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Differential
(Click to cross reference)
abdominal distention
abdominal muscle paralysis
abdominal protrusion
abscess, brainstem
abscess, intracerebral
abscess, lung
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
acute intermittant porphyria
acyl CoA dehydrogenase deficiency
addiction, heroin
addiction, heroin-neurologic complications with
adult polyglucosan body disease
advances in neurology
adverse drug reaction
alcoholism
alternating rapid movement, impaired
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anasarca
anemia
anemia, megaloblastic
aneurysm
aneurysm, abdominal aortic
aneurysm, aortic arch
aneurysm, intracranial
ankle clonous
ankle reflex, absent
ankle, swelling of
anoctaminopathy
anorexia
antecedent illness
anterior horn cell disease
anterior tibial muscle weakness
anti DNA agent
anti GQ1b IgG antibody
anti signal recognition particle antibody
antibodies to voltage-gated calcium channels
antiganglioside antibodies
antiviral agents
aorta, abdominal
aorta, abnormal
aortitis
arbovirus
areflexia
arm weakness
arthralgia
arthritis
aspartate aminotransferase
asthma
astrocytoma
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atrioventricular block
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
axonal degeneration
B 12 deficiency
Babinski sign
bacterial infection
basophilic stippling of red blood cells
bat bite
BCG treatment
Behcet's syndrome
bent spine syndrome
Bing-Neel syndrome
biologic markers
blacks
bladder dysfunction
blood cultures
bone biopsy
bone marrow biopsy
bone pain
bone scanning
botulism
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
bradycardia
bradykinesia
brain atrophy
brain biopsy
brain natriuretic peptide
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
Brown-Vialetto-Van Laere syndrome
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
burning paresthesia
cachexia
calf hypertrophy
camptocormia
campylobacter infection
cane
carcinoma
carcinoma of bladder
carcinoma of lung
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, chest
CAT scan, muscle
cauda equina
cauda equina, enhancement
cauda equina, lesion of
CD4 counts
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, location of
cerebrovascular accident, recurrent
cerebrovascular accident, topographic pattern
cerebrovascular disease
Charcot-Marie-Tooth
chelation therapy
chemotherapy, CNS treatment and complications with
chest pain
chest x-ray, abnormal
chewing, impaired
children
choreoathetosis
chromosome 5
chromosome 9
chronic progressive external ophthalmoplegia
Churg-Strauss syndrome
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
cognition
coinfection
cold temperature
coma
comorbidities
complications
conduction block
confusion
congenital heart disease
congenital myopathy
consanguinity
constipation
contractures, joint
controversies in neurology
conversion reaction
copper
copper deficiency
cranial nerve enhancement
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
critical care unit
cyclic vomiting
cyclosporine
cystoisospora belli
cytosine arabinoside
deafness
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, frontotemporal
demyelinating disease
denervation of muscle
denervation potentials
denture cream
depression
dermatitis
dermatomyositis
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diabetes mellitus, chemical
diagnostic criteria
diaphragmatic paralysis
diarrhea
diarrhea, bloody
differential diagnosis
difficulty climbing stairs
diplegia, brachial
diplopia
disorientation
distal muscle atrophy
distal muscle weakness
dizziness
down-beat nystagmus
dropped head syndrome
drug abuse
drug abuse, neurologic complications of
drug induced neurologic disorders
dying
dysarthria
dysdiadochokinesia
DYSF gene
dysferlinopathy
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dyspnea
dyspraxia
dystroglycanopathies
dystrophin
dystrophin associated proteins
efficacy
electrocardiogram, abnormal
electrocorticogram
electroencephalogram, abnormalities of
electromyogram
electromyogram, decremental response
electromyogram, incremental response
electron microscopy
electronystagmography
electrophoretic pattern, serum
Emery-Dreifuss muscular dystrophy
empty sella
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, episodic
encephalitis, Powassan
encephalitis, Rasmussen's
encephalitis, viral
encephalopathy
enteritis
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
eosinophilic granulomatosis with polyangiitis
epidemiology of neurology
epilepsia partialis continua
episodic disorders
episodic neurologic deficits
epistaxis
exercise
exercise intolerance
exercise-related muscle strength increase
extraocular muscle lesion
eye movement, disorders of
facial nerve palsy
facial nerve palsy, recurrent
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failed medical management
failure to thrive
falling
familial
fasciculation
fatigable chewing
fatigue
fever
fibrillations
fine motor function, impaired
Fisher's syndrome
flaccid paralysis
flavivirus
flu-like illness
foot deformity
foot drop
foot drop, bilateral
foot drop, differential diagnoses of
F-wave response
gadolinium
