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acid maltase deficiency
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyloidosis
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amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anterior horn cell disease
anterior tibial muscle weakness
apraxia of eye movements
areflexia
arthrogryposis multiplex
asymptomatic
ataxia
ataxia telangiectasia
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ataxia, truncal
benign congenital hypotonia
Brugada syndrome
bulbar palsy, progressive
calf hypertrophy
carcinoembryonic antigen
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central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
clinodactyly
coma
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congenital heart disease
congenital myopathy
congestive heart failure
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
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denervation of muscle
denervation potentials
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
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dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
Friedreich's ataxia
gait disorder
gait, waddling
gene
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gene therapy
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Guillain Barre syndrome
gynecomastia
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history of neurology
human T-lymphotropic virus type I(HTLV-I)
Huntington's chorea
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hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infant, evaluation of
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
mental retardation
misdiagnosis
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mortality
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MRI
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multiple system atrophy
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muscle weakness
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muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenic crisis
myelopathy
myelopathy, chronic progressive
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, carcinomatous
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myopathy, mitochondrial
myopathy, thyroid disease causing
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myotonia congenita
myotonia dystrophica
nemaline rod myopathy
nerve conduction studies
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neuropathy, hereditary peripheral
newborn, evaluation of
nusinersen
ocular motility, disorders of
Onufrowicz nucleus
Oppenheim muscular dystrophy
paraparesis, familial spastic
Parkinson disease
pathology
patient information and support
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phrenic nerve
placebo
poison, mercury
poison, neurologic problems with
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porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
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progeria
prognosis
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proximal muscle atrophy
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radiculopathy
Refsum's disease
respiratory failure
review article
RFLPs
risdiplam
risk-benefit assessment
Roussy Levy syndrome
safety
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
skin, lesions in neurologic disorders
SMN1 gene
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stiff man syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
sudden death
survival motor neuron gene
telangiectases
term infant
tongue, fasciculations of
torticollis
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
viral infection
vitamin E
vitamin E deficiency
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
West disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 800 to 850 of 7312 << Previous Next >>

Acute Obstructive Hydrocephalus complicating Bacterial Meningitis in Childhood
BMJ 316:1887-1889, Mactier,H.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Spontaneous Thoracic Spinal Cord Herniation Through an Anterior Dural Defect
AJNR 19:1345-1348, 11851998., Dix,J.E.,et al, 1998

Transdural Spinal Cord Herniation:Imaging and Clinical Spectra
AJNR 19:1337-1344, 11851998., Watters,M.R.,et al, 1998

CSF Spaces in Idiopathic Normal Pressure Hydrocephalus:Morphology and Volumetry
AJNR 19:1277-1284, 12851998., Kitagaki,H.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Progressive Multifocal Leukoencephalopathy, HIV, and Highly Active Antiretroviral Therapy
NEJM 339:848-849, Cinque,P.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

A Clinical Role for 99mTC-HMPAO SPECT in the Investigation of Dementia
JNNP 64:306-313, Talbot,P.R.,et al, 1998

Diagnosis of Cytomegalovirus Encephalitis in Pts with AIDS by Cytomegalovirus Genomes in Cells of Cerebrospinal Fluid
Neurol 50:693-697, Wildemann,B.,et al, 1998

Dural Arteriovenous Fistulas as a Cause of Intracranial Hypertension Due to Impairment of Cranial Venous Outflow
JNNP 65:308-316, Cognard,C.,et al, 1998

Herpes Simplex Encephalitis (HSE) and the Immunocompromised: A Clinical and Autopsy Study of HSE in the Settings of Cancer and Human Immunodeficiency Virus-Type 1 Infection
Hum Pathol 29:215-222, Schiff,D. &Rosenblum,M.K., 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Chronic Neutrophilic Meningitis Caused by Candida Albicans
Neurologia 13:362-366, del Pozo, M.M.,et al, 1998

Relationship Between Human Immunodeficiency Virus-Associated Dementia & Viral Load in Cerebrospinal Fluid & Brain
Ann Neurol 42:689-698, 6751997., McArthur,J.C.,et al, 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Cerebral Tuberculosis in Pts with AIDS, Report of 6 Cases & Review
Medicine 76:423-431, Lesprit,P.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Spinal MRI in Vacuolar Myelopathy, and Correlation with Histopathological Findings
et a, Neuroradiology 39:865-8691997., Sartoretti-Schefer,S., 1997

Diseases of the Spine and Spinal Cord
In AIDS and the Nervous System, Lippencott-Raven, Phila, Ch 13, p 3667., Whiteman,M.L.H.,et al, 1997

Dentate Nuclei Invol in AIDS Pts with CNS Cryptococcosis:Imaging Findings with Path Correl
J Comput Assist Tomogr 21:175-182, Ruiz,A.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Alteration of White Matter MR Signal Intensity in Frontotemporal Dementia
AJNR 18:367-378, Kitagaki,H.,et al, 1997

Correlation of MRI and Neuropathology in AIDS
JNNP 62:92-95, Everall,I.P.,et al, 1997

Diagnosis of AIDS-Related Focal Brain Lesions
Neurol 48:687-694, Antinori,A.,et al, 1997

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
Neurol 48:978-985, Kaufer,D.I.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Frontotemporal Dementia and Early Alzheimer Disease:Differentiation with Frontal Lobe H-1 MR Spectroscopy
Radiology 203:829-836, Ernst,T.,et al, 1997

A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997

Peripheral Neuropathy in HIV Infected Patients with the Diffuse Infiltrative Lymphocytosis Syndrome
Ann Neurol 41:438-445, Moulignier,A.,et al, 1997

Fulminating Encephal with Perivenular Demyel & Vacuolar Myelopathy as Initial Present of HIV Infection
Arch Neurol 54:647-650, Silver,B.,et al, 1997

Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,et al, 1997

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

MR Imaging of the Meninges, Part II, Neoplastic Disease
Radiology 201:605-612, Fukui,M.B.,et al, 1996

Clinicopath Conf
Noncaseating Granulomas Consistent with Sarcoidosis, Case 37-1996, NEJM 335:1668-1674996., , 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Zoster Myelitis:Improvement with Antiviral Therapy in Two Cases
Neurol 47:929-931, deSilva,S.M.,et al, 1996



Showing articles 800 to 850 of 7312 << Previous Next >>