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Differential
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abdominal distention

acyl CoA dehydrogenase deficiency

addiction, heroin

adverse drug reaction

alcohol intoxication

alcoholic withdrawal states, DT's, convulsions, etc.

alkalosis, respiratory

aminoacidopathies

anesthesia, general

anorexia nervosa

antibiotics, neurologic complications with

arrhythmia, cardiac

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bath salts, psychoactive

behavior, combative

behavioral disorder

behavioral disorder, acute

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

black toenail sign

blindness, sudden

buried bumper syndrome

calcification, intracranial

carbonic anhydrase II deficiency

carnitine deficiency

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, false negative

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral ischemia

cerebral palsy, risk factors

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

coma, sudden onset

compartment syndrome

compartment syndrome, abdominal

compression fracture

conjunctival biopsy

cornea, abnormal

cortical blindness

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes dialysis basal ganglia syndrome

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic ketoacidosis

diagnostic criteria

differential diagnosis

disability, neurological

disseminated intravascular coagulation(DIC)

D-lactate acidosis

downward deviation of eyes

drug abuse, toxic screen In

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

encephalitis, viral

encephalomalacia

encephalomyopathy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, marantic

episodic neurologic deficits

ethylene glycol

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

eye movement, disorders of

facial asymmetry

facial weakness

failure to thrive

feeding disorder

fingerprint bodies

fracture, pathologic

gastrointestinal bleeding

gastrostomy, percutaneous endoscopic

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

growth retardation

gyrus, abnormal

hallucination, auditory

headache, severe

hemianopia, transient

hemiparesis, transient

hemorrhagic diathesis

hemorrhagic shock encephalopathy syndrome

hepatic failure

heralding manifestation

herniated disc, differential diagnosis of

herpes simplex encephalitis

histochemistry of muscle

hyperammonemic encephalopathy

hypercoagulable state

hypoxia, newborn

iatrogenic neurologic disorders

ileus, paralytic

immunofluorescence

inborn errors of metabolism

inclusion bodies

intellectual deficit

intellectual deterioration

internal capsule

intracranial pressure, increased

intravenous drug abuse

isopropyl alcohol

Kearns-Sayre syndrome

keratoconjunctivitis

lactic acidemia

laminar necrosis, cortical

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lentiform fork sign

level of consciousness, decreased

level of consciousness, decreased acute

lipid storage myopathy

liver function enzymes

Lowe's syndrome

lysosomal storage disease

malignant hyperpyrexia

maple syrup urine disease

marche a petits pas

memory, impairment of

meningeal enhancement

meningitis, aseptic

mental retardation

mental status, abnormal

mental status, abnormal, acute

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylmalonic acidemia

methylmalonic aciduria

microangiopathic hemolytic anemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI lesion location

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral enhancement

MRI, gyral swelling

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple organ failure

multiple sclerosis, differential diagnosis of

muscle relaxant

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myoclonus, epilepsy

myopathy, mitochondrial

myopathy, proximal

myotonia congenita

myotonia, treatment of

nausea and vomiting

neonatal epileptic encephalopathy

nephrotic syndrome

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular blockade

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neurotoxicity, acute

next-generation sequencing

nutritional deficiency

nystagmus, rotary

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

ophthalmoplegia

ophthalmoplegia, progressive external

optic foramina, abnormal

ornithine transcarbamylase deficiency

pain, abdominal

paramyotonia congenita

Parkinsonism syndrome

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

peroxisomal disease

personality change

pleocytosis of cerebrospinal fluid

polymerase chain reaction

pons, lesion of

posterior cerebral artery territory infarction

precipitating factors

prevention of neurologic disorders

progressive neurologic disorder

propionic aciduria

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary edema

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

rabies prophylaxis

rabies, nervous system involvement with

ragged-red fibers

rapidly progressing neurologic illness

renal failure, acute

renal tubular acidosis

respiratory tract infection

retina, abnormal

retinitis pigmentosa

reversible neurologic disorder

salicylate intoxication

seizure, children

seizure, drug-induced

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, treatment of

sensorineural hearing loss

shock, hypovolemic

skin, lesions in neurologic disorders

skull x-ray, abnormal

small-bowel bypass

speech, loss of

spinal cord, infarction of

spontaneous remission

status epilepticus

stimulant drugs

stool, guaiac positive

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

symmetric brain lesions

sympathomimetic drugs

systemic illness

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

thrombocytopenia

thrombotic microangiopathy

toxic encephalopathy

toxins, nervous system

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

Trousseau's syndrome

uncal herniation

upgaze, paralysis of

urea-cycle enzymopathies

uremic encephalopathy

urinalysis, abnormal

urine test for metabolic disorders

urine test in toxic screen

violent behavior

viral infection

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual loss, progressive

visual loss, slow

vitamin deficiency

walking, difficulty with

weakness, fluctuating

weakness, generalized

weakness, proximal

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

whole genome sequencing

x-linked mental retardation

Showing articles 1000 to 1046 of 1046 << Previous

Specificity of the Urine Inhibitor Test for Leigh's Disease
Neurol 24:885, Pincus,J.H.,et al, 1974