gait disorder
gait, spastic
gait, waddling
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastric partitioning
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastrointestinal perforation
gastroparesis
gaze palsy
gaze palsy, vertical
gemfibrozil
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
geographic location
glioma
gliomatosis cerebri
glucose tolerance test, abnormal
glycogen storage disease
GM1 ganglioside antibodies
Google
Gowers maneuver
granuloma, eosinophilic
granulomatous disease
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, complications
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, etiology of
Guillain Barre syndrome, prognosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hallucination, auditory
hammertoes
hand deformity
hand weakness
headache
headache, positional
hearing loss
heart block
heart block, complete
heart murmur
heliotrope rash
hemiatrophy, cerebral
hemidiaphragm, paralysis of
hemiparesis
hemiplegia
hemiplegia, progressive
hemispherectomy
hemorrhagic diathesis
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
herpes simplex virus
herpes virus
herpes virus infection
herpes, genital
hiccoughs
high arched feet
highly active antiretroviral therapy
hip pain
histochemistry of muscle
HMGcoA reductase inhibitors
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
homocysteine, serum
homosexual
H-reflex testing
human diploid cell rabies vaccine
human immunodeficiency virus type 1
hydroxychloroquine
hypercalcemia
hyperhidrosis
hyperhomocysteinemia
hyperreflexia
hypertension
hypertension, intracranial causes of
hypertension, paroxysmal
hyperviscosity
hypoglycorrhachia
hypokalemia
hypokalemic paralysis
hypokinesia
hyponatremia
hyponatremia with cerebral disorders
hypoosmolality of serum
hypophonia
hypopituitarism
hyporeflexia
hypotelorism
hypotension, systemic
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immunohistochemistry
immunomodulation
immunosuppressive agents
inability to sit up
inappropriate antidiuretic(A.D.H.)hormone
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
infant, evaluation of
infection
intellectual deterioration
internet
intestinal pseudoobstruction
intracerebral hemorrhage
intrauterine
intrinsic hand muscles, wasting of
iododeoxyuridine
ipecac
jaundice
jaw jerk, abnormal
Jewish
Kernig's sign
ketogenic diet
kyphosis
lactic dehydrogenase(LDH)
lacunar infarction
lacunar infarction, progressive
laughing
laughing, pathologic
lead poisoning
learning disability
learning disability, in children
leg numbness
leg weakness, bilateral
leg weakness, unilateral
Leigh's disease
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
Lhermitte's sign
lid closure, weakness of
life expectancy
limbic encephalitis
liver function enzymes
low back pain
lung transplantation
lymph node biopsy
lymphadenopathy
lymphadenopathy, hilar
lymphadenopathy, paraaortic
lymphoma
lymphoma involving CNS
macroglobulinemia
malabsorption
malaise
malformation, vascular
malignant hyperpyrexia
malignant papulosis
Man-In-The-Barrel syndrome
masseter muscle wasting
mediastinum, mass of
medulla oblongata, lesion of
Melkersson's syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis, basilar
meningoencephalitis
mental status, abnormal
methylmalonic acid, serum
methylmalonic acidemia
microcephaly
Middle east
Mills syndrome
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mononeuritis multiplex, causes of
mononeuropathy
mortality
Morvan's fibrillary chorea
motor neuron disease
motor symptoms
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, brachial plexus
MRI, contrast enhanced
MRI, diffusion weighted
MRI, fetal
MRI, muscle
MRI, peripheral nerve
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRS
multiple sclerosis
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle strength, testing
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, causes of
muscle weakness, insidious onset of
muscle weakness, intermediate onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, treatment of
myasthenic syndrome
mycobacterial infection
mycobacterium bovis
mycotic aneurysm
myelitis, longitudinal
myelogram, cervical
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myeloradiculopathy
myoclonus
myoglobinuria
myokymia
myoneuropathy
myopathy
myopathy, amyloid
myopathy, autoimmune
myopathy, critically ill
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, genetic
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
myopathy, inclusion body, hereditary
myopathy, inflammatory
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, necrotizing
myopathy, necrotizing, autoimmune
myopathy, necrotizing, immune-mediated
myopathy, steroid induced
myopathy, toxic
myopathy, vacuolar
myositis
myositis, ocular
myotonic discharges
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, intracranial
neoplasm, intracranial assoc.with systemic hypertension
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve conduction studies, sensory
nerve root biopsy
nerve root enhancement
nerve root hypertrophy
neuroendocrinology
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyotonia
neuronal intranuclear inclusion disease
