Neudle.com: "facial nerve palsy congenital"

Differential
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abducens nerve paralysis

abscess, intracerebral

acute necrotizing encephalitis

agenesis of corpus callosum

Aicardi's syndrome

airway obstruction

alien hand syndrome

altered states of consciousness

aneurysm

aneurysm, berry

aneurysm, cavernous sinus

aneurysm, infraclinoid

aneurysm, intracranial

aneurysm, posterior communicating artery

aneurysm, supraclinoid

aneurysm, vertebral basilar system

angiography, cerebral

anterior horn cell disease

anterior tibial muscle weakness

antiviral agents

aphasia

apraxia

apraxia of eye movements

areflexia

arrhythmia, cardiac

arthritis

arthrogryposis multiplex

brainstem, hypoplasia

brainstem, infarction of

burst suppression pattern, electroencephalogram

calcification, intracranial

cataracts, congenital

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar pontine angle tumor

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, cytology

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, prevention of

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

chronic progressive external ophthalmoplegia

cleft palate

clubfoot as related to neurologic disease

Coats syndrome

coloboma

congenital bilateral perisylvian syndrome

congenital heart disease

congenital infection, CNS

congenital malformation

congenital malformation, non CNS

congenital myasthenic syndromes

congenital myopathy

conjunctival injection

conjunctivitis

consanguinity

contractures, joint

convergence, impaired

conversion reaction

corneal reflex, abnormal

corpus callosum

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial nerve palsies

cyst, porencephalic

cytomegalic inclusion disease

delivery, complicated

dementia

depression

depression, psychotic

developmental abnormality of brain

developmental retardation

differential diagnosis

diplopia

dislocated hip, congenital

drooling

dropped head syndrome

Duane syndrome

dysarthria

dyskinesia, buccal lingual facial

dyslexia

dysphagia

dystonia

ectatic basilar artery

edema, periorbital

Ehlers-Danlos syndrome

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, brainstem

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

episodic disorders

episodic neurologic deficits

erythema migrans

exome sequencing

exophthalmus

exophthalmus, bilateral

exophthalmus, pulsatile

exophthalmus, unilateral

eye closure

eye movement, disorders of

facial appearance, abnormal

facial asymmetry

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

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fluorescent treponema antibody absorption(FTA-ABS)

fluorescent treponema antibody absorption/false positive

foot drop

forceps delivery

fourth ventricle, floor

frontal balding

fundus, abnormality of

gag reflex, depressed

gait disorder

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gene mutation

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

Guillain Barre syndrome

hallucination

hallucination, visual

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, 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

Hirschprung's disease

histochemistry of muscle

immunofluorescent exam of CSF cells

immunohistochemistry

immunosuppression

inclusion bodies, intranuclear

infantile spasm

infectious mononucleosis

internuclear ophthalmoplegia

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

iododeoxyuridine

jaw pain

Kearns-Sayre syndrome

klippel feil syndrome

kyphoscoliosis, neurologic causes of

language disorders in children

level of consciousness, decreased

levitation

lid abnormalities

lid closure, weakness of

limbic encephalitis

limbic system

Lyme disease

malformation, CNS, congenital

malignant hyperpyrexia

median neuropathy

Melkersson's syndrome

meningitis

meningitis, aseptic

mental retardation

mental status, abnormal

mitral valve prolapse

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myotonia dystrophica, classification

nasal speech

nausea and vomiting

neck weakness

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

nerve conduction studies

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic examination, focal

neuromuscular junction

ocular motility, disorders of

ocular myopathy

opened mouth

operculum syndrome

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic atrophy

optic nerve

optic nerve, lesion of

optic neuritis

orbicularis oculi muscle

pacemaker, cardiac-transvenous

peroneal nerve, lesion of

personality change

photophobia

pleocytosis of cerebrospinal fluid

polyinosinic cytidic acid(poly IC)

