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Differential
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abdominal distention
abducens nerve paralysis
abiotrophy
acoustic nerve
agammaglobulinemia
alcohol intolerance
alkylating agents
alopecia
altered states of consciousness
alveolar hypoventilation
anesthesia, general
antimetabolite
aphasia
areflexia
arrhythmia, cardiac
arthralgia
asparginase
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
atonic bladder
autonomic dysfunction
baldness
basal ganglia, calcification of
blood dyscrasias, neurologic findings with
brainstem, dysfunction
cachexia
calcification, intracranial
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
central core disease
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chromosome 19
chronic progressive external ophthalmoplegia
cleft palate
Clinical Pathologic Conference(C.P.C.)
coma
congenital heart disease
congenital malformation
congenital myasthenic syndromes
congenital myopathy
consanguinity
cough
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
dementia
developmental retardation
diabetes mellitus
diarrhea
diplopia
distal muscle weakness
Duane syndrome
dysphagia
dyspnea
dyspraxia
dystonia
electrocardiogram, abnormal
electromyogram
encephalopathy
encephalopathy, progressive
exercise intolerance
extraocular muscle lesion
eye movement, disorders of
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fatigue
fever
fluorescein angiography
fluorouracil
flush syndrome
foot drop
gait disorder
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
granulomatosis with polyangiitis
granulomatous disease
hallucination
headache
hearing loss
heart block
hemianopia
hemiparesis
hepatic failure
hepatomegaly
heralding manifestation
high arched palate
Hirschprung's disease
Holt-Oram syndrome
hypercapnia
hypogonadism
hyponatremia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
intestinal pseudoobstruction
iris, abnormal
isoniazid
jaw pain
Kearns-Sayre syndrome
klippel feil syndrome
Korsakoff's psychosis
lactic acidemia
Leber's hereditary optic neuropathy
Leigh's disease
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
leukopenia
lymphoma involving CNS
lymphomatoid granulomatosis
MELAS syndrome
meningismus
meningoencephalopathy
mental retardation
MERRF syndrome
methotrexate
methylhydrazine derivatives
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoamine oxidase inhibitors
movement disorder
MRI
MRI, abnormal
muscle atrophy, progressive
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
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, familial incidence of
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, seronegative
myelopathy
myoclonus
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myotonia
myotonia dystrophica
nasal speech
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular blockade
neuromuscular junction
neuromuscular junction, abnormality of
neuroophthalmology
neuropathy
neuropathy, peripheral
neurotoxin
nitrogen mustard
normal
nystagmus
nystagmus, dissociated
nystagmus, vertical
ocular motility, disorders of
ocular myopathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic neuropathy
orthostatic hypotension
pain
pain, abdominal
pancytopenia
paraparesis
paraparesis, spastic
paresthesias
Parkinsonism syndrome
percussion induced muscle contraction
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polyneuropathy
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
prostigmine
pseudomyasthenia
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
ptosis, classification of
ptosis, familial
ptosis, unilateral
pulmonary infiltrates
ragged-red fibers
rash
retina, abnormal
retinal degeneration
retinal lesion
retinopathy
review article
seizure
sensorineural hearing loss
seronegative
short stature
skin, lesions in neurologic disorders
slit lamp examination
spasticity
spina bifida
splenomegaly
steroid therapy, CNS treatment and complications with
strokelike episodes
syringomyelia
systemic illness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
testicular atrophy
thrombocytopenia
tinnitus
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
vertigo
vinblastine
vincristine neurotoxicity
vocal cord paralysis
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weaning from respirator, failure to
web sites
weight loss
wheelchair
white matter disease
wide based gait
Wildervanck's syndrome
wrist drop
Showing articles 1500 to 1550 of 2049 << Previous Next >>

Wilson's Disease Studies with FDG & Positron Emission Tomography
Neurol 37:1707-1711, Hawkins,R.A.,et al, 1987

Essential Tremor:A Review
Neurol 37:1194-1197, Findley,L.J.&Koller,W.C., 1987

A Rating Scale for Gilles de la Tourette's Syndrome:Description, Reliability, & Validity Data
Neurol 37:1542-1544, Goetz,C.G.,et al, 1987

Alzheimer's Disease
Down's Syndrome, & Chromosome 21, Editorial, Lancet 1:1011-1012., , 1987

Risk Factors for Alzheimer's Disease:A Case-Control Study
Neurol 37:1630-1633, Shalat,S.T.,et al, 1987

Multiple Sclerosis & Systemic Lupus Erythematosus, Occurrence in Two Generations of the Same Family
Arch Int Med 147:1317-1320, Sloan,J.B.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Human T-Lymphotropic Virus Type I Antibodies in The Serum of Pts with Tropical Spastic Paraparesis in the Seychelles
Arch Neurol 44:605-607, Roman,G.C.,et al, 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Ice Pack Test for Myasthenia Gravis
Neurol 37:1383-1385, Sethi,K.D.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Bilateral Cerebral Ptosis
Neurol 37:1043-1046, Lepore,F.E., 1987

Familial Recurrent Bell's Palsy with Ocular Motor Palsies
Neurol 37:1369-1371, Aldrich,M.S.,et al, 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Magnetic Resonance Imaging in Isolated Noncompressive Spinal Cord Syndromes
Ann Neurol 22:714-723, Miller,D.H.,et al, 1987

The Aetiology of Mirror Writing:A New Hypothesis
JNNP 50:1572-1578, Tashiro,K.,et al, 1987

False Negative Results in Patients with fra (X) (q) Mental Retardation Taking Oral Vitamin Supplements
NEJM 316:1093, Froster-Iskenius,U.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Cervicomedullary Compression in Young Patients with Achondroplasia:Value of Neurologic & Respiratory Eval
J Pediatr 110:522-530, Reid,C.S.,et al, 1987

The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
Neurol 37:910-915, Boustany,R.M.N.,et al, 1987

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Magnetic Resonance Imaging in Pelizaeus-Merzbacher Disease
Neuroradiology 29:403-405, Journel,H.,et al, 1987

Neurofibromatosis
Editorial, Lancet 1:663-6641987., , 1987

Renal Cell Carcinoma in von Hippel-Lindau Syndrome
Am J Med 82:236-238, Malek,R.S.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Familial Occurrence of Spontaneous Dissection of the Internal Carotid Artery
Stroke 18:246-251, Mokri,B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

Evidence That the Gene for Tuberous Sclerosis is on Chromosome 9
Lancet 1:659-661, Fryer,A.E.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Caffeine & Tremor
Neurol 37:169-172, Koller,W.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Benign Sexual Headach within a Family
Arch Neurol 43:1158-1160, Johns,D.R., 1986

Unusual Clinical Variants & Signs in Guillain-Barre Syndrome
Arch Neurol 43:1150-1152, Ropper,A.H., 1986

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Orthostatic Tremor in Familial-Essential Tremor
Neurol 36:1241-1245, Wee,A.S.,et al, 1986

Computed Tomography of Familial Pineoblastoma
J Comput Assist Tomogr 10:32-33, Peyster,R.G.,et al, 1986

Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
JNNP 49:362-368, Battersby,R.D.E.,et al, 1986



Showing articles 1500 to 1550 of 2049 << Previous Next >>