Neudle.com: congenital paresis

Differential
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abdominal protrusion

abducens nerve paralysis

abscess, intracerebral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute necrotizing encephalitis

adolescent medicine

agenesis of corpus callosum

altered states of consciousness

alveolar hypoventilation

amaurosis fugax

amniotic fluid, infection

aneurysm

aneurysm, berry

aneurysm, cavernous sinus

aneurysm, infraclinoid

aneurysm, internal carotid artery

aneurysm, intracranial

aneurysm, posterior communicating artery

aneurysm, supraclinoid

aneurysm, vertebral basilar system

angiography, cerebral

angiography, posterior fossa

ankle clonous

anterior horn cell disease

anterior spinal artery infarction

anterior tibial muscle weakness

apraxia of eye movements

artery of Adamkiewicz

arthritis

arthrogryposis multiplex

asymmetric crying facies

basilar artery occlusion

brainstem, hypoplasia

brainstem, infarction of

brainstem, lesion of

brainstem, malformation

bulbar palsy, progressive

burst suppression pattern, electroencephalogram

calcification, intracranial

carotid artery disease

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid artery stenosis

CAT scan

CAT scan, abnormal

cataracts

cataracts, congenital

cavernous sinus, syndrome

central cord syndrome

central core disease

central hypoventilation, congenital

central nervous system, infection of

cerebellar peduncle

cerebral cortical atrophy

cerebral palsy

cerebral palsy, risk factors

cerebrospinal fluid

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cervical spine injury

children

chiropractic manipulation

chiropractic manipulation, neurologic complications with

chorea

chorioamnionitis

chorioretinitis

chromosomal abnormality

chromosome 11

chromosome 5

chronic progressive external ophthalmoplegia

cleft palate

clubfoot as related to neurologic disease

Coats syndrome

cognition

coloboma

congenital bilateral perisylvian syndrome

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myasthenic syndromes

congenital myopathy

congenital myopathy, inflammatory

congenital ocular motor apraxia

conus medullaris, lesion of

conversion reaction

corneal reflex, abnormal

corpus callosum

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost effectiveness

cranial nerve palsies

creatine phosphokinase(CPK)elevated

cyst, porencephalic

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

delivery, complicated

dementia

dementia, childhood

depression

depression, psychotic

developmental abnormality of brain

developmental disability

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

diplegia, brachial

diplopia

disability, neurological

disconnection syndrome

dislocated hip, congenital

doppler

drooling

dropped head syndrome

Duane syndrome

dysarthria

dyskinesia, buccal lingual facial

Ehlers-Danlos syndrome

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, brainstem

encephalitis, viral

encephalopathy

encephalopathy, neonatal

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

episodic disorders

episodic neurologic deficits

erythema migrans

exome sequencing

eye closure

eye movement, disorders of

eye, pain in

face, inexpressive

face, numbness of

facial appearance, abnormal

facial asymmetry

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, causes of

facial nerve palsy, congenital

facial nerve palsy, prognosis of

facial nerve, lesion of

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fibromuscular dysplasia

floppy infant

fluorescent treponema antibody absorption(FTA-ABS)

fluorescent treponema antibody absorption/false positive

foot drop

forceps delivery

fourth ventricle, enlargement of

fourth ventricle, floor

frontal balding

gag reflex, depressed

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gene

gene mutation

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

glioblastoma multiforme(astrocytoma Gr.III)

Gowers maneuver

Guillain Barre syndrome

hair, straight-unilateral

heralding manifestation

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

highly active antiretroviral therapy

Hirschprung's disease

histochemistry

histochemistry of muscle

hoarseness

Holt-Oram syndrome

Horner's syndrome

Horner's syndrome, bilateral

Horner's syndrome, congenital

Horner's syndrome, painful

human immunodeficiency virus type 1

hypoxic encephalopathy

iatrogenic neurologic disorders

IFA

imbalance

immunofluorescent exam of CSF cells

immunohistochemistry

immunosuppression

inclusion bodies, intranuclear

infant, evaluation of

infantile spasm

infectious mononucleosis

insular cortex

intellectual deficit

intellectual deterioration

interferon

interferon inducer

internal carotid artery

internuclear ophthalmoplegia

intracerebral hemorrhage

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

iododeoxyuridine

ipsilateral hemiplegia

jaw pain

joint hypermobility

juvenile paresis

Kearns-Sayre syndrome

klippel feil syndrome

kyphoscoliosis, neurologic causes of

language disorders in children

leg weakness, bilateral

leg weakness, unilateral

level of consciousness, decreased

levitation

lid closure, weakness of

malformation, CNS, congenital

malignant hyperpyrexia

Man-In-The-Barrel syndrome

meconium staining

median neuropathy

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

Melkersson's syndrome

memory, impairment of

meningitis

meningitis, aseptic

mental retardation

mental status, abnormal

mitral valve prolapse

monoclonal gammopathy

MRI, contraindications

MRI, diffusion tensor

MRI, diffusion weighted

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle diseases, characteristics of

