Neudle.com: progressive spinal muscular atrophy

Differential
(Click to cross reference)

acid maltase deficiency

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

alcoholic polyneuropathy

algorithm

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidurias

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, cluster

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, conjugal

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

analgesic

anatomy of

aneurysm, cavernous sinus

aneurysm, internal carotid artery

animal exposure

ankylosing spondylitis

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti Hu antibody

antibodies to voltage-gated calcium channels

apraxia of eye movements

arthrogryposis multiplex

aspiration

asymptomatic

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, truncal

ataxic gait

atlanto axial dislocation, congenital

autoantibodies

autoimmune disease

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

Bence Jones protein

benign congenital hypotonia

botulinum toxin, complications of

brachial neuritis

brain atrophy

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

C0ORF72

cachexia

CAG repeats

calcium channel dysfunction

calf hypertrophy

camptocormia

carbon monoxide poisoning

carcinoembryonic antigen

CAT scan, emission, abnormal

cataracts

cavernous sinus, syndrome

CD4 counts

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, young adult

cervical collar

cervical osteoarthritis

cervical osteophyte

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

chest x-ray, abnormal

chromosomal abnormality

chromosome 11

chromosome 5

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

concussion

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

constipation

controversies in neurology

coxsackievirus, myopathy with

CPAP

creatine phosphokinase(CPK)elevated

crying, pathologic

cycad seed flour

cyclosporine

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

depression

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diet

differential diagnosis

difficulty climbing stairs

diplegia, atonic

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dopamine

drooling

dropped head syndrome

electrical injury of nervous system

electrical sensation

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

encephalocele

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

ethics in neurology

euthanasia

evidence-based research

eye movement, disorders of

facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

football neurologic injuries

fragile-X syndrome

free radical

Friedreich's ataxia

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gag reflex, depressed

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gangliosides

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

GM1 ganglioside antibodies

growth retardation

guanidine

Guillain Barre syndrome

heavy metal intoxication

hemangioma

hemiparesis

hemiplegia

hemiplegia, progressive

heralding manifestation

herniated disc

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes zoster

highly active antiretroviral therapy

Hodgkin's disease, neurologic involvement with

hospice

human immunodeficiency virus type 1

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunologic disease

immunosuppression

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, ubiquitin

inclusion body myositis

infant, evaluation of

infantile tremor syndrome

insomnia

intellectual deficit

intermittent positive pressure breathing

internal capsule

internet

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

iron, brain

Isaacs syndrome

Jackson's syndrome

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

laminectomy, cervical

laughing, pathologic

lead and the nervous system

Leber's hereditary optic neuropathy

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukemia

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

lymphoma involving CNS

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

masseter muscle weakness

median neuropathy

medical-legal aspects of neurology

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mobility

mobility aids

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuropathy

mononeuropathy, motor

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, paramagnetic effect

MRI, spinal cord

MRI, spine

MRI, susceptibility weighted

MRS

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, treatment of

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, quadriceps

myopathy, thyroid disease causing

myositis

myotonia congenita

myotonia dystrophica

N-acetyl-L-aspartic acid

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic evaluation

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal migration disorder

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, bicycle

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuroprotective agents

newborn, evaluation of

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

opiate

Oppenheim muscular dystrophy

optic neuropathy

orthopnea

osteomalacia

owl's eye sign of spinal cord

pain, management of chronic

paraparesis, familial spastic

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

pathology

patient information and support

penicillamine

periodic paralysis

periodic paralysis, thyrotoxic

persistent vegetative state

personality change

phrenic nerve

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

Pick's disease

pigmentary retinopathy

placebo

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

porphyria

positive sharp waves

post polio syndrome

