Neurology Specific Literature Search   
 
[home][thesaurus]
    

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 121 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

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

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

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

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

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

Pyogenic Brain Abscesses in a Patient with Digital Clubbing
JAMA Neurol 77:129-130, Paliwal, V.K.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

Clinical Characteristics and Treatment Outcomes for Patients Infected with Mycobacterium haemophilum
Emerg Inf Dis 25:1648-1652, Nookeu,P.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Hearing and Vision Loss in an Older Man
JAMA Neurol 75:1439-1440, Ho, V.M.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

A 74-year-old Woman with Bilateral Foot Pain and a Palmar Rash
Neurol 88:e44-e50, Wynn, D.P.,et al, 2017

Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
Lancet 389:1367-1368, Vale, T.C.,et al, 2017

A Rare Case of Bilateral Optic Neuritis and Guillain-Barre Syndrome Post Mycoplasma Pneumoniae Infection
Neuro Opth 41:41-47, Baheerathan, A.,et al, 2017

Diabetic Sensory and Motor Neuropathy
NEJM 374:1455-1464, Vinik, A.I.,et al, 2016

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Foot Drop
BMJ 350:h1736, Stevens, F.,et al, 2015

Burning Hands and Feet
Neurol 84:e146-e152, Chan, A.C. & Wilder-Smith, E., 2015

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Chronic and Slowly Progressive Weakness of the Legs and Hands
BMJ 348:g459, Nightingale, H.,et al, 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Paroxysmal Burning Pain Caused by Erythromelalgia
Lancet 383:1692, Kondo, T.,et al, 2014

Polycythemia Vera Presenting with Ischemic Strokes in Multiple Arterial Territories
Neurol 82:e168-e170, Billakota, S. & Husseini, N.E., 2014

Copper Deficiency
BMJ 348:g3691, Chhetri, S.K.,et al, 2014

Erythromelalgia? A Clinical Study of People Who Experience Red, Hot, Painful Feet in the Community
Int J Vasc Med ID=864961, Friberg, D.,et al, 2013



Showing articles 0 to 50 of 121 Next >>