polymicrogyria

pons, infarction of

pregnancy, neurologic complications in

prognosis

progressive neurologic disorder

proptosis

proptosis, bilateral

proptosis, unilateral

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

rash

reading problem, causes of

remote effect of cancer on the nervous system

respiratory failure

review article

rheumatic heart disease

scoliosis, neurologic association with

scotoma

screening

sedimentation rate, elevated

seizure

seizure, neonatal

seizure, psychomotor-temporal lobe

seizure, recurrent

sensory loss

sensory loss, cortical

septicemia

serologic testing

skin, lesions in neurologic disorders

spinal muscular atrophy

spinal muscular atrophy, classification

spirochete infection

steroid therapy, CNS treatment and complications with

strokelike episodes

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

subarachnoid hemorrhage

subtemporal decompression

symmetric brain lesions

syringomyelia

talk

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

term infant

third nerve palsy

tinnitus

tongue, fasciculations of

tongue, impaired movements of

toxic encephalopathy

transient ischemic attack

transient neurologic deficit

transplacental virus infections

transposition of the great vessels

transverse smile

trauma

treatment of neurologic disorder

tremor

trigeminal neuralgia

trinucleotide repeats

ulnar nerve

ulnar neuropathy

vertebral-basilar insufficiency

viral infection, CNS

vision, blurred

visual acuity, decreased, monocular

visual loss

visual loss, sudden-unilateral

weakness

weakness, fatiguable

weakness, progressive

weakness, proximal

Wildervanck's syndrome

winging of scapula

xerophthalmia

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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

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

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

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

Performance of Bedside Stroke Recognition Tools in Discrimination Childhood Stroke from Mimics
Neurol 86:2154-2161, Mackay, M.T.,et al, 2016

Stroke and NonStroke Brain Attacks in Children
Neurol 82:1434-1440, Mackay, M.T.,et al, 2014

Ophthalmologic Features of Parkinson's Disease
Neurol 62:177-180, Biousse,V.,et al, 2004

MRI Findings in Mobius Syndrome: Correlation with Clinical Features
Neurol 55:1058-1060, Pedraza,S.,et al, 2000

Congenital Unilateral Facial Paralysis
Pediatrics 97:261-265, Shapiro,N.L.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Mobius Syndrome and Transposition of the Great Vessels
Neurol 38:1894-1895, Raroque,H.G.,et al, 1988

Lyme Disease, A Neuro-Ophthalmologic View
J Clin Neuro-ophthalmol 7:185-190, MacDonald,A.B., 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Dolichoectatic Basilar Artery:A Review of 23 Cases
Stroke 17:1277-1281, Nishizaki,T.,et al, 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Abnormalities of Eyelid Closure
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, 2:967, Miller,M.R., 1985

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

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

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

Neurologic Manifestations of Bacterial Endocarditis
Ann Int Med 71:21, Jones,H.,et al, 1969

The Carotid-Cavernous Fistula:Spontaneous & Traumatic, In Clinical Neuro-Ophthalmology
3rd Ed, Williams & Wilkins, Baltimore, p. 1714, Walsh,F.B.&Hoyt,W.F., 1969

Intracranial Aneurysms Causing Ophthalmoplegia
Arch Ophthal 70:75l, Cogan,D.,et al, 1963

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

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,et al, 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

Clinicopathological Conference, Systemic Lupus Erythematosus with Antiphospholipid Syndrome
NEJM 386:1560-1570, Case 12-2022, 2022

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 64-Year-Old Man with Multiple Cranial Neuropathies
Neurol 97:e215-e221, Lefland, A.,et al, 2021

A 47-Year-Old With Headache, Vertigo, and Double Vision
Neurol 97:e535-e539, Frey, J.,et al, 2021

A 42-Year-Old Woman with Mysterious Monocytic Meningitis
Neurol 97:449-454, Nothem, M.E., et al, 2021

The Tolosa-Hunt Syndrome
NJJP 71:577-582, Kline,L.B. & Hoyt,W.F., 2021

Cranial Nerve Disorders Associated with Immune Checkpoint Inhibitors
Neurol 96:e866-e875, Vogrig, A.,et al, 2021

Facial Nerve Palsy in COVID-19 Infection
Neurol 95:364-367, Goh, Y.,et al, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,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

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Facial Nerve Marginal Mandibular Branch Lesion
Neurol 94:e2069-e2071, Fleuren, K. & Staals, J., 2020

Showing articles 0 to 50 of 5680 Next >>