Neudle.com: chronic distal spinal muscular atrophy

Differential
(Click to cross reference)

acid maltase deficiency

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

advance directives

advances in neurology

adverse drug reaction

alcoholic polyneuropathy

algorithm

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

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

ankle edema

ankylosing spondylitis

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

antibodies to voltage-gated calcium channels

antiviral agents

anxiety

aphasia

aphasia, progressive, primary

aphonia

apnea

apraxia of eye movements

arthrogryposis multiplex

ascending paralysis

aspiration

asthma

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

atrioventricular block

autoantibodies

autoimmune disease

autonomic dysfunction

Babinski sign

basal ganglia, lesion of

behavioral disorder

Bence Jones protein

benign congenital hypotonia

botulinum toxin, complications of

botulism

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

C9orf72

cachexia

CAG repeats

calcium channel dysfunction

calf hypertrophy

camptocormia

cane

carbon monoxide poisoning

carcinoembryonic antigen

cardiovascular disease

CAT scan, emission, abnormal

cataracts

cavernous sinus, syndrome

CD4 counts

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

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

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

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

chewing, impaired

children

chills

Chinese paralytic syndrome

chorea

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chromosome 11

chromosome 5

chronic polyneuritis, children

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

concussion

conduction block

confusion

congenital heart disease

congenital myopathy

congestive heart failure

constipation

contractures, joint

controversies in neurology

coxsackievirus, myopathy with

CPAP

cranial neuropathy

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

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

diphtheria

diplegia, atonic

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dopamine

drooling

dropped head syndrome

dystrophic calcification

dystrophin

efficacy

electrical injury of nervous system

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

encephalitis

encephalitis, brainstem

encephalitis, paraneoplastic

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

ethics in neurology

euthanasia

evidence-based research

evoked potentials

excitotoxin

exercise intolerance

eye movement, disorders of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

fever

fibrillations

fine motor function, impaired

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

ganglionitis

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

Guillain Barre syndrome, differential diagnosis of

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

human T-lymphotropic virus type I(HTLV-I)

hypogammaglobulinemia

hypoglycemia

hypoglycemic coma

hypokalemia

hypokalemic alkalosis

hypoxic encephalopathy

iatrogenic neurologic disorders

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunosuppression

immunosuppressive agents

impotence

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, ubiquitin

inclusion body myositis

infant, evaluation of

infantile tremor syndrome

inflexibility, mental

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

jaw clonus

jaw closure weakness

jaw jerk, abnormal

klippel feil syndrome

Kugelberg-Welander syndrome

lactic acidemia

laminectomy, cervical

lathyrism

laughing, pathologic

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

masseter muscle weakness

median neuropathy

medical-legal aspects of neurology

meningitis

mental retardation

metabolic disorder, primary

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

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, 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 strength, testing

muscle tenderness

muscle twitching

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

mutism

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, treatment of

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

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, hormone producing

neoplasm, hormone producing, ectopic

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 vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal degeneration

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuroprotective agents

newborn, evaluation of

next-generation sequencing

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

orthopnea

osteomalacia

owl's eye sign of spinal cord

oxygen therapy

pain

pain, increased response

pain, management of chronic

palatal myoclonus

palliative care

paralysis, asymmetric

paraneoplastic ganglionopathy

paranoia

paraoxonase

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

pathology

patient information and support

penicillamine

periodic paralysis

periodic paralysis, thyrotoxic

peroxisomal disease

persistent vegetative state

personality change

pes cavus

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

Pick's disease

placebo

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis

polyclonal gammopathy

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

psychosis

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

radiation therapy, salivary gland

radiculopathy

release phenomena

remote effect of cancer on the nervous system

renal cell carcinoma

renal stones

repetitive nerve stimulation

respirator

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

scoliosis

scoliosis, neurologic association with

seizure, treatment of

sensory ganglia

sensory ganglia, abnormal

sensory symptoms

sensory testing

serologic testing

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

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, 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

stem cell transplantation

stereotyped behavior

sternocleidomastoid muscle

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

thalamus, lesion of

thoracic outlet syndromes

thrombophlebitis

thyrotropin-releasing hormone

tongue, fasciculations of

tongue, impaired movements of

treatment of neurologic disorder

tremor

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trigger finger

trinucleotide repeats

tripping

ubiquitin

ulnar nerve

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

valium

vasculopathy

venous thrombosis, non-cerebral

viral infection

viral infection, CNS

viral isolation

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 Nile fever

wheelchair

whistle, inability to

white matter disease

winging of scapula

word-finding difficulty

workup

xerostomia

X-linked bulbospinal neuronopathy

Showing articles 50 to 100 of 9067 << Previous Next >>

A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
Neurol 73:16-24,11, Wills,A.-M.,et al, 2009

