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Differential
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agitation
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, inflammatory type
anemia
angina pectoris
angiography, neurologic complications with
angioneurotic edema
ankle edema
anticholinergic drugs
anticholinergic drugs, side effects of
anticoagulant, complications of
aphasia
aphasia, global
areflexia
arrhythmia, cardiac
arsenic
arthralgia
ascending paralysis
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
atherosclerosis, generalized
autism
autonomic dysfunction
bacterial infection
bacterial infection, CNS
BAL
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basophilic stippling of red blood cells
behavioral disorder
bone marrow suppression
brain biopsy
BUN, elevated
Canavan's disease
cancer, cerebrovascular accident complicating patients with
carcinoma
carcinoma of lung
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
catatonia
catatonia, lethal
central nervous system, infection of
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glycine
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, multiple
cherry red spot
chest pain
chest x-ray, abnormal
children
chromosomal abnormality
chromosome 6
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cocaine
coma
confusion
conjunctivitis
coronary artery bypass
cortical blindness
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
dementia
dementia, rapidly progressive
demyelinating disease
dermatitis
developmental milestones, loss of
developmental retardation
diarrhea
diet
disseminated intravascular coagulation(DIC)
distal muscle weakness
drug abuse
drug abuse, neurologic complications of
drug abuse, toxic screen In
drug induced neurologic disorders
drug withdrawal
dystonia
ecchymoses
edema, pedal
electrocardiogram, abnormal
electromyogram
embolism
embolism, atheromatous
embolism, cholesterol
embolism, retinal
emergencies, neurologic
encephalopathy
encephalopathy, acute
encephalopathy, neonatal
endocarditis
endocarditis, marantic
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
erythrocyte
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
failure to thrive
familial
fatigue
feeding disorder
femoral artery catheterization
fever
fibrin split products
filariasis
fingernails, abnormal
gait disorder
gangliosidosis GM1
gangliosidosis GM2
gangrene
gastroenteritis
gastrointestinal bleeding
gene
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
glycogen storage disease
gram negative rod
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hallucination
hand weakness
head lag
headache
headache, severe
heart murmur
heavy metal intoxication
helminthic infection of CNS
hematuria, gross
hematuria, microscopic
hemiplegia
hemoglobinuria
hepatitis
hepatosplenomegaly
hyperammonemic encephalopathy
hyperamylasemia
hyperbilirubinemia
hyperglycinemia
hyperkeratosis
hypertension
hyperthermia
hyponatremia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
inborn errors of metabolism
infection
intraaortic balloon pump
ischemic exercise test
lactic dehydrogenase(LDH)
Legionella pneumophilia
Legionnaires'disease
Leigh's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, toxic
leukopenia
levamisole
lipid storage disorder of CNS
livedo reticularis
liver disease
liver function enzymes
Loa loa
loiasis
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
McArdle's disease
Mees lines
meningitis, aseptic
mental retardation
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
microangiopathic hemolytic anemia
misdiagnosis
mitochondrial disease
mitral valve vegetation
molecular genetics
mortality
MRI
MRI, abnormal
MRI, demyelinating disease
MRI, diffusion weighted
MRI, false negative
multinucleated giant cell
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle weakness
myoclonic jerks
myoglobinuria
myopathy
nausea and vomiting
nerve conduction studies
neuritis, heavy metals causing
neuroleptic
neuroleptic malignant syndrome
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuropathy
neuropathy, peripheral
neuropathy, toxic
neurotransmitter
opisthotonus
optic atrophy
ornithine transcarbamylase deficiency
pain
pain, back
pain, flank
pancreatitis
pancytopenia
paraphasias
parasitic infection, CNS
paresthesias
paresthesias, feet
paresthesias, hands
PAS positive
pathology
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
personality change
petechiae
phenylketonuria
phosphorylase b kinase deficiency
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
polyneuropathy
position sensation, abnormal
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proprioception, abnormal
proteinuria
pruritus
psychomotor retardation
pulmonary infiltrates
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
renal failure
renal infarct
respiratory failure
review article
rhabdomyolysis
rigidity
risk factors
Sandhoff's disease
screaming
second wind phenomena
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
self-mutilation
semialdehyde dehydrogenase deficiency
serologic testing
serotonin syndrome
skin, biopsy
skin, lesions in neurologic disorders
spinal cord, infarction of
splenic infarcts
splinter hemorrhages
spongy degeneration of brain
stuporous
sweating
sweating, abnormality of
thrombocytopenia
treatment of neurologic disorder
tropical disease
urea-cycle enzymopathies
uremia
urinalysis, abnormal
urinary casts
urine test for metabolic disorders
urine test in toxic screen
urine, dark
urine, white blood cells in
vasculitides
weakness
weight loss
white matter disease
Showing articles 300 to 350 of 3467 << Previous Next >>

