Neudle.com: muscle jerks unilateral

Differential
(Click to cross reference)

abducens nerve paralysis

abortion, spontaneous

abscess, intracerebral

abscess, intracerebral, multiple

abscess, intracerebral, treatment of

abscess, lung

acoustic nerve

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acute disseminated encephalomyelitis

acute intermittant porphyria

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic blackout

alcoholic coma

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

amaurosis fugax

amaurosis fugax, unilateral vs.bilateral

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

ANA

anemia

aneurysm

aneurysm, multiple intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

angiography, cerebral, false negative

angiokeratoma

angiotensin-converting enzyme

ankle reflex, absent

anorexia

antibiotics

antibiotics, neurologic complications with

antibodies to measles

anticardiolipin antibodies

anticonvulsants, untoward effects of

antimetabolite

antiphospholipid antibodies

antiviral agents

aphasia

aqueduct of Sylvius, obstruction

autonomic dysfunction

autonomic nervous system

Barkhof MR criteria for MS

basal ganglia

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

behavior, combative

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

biotin deficiency

biotinidase deficiency

blood dyscrasias, neurologic findings with

bone marrow transplantation

Borrelia miyamotoi infection

brachial plexus neuropathy

brain atrophy

brain biopsy

brain biopsy, false negative

brainstem, infarction of

burning feet, differential diagnosis of

burning paresthesia

burning skin

cachexia

calcification, intracranial

camptocormia

carbon monoxide poisoning

carbon monoxide poisoning, chronic

CAT scan, abscess, cerebral

CAT scan, disappearing lesion on

CAT scan, false negative

CAT scan, serial

cataracts

cauda equina

cauda equina, enhancement

cauda equina, lesion of

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar peduncle

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral infarction

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, atrial myxoma

cerebrovascular accident, bilateral

cerebrovascular accident, complications with

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisterna magna

Clinical Pathologic Conference(C.P.C.)