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
Neurol 73:1218-1226, Miller,R.G.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

What Are the Prospects of Stem Cell Therapy for Neurology?
BMJ 337:1325-1327, Chandran,S., 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

Primary Lateral Sclerosis With HIV-1 Infection
Neurol 70:575-577, Verma,A. &Berger,J.R., 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Palliative Care for Patients With Amyotrophic Lateral Sclerosis
JAMA 298:207-216,248, Mitsumoto,H. &Rabkin,J.G., 2007

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

The Natural History of Primary Lateral Sclerosis
Neurol 66:647-653, Gordon,P.H.,et al, 2006

Hemiplegic ALS:Mills Syndrome
Neurol 64:1984-1985, Rajabally,Y.A.,et al, 2005

Clinicopath Conf,Encephalomyelitis Due to West Nile Virus and CLL, Case 22-2005
NEJM 353:287-295, Hollande,H.,et al, 2005

ALS Corticospinal Degeration on DWI
Neurol 62:1834, Cabello,J.P.,et al, 2004

Occurrence of Amyotrophic Lateral Sclerosis Among Gulf War Veterans
Neurol 61:742-749, Horner,R.D.,et al, 2003

Excess Incidence of ALS in Young Gulf War Veterans
Neurol 61:750-756, Haleyl,R.W., 2003

Prognosis in Amyotrophic Lateral Sclerosis
Neurol 60:813-819, del Aguila,M.A.,et al, 2003

Early or Late Appearance of "Dropped Head Syndrome" in Amyotropic Lateral Sclerosis
JNNP 74:683-686, Gourie-Devi,M.,et al, 2003

Kennedy Disease
Arch Neurol 60:893-894, Paparounas,K.,et al, 2003

ALS Patients on TPPV
Neurol 61:135-137, Hayashi,H. &Oppenheimer,E.A., 2003

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Early Symptom Progression Rate is Related to ALS Outcome
Neurol 59:99-103, Chio,A.,et al, 2002

Jaw Drop in Kennedy's Disease
Neurol 59:1471-1472, Sumner,C.J. &Fischbeck,K.H., 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Euthanasia and Physician-Assisted Suicide Among Patients with Amyotrophic Lateral Sclerosis in the Netherlands
NEJM 346:1638-1644, Veldink,J.H.,et al, 2002

Results of Radiotherapy for Drooling in Amyotrophic Lateral Sclerosis
Neurol 58:1308, Stalpers,L.J.A. &Moser,E.C., 2002

Mimic Syndromes in Sporadic Cases of Progressive Spinal Muscular Atrophy
Neurol 58:1593-1596, Visser,J.,et al, 2002

The Final Month of Life in Patients with ALS
Neurol 59:428-431, Ganzini,L.,et al, 2002

Reversible ALS-Like Disorder in HIV Infection
Neurol 57:995-1001,945, Moulignier,A.,et al, 2001

Hospitalization in Amyotrophic Lateral Sclerosis, Causes, Costs, and Outcomes
Neurol 56:753-757, Lechtzin,N.,et al, 2001

Amyotrophic Lateral Sclerosis
NEJM 344:1688-1700, Rowland,L.P. & Shneider,N.A., 2001

Inclusiong Body Myositis Mimicking Motor Neuron Disease
Arch Neurol 58:1253-1256, Dabby,R.,et al, 2001

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

The Split Hand in ALS has a Cortical Basis
J Neurol Sci 180:66-70, Weber,M.,et al, 2000

Disorders of Upper & Lower Motor Neurons
Neurol in Clin Practice, 3rd Ed., Butterworth, Boston: Ch. 78 p. 2007, Mitasumoto,H., 2000

Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
Arch Neurol 57:109-113, Traynor,B.J.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Injections of Botulinum Toxin A Into the Salivary Glands Improve Sialorrhoea in Amyotrophic Lateral Sclerosis
JNNP 69:121-123, Giess,R. et al, 2000

An Algorithm for ALS Diagnosis and Management
Neurol 53:S58-S62, Swash,M., 1999

Atypical Form of Amyotrophic Lateral Sclerosis
JNNP 66:581-585, Sasaki,S.&Iwata,M., 1999

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998

Showing articles 50 to 100 of 9067 << Previous Next >>