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Differential
(Click to cross reference)
airway obstruction
angiitis
ankle reflex, absent
anosmia
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
aspartate aminotransferase
asthma
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
autonomic dysfunction
autonomic neuropathy
autonomic neuropathy, idiopathic
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
benign essential tremor
bladder dysfunction
brainstem, atrophy
bulbar palsy
calf hypertrophy
carcinoma
carcinoma of thyroid
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central core disease
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebral cortical atrophy
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
chromosome 9
Churg-Strauss syndrome
clubfoot as related to neurologic disease
cognition
compression fracture
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
degenerative diseases of CNS
developmental abnormality of brain
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, ocular complications in
diabetic cranialneuropathies
differential diagnosis
dimple
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
drooling
dysarthria
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dysraphism, spinal
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
endemic area
eosinophilia
eosinophilic granulomatosis with polyangiitis
evoked potentials
exome sequencing
facial weakness
facial weakness, bilateral
falling
familial
fatigue
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
foot ulcer, neuropathic
frataxin
Friedreich's ataxia
gag reflex, depressed
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
giant axonal neuropathy
granuloma, eosinophilic
hammertoes
hand deformity
hand weakness
hearing loss
high arched feet
high arched palate
hydrocephalus
hyperphosphatasia
hyperreflexia
hypertrichosis
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hyposmia
hypotonia
hypotonia, infants
imbalance
incontinence, fecal
incoordination
intellectual deficit
intrinsic hand muscles, wasting of
iritis
kyphoscoliosis, neurologic causes of
kyphosis
L-dopa
leg weakness, bilateral
leg weakness, unilateral
leprosy
Lhermitte's sign
light-near dissociation, causes of
lipoma of CNS
lipoma of skin
liver function enzymes
lordosis
malaise
malformation, CNS, congenital
malignant hyperpyrexia
Marinesco-Sjogren syndrome
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
myelomalacia
myelomeningocele
myopathy
myotonia congenita
myotonia dystrophica
nasal speech
nerve conduction studies
nerve enlargement
nerve hypertrophy
neuroendocrinology
neurologic disease, diagnoses of
neuroma
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, small-fiber, painful sensory
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
pain
pain, anal
pain, foot
pain, leg
pain, perineum
palmar erythema
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paresthesias
Parkinson disease
past pointing
peroneal muscle atrophy, causes of
peroxisomal disease
pes cavus
petechiae
phytanic acid
polymerase chain reaction
polymicrogyria
polyneuropathy
polyneuropathy, familial
pons, lesion of
prognosis
progressive neurologic disorder
pseudobulbar palsy
pseudohypertrophy
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pyramidal tract dysfunction
radiculopathy
rash
rash, hand
Red flags
Refsum's disease
respiratory failure
retinitis pigmentosa
review article
Romberg's sign
Samoa
scoliosis
scoliosis, neurologic association with
seizure
sensorineural hearing loss
sensory loss
skin, biopsy
skin, lesions in neurologic disorders
smell
spasticity
spinal stenosis
steppage gait
sudden death
synkinesis
temporalis muscle wasting
term infant
tethered spinal cord
toe walking
trauma
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
trinucleotide repeats
tripping
urinary incontinence
uveitis
vibratory sensation, abnormal
visual evoked response
visual fields, constricted
vitamin deficiency
vitamin E
vitamin E deficiency
walking
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
Wolfram syndrome
x-ray, lumbar spine
Showing articles 0 to 50 of 435 Next >>

Skin Lesions, Foot Drop, and Hand Contractures
JAMA doi:10.1001/JAMA.2023.9915, Filley,A.R.,et al, 2023

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

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

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

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

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

Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
Neurol 62:13-16, Bruno,C.,et al, 2004

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

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

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

Hand Contractures in Parkinson's Disease
JNNP 51:1221-1223, Kyriakides,T.&Hewer,R.L., 1988

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

Tethered Cord Syndrome in Adults
J Neurosurg 57:32-47, Pang,D.&Wilberger,J.E.Jr., 1982

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

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

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

A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
Neurol 103:e209900, Jones,F.J.S.,et al, 2024

Clinical Outcomes and Safety Comparison of Vertebroplasty, Balloon Kyphoplasty,and Vertebral Implant for Treatment of Vertebral Compression Fractures
AJNR 44:1345-1351, Li,T.,et al, 2023

A 22-Year-Old Man with Multifocal Brain and Osseous Lesions
Neurol 101:1025-1031, Reddy,S.,et al, 2023

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

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Spina Bifida
NEJM 387:444-450, Iskandar, B.J. & Finnell, R.H., 2022

Reversible Parkinsonism Caused by Lumboperitoneal Shunt Overdrainage
Neurol 99:486-488, Takeuchi, H.,et al, 2022

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

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

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,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

Spinal Metastases
JAMA 323:2438, Chiu, R.G.,et al, 2020

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

A Pregnant Woman with Chin Numbness
Neurol 92:e996-e999, Arnold, A.J.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Antiepileptic Drug Treatment Patterns in Women of Childbearing Age with Epilepsy
JAMA Neurol 76:783-790, Kim, H.,et al, 2019



Showing articles 0 to 50 of 435 Next >>