Ophthalmol 12:21-25, Capo,H.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Wegener's Granulomatosis Mimicking Temporal Arteritis
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Sarcoid Peripheral Neuropathy
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Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
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MR Imaging of Primary Trochlear Nerve Neoplasms
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

A Genetic Study of Idiopathic Focal Dystonias
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Long-Term Suppression of Tremor by Chronic Stimulation of the Ventral Intermediate Thalamic Nucleus
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Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Showing articles 700 to 750 of 5743 << Previous Next >>