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Cerebral Venous Thrombosis-A Review of 38 Cases
Stroke 16:199-213, Bousser,M.,et al, 1985

Subcortical Arteriosclerotic Encephalopathy, (Binswanger's Disease)
Arch Neurol 42:951-959, Kinkel,W.R.,et al, 1985

Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
Arch Neurol 41:1293-1296, Dave,P.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984

CT Abnormalities & Altered Methotrexate Clearance in Children with CNS Leukemia
Neurol 34:229-233, Duffner,P.K.,et al, 1984

Detection of Urea Cycle Enzymopathies in Childhood
Arch Neurol 41:758-760, Trauner,D.A.,et al, 1984

Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983

Sphenoid Sinusitis
NEJM 309:1149-1154, Lew,D.,et al, 1983

Brain Biopsy in the Diagnosis of Cerebral Mycosis Fungoides
JNNP 45:175-178, Tremblay,G.F.,et al, 1982

Carbamazepine & Hematological Monitoring
Ann Neurol 11:309-312, Hart,R.G.,et al, 1982

Subcortical Arteriosclerotic Encephalopathy:A Clinical & Radiological Investigation
JNNP 44:294-304, Loizou,L.A.,et al, 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Leukoencephalopathy & Elevated Levels Of Myelin Basic Protein In The CSF Of Patients With Acute Lymphoblastic Leukemia
NEJM 303:19-21, Gangji,D.,et al, 1980

Phencyclidine:The New American Street Drug
Editorial, BMJ 281:1511-15121980., , 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Long-term Neurological Implications of Somnolence Syndrome in Children with Acute Lymphocyte Leukemia
Ann Neurol 8:273-277, Ch'ien,L.T.,et al, 1980

Status Epilepticus
Am J Med 69:657-665, Aminoff,M.J.,et al, 1980

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Phenytoin Hypersensitivity:38 Cases
Neurol 29:1480-1485, Harunda,F., 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

Subcortical Arteriosclerotic Encephalopathy (Binswanger) :Computerized Tomography
Neurol 29:1102-1106, Rosenberg,G.A.,et al, 1979

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979

Clinical Features of Subcortical Arteriosclerotic Encephalopathy (Binswanger Disease)
Neurol 28:1206-1215, Caplan,L.R.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Subarachnoid Hemorrhage Complicating Acute Poststreptococcal Glomerulonephritis
Arch Neurol 35:473, DeBeukelaer,M.M.,et al, 1978

Neurologic Manifestations of Cogan Syndrome
Neurol 28:278, Bicknell,J.M.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Neuropathology of Sanfilippo Syndrome
Ann Neurol 2:161, Ghatak,N.R.,et al, 1977

Spinal Cord Compression Due to Pseudomonas in a Heroin Addict
Neurol 27:1034, Jabbari,B.,et al, 1977

Purine Phosphoribosyltransferase in Gilles de la Tourette Syndrome
NEJM 296:210, VanWoert,M.H.,et al, 1977

Eosinophilic Polymyositis
Ann Neurol 1:65, Layzer,R.B.,et al, 1977

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Abnormality of a Thiamine-Requiring Enzyme in Patients with Wernicke-Korsakoff Syndrome
NEJM 297:1367, Blass,J.P.,et al, 1977

Leukoencephalopathy in Childhood Leukemia
et al. , Neurol 27:609977., Devivo,D.C., 1977

Cardiac Myxoma:A Diagnostic Challenge for the Neurologist
Neurol 26:1060, Yufe,R.,et al, 1976

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

Case Records of the MGH
Giant cell Angiitis, intracranial NEJM 295:9441976., , 1976



Showing articles 300 to 350 of 3467 << Previous Next >>