neuronopathy
neuropathology
neuropathy
neuropathy, acute
neuropathy, asymptomatic
neuropathy, hereditary peripheral
neuropathy, iatrogenic
neuropathy, medication induced
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, peripheral
neuropathy, sensory
neuropathy, toxic
neurotoxic
newborn, evaluation of
next-generation sequencing
nitrous oxide
numbness, ascending
numbness, extremity
numbness, generalized
nusinersen
nutritional deficiency
nystagmus
ocular motility, disorders of
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
optic neuritis
oral contraceptives
orthopnea
overlap syndrome
pacemaker, cardiac-transvenous
Paget's disease
pain
pain, abdominal
pain, foot
pain, leg
pain, severe
pain, total body
pancytopenia
papovavirus
paralysis, acute
paralysis, asymmetric
paraparesis
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
paresthesias
paresthesias, feet
paresthesias, generalized
paresthesias, hands
Parkinson disease
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathology
pedicles of vertebrae, erosion of
periarteritis nodosa
perineurioma
peripheral blood smear
pernicious anemia
personality change
pes cavus
pheochromocytoma
phosphorylase b kinase deficiency
plasmapheresis
PLEDs
PLEDs, bilateral independent
pleocytosis of cerebrospinal fluid
pleural effusion
POLG1 gene
polyglucosan body
polyglucosan body disease
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, childhood
polyneuropathy, subacute idiopathic demyelinating
pons, infarction of
porphyria
positive sharp waves
posterior column disease
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive spinal muscular atrophy
proprioception, abnormal
proteinuria
protozoan infection
proximal muscle atrophy
pruritus
pseudobulbar palsy
pseudomyotonia
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
psychotic behavior
ptosis
ptosis, bilateral
puerperium
pulmonary embolism
pulmonary infiltrates
pulmonary nodules
pupil, abnormality in neurologic disorders
pupil, dilated, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriparesis, acute
quadriparesis, progressive
quadriplegia
quadriplegia, transient
quality of life
rabies, nervous system involvement with
radiation therapy, CNS treatment and complications with
radiculopathy
ragged-red fibers
rapidly progressing neurologic illness
rash
recurrent
regional enteritis
release phenomena
remote effect of cancer on the nervous system
renal failure
renal tubular acidosis
repetitive nerve stimulation
respirator
respiratory failure
respiratory tract infection
retina, abnormal
retinal hemorrhages
retinal lesion
retinopathy
retroperitoneal mass
reversible neurologic disorder
review article
rhabdomyolysis
riboflavin
riboflavin transporter deficiency
rituximab
Romberg's sign
safety
sarcoglycan
sarcoidosis
sarcoidosis, CNS
schizophrenia
sclerosis, bone
scoliosis
scoliosis, neurologic association with
screening
season
sedimentation rate
sedimentation rate, elevated
seizure
seizure, focal
seizure, intractable
seizure, repetitive
seizure, surgical treatment of
seizure, treatment of
sensorineural hearing loss
sensory loss
sensory loss, band distribution
sensory loss, patchy
serum alanine aminotransferase
sex reassignment surgery
Sheehan's syndrome
shoulder, pain in
simvastatin
skin, biopsy
skin, lesions in neurologic disorders
sloped shoulders
slow virus infection of CNS
small vessel disease
small vessel vasculitis
small-bowel resection
SMN1 gene
solitary scerlosis
somnolence
spasticity
speech disorder, childhood
speech, delayed development of
spinal cord, cervical
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary
spinal cord, neoplasm, intramedullary
spinal cord, vascular malformation of
spinal muscular atrophy
spinal muscular atrophy, classification
splenomegaly
standing difficulty
statin therapy
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stooped posture
stroke, progression of
subarachnoid hemorrhage
sudden death
suspended sensory loss
syringomyelia
systemic illness
systemic lupus erythematosus
temporalis muscle wasting
term infant
thrush
thymoma
thymus and neuromuscular function
tick bite
tick-borne encephalitis
tinnitus
titinopathy
toe walking
tongue, atrophy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
tonsillar herniation of cerebellum
torticollis
transgender
transient ischemic attack
transverse smile
treatment of neurologic disorder
treatment, empirical
tremor
tremor, postural
tripping
tuberculosis
ulcerative colitis
unconsciousness
upgaze, paralysis of
urinary incontinence
urine osmolality, elevated
urine, dark
vasculitides
vasculopathy
vasopressin
vectors of infection
vertigo
vibratory sensation, abnormal
vincristine neurotoxicity
viral infection
viral infection, CNS
viral myopathy
vision, blurred
visual loss
vital capacity
vitamin D
vitamin deficiency
Waldenstrom's macroglobulinemia
walking frame
walking, difficulty with
Watson-Schwartz reaction
weakness
weakness, acute
weakness, congenital
weakness, episodic
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
workup
wrist drop
xerostomia
X-linked myopathy
x-linked myopathy with excessive autophagy
zinc
Showing articles 200 to 250 of 3889 << Previous Next >>

