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Differential
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abulia
acanthosis nigricans
acquired immunodeficiency syndrome
acrochordon
acromegaly
acute intermittant porphyria
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
adrenal crisis, acute
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
affect, inappropriate
agitation
Albright disease
alcohol
alcohol, neurologic complications with
alcoholism
alopecia
amenorrhea
aminoacidurias
anasarca
anemia
anemia, megaloblastic
anesthesia, general
ankle, swelling of
anorexia
anorexia nervosa
anterior horn cell disease
antibiotics
anticholinergic drugs
anticholinergic drugs, side effects of
arachnodactyly
areflexia
arrhythmia, cardiac
arteritides
arteritis, temporal
arthralgia
arthritis
ascites
aspartate aminotransferase
aspergillosis
asterixis
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxic gait
autoantibodies
autoimmune disease
autonomic dysfunction
azidodeoxythymidine
B 12 deficiency
B 12 deficiency, infants
Babinski sign
bacterial infection
bacterial infection, CNS
Bannayan-Riley-Ruvalcaba syndrome
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
bladder dysfunction
blindness
bone age
bone marrow biopsy
bone marrow transplantation
bone pain
bone survey
bone survey, metastatic
brain atrophy
brain biopsy
brain natriuretic peptide
brain scan, abnormal
breast feeding
bulbar palsy
bulimia
bulimia nervosa
burning hands
burning paresthesia
cachexia
calcification, intracranial
calf hypertrophy
carbamazepine
carbon monoxide poisoning
cardiomyopathy
cardiovascular disease
carnitine deficiency
carnitine deficiency myopathy
carotid artery disease
carotid artery stenosis
carpal tunnel syndrome
Castleman's disease
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, disappearing lesion on
CAT scan, muscle
CAT scan, pelvis
cataracts
catatonia
catatonia, lethal
cathartic
cecum perforation
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cephalosporins
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, secondary
cerebellar degeneration
cerebellum, disease of
cerebral cortical atrophy
cerebral edema
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, red cells in
cerebrovascular accident
cervical spondylosis
chemotherapy, CNS treatment and complications with
children
chorionic gonadotropin
chromosome 19
cirrhosis
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clofibrate
clubbing of fingers
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
cognition
cogwheel rigidty
colchicine
collagenous sprue
coma
compartment syndrome
compartment syndrome, gluteal
complications
compression fracture
compression neuropathy
confusion
confusional state, acute
congenital malformation
congenital myopathy
conjunctivitis
contractures, joint
contraindications
cortical blindness
cortisol, low
cough
craniopharyngioma
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
cyst
cyst, parenchymal
dantrolene sodium
dark adaptation
D-dimer
deafness
decerebrate posture
delay in diagnosis
delirium
dementia
dementia, childhood
demyelinating disease
depression
dermal sinus tract
dermatitis
dermatitis herpetiformis
dermatomyositis
dermoid
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diarrhea
diastematomyelia
diet
differential diagnosis
difficulty climbing stairs
dimple
diplopia
dizziness
down-beat nystagmus
drug abuse
drug abuse, neonatal abstinence syndrome with
drug abuse, neurologic complications of
drug addiction
drug induced neurologic disorders
drug induced neurologic disorders in children
drug interactions
drug withdrawal
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dysphasia
dyspraxia
dysproteinemia
dysraphism, spinal
dystonia
dystonia musculorum deformens
dystrophin
eating disorder
ecchymoses
ECHO virus
ectopic pinealoma
edema, leg
edema, pedal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electrophoretic pattern, serum
emergencies, neurologic
emotional lability
encephalomyopathy
encephalopathy
encephalopathy, metabolic
endarterectomy, carotid
endocarditis, infectious
endophthlamitis
enterovirus
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
eosinophilia-myalgia syndrome
