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Differential
(Click to cross reference)
ankle reflex, absent
areflexia
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
benign essential tremor
Brown-Vialetto-Van Laere syndrome
calf hypertrophy
cardiomyopathy
central core disease
cerebellar atrophy, primary
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
clubfoot as related to neurologic disease
cognition
consanguinity
contractures, joint
corpus callosum, thinning
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
developmental milestones, loss of
differential diagnosis
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
dysarthria
dystonia
endemic area
evoked potentials
facial weakness
failure to thrive
falling
familial
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hammertoes
hand deformity
hand weakness
hearing loss
high arched feet
hyperreflexia
hyporeflexia
hypotonia
hypotonia, infants
imbalance
incoordination
intrinsic hand muscles, wasting of
kyphoscoliosis, neurologic causes of
L-dopa
leg weakness, bilateral
leprosy
lordosis
malignant hyperpyrexia
microcephaly
mitral valve prolapse
molecular genetics
MRI, abnormal
muscle atrophy, static
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
myopathy
nerve conduction studies
nerve enlargement
nerve hypertrophy
neuropathy
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, peripheral
nystagmus
pain, foot
Parkinson disease
past pointing
pes cavus
polymerase chain reaction
polyneuropathy
polyneuropathy, familial
pons, lesion of
prognosis
progressive neurologic disorder
pseudohypertrophy
pyramidal tract dysfunction
rash
Red flags
renal tubular acidosis
review article
riboflavin transporter deficiency
Romberg's sign
Samoa
scoliosis
scoliosis, neurologic association with
sensory loss
skin, biopsy
skin, lesions in neurologic disorders
steppage gait
toe walking
treatment of neurologic disorder
tremor
tremor, intention
tripping
visual evoked response
walking
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
wide based gait
wrist drop
Showing articles 100 to 150 of 857 << Previous Next >>

Precentral Gyrus Infarct Presenting as Isolated Contralateral Peripheral-Type Facial Palsy
Neurol 91:421-422, Hebant, B.,et al, 2018

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

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Clinicopathologic Conference, Lyme Meningoradiculitis
NEJM 379:1862-1868, Case 34-2018, 2018

Complex Bilateral Corpus Callosum Infarction after Paradoxical Embolism
Neurol 91:e1947-e1948, Calheiros de Oliveira Costa, G.V.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,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

Wilson Disease
NIDDK Oct2018, , 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

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

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

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

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,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

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

A Young Woman with Progressive Headache and Pancytopenia
Neurol 88:e132-e136, Conrad, E.C.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

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

Outcomes of Colorado Children with Acute Flaccid Myelitis at 1 Year
Neurol 89:129-137, Martin, J.A.,et al, 2017

Abdominal Tremor in Thyrotoxicosis
Neurol 89:1424-1425, Kelly, D.M.,et al, 2017

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

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

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

Safety and Efficacy of Focused Ultrasound Thalamotomy for Patients with Medication-Refractory, Tremor-Dominant Parkinson Disease
JAMA Neurol 74:1412-1418, Bond, A.E.,et al, 2017

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

Purple Hands in Multiple System Atrophy
Neurol 86:2314, Coon, E.A.,et al, 2016

50 Year Old Man with Cloudy Vision, Hearing Loss, and Unsteadiness
NEJM 374:2586-2593, Eliott, D.,et al, 2016

Spontaneous Limb Withdrawal Heralding Hyperacute Stroke or Stroke Worsening
Neurol 87:636-638, Delgado, M.G.,et al, 2016

A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
Neurol 87:e110-e113, Paliwal, V.K.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

A 2-year-old Child with Acute Flaccid Paralysis
Neurol 87:e149-e154, Al-Ghamdi, F. & Ghosh, P.S., 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

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

Pseudoradial Nerve Palsy Caused by Acute Ischemic Stroke
J Invest Med Case Report doi:10.1177/2324709616658310, Tahir, H.,et al, 2016

Orthostatic Tremor
Neurol 86:458-464, Hassan, A.,et al, 2016

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 73:1297-1307, Fang, B.,et al, 2016

Syphilitic Optic Neuropathy: Re-Emerging Cases Over a 2-Year Period
Neuro-Ophthalmol 40:69-73, Apinyawasisuk, S.,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

Holmes Tremor
Neurol 86:931-938, Raina, G.B.,et al, 2016

Differential Diagnosis
Thoracic Key, Southerland,A.W.,et al, 2016

Acute Flaccid Myelitis of Unknown Etiology in California 2012-2015
JAMA 314:2663-2671, Van Haren, K.,et al, 2015

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015

A Case of Hirayama Disease Presenting with Polymyoclonus
Neurol 85:e156, Ong, J.J.Y.,et al, 2015

MRI Findings in Children with Acute Flaccid Paralysis and Cranial Nerve Dysfunction Occurring during the 2014 Enterovirus D68 Outbreak
AJNR 36:245-250, Maloney, J.A.,et al, 2015



Showing articles 100 to 150 of 857 << Previous Next >>