Neudle.com: distal spinal muscular atrophy

Differential
(Click to cross reference)

acid maltase deficiency

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

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

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

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

carcinoma

carcinoma of breast

cardiomyopathy

cardiovascular disease

CAT scan, emission, abnormal

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

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

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

concussion

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

constipation

contractures, joint

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

dystrophic calcification

dystrophin

efficacy

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

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

jaw clonus

jaw closure weakness

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

klippel feil syndrome

Kugelberg-Welander syndrome

laminectomy, cervical

laughing, pathologic

lead and the nervous system

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

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

meningitis

mental retardation

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

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, disappearing lesion on

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 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

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 vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

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

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

orthopnea

osteomalacia

owl's eye sign of spinal cord

oxygen therapy

pain

pain, elbow

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

placebo

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis-like illness

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

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

radiation therapy, salivary gland

radiculopathy

rash

release phenomena

remote effect of cancer on the nervous system

renal stones

repetitive nerve stimulation

respirator

respiratory depression

respiratory failure

retrovirus

reverse split hand sign

risk-benefit assessment

safety

salivation, excessive

sarcoidosis

scoliosis

scoliosis, neurologic association with

seizure, treatment of

sensory ganglia

sensory ganglia, abnormal

sensory symptoms

sensory testing

serologic testing

serum alanine aminotransferase

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, enlargement

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion 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

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

West Nile fever

wheelchair

whistle, inability to

white matter disease

winging of scapula

workup

X-linked bulbospinal neuronopathy

Showing articles 1000 to 1050 of 6886 << Previous Next >>

Longitudinally Extensive Spinal Cord Lesions in a Middle-Aged Man
Neurol 98:419-424, Xi, N. & Zhou, Y., 2022

Bilateral Trigeminal Neuralgia - A Condition of the Upper Neck
Head Pain Disorder, Jan, , 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Thalamus L-Sign: A Potential Biomarker of Neonatal Partial, Prolonged Hypoxic-Ischemic Brain Injury or Hypoglycemic Encephalopathy
AJNR 43:919-925, Misser, S.K.,et al, 2022

Durability of Clinical and Quality-of-Life Outcomes of Closed-Loop Spinal Cord Stimulation of Chronic Back and Leg Pain
JAMA Neurol 79:251-260, Mekhail, N.,et al, 2022

Stroke Prevention in Symptomatic Large Artery Intracranial Atherosclerosis Practice Advisory
Neurol 98:486-498, Turan, T.N.,et al, 2022

Toward Simpler, Safer Treatment of Cryptococcal Meningitis
NEJM 386:1179-1181, Moosa, M.Y.S. & Lessells, R.J., 2022

In Stroke, When is a Good Outcome Good Enough?
NEJM 386:1359-1361, Schwamm, L.H., 2022

Laboratory Diagnosis of Creutzfeldt-Jakob Disease
NEJM 386:1345-1350, Zerr, I., 2022

A 72-Year-Old Woman with Rapidly Progressive Bilateral Hearing Loss
Neurol 98:632-637, Alsalem, A.,et al, 2022

Reversal of Imaging Findings of Idiopathic Intracranial Hypertension after Lumbar Puncture
JAMA Neurol 79:416-417, Kapadia, A.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 73-Year-Old Woman with Episodic Dysarthria and Horizontal Binocular Diplopia
Neurol 98:767-772, Bower, A.S.,et al, 2022

A 64-Year-Old Man with History of Meningitis Presenting with Proximal Weakness of the Arms
Neurol 98:208-213, Karschnia, P.,et al, 2022

A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Glial Fibrillary Acidic Protein Autoimmunity
Neurol 98:e653-e668, Gravier-Dumonceau, A.,et al, 2022

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

Endovascular Therapy for Acute Stroke with a Large Ischemic Region
NEJM 386:doi.10.1056/NEJMoa2118191, Yoshimura, S.,et al, 2022

A Woman with Eosinophilic Brainstem Meningoencephalitis
JAMA Neurol 79:198-199, Fernandes Ferreira, L.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Severe High Cervical Cord Compression Due to Large Bilateral Neurofibromas in a Patient with Neurofibromatosis Type 1: A Case Report and Review of Literature
CUREUS doi:10.7759/CUREUS.27211, Sadeh,M. & Farhat, H., 2022

Mild Encephalitis/Encephalopathy with a Reversible Splenial Lesion Associated with Systemic Mycoplasma Pneumoniae Infection in North America: A Case Report
J Med Case Reports doi:10.1186/s13256-022-03299-6, Talukder,N.T.,et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Neurobrucellosis:The Great Mimicker
Rev Soc Bras Med Trop 55:e0567-e2012, Soares,C.N.,et al, 2022

Sweet Syndrome
Stat Pearls www.ncbi.nlm.gov, Sept, Goyal,V.P. & Holmes,H, 2022

Case 302:Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids
Radiology 303:726-730, Vattoth,S.,et al, 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Spontaneous Escherichia Coli Meningitis and Brain Abscess in an Immunocompetent Adult
Cureus doi.10.7759/CUREUS.208728, Jeter,K.et al, 2022

Saturday Night Myelopathy Flexion Myelopathy Related to Drug Intoxication
Neurologist 27:27-29, Martin, A.J.&Garcia,M.C., 2022

HSV-Encephalitis Resembling Acute Cerebral Infarction in a Patient with Atrial Fibrillation, Beware of Stroke Mimics
Neurologist 27:30-33, Kargiotis,O.,et cl, 2022

Acute Myelopathy in a Man with Cutaneous Papules
JAMA Neurol 79:84-85, Neo, S.,et al, 2022

Noncontrast Computed Tomography vs Computed Tomography Perfusion or Magnetic Resonance Imaging Selection in Late Presentation of Stroke with Large-Vessel Occlusion
JAMA Neurol 79:22-31, Nguyen, T.N.,et al, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Thrombectomy for Anterior Circulation Stroke Beyond 6 h from Time Last Known Well (AURORA): A Systematic Review and Individual Patient Data Meta-Analysis
Lancet 399:249-258, Jovin, T.G.,et al, 2022

Pontine Owl-Eyes Lesions in a Case of Neuroborreliosis
Neurol 98:e443-e444, Borgeaud, S.,et al, 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

Encephalopathies Associated with Severe COVID-19 Present Neurovascular Unit Alterations without Evidence for Strong Neuroinflammation
Neurol Neuroimmunol Neuroinflamm 8:e1029, Bernard-Valnet, R.,et al, 2021

Fluorosis
Neurol 97:e1973-e1974, Saluja, A.,et al, 2021

Automated Brain Perfusion Imaging in Acute Ischemic Stroke: Interpretation Pearls and Pitfalls
Stroke 52:3728-3738, Nicolas-Jilwan, M. & Wintermark, M., 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
AJNR 42:1942-1948, Morzage, M.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

Direct to Angiography Suite Without Stopping for Computed Tomography Imaging for Patients with Acute Stroke
JAMA Neurol 78:1099-1107, Requena, M.,et al, 2021

Lumbar Sediment Sign Seen in an Unusual Presentation of Meningitis
Lancet 398:1436, Hegde, A.,et al, 2021

An Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,et al, 2021

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,et al, 2021

Showing articles 1000 to 1050 of 6886 << Previous Next >>