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accomodation, abnormal

advances in neurology

adverse drug reaction

alcohol intolerance

alternating rapid movement

alternating rapid movement, impaired

anesthesia, general

anterior tibial muscle weakness

anti Yo antibody

antiviral agents

arrhythmia, cardiac

arthrogryposis multiplex

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

atrial fibrillation

atrial paralysis

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

biopterin deficiency

blinking, reduced

bone marrow transplantation

brainstem, atrophy

Brown-Vialetto-Van Laere syndrome

burning paresthesia

calcification, intracranial

calf hypertrophy

carcinoma of breast

cardiovascular disease

carpal tunnel syndrome

CAT scan, abnormal

central core disease

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, carotid origin

cerebrospinal fluid, abnormal

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, young adult

cervical spine abnormality

Charcot-Marie-Tooth

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

cognition, slowed

cogwheel rigidty

congenital infection, CNS

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contractures, joint

contrast agents, neurotoxicity of

convergence, impaired

cornea, opacity of

corpus callosum, lesion of

cranial neuropathy

cranial neuropathy, multiple

crawl regression

C-reactive protein, elevated

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cytomegalovirus infection

cytomegalovirus infection, congenital

decision analysis

deep gray nuclei

dementia, familial

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability rating scale, neurological

disability, neurological

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

drug induced neurologic disorders

dysdiadochokinesia

dysostosis multiplex

dystonia, children

dystonia, treatment of

dystrophic calcification

electrocardiogram, abnormal

Emery-Dreifuss muscular dystrophy

encephalopathy, progressive

entrapment neuropathy

enzyme, muscle disease

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

epileptic encephalopathy

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

FARS2 deficiency

feeding disorder

fetal movements, reduced

fine motor function, impaired

finger nose finger test

gait, festinating

gamma amino butyric acid

genetic counselling

genetic neurologic disorders

genetic testing

glutamic acid decarboxylase, antibody

Gowers maneuver

growth retardation

Guillain Barre syndrome

heart block, complete

heel-knee-shin test

hepatosplenomegaly

high arched feet

histochemistry of muscle

hot cross bun sign

hyperpigmentation of skin

hypoparathyroidism

hypotonia, infants

iatrogenic neurologic disorders

immunohistochemistry

immunosuppressive agents

implantable cardioverter defibrillator

inclusion body myositis

infection, recurrent

inferior calcaneal neuropathy

influenza A virus

influenza B virus

injection neuropathy

intellectual deficit

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

joint hypermobility

kinesia paradoxica

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lateral cutaneous nerve of forearm

lid closure, weakness of

life expectancy

liver function enzymes

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lysosomal storage disease

malignant hyperpyrexia

marche a petits pas

median neuropathy

memory, impairment of

meningitis, CSF cell count-normal

mental retardation

midbrain, atrophy

mitochondrial disease

mitral valve prolapse

molecular genetics

monoclonal antibodies

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, complications with

MRI, contraindications

MRI, contrast enhanced

MRI, diffusion weighted

MRI, punctate pattern

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle stiffness

muscle strength, testing

muscle tenderness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenic syndrome

myocardial biopsy

myopathy, centronuclear

myopathy, distal

myopathy, distal, vacuolar

myopathy, hypocalcemic

myopathy, mitochondrial

myopathy, quadriceps

myopathy, vacuolar

myositis, acute of childhood

myositis, post infectious

myotonia dystrophica

myotonic discharges

nausea and vomiting

nemaline rod myopathy

nephrogenic systemic fibrosis

nerve conduction studies

nerve enlargement

nerve hypertrophy

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, peripheral

neuropathy, sensory

optic neuropathy

orange peel appearance of skin

overlap syndrome

pacemaker, cardiac-transvenous

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinsonism syndrome

periventricular leukomalacia

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymyalgia rheumatica

polyneuropathy, chronic inflammatory demyelinating

positional head-hanging test

positive sharp waves

practice guidelines

premature infant

prenatal diagnosis by amniocentesis

progressive neurologic disorder

prolactin, elevated

proximal muscle atrophy

pseudohypertrophy

psychomotor retardation

pulmonary infiltrates

pursuit eye movements, abnormal

pyramidal tract dysfunction

reading disorder, acquired

real-time quaking-induced conversion

reflex sympathetic dystrophy

remote effect of cancer on the nervous system

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

riboflavin transporter deficiency

rigid spine syndrome

rippling muscle disease

saccadic eye movements, abnormal

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorineural hearing loss

shoulder, pain in

skin, lesions in neurologic disorders

skin, thickened

sloped shoulders

spastic diplegia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 7

sports medicine, neurology of

startle myoclonus

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

systemic illness

systemic juvenile idiopathic arthritis

tandem gait, ataxic

toxic oil syndrome

transverse smile

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, resting

trinucleotide repeats

type 1 muscle fiber

type 2 muscle fiber

tyrosine hydroxylase deficiency

upgaze, paralysis of

urea-cycle enzymopathies

vibratory sensation

vibratory sensation, abnormal

viral infection

visual acuity, decreased

voice, abnormality of

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

weakness, congenital

weakness, generalized

weakness, progressive

whistle, inability to

white matter disease

wide based gait

winging of scapula

x-ray, cervical spine

Showing articles 0 to 50 of 60 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Skin Lesions, Foot Drop, and Hand Contractures
JAMA doi:10.1001/JAMA.2023.9915, Filley,A.R.,et al, 2023

Polymyalgia Rheumatica
Lancet 402:1459-1472, Espigol-Frigole,G.,et al, 2023

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

Gadolinium-Based MR Contrast Agents and Nephrogenic Systemic Fibrosis
Radiology 242:647-649, Kuo,P.H.,et al, 2007

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Isolated Inferior Calcaneal Neuropathy
Muscle & Nerve 19:106-108996., Park,T.A.&DelToro,D.R., 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
Neurol 44:962-964, Horowitz,S.H., 1994

Tibial Muscular Dystrophy
Arch Neurol 50:604-608, Udd,B.,et al, 1993

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Showing articles 0 to 50 of 60 Next >>