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

muscular dystrophy, LAMA2

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, treatment of

myopathy, centronuclear

myotonia dystrophica, classification

nasal speech

nausea and vomiting

neck weakness

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-infants

nerve conduction studies

nerve injury

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic examination, focal

neuromuscular junction

neuroophthalmology

neuropathology

neurosyphilis

newborn, evaluation of

obstetric neurologic injuries

ocular motility, disorders of

operculum syndrome, bilateral

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic nerve

optic nerve, lesion of

optic neuritis

optokinetic nystagmus, abnormal

orbicularis oculi muscle

pacemaker, cardiac-transvenous

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

paratrigeminal syndrome

pathology

peroneal nerve palsy

peroneal nerve, lesion of

personality change

photophobia

phrenic nerve

phrenic nerve pacemaker

phrenic nerve, injury of

pitfalls

placenta

placenta, infection of

pleocytosis of cerebrospinal fluid

polyinosinic cytidic acid(poly IC)

polymicrogyria

polymyositis

polymyositis, infantile

pons, hypoplasia

positive sharp waves

posterior spinal artery infarction

pregnancy, neurologic complications in

prenatal

prognosis

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary infiltrates

pulse oximeter

pupil, abnormality in neurologic disorders

pyramidal tract dysfunction

pyramidal tract, uncrossed

remote effect of cancer on the nervous system

renal artery stenosis

respiratory failure

retinopathy

review article

rheumatic heart disease

rigidity

risk factors

rubella encephalitis

rubella encephalitis, progressive

scoliosis, neurologic association with

scotoma

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, neonatal

seizure, psychomotor-temporal lobe

seizure, recurrent

sensory ganglia

sensory loss

sensory loss, cortical

septicemia

serologic testing

skin, lesions in neurologic disorders

spinal cord vasculature

spinal cord, enlargement

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, New Born

spinal cord, intramedullary cyst of

spinal cord, ischemic lesion of

spinal cord, neoplasm

spinal cord, neoplasm, infants and children

spinal cord, transection

spinal cord, vascular disorders Affecting

spinal muscular atrophy

spinal muscular atrophy, classification

spirochete infection

standing difficulty

stem cell transplantation

stent, carotid artery

steroid therapy, CNS treatment and complications with

stooped posture

strokelike episodes

subacute myelo-opticoneuropathy(S.M.O.N.)complex

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

subarachnoid hemorrhage

subtemporal decompression

symmetric brain lesions

syncope

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syringomyelia

talk

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tongue, fasciculations of

tongue, impaired movements of

TORCH infections

torticollis

torticollis, infants and children

toxic encephalopathy

toxoplasmosis, CNS

toxoplasmosis, congenital

transient ischemic attack

transient neurologic deficit

transluminal angioplasty, carotid artery

transplacental virus infections

transposition of the great vessels

transverse smile

trauma

treatment of neurologic disorder

tremor

trigeminal neuralgia

trinucleotide repeats

ulnar nerve

ulnar neuropathy

ultrasonography

ultrasonography, carotid artery

weakness, generalized

weakness, progressive

Wildervanck's syndrome

winging of scapula

workup

xerostomia

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EEG Recognition of Aicardi's Syndrome
Arch Neurol 34:563, Fariello,R.G.,et al, 1977

Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence
Arch Neurol 34:174, Okihiro,M.M.,et al, 1977

Herpes Simplex & the Human Nervous System
Milit Med 140:765, Finelli,P.F., 1975

Progressive Rubella Encephalitis
NEJM 292:990-993, 994-998, 1023-1024975., Townsend,J.J., 1975

Neurologic Manifestations of Bacterial Endocarditis
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Internal Carotid Aneurysm as a Cause of Raeder's Para-trigeminal Syndrome
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Intracranial Aneurysms Causing Ophthalmoplegia
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Sarcoidosis of the Pituitary Gland and Stalk in a Man Presenting Asthenia, Impotence, Loss of Libido, Polyuria, and Polydipsia
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Congenital and Acquired Chiari Syndrome
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Infective Endocarditis
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Photophobia as the Presenting Symptom of Internal Carotid Artery Dissection
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Neonatal Seizures
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Showing articles 50 to 100 of 2146 << Previous Next >>