eosinophilic fasciitis
epidemiology of neurology
epidermal nevus syndrome
epsilon-aminocaproic acid(E.A.C.A.)
etonogestrel
exercise
exercise intolerance
eye movement, disorders of
eye, pain in
face, numbness of
facial anomalies
facial appearance, abnormal
facial nerve
facial nerve palsy
facial pain
facial pain, atypical
facial weakness
falling
familial
fatigue
fatty acid, elevated plasma content
fever
fibrillations
fibrous dysplasia
fibrous dysplasia of orbit
fine motor function, impaired
fingernails, abnormal
fingernails, white
fingers, abnormal
folic acid deficiency
follicle stimulating hormone
foot numbness
fungal infection
gait disorder
gait, waddling
gasoline sniffing
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
glossitis
glossopharyngeal nerve
glossopharyngeal neuralgia
glucose tolerance test, abnormal
glycogen storage disease
Gowers maneuver
gram positive rod
grimacing
groove sign
growth retardation
gynecomastia
hair, darkening of
hand pain
hand weakness
head injury
headache
headache, positional
headache, severe
hearing loss
hemangioma
hematuria, microscopic
hemochromatosis
hemochromatosis, primary
hemorrhagic diathesis
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes simplex virus
herpes simplex virus, human nervous system and
herpes simplex, neurocutaneous lesions in
hirsutism
histochemistry of muscle
HMGcoA reductase inhibitors
homocystinuria
hormone replacement
hormone therapy
human immunodeficiency virus type 1
hung reflex
hydrocephalus
hypercapnia
hyperglycemia
hyperhidrosis
hyperhomocysteinemia
hyperkalemia
hypernatremia
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypersomnia
hyperthermia
hypertrichosis
hypoalbuminemia
hypocalcemia
hypoglycemia
hypoglycemic coma
hypogonadism
hypokalemia
hypomagnesemia
hyponatremia
hyponatremic encephalopathy
hypopigmentation of skin
hypoproteinemia
hypoprothrombinemia
hyporeflexia
hypotension, systemic
hypothalamus
hypothalamus, disturbance of
hypothalamus, neoplasm of
hypothermia
hypothermia, causes of
hypothyroidism
hypotonia, infants
iatrogenic neurologic disorders
immunoelectrophoresis, serum
immunosuppressive agents
implant contraceptives
impotence
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
inclusion body myositis
incontinentia pigmenti
infant, evaluation of
infantile tremor syndrome
infection
injection neuropathy
insulin resistance
intellectual deficit
intellectual deterioration
intestinal biopsy
intracranial hypertension, benign
intracranial pressure, increased
intravenous drug abuse
irritability
ischemic exercise test
jaundice
jaw pain
lactic acidemia
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
leg swelling
leg weakness, bilateral
leg weakness, unilateral
lethargy
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, toxic
level of consciousness, decreased
limb-girdle weakness
lipid lowering agent
lipoma of CNS
lipoma of skin
lipomatosis
lithium
liver disease
liver function enzymes
liver transplantation
Lorenzo's oil
L-tryptophan
luteinizing hormone
lymph node biopsy
lymphadenopathy
lymphoid hyperplasia
lymphoma involving CNS
macrocephaly
malabsorption
malabsorption syndrome
malformation, CNS, congenital
malignant hyperpyrexia
McArdle's disease
McArdle's disease, adult onset
McCune-Albright syndrome
memory, impairment of
mental retardation
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methylmalonic acid, serum
microcephaly
midbrain, lesion of
mimics
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mood change
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, muscle
MRI, negative
MRI, serial
MRI, spinal cord
MRI, spine
multiple myeloma
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myeloma, osteosclerotic
myelopathy
myoclonus
myocytolysis
myoedema
myoglobinuria
myopathy
myopathy, acute
myopathy, drug-induced
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, necrotizing, autoimmune
myopathy, proximal
myopathy, toxic
myositis
myotonia dystrophica
myxedema, neurologic manifestations of
nausea and vomiting
neck trauma
neoplasm, pituitary
nephrotic syndrome
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurofibromatosis 1
neuroleptic
neuroleptic malignant syndrome
