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Differential
(Click to cross reference)
airway obstruction
anosmia
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, truncal
ataxic gait
autonomic dysfunction
autonomic neuropathy
autonomic neuropathy, idiopathic
Babinski sign
benign essential tremor
bulbar palsy
calf hypertrophy
carcinoma
carcinoma of thyroid
cardiomyopathy
cataracts
cataracts, congenital
central core disease
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
chromosome 9
clubfoot as related to neurologic disease
congenital bilateral perisylvian syndrome
congenital malformation
congenital myasthenic syndromes
consanguinity
constipation
contractures, joint
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
deafness
deep tendon reflexes
developmental abnormality of brain
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, ocular complications in
diabetic cranialneuropathies
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
drooling
dysarthria
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
evoked potentials
exome sequencing
facial weakness
facial weakness, bilateral
familial
fatigue
fine motor function, impaired
foot deformity
foot drop
frataxin
Friedreich's ataxia
gag reflex, depressed
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
hammertoes
hand deformity
hand weakness
hearing loss
high arched feet
high arched palate
hydrocephalus
hyperreflexia
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hyposmia
hypotonia
hypotonia, infants
intellectual deficit
intrinsic hand muscles, wasting of
iritis
kyphoscoliosis, neurologic causes of
kyphosis
leg weakness, bilateral
light-near dissociation, causes of
lordosis
malformation, CNS, congenital
malignant hyperpyrexia
mental retardation
mestinon
micrognathia
mitral valve prolapse
molecular genetics
MRI
MRI, abnormal
multiple endocrine neoplasia
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
myopathy
myotonia congenita
myotonia dystrophica
nasal speech
nerve conduction studies
nerve hypertrophy
neuroendocrinology
neurologic disease, diagnoses of
neuroma
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, sensory
neuropathy, sensory, hereditary
night blindness
nonverbal
nystagmus
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
opened mouth
operculum syndrome, bilateral
ophthalmoplegia
optic atrophy
optic disc cup
paraparesis
paraparesis, familial spastic
paraparesis, spastic
peroneal muscle atrophy, causes of
peroxisomal disease
pes cavus
phytanic acid
polymicrogyria
polyneuropathy
polyneuropathy, familial
prognosis
pseudobulbar palsy
pseudohypertrophy
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pyramidal tract dysfunction
Refsum's disease
respiratory failure
retinitis pigmentosa
review article
Romberg's sign
scoliosis
scoliosis, neurologic association with
seizure
sensorineural hearing loss
sensory loss
skin, lesions in neurologic disorders
smell
spasticity
steppage gait
sudden death
synkinesis
temporalis muscle wasting
term infant
treatment of neurologic disorder
tremor
trinucleotide repeats
uveitis
vibratory sensation, abnormal
visual evoked response
visual fields, constricted
vitamin deficiency
vitamin E
vitamin E deficiency
weakness
weakness, fatiguable
weakness, proximal
wheelchair
Wolfram syndrome
Showing articles 0 to 50 of 23264 Next >>

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Neurologic Findings in Men with Isolated Hypogonadotropic Hypogonadism
Neurol 39:223-226, Schwankhau,J.D.,et al, 1989

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Juvenile Diabetes Mellitus & Optic Atrophy
Arch Neurol 34:759, Lessell,S.,et al, 1977

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 1976

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

Surgical Versus Nonsurgical Treatment for Back Pain
NEJM 357:1255, Copeland,B., 2007

Treatment of Physicians With Epilepsy
Neurol 69:1374-1379, Allen,J.W. &Devinsky,O., 2007

Conditions That Mimic Stroke in the Emergency Department
Arch Neurol 52:1119-1122, Libman,R.B.,et al, 1995

Weeping as a Common Element of Pseudoseizures
Arch Neurol 50:1059-1060, Bergen,D.&Ristanovic,R., 1993

Brain Tumor Presenting as an Acute Pure Motor Hemisparesis
Stroke 20:288-291, Fisher,M.&Recht,L.D., 1989

Hypothalamic Hamartomas & Ictal Laughter:Evolution of Charact Epileptic Syndrome & Diagnostic Value of MRI
Ann Neurol 23:429-439, Berkovic,S.F.,et al, 1988

If I Had a Transient Ischemic Attack at the Age of 55
BMJ 1:969, Pearce,J.M.S., 1978

Remote Cerebral Infarction as a Presenting Manifestation of Brain Tumor
Milit Med 141:548, Finelli,P.F., 1976

Eletrophoretic Analy. of CSF Proteins in Pts with CNS Mass Lesions
J Neurosurg 36:679, Weber,E.L., 1972

Oculomotor Palsy From Minor Head Trauma
JAMA 220:1083, Eyster,E.F.,et al, 1972

Acquired Sixth-Nerve Paresis in Children
Arch Ophthal 83:574-579, Robertson,D.M.,et al, 1970

Addressing Systemic Complications of Acute Stroke: A Scientific Statement From the American Heart Association
Stroke 56:e15-e29, Kumar,S.,et al, 2025

Rocky Mountain Spotted Fever Encephalitis and "Starry Sky" Pattern on MRI, A Case Report
Neurologist 30:34-38, Mikhaiel,J.P.,et al, 2025

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

Angioedema Following Tenecteplase for Acute Ischemic Stroke
Stroke 55:e242-e244, Dellabella,A., 2024

A 32-Year-Old Man with Painless Bilateral Shoulder Girdle Weakness and Atrophy
Neurol 103:e209915, Gutti,N.B.,et al, 2024

An Unusual Etiology of Lumbosacral Plexopathy in a Patient with HIV
Neurol 103:e209930, Madduluri,B.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Safety and Efficacy of Staged, Bilateral Focused Ultrasound Thalamotomy in Essential Tremor, An Open-Label Clinical Trial
JAMA Neurol 81:939-946, Kaplitt,M.G.,et al, 2024

Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
Ann Neurol 96:1086-1091, Fadda,G.,et al, 2024

Miyazaki Syndrome as a Complication of Shunt Drainage
Ann Neurol 96:1230-1231, vanLanen,R.H.G.J., et al, 2024

Sarcoidosis of the Pituitary Gland and Stalk in a Man Presenting Asthenia, Impotence, Loss of Libido, Polyuria, and Polydipsia
Lancet 404:2460-2461, Clement,J., et al, 2024

Clinical Reasoning: A 39-Year-Old Returning traveler with Acute Encephalopathy and Strokes
Neurol 104:e210177, Buback,ClT.,et al, 2024

Clinicopathologic Conference, Cryptococcal Meningoencephalitis
NEJM 391:2361-2369, Case 40-2024, 2024

Effect of IV Thrombolysis With Alteplase in Patients with Vessel Occlusion in the WAKE-UP Trial
Neurol 104:e209871, Galinovic,I.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

Face to Face - A Neurologists Perspective on Teleeducation
NEJM 391:2286-2287, Schelke,M.W., 2024

Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
Neurol 102:e209396, Yang,Y.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024



Showing articles 0 to 50 of 23264 Next >>