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Differential
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abducens nerve paralysis
acoustic nerve
acral sensory symptoms
Adies pupil
advances in neurology
alcohol intolerance
alkylating agents
altered states of consciousness
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ankle reflex, absent
anterior tibial muscle weakness
antimetabolite
areflexia
arthrogryposis multiplex
asparginase
ataxia
ataxia, cerebellar
atonic bladder
autonomic dysfunction
Babinski sign
benign essential tremor
blood dyscrasias, neurologic findings with
burning paresthesia
caloric testing
CAT scan, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central core disease
cerebrospinal fluid, pressure low
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chromosomal abnormality
chromosome 17
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
corpus callosum, lesion of
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
dermatomyositis
differential diagnosis
diplopia
diplopia, transient
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dysarthria
dysphagia
electroencephalogram, inflammatory disease
electromyogram
encephalopathy
epidemiology of neurology
episodic neurologic deficits
evoked potentials
facial nerve palsy, bilateral
facial pain
falling
familial
fasciculation
Fazio-Londe's disease
fever
fine motor function, impaired
fluorouracil
flush syndrome
foot deformity
foot drop
gadolinium
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genu of corpus callosum
Guillain Barre syndrome
hallucination
hammertoes
hand deformity
hand weakness
headache
hearing loss
heavy metal intoxication
hemiparesis
hemiparesis, transient
high arched feet
human genome
hyperreflexia
hyponatremia
hyporeflexia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intrinsic hand muscles, wasting of
Isaacs syndrome
isoniazid
jaw pain
klippel feil syndrome
Korsakoff's psychosis
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
laminectomy, cervical
laminectomy, lumbar
leg weakness, bilateral
leukemia, neurologic findings assoc.with
leukoencephalopathy
lumbosacral plexopathy
meningismus
meningoencephalopathy
methotrexate
methylhydrazine derivatives
misdiagnosis
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
monoparesis
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelin protein zero gene
myelogram
myelopathy
myeloradiculopathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nausea and vomiting
nerve biopsy
nerve conduction studies
nerve growth factor
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neuritis, causes of
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuropathy
neuropathy, classification of
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, work up for
neurotoxin
neurotrophin-3
night blindness
nitrogen mustard
numbness, extremity
optic atrophy
optic atrophy, hereditary
orthostatic hypotension
pain
pain, foot
paralysis
paralysis, recurrent
paraparesis
paresthesias
paresthesias, feet
paresthesias, lower extremity
patient information and support
peroneal muscle atrophy, causes of
pes cavus
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, familial
porphyria
post polio syndrome
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
proptosis
ptosis
ptosis, bilateral
pulmonary function tests
pupil
pupil, dilated and fixed, bilateral
pyramidal tract dysfunction
quadriparesis
quadriplegia, transient
quality of life
radiculopathy
recombinant DNA
recurrent
Refsum's disease
respiratory failure
reversible neurologic disorder
review article
RFLPs
Romberg's sign
Roussy Levy syndrome
sarcoidosis
seizure
sensorineural hearing loss
sensory loss
spinal cord, compression of
spinal muscular atrophy
spinal stenosis
spinal stenosis, familial
splenium of corpus callosum
spontaneous remission
steppage gait
stiff man syndrome
strokelike episodes
subdural hematoma
symmetric brain lesions
syncope
tinnitus
toe walking
tomaculous neuropathy
torticollis
transient neurologic deficit
treatment of neurologic disorder
tremor
tricresylphosphate
trigeminal nerve
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
ultrasonography, nerve
vestibular function, tests of
vinblastine
vincristine neurotoxicity
visual evoked response
visual impairment
vocal cord paralysis
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
white matter disease
wrist drop
X-linked neuropathy
x-ray, spine
Showing articles 350 to 400 of 7753 << Previous Next >>