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronopathy, sensory
neuropathy
neuropathy, acute
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neurotoxic
nicotinic acid
night blindness
nutritional deficiency
nystagmus
ochronosis
oculomasticatory myorhythmia
ophthalmoplegia
optic atrophy
orange peel appearance of skin
organomegaly
osteoarthrosis
osteopetrosis
osteoporosis
pain
pain, abdominal
pain, buttock
pain, leg
papilledema
paradichlorobenzene
paraparesis
paraparesis, spastic
paresthesias
paresthesias, hands
PAS positive
PAS positive material in the brain
pellagra
penis, pigmented macules
periarteritis nodosa
periodic paralysis
peripheral blood smear, abnormal
pernicious anemia
peroxisomal disease
perseveration
personality change
petechiae
phlebotomy
phosphorylase b kinase deficiency
photic stimulation
photophobia
photosensitivity, skin
pigmentary retinopathy
pigmented macules
pituitary, adenoma
plasma cell dyscrasia
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
POEMS syndrome
polycythemia, primary
polycythemia, secondary
polymerase chain reaction
polymyalgia rheumatica
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyps, gastrointestinal tract
porphyria
post herpetic neuralgia
posterior column disease
precipitating factors
precocious puberty
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
progeria
prognosis
progressive neurologic disorder
prolactin, elevated
proteinuria
proximal muscle atrophy
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
ptosis, unilateral
pupil, dilated, unilateral
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
rash
Raynaud's phenomenon
recurrent
red eye
refractory sprue
remote effect of cancer on the nervous system
renal failure
renal failure, acute
renal stones
respiratory failure
reticulum cell sarcoma
reversible neurologic disorder
review article
RFC1 gene
rhabdomyolysis
rigidity
risk factors
Romberg's sign
sarcoglycan
sarcoglycanopathy
scalp necrosis
sciatic neuropathy
sclerae, hyperpigmented
sclerosis, bone
screening
second wind phenomena
sedimentation rate, elevated
seizure
seizure, darkness induced
seizure, eye closure inducing
seizure, neonatal
seizure, neonatal abstenence syndrome
seizure, photosensitive
seizure, stimulus sensitive
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss, leg
serotonin syndrome
serum alanine aminotransferase
sex reassignment surgery
shock, hypovolemic
short stature
skin, biopsy
skin, darkening of
skin, discoloration
skin, lesions in neurologic disorders
skin, thickened
skull x-ray, abnormal
skull x-ray, bony defect on
sleep apnea
somnolence
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spina bifida
spinal cord, lesion of
splenomegaly
spondylolysis
sprue
statin therapy
status epilepticus
steatorrhea
stem cell transplantation
steroid therapy, CNS treatment and complications with
strychnine poisoning
stuporous
subarachnoid hemorrhage
subdural hematoma
substantia nigra
superior sagittal sinus thrombosis
systemic illness
tachycardia
tachypnea
tandem gait, ataxic
teratoma
testicular atrophy
testicular biopsy
tetanus
tetany
tethered spinal cord
third ventricle, mass of
thrombocytosis
toe walking
toilet seat neuropathy
tongue, black
tongue, discoloration
tongue, smooth
tongue, swelling
transgender
treatment of neurologic disorder
tremor
tremor, intention
trifluoperazine
trigeminal neuropathy
trigeminal neuropathy, sensory
trimethoprim-sulfamethoxazole
tripping
unconsciousness
undiagnosed
urinary incontinence
urine osmolality, elevated
urine test in toxic screen
urine, dark
urticaria
uveitis
vascular endothelial growth factor
vegetarianism
very long chain fatty acids
vestibular areflexia
viral infection
viral myopathy
Virchow-Robin spaces, dilated
vision, blurred
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual loss
visual loss, slow
vitamin B3, deficiency
vitamin deficiency
vitritis
vomiting, recurrent
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, acute
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight gain
weight loss
Whipple's disease
white hair
white matter disease
whites
wide based gait
winging of scapula
workup
x-ray, lumbar spine
Showing articles 50 to 98 of 98 << Previous