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

practice guidelines

preclinical

pregnancy, neurologic complications in

pressure sores

prevention of neurologic disorders

primary lateral sclerosis

progeria

prognosis

progranulin

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

radiation therapy, salivary gland

radiculopathy

ragged-red fibers

release phenomena

remote effect of cancer on the nervous system

renal stones

repetitive nerve stimulation

respirator

respiratory depression

respiratory failure

retinopathy

retrovirus

reverse split hand sign

risk-benefit assessment

safety

salivation, excessive

sarcoidosis

scoliosis

scoliosis, neurologic association with

seizure, treatment of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

serum alanine aminotransferase

short stature

shoulder, subluxation

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

smell

Smell Identification Test

SMN1 gene

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar degeneration

spirometry

spondylosis

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

sternocleidomastoid muscle

stiff legs

stiff man syndrome

strangulation

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

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

subarachnoid hemorrhage

survival motor neuron gene

temporal lobe, atrophy

temporalis muscle wasting

tensilon test

tensilon test, false positive

term infant

testicular atrophy

thoracic outlet syndromes

thrombophlebitis

thyrotropin-releasing hormone

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

treatment of neurologic disorder

tremor

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trinucleotide repeats

ulnar nerve, deep palmar branch of

venous thrombosis, non-cerebral

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

web sites

Weber's syndrome

weight loss

Werdnig-Hoffman disease

West disease

wheelchair

whistle, inability to

white matter disease

winging of scapula

workup

X-linked bulbospinal neuronopathy

Showing articles 950 to 1000 of 7323 << Previous Next >>

Candidal Meningitis in HIV-Infected Patients: Analysis of 14 Cases
Clin Inf Dis 25:473-476, Casado, J.L.,et al, 1997

MR Imaging of the Meninges, Part II, Neoplastic Disease
Radiology 201:605-612, Fukui,M.B.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Clinicopath Conf
Noncaseating Granulomas Consistent with Sarcoidosis, Case 37-1996, NEJM 335:1668-1674996., , 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
NEJM 335:924-930, 9631996., Hsich,G.,et al, 1996

Diagnosis of Creutzfeldt-Jakob Disease in Two-Dimensional Gel Electrophoresis of Cerebrospinal Fluid
Lancet 348:846-849, Zerr,I.,et al, 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies
JAMA 275:1335-1338, Politano,L.,et al, 1996

Tuberculous Meningitis Among Adults with and without HIV Infection
Arch Int med 156:1710-1716, Yechoor,V.K.,et al, 1996

Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
ARch Neurol 53:814-818, Duffey,P.,et al, 1996

Prenatal Diagnosis of Duchenne Muscular Dystrophy Using a Single Fetal Nucleated Erythrocyte in Maternal Blood
Neurol 46:1350-1353, Sekizawa,A.,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

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Acute Focal Neuropathy in Male Weight Lifters
Muscle & Nerve 19:897-899996., Bird,S.J.&Brown,M.J., 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

Human T-Cell Lymphotropic Virus Type 1-Associated Myelopathy, Sjogren Syndrome, and Lymphocytic Pneumonitis
Arch Neurol 53:940-942, Kompoliti,A.,et al, 1996

Delayed Radiation-Induced Bulbar Palsy
Neurol 46:1604-1606, Shapiro,B.E.,et al, 1996

Lyme Neuroborreliosis Disguised as Normal Pressure Hydrocephalus
Neurol 46:1743-1745, Danek,A.,et al, 1996

Manganese Toxicity in Children Receiving Long-Term Parental Nutrition
Lancet 347:1218-1221, Fell,J.M.E.,et al, 1996

A 64-Year-Old Man with Diabetes and Ascending Paraplegia
Lancet 347:516, Gliemroth,J.,et al, 1996

Serial Gadolinium-Enhanced MRI of the Brain and Spinal Cord in Early Relapsing-Remitting MS
Neurol 46:373-378, Thorpe,J.W.,et al, 1996

Evolution of High-Intensity Basal Ganglia Lesions on T1-Weighted MR in Neurofibramotisis Type 1
AJNR 17:755-760, Terada,H.A.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

Cerebrovascular complic of Neurocysticercosis, Clin & Neuroimaging Spectrum
Arch Neurol 53:233-239, Cantu,C.&Barinagarrementeria,F., 1996

Idiop Hypertrophic Cranial Pachymeningitis Assoc with Hydrocep & Myocarditis:Steroid-Induced Remission
Neurol 46:554-556, Tanaka,M.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

Post-Traumatic Syringomyelia (Cystic Myelopathy) :A Prospective Study of 449 People with Spinal Cord Injury
JNNP 60:61-67, Schurch,B.,et al, 1996

Wilson Disease:Findings at MR Imaging and CT of the Brain with Clinical Correlation
Radiology 198:531-536, van Wassenaer-van Hall,H.N.,et al, 1996

Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
NEJM 333:832-838, 8711995., Mendell,J.R.,et al, 1995

Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Diagnostic Value of Detecting JC Virus DNA in Cerebropsinal Fluid of Patients with Progressive Multifocal Leukoencephalopathy
J Clin Microbiol 33:484-486, Fong,I.W.,et al, 1995

Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
Muscle & Nerve 18:283-291995., Nigro,G.,et al, 1995

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Neurofibromatosis Type 1:Pathologic Substrate of High-Signal-Intensity Foci in the Brain
Radiology 195:721-724, DiPaolo,D.P.,et al, 1995

Showing articles 950 to 1000 of 7323 << Previous Next >>