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Differential
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abdominal distention

abducens nerve paralysis

abducens nerve paralysis, bilateral

acute intermittant porphyria

airway obstruction

alveolar hypoventilation

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, sensory symptoms in

anal wink response

anesthesia, general

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

arrhythmia, cardiac

arterial dissection

arterial dissection, bilateral

arterial dissection, carotid

ataxia, cerebellar

atrophy, muscle

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

axonal degeneration

Bickerstaff's brainstem encephalitis

bone marrow biopsy

botulism antitoxin

botulism, infant

brain biopsy, false negative

brainstem, hypoplasia

brainstem, ischemia

brainstem, lesion of

bulbar palsy, acute

bulbar palsy, juvenile

bulbar palsy, progressive

calcification, intracranial

campylobacter infection

carcinoembryonic antigen

carcinoembryonic antigen, cerebrospinal fluid

carcinoma of lung

CAT scan, abnormal

cauda equina, enhancement

central nervous system, infection of

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

chest x-ray, abnormal

cholesterol, HDL

choreoathetosis

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

conduction block

congenital bilateral perisylvian syndrome

congenital heart disease

congenital malformation

congenital myopathy

congestive heart failure

corneal dystrophy

corneal reflex, abnormal

corneal reflex, absent

corneal transplant

corpus callosum

corpus callosum, thinning

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, recurrent

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

crying, pathologic

deafness, bilateral

deafness, unilateral

delay in diagnosis

denervation of muscle

denervation potentials

descending paralysis

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus, chemical

differential diagnosis

difficulty climbing stairs

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, brachial

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dyskinesia, buccal lingual facial

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram, decremental response

emotional lability

encephalitis, brainstem

epidemiology of neurology

erythema migrans

face, inexpressive

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, congenital

facial nerve palsy, recurrent

facial swelling

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

Fisher's syndrome

flaccid paralysis

fontanel, bulging

fourth ventricle, floor

F-wave response

gag reflex, depressed

gastrointestinal perforation

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, neuropathology of inflammatory lesion of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

hallucination, auditory

head circumference

hearing loss, unilateral

herpes simplex encephalitis

high arched feet

high arched palate

hydrocephalus, communicating

hypoglycorrhachia

hypokalemic periodic paralysis

hypoosmolality of serum

hypotonia, infants

IgG4-related disease

ileus, paralytic

immunofluorescence

immunohistochemistry

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

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

intellectual deficit

intracranial hypertension, benign

intracranial pressure, increased

intrinsic hand muscles, wasting of

language disorders in children

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

level of consciousness, decreased

lid closure, weakness of

life expectancy

lumbosacral radiculopathy

lymphadenopathy

lymphocytic meningoradiculitis

lymphoma involving CNS

malformation, CNS, congenital

maple syrup urine disease

masseter muscle wasting

meningeal biopsy

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

meningitis, lymphomatous

meningitis, monocytic

meningitis, plasma cell

mental retardation

Moebius syndrome

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

motor neuron disease

MRI, contrast enhanced

MRI, cranial nerves

MRI, spinal cord

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, infantile and juvenile

myeloradiculopathy

myopathy, mitochondrial

myotonia congenita

myotonia dystrophica

nausea and vomiting

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

nerve root enhancement

neurogenic vs.myopathic atrophy

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neurological intensive care

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronopathy, sensory and motor

