Neudle.com: proximal muscle atrophy

Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

adverse drug reaction

alcohol

alcohol, heart involvement with

alcohol, neurologic complications with

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

anterior horn cell disease

anti signal recognition particle antibody

arthrogryposis multiplex

aspartate aminotransferase

atrioventricular block

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, children

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

calcification, intracranial

cardiovascular disease

carpal tunnel syndrome

case studies

CAT scan

CAT scan, abnormal

CAT scan, false negative

central core disease

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chewing, impaired

children

chromosomal abnormality

chromosome 5

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

cold temperature

coma

conduction block

congenital heart disease

congestive heart failure

consanguinity

contractures, joint

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

deafness

delay in diagnosis

dementia

dementia, frontotemporal

dermatomyositis

developmental milestones

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diarrhea

differential diagnosis

difficulty climbing stairs

diplopia

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dystrophic calcification

dystrophin

echocardiogram

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalomyelitis

encephalomyelitis, parainfectious

encephalopathy

encephalopathy, progressive

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

exercise

extraocular muscle lesion

facial weakness

facial weakness, bilateral

finger flexor weakness

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic neurologic disorders

genetic screening

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

gray matter

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

headache, worst of life

hearing loss

heart block

heart block, complete

heart murmur

hepatomegaly

heralding manifestation

hip flexor weakness

histochemistry of muscle

hoarseness

Hoesch test

human immunodeficiency virus type 1

immunosuppressive agents

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

leg atrophy

leg numbness

leg weakness, bilateral

leg weakness, unilateral

leukodystrophy

level of consciousness, decreased

lid closure, weakness of

life expectancy

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lymphadenopathy

lymphadenopathy, cervical

lysosomal storage disease

lysosomes, abnoral

malignant hyperpyrexia

McArdle's disease

medulla oblongata, lesion of

MELAS syndrome

meningeal enhancement

meningismus

meningoencephalomyelitis

mental retardation

mental status, abnormal

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

motor neuron disease, spontaneous recovery

MRI, spinal cord, increased intramedullary cord signal

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle pain

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenic crisis

mycoplasma

mycoplasma pneumoniae

myopathy, carcinomatous

myopathy, drug-induced

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, mitochondrial

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

neuritis, causes of

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neurotoxin

next-generation sequencing

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

osteomalacia

pacemaker, cardiac-transvenous

paraspinal muscle weakness

parathyroid adenoma

paresthesias

photophobia

plasma cell dyscrasia

plasmapheresis

pleocytosis of cerebrospinal fluid

poliomyelitis

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyradiculoneuropathy

Pompe's disease of glycogen storage

porphyria

positive sharp waves

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

rash

recurrent

renal stones

repetitive nerve stimulation

respiratory failure

respiratory tract infection

scoliosis, neurologic association with

screening

seizure

sensorineural hearing loss

sensory symptoms

serologic testing

short stature

shoulder, subluxation

SMN1 gene

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

standing difficulty

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

sudden death

survival motor neuron gene

systemic illness

tandem gait, ataxic

temporalis muscle wasting

toe walking

tongue, enlarged

tongue, fasciculations of

tongue, weakness

torticollis

toxins, nervous system

transverse smile

treatment of neurologic disorder

trinucleotide repeats

upgaze, paralysis of

upward deviation of eyes

urine, dark

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

wheelchair

white matter disease

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 350 to 400 of 4234 << Previous Next >>

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

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Distal Myasthenic Gravis
Neurol 52:632-634, Nations,S.P.,et al, 1999

Cervical Root Stimulation in a Case of Classic Neurogenic Thoracic Outlet Syndrome
Muscle & Nerve 22:1287-1292, Felice,K.J.,et al, 1999

Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
JNNP 67:685-687, Duarte,J.,et al, 1999

Suprascapular Neuropathy
J Am Acad Orthop Surg 7:358-367, Romeo, A.A.,et al, 1999

Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

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

Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
Neurol 51:1226-1227, Wasay,M.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

Attitudes of Patients with Amyotrophic Lateral Sclerosis and Their Care Givers Toward Assisted Suicide
NEJM 339:967-973,987, Ganzini,L.,et al, 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

An Analysis of Extended Survival in Patients with Amyotrophic Lateral Sclerosis Treated with Riluzole
Arch Neurol 55:526-528, Riviere,M.,et al, 1998

Magnetic Resonance Imaging of Muscle in Amyotrophic Lateral Sclerosis
Neurol 51:110-113, Bryan,W.W.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Myasthenic Hand
Neurol 51:913-914, Janssen,J.C.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Isolated Weakness of the Fingers in Cortical Infarction
Neurol 50:823-824, Lee,P.,et al, 1998

MR Findings of Werdnig-Hoffmann Disease in Two Infants
AJNR 19:550-552, Hsu,C.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Estimation of Brainstem Neuronal Loss in ALS with in Vivo Proton Magnetic Resonance Spectroscopy
Neurol 50:72-77, Cwik,V.A.,et al, 1998

Risk of Amyotrophic Lateral Sclerosis & History of Physical Activity, A Population Study
Arch Neurol 55:201-206, Longstreth,W.T.,et al, 1998

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
Neurol 50:764-767, Levin,M.I.,et al, 1998

Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

High Signal Intensity on T1 Weighted MRI of Anterolateral Column of Spinal Cord of Amyotrophic lateral Sclerosis
JNNP 62:88-91, Waragai,M.,et al, 1997

Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

Mononeuropathy of a Distal Branch of the Femoral Nerve in a Body Building Champion
JNNP 63:669-671, Padua,L.,et al, 1997

Clinical Characteristics of Patients with Motor Disability Due to Conversion Disorder:A Prospective Study
JNNP 63:83-88, Binzer,M.,et al, 1997

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Steroid Myopathy in Cancer Patients
Neurol 48:1234-1238, Batchelor,T.T.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Showing articles 350 to 400 of 4234 << Previous Next >>