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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 550 to 600 of 2020 << Previous Next >>

Neuropsychological and Quality of Life Outcomes 12 Months After Unilateral Thalamic Stimulation for Essential Tremor
JNNP 74:305-311, Fields,J.A.,et al, 2003

Rest Tremor in Patients with Essential Tremor
Arch Neurol 60:405-410, Cohen,O.,et al, 2003

Treatment of Wilson Disease With Ammonium Tetrathiomolybdate, III. Initial Therapy in a Total of 55 Neurologically Affected Patients and Follow-up With Zinc Therapy
Arch Neurol 60:379-385, Brewer,G.J.,et al, 2003

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
Lancet 361:1552-1554, Reynolds,R.M., et al, 2003

Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
NEJM 348:1442-1448,1480, Siddiqui,A.,et al, 2003

Alzheimer's Disease and Parkinson's Disease
NEJM 348:1356-1364, Nussbaum,R.L. &Ellis,C.E., 2003

Diffusion MR Imaging Changes Associated with Wilson Disease
AJNR 24:965-967, Sener,R.N., 2003

Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
BMJ 326:1078-1079, Plunkett,A.,et al, 2003

Should Asymptomatic Patients with Hereditary Haemorrhagic Telangiectasia (HHT) be Screened for Cerebral Vascular Malformations? Data from 22 061 years of HHT Patient Life
JNNP 74:743-748, Easey,A.J.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

von Hippel-Lindau Disease
Lancet 361:2059-2067, Lonser,R.R.,et al, 2003

Autosomal Dominant Acute Necrotizing Encephalopathy
Neurol 61:226-230, Neilson,D.E.,et al, 2003

Mental Retardation
Neurol 61:156-157, Patterson,M.C. &Zoghbi,H.Y., 2003

The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003

Learning Disability
Lancet 362:811-821, Gillberg,C.&Soderstrom,H., 2003

Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
Ann Neurol 43:367-375, Rolfs,A.,et al, 2003

Hypoglossal Neuropathy in Hereditary Neuropathy with Liability to Pressure Palsy
Neurol 61:1154-1155, Winter,W.C. &Juel,V.C., 2003

Can We Prevent Cerebral Palsy?
NEJM 349:1765-1769, Nelson,K.B., 2003

Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003

A ripping roller coaster ride
Neurol 61:1255, Blacker, D.J. & Wijdicks, E.F.M., 2003

Hypertrophic Cardiomyopathy A Systematic Review
JAMA 287:1308-1320, Maron, B.J., 2002

Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
J Am Coll Cardiol 39:301-307, Maron,B.J.,et al, 2002

Paraganglioma of the Cervical Sympathetic Trunk
Ann Otol Rhinol Laryngol 111:1087-1091, Birchler,M.T., et al, 2002

Ptosis in Patients with Hemispheric Strokes
Neurol 58:620-624, Averbuch-Heller,L.,et al, 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
J Pediatr 140:242-246, Wolf,B.,et al, 2002

Clinicopath Conf,Mucormycosis, rhino-orbital
NEJM 346:924-929, Case 9-2002, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Therapies for Movement Disorders
Arch Neurol 59:699-702, Goetz,C.G &Hinson,V.K., 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Spontaneous Regression of Cerebral Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia
AJNR 23:1049-1050, Cloft,H.J., 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

A Double-blind Placebo-controlled Trial of Topiramate Treatment for Essential Tremor
Neurol 59:132-134, Connor,G.S., 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Familial Dementia With Lewy Bodies
Arch Neurol 59:1622-1630, Tsuang,D.W.,et al, 2002

Indications and Usefulness of Nerve Biopsy
Arch Neurol 59:1532-1535, Said,G., 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Tranexamic Acid in Hereditary Hemorrhagic Telangiectasia
NEJM 346:457, Sabra,C.,et al, 2002

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

Jaw Drop in Kennedy's Disease
Neurol 59:1471-1472, Sumner,C.J. &Fischbeck,K.H., 2002

Ptosis as a Remote Effect of Therapeutic Botulinum Toxin B Injection
Neurol 59:1445-1447, Racette,B.A.,et al, 2002

New Players in the Genetics of Stroke
NEJM 347:1711-1712, Tournier-Lasserve,E., 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Is Patent Foramen Ovale a Family Trait?
Stroke 32:1563-1566, Arquizan,C.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001



Showing articles 550 to 600 of 2020 << Previous Next >>