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

ocular myopathy

operculum syndrome

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, neonatal

ophthalmoplegia, total

optic neuropathy

optic neuropathy, bilateral

oral contraceptives

pain, abdominal

palate, paralysis

paralysis, acute

paralysis, acute areflexic

paraparesis, spastic

paresthesias, feet

percussion induced muscle contraction

periodic paralysis

perioral numbness

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, lymphomatous

polyradiculoneuropathy

pregnancy, neurologic complications in

primary CNS histiocytic sarcoma

primary lateral sclerosis

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, light reflex, abnormal

pyramidal tract dysfunction

quadriparesis, progressive

rabies, nervous system involvement with

renal failure, acute

repetitive nerve stimulation

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

root lesion, nerve

sarcoidosis, CNS

scoliosis, neurologic association with

sedimentation rate, elevated

seizure, recurrent

sensorineural hearing loss

sensory loss, truncal

sensory symptoms

serologic testing

shoulder, numbness

shoulder-girdle wasting

skin, lesions in neurologic disorders

slit lamp examination

sloped shoulders

speech disorder

speech, loss of

spinal muscular atrophy

spinal muscular atrophy, classification

spontaneous muscle activity

steroid therapy, CNS treatment and complications with

symmetric brain lesions

Tangier's disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

third nerve palsy

thrombocytopenia

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

transient neurologic deficit

transposition of the great vessels

transverse smile

treatment of neurologic disorder

tremor, intention

trigeminal nerve, abnormality of

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

unconsciousness

urine osmolality, elevated

viral infection

viral infection, CNS

viral isolation

vocal cord paralysis

Waldenstrom's macroglobulinemia

walking, difficulty with

Watson-Schwartz reaction

weakness, generalized

weakness, progressive

whistle, inability to

winging of scapula

Showing articles 0 to 50 of 642 Next >>

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

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

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

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

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Bilateral Facial Diplegia:A Rare Presenting Symptom of Lyme
Case Reports Infect Dis doi.10.1155/2017/4521526, Ashurst,J. & Perry,M., 2017

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

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

Juvenile Myasthenia Gravis: Recommendations for Diagnostic Approaches and Treatment
Neuropediatrics 45:75-83, Marina, A.D.,et al, 2014

Woke Up Paralysed--Without Injury or Stroke
Lancet 371:870, Bawaskar,H.S. &Bawaskar,P.H., 2008

Acute Facial Diplegia and Hyperreflexia
Neurol 62:825-827, Susuki,K.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

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

Acute Renal Failure with Neurological Involvement in Adults Associated with Measles Virus Isolation
Lancet 354:992-995, Wairagkar,N.S.,et al, 1999

Facial Diplegia Complicating a Bilateral Internal Carotid Artery Dissection
Stroke 30:681-686, Gout,O.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Adult-Onset "Infant" Botulism:An Unusual Cause of Weakness in the Intensive Care Unit
Neurol 53:891, Li,L.Y.J.,et al, 1999

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Anterior Opercular Syndrome, Caused by Herpes Simplex Encephalitis
Neurol 49:494-497, McGrath,M.N.,et al, 1997

Magnetic Resonance Imaging in a Patient with Segmental Zoster Paresis
Neurol 49:631-632, Hanakawa,T.,et al, 1997

Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
Muscle & Nerve 20:347-351997., Pringle,C.E.,et al, 1997

Clinicopath Conf
Botulism, Case 22-1997, NEJM 337:184-190997., , 1997

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Idiopathic Intracranial Hypertension and Facial Diplegia
Neurol 44:357, Selky,A.K.,et al, 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

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

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Moebius Sequence and Prenatal Brainstem Ischemia
Pediatrics 84:570-573, Govaert,P.,et al, 1989

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Clinicopath Conf
Lymphoma, Large-Cell (B type) of CNS, (Temporal & Frontal Lobes, Br Stem, Sp Cord, Meninges, & Nr Ro, t) , Case RecM 319:426-436,1988., 1988

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

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

Clinicopath Conference
Adenocarcinoma of Lung, with Metastases to Leptomeninges, Medulla Oblongata, Spinal Cord, & Liver, C, se 32-JM 317:366-375,1987., 1987

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

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

Facioscapulohumeral Dystrophy Presenting in Infancy with Facial Diplegia & Sensorineural Deafness
Ann Neurol 17:513-516, Korf,B.R.,et al, 1985

Polyneuritis Cranialis Associated with Borrelia Burgdorferi
JNNP 48:1182-1184, Schmutzhard,E.,et al, 1985

Clin. Path. Conference
Lyme Disease, with Meningo-polyneuritis (Bannwarth's Syndrome) , Case Record 29-1984, NEJM 311:172-1, 1, 198, 1984

Benign Intracranial Hypertension & Facial Diplegia
Arch Neurol 41:787-788, Kiwak,K.J.,et al, 1984

Juvenile Progressive Bulbar Palsy
Arch Neurol 40:351-353, Albers,J.W.,et al, 1983

Demyelinating Neuropathy Accompanying Lyme Disease
Neurol 32:1302-1305, Sterman,A.B.,et al, 1982

Clin. Path. Conference
Type B Botulism, Unclassified Form, Case Record 48-1980, NEJM 303:1347-135580., , 1980

Ophthalmoplegia & Bulbar Palsy in Variant Form of Maple Syrup Urine Disease
Ann Neurol 6:71-72, Chhabria,S.,et al, 1979

Showing articles 0 to 50 of 642 Next >>