CLOVES syndrome

coenzyme Q10

coenzyme Q10 deficiency

cognition

collagen vascular disease

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congestive heart failure

conversion reaction, children

Coombs test, positive

cortical blindness

cortical blindness, transient

cortical deafness

cortical hemorrhage

cough

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cryptorchidism

cultured skin fibroblasts

cyclophosphamide

cyst

cyst, cortical parenchyma

cyst, parenchymal

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cytoid bodies

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

deafness

deafness, unilateral

deep gray nuclei

degenerative diseases of CNS

delirium

dementia

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

developmental disability

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

disability, neurological

disorientation

distal muscle weakness

disulfiram

dizziness

drowsiness

drug induced neurologic disorders

dysarthria

dysequilibrium syndrome

dystonic reaction, acute

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

embolism

emergencies, neurologic

encephalitis

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, Rasmussen's

encephalitis, recurrent

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyopathy

encephalopathy

encephalopathy, metabolic

encephalopathy, progressive

endemic area

enzyme, defect

epidemic

epidemiology of neurology

epidermal nevus syndrome

epilepsia partialis continua

episodic neurologic deficits

epistaxis

evoked potentials

exercise intolerance

eye movement, disorders of

eye movement, painful

eye, pain in

face, numbness of

facial anomalies

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial pain

facial pain, atypical

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

fetal alcohol syndrome

fever

fine motor function, impaired

floaters

fluorescent treponema antibody absorption/false positive

fourth ventricle, cyst

frontal lobe, pathologic signs of

fucosidosis

fundus, abnormality of

fungal infection, CNS

gadolinium

gait disorder

gaze palsy

gaze palsy, supranuclear

gene

gene mutation

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

gliomatosis cerebri

glycoprotein

granulomatous disease

grasp reflex

growth retardation

Guillain Barre syndrome

hallucination

hallucination, visual

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

heart murmur

helminthic infection of CNS

hemianopia

hemianopia, homonymous

hemianopia, transient

hemiatrophy, cerebral

hemiballismus

hemichorea

hemihypertrophy, congenital

hemihypertrophy, facial

hemimegalencephaly

hemimyoclonic jerks

hemiparesis

hemiparesis, transient

hemiplegia, progressive

hemispherectomy

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatomegaly

hepatosplenomegaly

heralding manifestation

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hypergammaglobulinemia

hypertensive encephalopathy

hypertonia

hypertrophic cardiomyopathy

hypothalamus, disturbance of

immunosuppressive agents

immunotherapy

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

incidence

inclusion body myositis

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

intrinsic hand muscles, wasting of

irritability

isoniazid

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

ketogenic diet

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

lactate

lactic acidemia

laminar necrosis, cortical

lateropulsion

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocytosis

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

limbic encephalitis

liver function enzymes

lumbar puncture, complications of

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malformation, CNS, congenital

malignant papulosis

Marchiafava-Bignami disease

mastoiditis

MELAS syndrome

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, children

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, factors influencing mortality in

meningitis, late neurologic sequelae in

meningitis, neurologic aspects and complications of

meningitis, neutrophilic

meningitis, treatment of

meningoencephalitis

meningoencephalopathy

mental retardation

mental status, abnormal

mental status, abnormal, acute

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

methotrexate

methylhydrazine derivatives

Mexican

Mexico

microangiopathy, brain

microcephaly

middle cerebellar peduncle, lesion

migraine

migraine, seizures in

Mills syndrome

mimics

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, angiography

MRI, angiography, false negative

MRI, brachial plexus

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, sulcal hyperintensity

MRS

multiple sclerosis

multiple sclerosis, misdiagnosis

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myasthenic syndrome

myelitis

myelopathy

myelopathy, chronic progressive

myocardial infarction

myopathy, mitochondrial

nasal septum, perforation of

neonatal infection, viral

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplastic angioendotheliosis

nephritis

nephrotic syndrome

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathy

neuropathy, medication induced

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

nutritional deficiency

nystagmus

nystagmus, monocular

occipital lobe, lesion of

ophthalmoplegia

ophthalmoplegia, progressive external

optic neuritis, bilateral

optic neuropathy

optic neuropathy, nutritional

orthostatic hypotension

otitis, neurologic complications with

parasitic infection, CNS

paresthesias

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinsonism syndrome

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

partial thromboplastin time, prolonged

pigmentary retinopathy

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleurisy

POLG1 gene

polycythemia, primary

polyhydramnios

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, uremic

polyuria

pons, lesion of

porphyria

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

potassium channel antibodies

precipitating factors

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

procarbazine

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proteinuria

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pulmonary infiltrates

pulmonary stenosis

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, dilated, episodic

pupil, tonic

pyramidal tract dysfunction

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

Rankin score

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

reading disorder, acquired

renal transplantation

respiratory failure

restless leg syndrome

reticulum cell sarcoma

retinal artery occlusion

rheumatoid arthritis factor(R.A.factor)

scoliosis, neurologic association with

scotoma

sedimentation rate, elevated

seizure, injury following

seizure, intractable

seizure, neonatal

seizure, repetitive

seizure, surgical treatment of

seizure, treatment of

seizure, withdrawal

sensorineural hearing loss

sensory loss

sensory testing

sensory testing, split midline on

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

short stature

shunt procedure, ventricular

sicca syndrome

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

slurred speech

small for dates infant, problems in

speech, unintelligible

spinal cord

spinal cord, lesion of

spirochete infection

splenomegaly

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

strokelike episodes

stuporous

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

subcutaneous nodules

subdural hematoma

symmetric brain lesions

syncope

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tachycardia

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

Trousseau's sign

ulcerative colitis

ultrasonography, head

unconsciousness

unconsciousness, transient

upgaze, paralysis of

uremia

uremic encephalopathy

Venereal Disease Research Laboratory test

ventricular enlargement

vertigo

Vietnamese

vinblastine

vincristine neurotoxicity

viral infection

viral infection, CNS

vision, blurred

vision, blurred, monocular

visual acuity, decreased

visual field defect

visual fields, constricted

visual impairment

visual loss

visual symptoms

visuospatial disturbance

vocal cord paralysis

vomiting, recurrent

walking, difficulty with

weakness

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

web sites

weight loss

Wernicke's encephalopathy

word-finding difficulty

Showing articles 250 to 300 of 6950 << Previous Next >>

Tumefactive Multiple Sclerosis
www.medlink.com, JUne, Bunyan, R.F. and Lucchinetti, C.F., 2010

