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Differential
(Click to cross reference)
anticonvulsants, discontinuation in seizure-free epileptics
apraxia
asymptomatic
ataxia
behavioral disorder
bone pain
calcification, intracranial
CAT scan
CAT scan, abnormal
CAT scan, false negative
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
chromosome 8
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
color vision, impaired
coma
degenerative diseases of CNS
dementia
dementia, presenile
dementia, rapidly progressive
depression
diplopia
electroencephalogram
electroencephalogram, abnormalities of
encephalopathy
encephalopathy, progressive
familial
familial adult myoclonic epilepsy
Gaucher's disease
Gaucher's disease, adult onset
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hallucination
hallucination, visual
headache
hearing loss
hepatosplenomegaly
inclusion bodies
inclusion bodies, intracytopasmic
intellectual deficit
intellectual deterioration
juvenile myoclonus epilepsy
lactic acidemia
Lafora body
Lafora's disease
Leigh's disease
Leigh's disease, adult variety
lethargy
MELAS syndrome
mental retardation
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
MRI, abnormal
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myoclonic jerks
myoclonus
myoclonus, epilepsy
negative
neuroendocrinology
neurologic disease, diagnoses of
neuroophthalmology
neuropathology
neuropathology, brain
neuropsychiatry
normal
ophthalmoplegia
optic atrophy
optic atrophy, hereditary
paraparesis, spastic
PAS positive
PAS positive material in the brain
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
ragged-red fibers
review article
seizure
seizure, children
seizure, diagnosis of
seizure, familial
seizure, intractable
seizure, prognosis in adults
seizure, teenager
seizure, treatment of
short stature
skin, biopsy
sodium valproate
sphingolipodoses
strokelike episodes
treatment of neurologic disorder
upgaze, paralysis of
weakness
Showing articles 600 to 650 of 5884 << Previous Next >>

Early Prognosis of Epilepsy
BMJ 285:1699-1701, Shorvon,S.D.,et al, 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Prognosis In Childhood Epilepsy
NEJM 306:831-836, Thurston,J.H.,et al, 1982

Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
Ann Neurol 11:372-376, Murphy,M.J.,et al, 1982

Valproate & Clonazepam in the Treatment of Severe Progressive Myoclonus Epilepsy
Arch Neurol 39:236-238, Iivanainen,M.,et al, 1982

Seizure Recurrence After A First Unprovoked Seizure
NEJM 307:522-528, Hauser,W.A.,et al, 1982

Epileptic Patients Who are Refractory to Anticonvulsant Medications
Neurol 32:1382-1384, Rodin,E.,et al, 1982

Prognosis of Isolated Seizures in Adult Life
BMJ 283:1364-1365, Cleland,P.G.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Spinal Seizures Following Intravenous Contrast in a Patient with a Cord AVM
Ann Neurol 10:580-581, Uhl,G.R.,et al, 1981

Cephaloridine Encephalopathy
BMJ 283:409-410, Taylor,R.,et al, 1981

Myoclonic Seizures Following Chlorambucil Overdose
Jr. , Ann Neurol 9:191-194981., Byrne,T.N., 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

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

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Familial Stroke Syndrome Associated with Mitral Valve Prolapse
Ann Neurol 7:130-134, Rice,G.P.A.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Acquired Aphasia with Convulsive Disorder:Course & Prognosis
Neurol 30:524-529, Mantovani,J.F.,et al, 1980

Neonatal Polycythemia Causing Multiple Cerebral Infarcts
Arch Neurol 37:109-110, Amit,M.,et al, 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Benign Familial Neonatal Seizures
E. , Arch Neurol 37:47-48980., Pettit,R., 1980

Neurologic Prognosis after Cardiopulmonary Arrest:III. Seizure Activity
Neurol 30:1292-1297, Snyder,B.D.,et al, 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Reye's Syndrome in the Adult Patient
Am J Med 67:672-678, Atkins,J.N.,et al, 1979

Intracranial Hemorrhage in the Newborn:Current Understanding & Dilemmas
Neurol 29:632-635, Volpe,J.J., 1979

Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Microangiopathy of the Brain & Retina
Neurol 29:313-316, Susac,J.O.,et al, 1979

Cerebral Infarcts with Arterial Occlusion in Neonates
Ann Neurol 6:495-502, Barmada,M.A.,et al, 1979

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

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Clinical Pathological Conference, Reticulum Cell Sarcoma of Brain
NEJM 299:1349-1359, Case Record 49-1978,Mass.Gen.Hosp., 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Imipramine in Absence & Myoclonic-astatic Seizures
Neurol 28:953-957, Fromm,G.H.,et al, 1978

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

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

Familial Cavernous Angiomas
Arch Neurol 35:746-749, Bicknell,J.M.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Increased Prevalence of Epilepsy in Coeliac Disease
BMJ 2:250, Chapman,R.W.G.,et al, 1978

Drug Therapy, Clonazepam
NEJM 299:812-816, Brown,T.R., 1978

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

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

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978



Showing articles 600 to 650 of 5884 << Previous Next >>