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Differential
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abdominal cramps
abducens nerve paralysis
acoustic nerve
adult polyglucosan body disease
ageusia
akathisia
alcohol intolerance
alkylating agents
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
amyloidosis
anatomy of
angina pectoris
anhidrosis
anosmia
antimetabolite
areflexia
asparginase
asystole
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atonic bladder
attention deficit disorder with hyperactivity
autonomic dysfunction
autonomic dysfunction, acute
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
autosomal dominant leukodystrophy
axonal degeneration
Babinski sign
bacterial infection
baroreceptors
bladder dysfunction
blood dyscrasias, neurologic findings with
botulism
bradycardia
brain atrophy
brainstem, infarction of
bulbar palsy
burning paresthesia
carbamazepine
carcinoma
carcinoma of thyroid
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cataracts, congenital
catecholamine
cerebellar atrophy, secondary
cerebellar vermis
cerebral cortical atrophy
cerebral ischemia
cerebral vasculature
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
chewing movements
children
chorea
choreoathetosis
cingulate island sign
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
coat-hanger pain
coma
confabulation
congestive heart failure
constipation
cranial neuropathy, multiple
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, rapidly progressive
dementia, subcortical
developmental retardation
diabetes mellitus
diarrhea
differential diagnosis
diplopia
dopamine
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dystonia
dystonia musculorum deformens
encephalopathy
erectile dysfunction
exome sequencing
eye, pain in
Fabry's disease
facial nerve palsy
facial nerve palsy, bilateral
facial pain
failure to thrive
falling
familial
familial rectal pain
fatal familial insomnia
fever
flunarizine
fluorouracil
flush syndrome
flushing
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
gait disorder
gait, spastic
gamma amino butyric acid
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
glycogen storage disease
hallucination
head injury
headache
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
homovanillic acid
Horner's syndrome
human immunodeficiency virus type 1
hydrocephalus
hyperhidrosis
hyperreflexia
hypertension
hyperthermia
hyponatremia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypotonia
imbalance
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inattention
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
isoniazid
jaw pain
Jewish
karyotyping
Korsakoff's psychosis
laughing
laughing, pathologic
L-dopa
leprosy
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningismus
meningoencephalopathy
mental retardation
methotrexate
methylhydrazine derivatives
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
monoamine oxidase inhibitors
monoamines
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
multiple endocrine neoplasia
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle pain
muscle weakness
myelomalacia
myeloneuropathy
myocardial infarction
myoclonic jerks
myoclonus
nausea and vomiting
neck pain
nerve biopsy
nerve growth factor
neuroendocrinology
neurofibromatosis 1
neurogenic bladder
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuroma
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, work up for
neurotoxin
neurotransmitter
next-generation sequencing
nitrogen mustard
norepinephrine
NOTCH2NLC
nystagmus
ocular dysmetria
orthostatic hypotension
orthostatic hypotension, idiopathic
pain
pain, anal
paraparesis
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, atypical
Parkinson disease, familial
Parkinsonism syndrome
paroxysmal extreme pain disorder
paroxysmal neurologic deficits
peroneal muscle atrophy, causes of
phenylketonuria
pleocytosis of cerebrospinal fluid
polyglucosan body
polyglucosan body disease
polyneuropathy, familial
precipitating factors
prion disease
procarbazine
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
radiculopathy
review article
Riley-Day syndrome
Romberg's sign
screening
seizure
seizure, children
seizure, differential diagnosis of
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
shoulder, pain in
Shy-Drager syndrome
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
smell
SNCA duplication
sodium channel dysfunction
spasticity
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 3/Machado Joseph disease
stuporous
subcortical U fibers
syncope
tachycardia
tardive dyskinesia
taste
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
torticollis
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
trinucleotide repeats
urinary frequency
urinary incontinence
valsalva maneuver
vasospasm, cerebral
vinblastine
vincristine neurotoxicity
viral infection
visual loss, transient
vocal cord paralysis
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
wrist drop
Showing articles 950 to 1000 of 1945 << Previous Next >>

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Familial Autoimmune Myasthenia Gravis
Neurol 44:551-554, Bergoffen,J.,et al, 1994

Progressive Spastic Paraparesis Revealing Primary Hyperparathyroidism
Neurol 44:178-179, Thomas,P.&Lebrun,C., 1994

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
Stroke 25:889-903, Schievink,W.I.,et al, 1994

Progressive Multifocal Leukoencephalopathy Complicating Wiskott-Aldrich Syndrome
Arch Neurol 51:422-426, Katz,D.A.,et al, 1994

Clinicopath Conf
Chronic Idiopathic Anhidrosis, Case 29-1994, NEJM 331:259-265994., , 1994

Idiopathic Autonomic Neuropathy:Clinical Neurophysiologic, and Follow-up Studies on 27 Patients
Neurol 44:1675-1682, Suarez,G.A.,et al, 1994

The Importance of Family History in Cerebrovascular Disease
Stroke 25:1599-1604, Graffagnini,C.,et al, 1994

Study of Antiphospholipid Antibodies in a Patient with Sneddon's Syndrome and Her Family
Stroke 25:1071-1074, Lousa,M.,et al, 1994

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
JNNP 57:1260-1262, Silander,K.,et al, 1994

Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities
Neurol 44:2250-2252, Gouider,R.,et al, 1994

Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
Neurol 44:2253-2257, Chance,P.F.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

Twinning and Cerebral Palsy:Experience in Four Northern California Counties, Births 1983 Through 1985
Pediatrics 92:854-858, Grether,J.K.,et al, 1993

Choroido-Cerebral Calcification Syndrome with Retardation
Neurol 43:2387-2389, Singh,B.,et al, 1993

Autosomal Dominant Parkinsoniam with Benign Course and Typical Lewy-Body Pathology
Neurol 43:2222-2227, Golbe,L.I.,et al, 1993

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
JAMA 270:2316-2320, MacCollin,M.,et al, 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Copper-Histidine Therapy for Menkes Disease
J Pediatr 123:828-830, Sarkar,B.,et al, 1993

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

A Neurological Gene Map
Arch Neurol 50:1269-1271, Rosenberg,R.N., 1993

Validity of Family History Data on Severe Headache and Migraine
Neurol 43:1954-1960, Ottman,R.,et al, 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and Von Hippel-Lindau Disease
NEJM 329:1531-1538, Neumann,H.P.H.,et al, 1993

Aicardi's Syndrome:MR Appearance of Unusual Orbital and Ventricular Cystic Lesions
AJR 160:601-603, Mehta,r.C.,et al, 1993

Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993

Twin Birth is Not a Risk Factor for Seizures
Neurol 43:2515-2519, Berkovic,S.F.,et al, 1993

Intensive Management and Treatment of Severe Guillain-Barre Syndrome
Crit Care Med 21:433-446, Hund,E.F.,et al, 1993

Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
Neurol 43:36-41, Silver,K.&Andermann,F., 1993

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

Tolrestat for Mild Diabetic Neuropathy, A 52-Week Randomized, Placebo-Controlled Trial
Ann Int Med 118:7-11, Guigliano,D.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993

A Population-Based Study of Multiple Sclerosis in Twins:Update
Ann Neurol 33:281-285, Sadovnick,A.D.,et al, 1993

Use of Twin Cohorts for Research in Alzheimer's Disease
Neurol 43:261-267, Breitner,J.C.S.,et al, 1993

Sleep Paralysis
Lancet 341:406-407, Dahlitz,M.&Parkes,J.D., 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993



Showing articles 950 to 1000 of 1945 << Previous Next >>