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Diagnosis & Treatment of Metastases to the Brain
Clin Bull 4:47, Posner,J., 1974

Clinical Advances in the Evaluation of Deep Coma
MCV Quart 10:152, Suter,C., 1974

Unrecognized Adult Phenylketonuria
NEJM 289:395, 1973, 289:1040, 1973, 290:1084., Perry,T.,et al, 1974

Neuropathy Due to Cytosine Arabinoside
BMJ 2:652-653, Russell,J.A.,et al, 1974

Vincristine Neurotoxicity
Ann Int Med 80:733-737, Rosenthal,S.,et al, 1974

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Central Nervous System Infections in Patients with Cancer
Medicine 52:563, Chernik,N.L.,et al, 1973

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Case Records of MGH-NEJM 286:309
1972 Pseudomonas Meningitis with Cavernous Sinus, Carotid Artery & Sphenoid Sinus Involvement., , 1972

Neurotoxicity of Sulfones
Arch Derm 106:598, Hubler,W.R., 1972

Vincristine Neurotoxicity-Correspondence
NEJM 286:1369, 1972, 287:517972., , 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

Differential Diagnosis of Tremors
Med Clin North Am 56:1363, Fahn,S., 1972

Important Drug Warning-Methotrexate-Chemotherapy-Director
Lederle Laboratories 17 Nov 1971., Sweeney,Wm., 1971

Aphasia Current Conceps
NEJM 284:654, Geschwind,N., 1971

Neurological Complications of Systemic Cancer
Med Clin North Am 55:625, Posner,J., 1971

Organophosphate Poisoning
Am J Med 50:475-492, Namba,T., 1971

Infectious Complications of Neoplastic Disease
Med Clin North Am 55:729, Armstrong,D.,et al, 1971

New Kind of PKU
Pediatrics Consultant Sept 1971, pp 68-70., Johnson,C., 1971

Neurology of the Leukemias & Lymphomas-Editorial
BMJ 442, 1971 Nov., , 1971

Newer Concepts of Cerebral Vascular Disease
Med Clin North Am 54:1970., Meyer,J., 1970

Clinical Spectrum of Ocular Bobbing
JNNP 33:771, Susac,J.O.,et al, 1970

Facial Nerve Latency Studies in Man:Effects of Trichlorethylene Intoxication
Electromyog 93, Feldman,R., 1970

Diaschisis Resulting from Acute Unilateral Cerebral Infarction
Arch Neurol 23:241, Meyer,J.S.,et al, 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

Neurologic Disorders Seen In the Uremic Patient
Arch Int Med 126:781, Tyler,H.R., 1970

The Neuromyopathy of Vincristine in Man, Clinical, Electrophysiol & Pathological Studies
J Neurol Sci 10:107-131, Bradley,W.G.,et al, 1970

Current Trends in the Chemotherapy of Brain Tumors with Special Reference to Glioblastomas
J Neurosurg 31:589, Wilson,C.,et al, 1969

Hemispheric Blood Flow & Metabolism in Neurological Disease
Metabolic Accompaniments of Diaschisis, Trans of Am Neuro Assoc 94:303:1969., Meyer,J.S.,et al, 1969

Neurologic Disorders in Renal Failure
Am J Med 44:734, Tyler,H.R., 1968

Neurological Dysfunction Associated with Nonketonic Hyperglycemic
Arch Neurol 19:525, Maccario,M., 1968

Subacute Necrotizing Encephalopathy in Late Adolescence
Arch Neurol 18:478, Hardman,J.M.,et al, 1968

Ataxia In Childhood
Dev Med Child Neurol 10:388-389, Wilson,J., 1968

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Ocular Complications of Vincristine Therapy
Arch Ophthalmol 78:709, Albert,D.M.,et al, 1967

Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both
NEJM 274:384, Renuart,A., 1966

Inherited Aminoacidopathies Demonstrating Vitamin Dependency
NEJM 281:145, Rosenberg,L., 1965

Metabolic Defects Associated with Mental Retardation
Am J Dis Child 104:401, Garell,D., 1962

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Neurologic Manifestations of Chronic Carbon Monoxide Poisoning
NEJM 261:1217-1220, Gilbert,G.J.,et al, 1959

Carbon Monoxide Asphyxia, A Common Clinical Entity
Canad M A J 78:182-185, Katz,M., 1958

Minamata:A Living Death
Text by D. Johnson Maryknol Missions, , 1850

Showing articles 1000 to 1046 of 1046 << Previous