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Differential
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acanthocytosis
adrenoleukodystrophy
adverse drug reaction
anosmia
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
Bassen-Kornzweig syndrome
bladder dysfunction
blindness
brainstem, atrophy
cardiomyopathy
cataracts
cerebellar ataxia, children
cerebellar atrophy, primary
cerebral cortical atrophy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
choreoathetosis
chronic progressive external ophthalmoplegia
clubfoot as related to neurologic disease
Cockayne's syndrome
coenzyme Q10 deficiency
cone-rod dystrophy
consanguinity
cornea, abnormal
deafmute
deafness
degenerative diseases of CNS
dementia
diabetes insipidus
diabetes mellitus
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dysmetria
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electronystagmography
electroretinograph
eye movement, disorders of
familial
foot deformity
Friedreich's ataxia
fundus, abnormality of
gait disorder
gargoylism
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
globus pallidus
globus pallidus, lesion of
Hallervorden Spatz disease
Hallgren's syndrome
headache
hearing loss
heart block
Hurler's syndrome
hydrocephalus
hyperreflexia
hyposmia
intellectual deficit
intestinal pseudoobstruction
iron, brain
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
macular degeneration
malformation, CNS, congenital
MELAS syndrome
mental retardation
MERRF syndrome
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
mucopolysaccharidoses
muscle atrophy, progressive
myelopathy
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
myopia
neuritis
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
night blindness
nystagmus
obesity
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic nerve
optic neuropathy
optical coherence tomography
pancytopenia
peroxisomal disease
pes cavus
phytanic acid
pigmentary retinopathy
polydactyly
polyneuropathy
prognosis
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
ptosis
pyramidal tract
pyramidal tract dysfunction
ragged-red fibers
refractive errors
Refsum's disease
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
rigidity
Romberg's sign
schizophrenia
sea-blue histiocytes
seizure
sensorineural hearing loss
sensory loss
short stature
spasticity
speech disorder
speech disorder, childhood
Spielmeyer Vogt syndrome
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 7
spinocerebellar degeneration
substantia nigra
sudden death
tapetoretinal degeneration
treatment of neurologic disorder
tremor
trinucleotide repeats
Usher's syndrome
visual evoked response
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
weakness
weight loss
Wolfram syndrome
Showing articles 50 to 100 of 4537 << Previous Next >>

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

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

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

A Woman with Progressive Painless Sequential Monocular Vision Loss
Neurol 101:e2197-e2201, Ditrapani,J.,et al, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

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

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Autoimmune Nodopathies, An Emerging Dignostic Category
Curr Opin Neurol 35:579-585, Martin-Agullar, L.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

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

A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Chorioretinopathy After Corticosteroid Treatment for Optic Neuritis
Neurol 96:e305-e306, Ling, J. and Micieli, J.A., 2021

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

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

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

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

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

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
Neurol 86:742-747, Kim, J.K.,et al, 2016



Showing articles 50 to 100 of 4537 << Previous Next >>