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

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

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

Missed Neuroleptic Malignant Syndrome
BMJ 304:831-832, Renwick,D.S.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Pituitary Adenoma in McCune-Albright Syndrome:MR Demonstration
J Comput Assist Tomogr 13:685-688, O'Laughlin,R.L.,et al, 1989

Brain Malformations in Linear Nevus Sebaceous Syndrome:An MR Study
J Comput Assist Tomogr 12:338-340, Sarwar,M.&Schafer,M.E., 1988

The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

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

Clinicopath Conf
Castleman's Disease, Synd of Polyneuropathy, Organomegally, Endocrinopathy, Monoclonal Gammopathy, &, Skin CPOEM Synd),NEJM 316:606-618,1987., 1987

Peripheral Neuropathy Associated with Dysproteinaemia, Skin Changes, & Endocrinopathy
BMJ 292:1415-1416, Burton,J.L., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Acute Ventilatory Failure & Myoglobinuria
Neurol 34:369-371, Taverner,D.,et al, 1984

Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Idiopathic Recurrent Myoglobinuria & Persistent Weakness
Neurol 33:1613-1615, Bermils,C.,et al, 1983

Osteosclerotic Myeloma & Peripheral Neuropathy
Neurol 33:202-210, Kelly,J.J.,et al, 1983

Acute Myopathy Associated with Gasoline Sniffing
Neurol 33:629-631, Kovanen,J.,et al, 1983

Severe Dystonia & Myoglobinuria
Neurol 32:1195-1197, Jankovic,J.,et al, 1982

Rhabdomyolysis During Treatment With Epsilon-Aminocaproic Acid
Arch Neurol 37:187-188, Britt,C.W.,et al, 1980

Plasma Cell Dyscrasia with Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, & Skin Changes:The POEMS Syndrome
Medicine 59:311-322, Bardwick,P.A., 1980

Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Arch Neurol 37:457-458, Jehn,U.W.,et al, 1980

Acute Rhabdomyolysis Associated With An Echovirus 9 Infection
Arch Int Med 140:1671-1672, Josselson,J.,et al, 1980

Conversion of Photosensitive to Scotosensitive Epilepsy:Report of a Case
Neurol 29:1550-1554, Panayiotopoulos,C.P., 1979

Clinical Pathological Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 18-1979, NEJM 300:1037-104579., , 1979

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Myoglobinuria & Renal Failure after Status Epilepticus
Neurol 28:200, Singhal,P.C.,et al, 1978

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Polyneuropathy, Skin Hyperpigmentation, Edema, & Hypertrichosis in Localized Osteosclerotic Myeloma
Neurol 27:675, Iwashita,H.,et al, 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Bilateral Scalp Necrosis in Temporal Arteritis
Am J Med 61:541, Soderstrom,C.W.,et al, 1976

Herpes Simplex Neuropathy
Neurol 26:596, 1976, Krohel,G.B.,et al, 1976

Germinoma of third Ventricle (Case Record of MGH)
NEJM 293:653, Locke,S.,et al, 1975

Narcotic Abuse:Neurologic Complications in Pedi & Adolescent Pts
JAMA 66:426, French,J.H.,et al, 1974

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Whipple's Disease:A Review of 19 Pnts from one Hospital & a Review of the Literature since 1950
Medicine 49:175, Maizel,H.,et al, 1970

Fibrous Dysplasia, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 165., Bray,P.F., 1970

Addison's Disease, In The Diagnosis of Stupor & Coma
& Posner, J. , FA Davis Co. 1966, p. 145-146., Plum,F., 1966



Showing articles 50 to 98 of 98 << Previous