Neudle.com: speech absence of

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

ataxia telangiectasia

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

chromosomal abnormality

chromosome 9

Clinical Pathologic Conference(C.P.C.)

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

dopa responsive dystonia

dysarthria

dysdiadochokinesia

dyskinesia, buccal lingual facial

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

Friedreich's ataxia, late onset

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

immunoelectrophoresis, serum

incoordination

intellectual deficit

L-dopa

leg weakness, bilateral

leg weakness, unilateral

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

misdiagnosis

mitochondrial disease

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

next-generation sequencing

numbness, ascending

numbness, extremity

nystagmus

nystagmus, gaze-evoked

nystagmus, vertical

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

paralysis, acute areflexic

parenteral alimentation

paresthesias

Parkinson disease

Parkinsonism syndrome

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

sensory nerve action potentials

short stature

single photon emission computed tomography

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

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

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 350 to 400 of 845 << Previous Next >>

Botulinum Toxin as a Biological Weapon
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Confusion After Antibiotics
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Dysarthria in Acute Ischemic Stroke
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MR Brain Imaging of Fucosidosis Type I
AJNR 22:777-780, Galluzzi,P.,et al, 2001

Postictal Language Dysfunction in Complex Partial Seizures: Effect of Contralateral Ictal Spread
Neurol 56:1590-1592, Ficker,D.M.,et al, 2001

Diffusion-Weighted Magnetic Resonance Imaging in Nonconvulsive Status Epilepticus
Arch Neurol 58:993-998, Chu,K.,et al, 2001

Nonpoliovirus Poliomyelitis Simulating Guillain-Barre Syndrome
Arch Neurol 58:1460-1464, Gorson,K.C.&Ropper,A.H., 2001

Continuous EEG Monitoring and Midazolam Infusion for Refractory Nonconvulsive Status Epilepticus
Neurol 57:1036-1042, Claasen,J.,et al, 2001

Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
JAMA 286:2437-2440, Becher,M.W.,et al, 2001

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Clinical Features of Nipah Virus Encephalitis Among Pig Farmers in Malaysia
NEJM 342:1229-1235, Goh,K.J.,et al, 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Echolalia-Palilalia as the Sole Manifestation of Nonconvulsive Status Epilepticus
Neurol 55:733-734, Linetsky,E. et al, 2000

Holmes-Adie Syndrome
Lancet 356:1760-1761, Martinelli,P., 2000

Prevalence of Nonconvulsive Status Epilepticus in Comatose Patients
Neurol 54:340-345, Towne,A.R.,et al, 2000

Language Disturbances in Corticobasal Degeneration
Neurol 54:990-992, Frattali,C.M.,et al, 2000

Nitrous Oxide Anesthesia-Associated Myelopathy
ArchNeurol 57:380-382, Marie,R.,et al, 2000

Thrombotic Thrombocytopenic Purpura Associated with Clopidogrel
NEJM 342:1773-1777,1824, Bennett,C.L.,et al, 2000

Status Epilepticus Associated with Cefepime
Neurol 54:2153-2155, Dixit,S.,et al, 2000

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Treatment of Absence Status with Intravenous Valproate
Neurol 52:889-890, Alehan,F.K.,et al, 1999

MRI Abnormalities Associated with Partial Status Epilepticus
Neurol 52:1021-1027, Lansberg,M.G.,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

Bilateral Thalamic Stimulation for the Treatment of Essential Tremor
Neurol 53:1447-1450, Pahwa,R.,et al, 1999

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

Unilateral Pallidotomy for Parkinson's Disease:Results after More Than 1 Year
JNNP 67:511-517, Schrag,A.,et al, 1999

Bilteral Caudate Infarct--A Case Report
Ann Acad Med Singapore 28:569-571, Lim,J.K.H., 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

MRI Abnormalities Associated with Partial Status Epilepticus
Neurol 52:1021-1027, Lansberg, M.G.,et al, 1999

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Secondary Hyperkalaemic Paralysis
JNNP 64:249-252, Evers,S.,et al, 1998

Do Nonconvulsive Seizures Damage the Brain? Yes
Arch Neurol 55:117-120, Young,G.C.&Jordan,K.G., 1998

Do Nonconvulsive Seizures Damage the Brain? No
Arch Neurol 55:119-120, Aminoff,M.J., 1998

Infarction in the Territory of the Anterior Cerebral Artery
Neurol 51:620-622, Klatka,L.A.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Guillain-Barre Syndrome
Lancet 352:635-641, Hahn,A.F., 1998

Effects of Resective Surgery for Left-Sided Intracranial Tumors on Language Function:A Prospective Study
Lancet 351:1014-1018, Whittle,I.R.,et al, 1998

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

Clinicopath Conf
Demyelinating Process Consistent with Multiple Sclerosis, Case 26-1998, NEJM 339:542-549998., , 1998

Clinicopath Conf
Wegener's Granulomatosis Involving Sinuses, Skull, and Cranial Nerves, Case 28-1998, NEJM 339:755-76, , 199, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Treatment of Aphasia
Arch Neurol 55:1417-1419, Albert,M. L., 1998

Pregnant,Vomiting,and Going Blind
Lancet 352:1594, Tesfaye,S.,et al, 1998

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Showing articles 350 to 400 of 845 << Previous Next >>