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Differential
(Click to cross reference)
acanthocytosis
accomodation, abnormal
acral sensory symptoms
alternating rapid movement
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
anal wink response
anorexia
antecedent illness
anti GQ1b IgG antibody
antiganglioside antibodies
antioxidant
areflexia
arrhythmia, cardiac
ascending paralysis
astrocytoma
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
athetosis
atypical
autoantibodies
axonal degeneration
Babinski sign
botulism
brain atrophy
Brown-Vialetto-Van Laere syndrome
bulbar palsy
bulbar palsy, acute
burning paresthesia
campylobacter infection
cardiomyopathy
CAT scan
CAT scan, abnormal
caudate nucleus, atrophy
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellum, disease of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrospinal fluid, xanthochromia of
Charcot-Marie-Tooth
children
chorea
chorein
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Collier's sign
congestive heart failure
consanguinity
constipation
contractures, joint
corneal reflex, abnormal
corpus callosum, hypoplastic
corpus callosum, lesion of
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
denervation of muscle
denervation potentials
developmental disability
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
dopa responsive dystonia
dysarthria
dysdiadochokinesia
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dystonia
dystonia, children
electromyogram
electromyogram, decremental response
encephalopathy
encephalopathy, progressive
enteritis
enzyme, defect
episodic neurologic deficits
exome sequencing
eye movement, disorders of
facial appearance, abnormal
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fever
Fisher's syndrome
flaccid paralysis
flu-like illness
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
F-wave response
gait disorder
galactorrhea
gaze palsy
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
glioma
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hammertoes
hand deformity
hearing loss
heel-knee-shin test
hoarseness
hydrocephalus
hyperreflexia
hypertonia
hypophosphatemia
hyporeflexia
hypotonia
imbalance
immunoelectrophoresis, serum
incoordination
intellectual deficit
L-dopa
leg weakness, bilateral
leg weakness, unilateral
lethargy
lid
lid abnormalities
lip, biting
liver disease
lymphadenopathy
malabsorption
meningismus
mental retardation
microcephaly
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, spinal cord
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
myelomalacia
nasal speech
nausea and vomiting
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, sensory
neurotoxin
next-generation sequencing
numbness, ascending
numbness, extremity
nystagmus
nystagmus, gaze-evoked
nystagmus, vertical
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
overlap syndrome
pain, abdominal
palatal myoclonus
papilledema
paralysis
paralysis, acute
paralysis, acute areflexic
parenteral alimentation
paresthesias
Parkinson disease
Parkinsonism syndrome
perioral numbness
pes cavus
philtrum, tented
POLG1 gene
positional head-hanging test
postoperative neurologic complications
prevention of neurologic disorders
prion disease
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
prolactin, elevated
proprioception, abnormal
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
Purkinje cell
quadriparesis
quadriplegia
reading disorder, acquired
recurrent
renal tubular acidosis
ReNU syndrome
repetitive nerve stimulation
respiratory failure
respiratory tract infection
reversible neurologic disorder
review article
riboflavin transporter deficiency
Romberg's sign
saccadic eye movements, abnormal
scannig speech
scoliosis
seizure
sensory loss
sensory nerve action potentials
short stature
single photon emission computed tomography
slurred speech
spastic ataxia
spasticity
speech arrest
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, absence of
speech, loss of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spinopontine atrophy, dominant
spontaneous remission
stool culture
subdural hematoma
tandem gait, ataxic
tauopathy
telangiectases
temporal lobe, status
thalamus, lesion of
thalamus, lesion of-bilateral
tick bite
tick paralysis
tongue, biting
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, postural
trinucleotide repeats
tyrosine hydroxylase deficiency
upgaze, paralysis of
vestibulopathy
vibratory sensation, abnormal
vision, blurred
vital capacity
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin supplementation
vocalizations
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
white matter disease
whole genome sequencing
wide based gait
workup
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 550 to 600 of 845 << Previous Next >>

Paravermal Infarct and Isolated Cerebellar Dysarthria
Ann Neurol 30:211-213, Amarenco,P.,et al, 1991

Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy
Stroke 22:933-937, Gordon,D.L.,et al, 1991