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

Horners Syndrome-Not To Be Sneezed At
Lancet 375:776, Bazari,F.,et al, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

Primary Central Nervous System Post-Transplantation Lymphoproliferative Disorder
CANCER 16:863-870, Cavaliere, R.,et al, 2010

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Epilepsy in Children with Infantile Thiamine Deficiency
Neurol 73:828-833, Fattal-Valevski,A.,et al, 2009

Unexplained Seizures in an Infant
Lancet 373:94, Astuto,M.,et al, 2009

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
NEJM 360:1960-1970, Bockenhauer,D.,et al, 2009

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

Clinicopath Conf, Neurosarcoidosis
NEJM 360:802-809, Case 6-2009, 2009

Long-Term Outcomes Among Adult Survivors of Childhood Central Nervous System Malignancies in the Childhood Cancer Survivor Study
J Natl Cancer Inst 101:946-958, Armstrong,G.T.,et al, 2009

Clinicopath Conf., Eastern Equine Encephalitis
NEJM 359:294-303, Case 22-2008, 2008

Polymyalgia Rheumatica and Giant-Cell Arteritis
Lancet 372:234-245, Salvarani,C.,et al., 2008

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Opsoclonus-Myoclonus-Ataxia Syndrome with Autoantibodies to Glutamic Acid Decarboxylase
Clin Neurol Neurosurg 110:619-621, Markakis,I.,et al, 2008

Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome
Acta Neurol Taiwan 17:177-183, Shen, F.,et al, 2008

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

CT and MR Characteristics of Cerebral Sparganosis
AJNR 28:1700-1705, Song,T.,et al, 2007

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

A Young Man with Rapidly Progressive Multifocal Disease Affecting the White matter
Pract Neurol 7:172-181, Hilton-Jones,D.,et al, 2007

Neurological Findings in Aminoacylase 1 Deficiency
Neurol 68:2151-2153, Sass,J.O.,et al, 2007

CNS Lupus: A Study of 41 Patients
Neurol 69:644-654, Joseph,F.G.,et al, 2007

Segmental Zoster Paresis of Limbs: Report of Three Cases and Review of Literature
Neurologist 13:313-317, Kawajiri,S.,et al, 2007

Clinicopath Conf., Left Atrial Myxoma with Systemic Embolization
NEJM 357:1137-1145, Case 28-2007, 2007

Managing Acute Organophosphorus Pesticide Poisoning
BMJ 334:629-634, Roberts,D.M.&Aaron,C.K., 2007

Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
Neurol 68:1843-1850, Juhasz-Pocsine,K.,et al, 2007

Orthostatic Myoclonus: A Contributor to Gait Decline in Selected Elderly
Neurol 68:1826-1830, Glass,G.A.,et al, 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

A 16-Year-Old Girl With Progressive Weakness of the Left Leg
Neurol 69:84-90, Hahn,A.F.,et al, 2007

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Tiagabine-Induced Myoclonic Status Epilepticus in a Nonepileptic Patient
Neurol 68:310, Vollmar,C. &Noachtar,S., 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Adult Onset Subacute Sclerosing Panencephalitis: Clinical Profile of 39 Patients From a Tertiary Care Centre
JNNP 77:630-633, Prashanth,L.K.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Community-Acquired Bacterial Meningitis in Adults
NEJM 354:44-53, van de Beek,D.,et al, 2006

Update on Susacs Syndrome
Curr Opin Neurol 18:311-314, Gross,M. &Eliashar,R., 2005

Reversible Posterior Leukoencephalopathy Syndrome
Intern Med J 35:83-90, Stott,V.L.,et al, 2005

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Cardiac Pathology in Status Epilepticus
Ann Neurol 58:954-957, Manno,E.M.,et al, 2005

Showing articles 250 to 300 of 6950 << Previous Next >>