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Neurology Specific Literature Search

Differential
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accomodation, abnormal

acral sensory symptoms

alternating rapid movement

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anal wink response

antecedent illness

anti GQ1b IgG antibody

antiganglioside antibodies

arrhythmia, cardiac

ascending paralysis

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

axonal degeneration

Brown-Vialetto-Van Laere syndrome

bulbar palsy, acute

burning paresthesia

campylobacter infection

CAT scan, abnormal

caudate nucleus, atrophy

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellum, disease of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrospinal fluid, xanthochromia of

Charcot-Marie-Tooth

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

congestive heart failure

contractures, joint

corneal reflex, abnormal

corpus callosum, hypoplastic

corpus callosum, lesion of

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

denervation of muscle

denervation potentials

developmental disability

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

dopa responsive dystonia

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystonia, children

electromyogram, decremental response

encephalopathy, progressive

episodic neurologic deficits

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

failure to thrive

feeding disorder

Fisher's syndrome

flaccid paralysis

flu-like illness

Friedreich's ataxia

Friedreich's ataxia, late onset

F-wave response

gaze palsy, horizontal

genetic counselling

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

heel-knee-shin test

hypophosphatemia

immunoelectrophoresis, serum

intellectual deficit

leg weakness, bilateral

leg weakness, unilateral

lid abnormalities

lymphadenopathy

mental retardation

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

molecular genetics

motor neuron disease

movement disorder

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, spinal cord

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

nausea and vomiting

neoplasm, primary intracerebral

nerve conduction studies

nerve conduction studies, motor

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronopathy, sensory

neuroophthalmology

neuropathy, sensory

next-generation sequencing

numbness, ascending

numbness, extremity

nystagmus, gaze-evoked

nystagmus, vertical

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

overlap syndrome

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

parenteral alimentation

Parkinson disease

Parkinsonism syndrome

perioral numbness

philtrum, tented

positional head-hanging test

postoperative neurologic complications

prevention of neurologic disorders

progressive neurologic disorder

progressive spinal muscular atrophy

prolactin, elevated

proprioception, abnormal

ptosis, bilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

reading disorder, acquired

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

respiratory tract infection

reversible neurologic disorder

riboflavin transporter deficiency

saccadic eye movements, abnormal

sensory nerve action potentials

single photon emission computed tomography

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, absence of

speech, loss of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

spontaneous remission

subdural hematoma

tandem gait, ataxic

temporal lobe, status

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, postural

trinucleotide repeats

tyrosine hydroxylase deficiency

upgaze, paralysis of

vibratory sensation, abnormal

vision, blurred

vitamin deficiency

vitamin E deficiency

vitamin supplementation

voice, abnormality of

walking, difficulty with

weakness, generalized

weakness, progressive

white matter disease

whole genome sequencing

wide based gait

X-linked bulbospinal neuronopathy

Showing articles 800 to 845 of 845 << Previous

Lumbosacral Radiculomyelitis Assoc with Pandemic Acute Hemorrhagic Conjunctivitis
Letter Lancet Feb 1973., Wadia,N.H.,et al, 1973

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

Determinations of Plasma Ethosuximide Concentration & Management of Absence (Petit Mal) Seizures
Neurol 22:410, Penry,J.K.,et al, 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

Language Disturbances Following Anterior, Cerebral Artery Occlusion
Neurol 22:430, Rubens,A.B., 1972

Stuttering & Cerebral Ischemia
Letter, NEJM 287:9911972., Rosenfield,D., 1972

Children with Develpmental Language Diorders
Neurol 2:421, Wilson,J.,et al, 1972

Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
Neurol 22:49, Nakano,K.K.,et al, 1972

Enlargement of the Sylvian Aqueduct:A Sequel of Head Injuries
JNNP 35:463-467, Boller,F.C.,et al, 1972

Brain Stem Encephalitis Caused by Herpevirus Hominis
BMJ 4:405-406, Dayan, A.D.,et al, 1972

Spike-Wave Stupor
Amer J Dis Child 121:307, Moe,P., 1971

Learning & Language Disorders in Children
Part II:The School-age Child, Curr Prob Pediatr 1:, 1971 Sept., Gofman,H.,et al, 1971

Neurologic Aspects of Malignant External Otitis:Report of Three Cases
Mayo Clin Proc 46:339, Dinapoli,R.P.,et al, 1971

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

Whipple's Disease-Dementia
ed. by Charles G. Wells, Chap. 10 by Gunther Haas-Contemporary Neuro. Series 192, 1971 Published by, . A. Davila., 1971

Mercury Poisoning & its Treatment with N-Acetyl-D, L-Penicillamine
NEJM 285:10, Kark,R.A.,et al, 1971

Learning & Language Disorders in Children
Part I:The School-age Child, Current Problems in Pediatrics 1:1971 Aug., Gofman,H.,et al, 1971

Acute Intermittent Porphyria
Medicine 49:1, Stein,J.,et al, 1970

Three Pediatric Problems That Worry Parents
Consultant, MayJun, p. 1270., Bakwin,H.,et al, 1970

Brain Stem Tumors of Childhood & Adolescence
Am J Dis Child 119:465-472, Panitch,H.S.,et al, 1970

Petit Mal:A Critique Review
Neurol 17:197, Hanotia,P., 1969

Epilepsy & 3 per sec Spike & Wave Rhythms
Acta Neuro Scand Supp 40, Vol 451969., Dalby,M., 1969

Automatisms Associated with the Absence of Petit Mal Epilepsy
Arch Neurol 21:142, Penry,J.,et al, 1969

Petit Mal Status in Adults
Ann Int Med 68:1271, Thompson,S.&Greenhouse,A., 1968

Isolation of the Speech Area
Neuropsychologia 6:327-340, Geschwind,N.,et al, 1968

Cerebral Dominance & Its Disturbances
Ped Clin North Am 15:759-769, Benson,D.F.,et al, 1968

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

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

Long-Term Follow-up of Patients with Petit Mal
Arch Neurol 16:595, Charlton,M.H.,et al, 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Brief Focal Seizures vs Petit Mal Epilepsy
JAMA 198:181, Stevens,J., 1966

Epilepsy in Children
Current Therapy, 1966, p. 574., Scholl,M.L., 1966

Clinical Features of Petit Mal
Acta Neurol Scand 42:176, Givverd,F.B., 1966

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

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

On the Nature of the"Absence"in Centrecephalic Epilepsy
Electroenceph Clin Neurophysiol 18:334, Mirsky,A.,et al, 1965

Petit Mal Epilepsy
JAMA 194:113, Livingston,S.,et al, 1965

Non-Aphasia Disorders of Speech
International Jour Neurol 4:207-214, Geschwind,N., 1964

Neuro CPC of MGH
Multiple Sclerosis, Cerebral Infarcts, & Colitis, NEJM 268:607-615., , 1963

Acute Cerebellar Syndrome Secondary to Infectious Mononucleosis in a Fifty-Two Yealr Old Man
Ann Int Med 55:147-149, Bennett,D.R.&Peters,H.A., 1961

Pathologic Findings in Patients with"centrecephalic"Electroencephalographic Patterns
Neurol 10:992, Marsan,C.,et al, 1960

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

Mirror Writing (Book)
Psyche Miniatures Med. Series1928., Critchley,M., 1928

Showing articles 800 to 845 of 845 << Previous