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Rapid Improvement in Nerve Conduction Velocity Following Renal Transplantation
Ann Neurol 4:369-373, Oh,S.J.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Polyneuropathy in Waldenstrom's Macroglobulinemia
Arch Neurol 35:423, Julien,J.,et al, 1978

Neuropathy Following Abuse of Nitrous Oxide
. et al, Neurol 28:504978., Layzer,R.B., 1978

Nerve Growth Factor (three parts)
NEJM 297:1096, 1149, 1211977., Mobley,W.C.,et al, 1977

Subacute Sensory Neuropathy:A Remote Effect of Carcincoma
Ann Neurol 2:7, Horwich,M.S.,et al, 1977

Alcoholic Neuropathy:Clinical, Electrophysiological, & Biopsy Findings
Ann Neurol 2:95, Behse,E.,et al, 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Mercury Poisoning in a Dentist
Arch Neurol 33:788, Iyer,K.,et al, 1976

Myasthenic Abduction Nystagmus in a Patient with Hyperthyroidism
Neurol 26:589, Finelli,P.F.&Hoyt,W., 1976

Herpes Simplex Virus in Idiopathic Facial Paralysis (Bell Palsy)
JAMA 233:527, Adour,K.K.,et al, 1975

Carpal Tunnel Syndrome-Importance of Sensory Nerve Conduction Studies in Diagnosis
JAMA 233:983, Hoffman,D.E., 1975

Scalloped Pupils in Familial Amyloidosis
NEJM 293:914, Lessell,S.,et al, 1975

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971

Radial Nerve-Handbook of Clinical Neurology
Vol 7, p 309, Ed, Vinken & Bruyn., Staal,A., 1970

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Intracavernous Carotid Aneur
Clinical Neuro-Ophthalmology, Third Ed. , Baltimore, The Williams & Wilkins Co. , 1969, Vol 2, Chap, 1, ph,F.B.&Hoyt,W.F., 1969

Ophthalmoplegia in Diabetes Mellitus
Ann Int Med 67:968, Zorrilla,E.,et al, 1967

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Mononeuritis Multiplex in Polyarteritis Nodosa
Neurol 14:434, Lovelace,R.E., 1964

Intracranial Aneurysms Causing Ophthalmoplegia
Arch Ophthal 70:75l, Cogan,D.,et al, 1963

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

Ribbon-Like Sign in Convexity Subarachnoid Hemorrhage
Ann Neurol 99:881-882, Liu,S-X.,et al, 2026

A 41-Year-Old Man Presenting with Right Foot Tingling
Neurol 106:214781, Lu,V.,et al, 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

A 55-Year-Old Man with Rapidly Progressive Weakness and Numbness
Neurol 106:e218063, Li,X.,et al, 2026

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

A 16-Year-Old Adolescent Boy with Ophthalmoplegia and Unilateral Ptosis
Neurol 105:e214430, Lu,Y.,, 2025

A 50-Year-Old Male Patient With Acute Severe Sensory Deafferentation and Bilateral Ptosis with Rapid Recovery
Neurol 106:e214435, Pseruk,F.,et al, 2025

An 83-Year-Old Female Patient with a Pupil Involving Oculomotor Nerve Palsy
Neurol 105:e214383, Riegel,D.C.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
Stroke 56:e359-362, deLima, M.M.,et al, 2025

Infantile Epileptic Spasms Syndrome (West Syndrome)
Stat Pearls PMID:30725936, Smith,M.S.,et al, 2025

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
Neurol 105:e214183, Costa,R., et al, 2025

Atypical Diabetic Neuropathies
BMJ 390:e081109, McCray,B.A.,et al, 2025

Pan-Neurofascin Nodo-Paranodopathy Presenting as Fulminant Guillain-Barre Syndrome
Neurol 105:e213848, Cabral,A.,et al, 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

Clinicopathological Conference, Powasan Virus Encephalitis
NEJM 393:176-184, Case 19-2025, 2025



Showing articles 350 to 400 of 7753 << Previous Next >>