A 35-Year-Old Bricklayer with Hemimyoclonic Jerks
Lancet 351:1926, Grunewald,T.,et al, 1998

Poliomyelitis-Like Illness Due to Japanese Encephalitis Virus
lancet 351:1094-1097, Solomon,T.,et al, 1998

An Infant with Encephalitis
Lancet 350:1594, Yeung,W.L.,et al, 1997

Clinicopath Conf
Placental Vascular Thrombosis Due to Listeria Infection, Cerebral Embolism and Infarction, Case 15-1, 97EJM 336:1439-1446,1997., 1997

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

Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
Mov Dis 12:342-353, Singer,C.,et al, 1997

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Diagnosing the Severe Headache
Neurol 44:S6-S12, Dalessio,D.J., 1994

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
Muscle & Nerve 17:946-948994., Ionasescu,V.,et al, 1994

Prevalence of Headache and Migraine in Schoolchildren
BMJ 309:765-769, Abu-Arefeh,I.&Russell,G., 1994

Myositis-Specific Autoantibodies, Touchstones for Understanding the Inflammatory Myopathies
JAMA 270:1846-1849, Miller,F.W., 1993

Evaluation Times for Patients with In-Hospital Strokes
Stroke 24:1817-1822, Alberts,M.J.,et al, 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
Neurol 43:937-941, Stacy,M.,et al, 1993

Acute Paralytic Syndrome in Three American Men:Comparison with Chinese Cases
Arch Neurol 50:732-735, Jackson,C.E.,et al, 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Clin & Lab Obser Neurologic Sequelae in Transient Nonketotic Hyperglycinemia of the Neonate
J Pediatr 121:620-621, Eyskens,F.J.M.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

'De Novo'Absence Status of Late Onset:Report of 11 Cases
Neurol 42:104-110, Thomas,P.,et al, 1992

Neonatal Idiopathic Cerebral Venous Thrombosis:An Unrecognized Cause of Transient Seizures or Lethargy
Ann Neurol 32:51-56, Rivkin,M.J.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

Clinical and Electrophysiological Aspects of Acute Paralytic Disease of Children and Young Adults in Northern China
Lancet 338:593-597, McKhann,G.M.,et al, 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Neonatal Seizures:Current Concepts and Revised Classification
Pediatrics 84:422-428, Volpe,J.J., 1989

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Acute Paralysis from Inhaled Barium Carbonate
Arch Neurol 45:579-580, Shankle,R.&Keane,J.R., 1988

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Nemaline Myopathy Appearing in Adults as Cardio-myopathy
Arch Neurol 41:443-445, Meier,C.,et al, 1984

Nemaline Myopathy Presenting as Cardiomyopathy
NEJM 308:1536-1537, Meier,C.,et al, 1983

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Acute Hypokalemic Myopathy in Alcoholism
Arch Neurol 34:553, Rubenstein,A.E.,et al, 1977

A Pseudohemiparetic Form of Parkinson's Disease
Lancet 442, 1976, August., Gilbert,G.J., 1976



Showing articles 200 to 250 of 3889 << Previous Next >>