Clinical Anatomic Study of Pure Dysarthria
Stroke 22:809-812, Ichikawa,K.&Kageyama,Y., 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Clinical and Electrophysiological Aspects of Acute Paralytic Disease of Children and Young Adults in Northern China
Lancet 338:593-597, McKhann,G.M.,et al, 1991

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

Pontine Supranuclear Facial Palsy
Stroke 21:1754-1757, Hopf,H.C.,et al, 1990

Treatment of Speech and Voice Disorders with Botulinum Toxin
JAMA 264:2671-2675, Ludlow,C.L., 1990

Clinicopath Conf
Cerebral Mucormycosis, Case 52-1990, NEJM 323:1823-1833990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Prolonged Confusion Following Convulsions Due to Generalized Nonconvulsive Status Epilepticus
Neurol 40:1689-1694, Fagan,K.J.&Lee,S.I., 1990

Dysphagia, Speech Disorders and Centrotemporal Spikes-Waves
Arch Francaises De Pediatrie 47:115-117, Boulloche,J.,et al, 1990

Anterior Cerebral Artery Territory Infarction in the Lausanne Stroke Registry
Arch Neurol 47:144-150, Bogousslavsky,J.&Regli,F., 1990

Caudate Infarcts
Arch Neurol 47:133-143, Caplan,L.R.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Acute Paraneoplastic Sensory Ganglionitis, NEJM 322:531-5431990., , 1990

Clinical Features of Proven Basilar Artery Occlusion
Stroke 21:1135-1142, Ferbert,A.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

The Syndrome of Acute Sensory Neuropathy:Clinical Features and Electrophysiologic and Pathologic Changes
Neurol 40:584-591, Windebank,A.J.,et al, 1990

Extensive Brain Calcif & Prog Dysarthris & Dysphagia Assoc with Chronic Hypoparathyroidism
Arch Neurol 47:1038-1039, Cheek,J.C.,et al, 1990

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Complex Partial Status Epilepticus in a Patient with Leptomeningeal Carcinomatosis
Neurol 40:858-859, Dexter,D.D.,et al, 1990

Acquired Childhood Aphasia
Arch Neurol 47:1324-1328, Loonen,M.C.B.&vanDongen,H.R., 1990

Slowly Progressive Aphasia:Three Cases with Language, Memory, CT and PET Data
JNNP 53:987-993, Kempler,D.,et al, 1990

Paramedian Thalamic and Midbrain Infarcts Associated with Palilalia
JNNP 53:797-799, Yasuda,Y.,et al, 1990

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

Valproate Prevents the Recurrence of Absence Status
Neurol 39:1294-1297, Berkovic,S.F.,et al, 1989

Nonconvulsive Status Epilepticus Following Cerebral Angiography
Ann Neurol 25:199-201, Vickrey,B.G.&Bahls,F.H., 1989

Complex Partial Status Epilepticus Provoked by"Crack"Cocaine
Ann Neurol 26:785-786, Ogunyemi,A.O.,et al, 1989

Complex Partial Status Epilepticus Associated with Cyclosporin A Therapy
JNNP 52:1068-1071, Appleton,R.E.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Progressive Aphasia without Dementia:Further Documentation
Ann Neurol 25:411-413, Sapin,L.R.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Anterior Operculum Syndrome
Neurol 39:1169-1172, Mao,C.C.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

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

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Delayed Speech in Children
BMJ 297:1281-1282, Hall,D., 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Absence Status Epilepticus with Computed Tomographic Brain Changes Following Mitrizamide Myelography
Ann Neurol 24:582-584, Obeid,T.,et al, 1988

Comparison of Monotherapy with Valproate and Other Antiepileptic Drugs in the Treatment of Seizure Disorders
Am J Med 84: (Supp1A) , 3-688., Chadwick,D., 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Effect of Vitamin E Deficiency on Neurologic Function in Patients with Cystic Fibrosis
J Pediatr 113:637-640, Cynamon,H.A.,et al, 1988

Sensory Form of Acute Polyneuritis
Neurol 38:1728-1731, Dawson,D.M.,et al, 1988



Showing articles 550 to 600 of 845 << Previous Next >>