Neudle.com: myopathy distal

Differential
(Click to cross reference)

abdominal muscle paralysis

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

ACTH, ectopic syndrome of

Addison's disease

advances in neurology

algorithm

alveolar hypoventilation

amyloid

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

arthrogryposis multiplex

ascending paralysis

aspiration

asthma

asthma, poliomyelitis-like syndrome with

atrioventricular block

basal ganglia, infarction

basophilic stippling of red blood cells

benign congenital hypotonia

bitemporal visual field defect

bone marrow suppression

calcification, intracranial

cardiovascular disease

carpo-pedal spasm

cataracts

central core disease

cerebellar degeneration

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

Charcot-Marie-Tooth

chewing, impaired

children

chromosomal abnormality

chronic polyneuritis, children

Chvostek sign

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

collagen vascular disease

coma

complications

compression neuropathy

concussion

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

coxsackievirus, myopathy with

CPAP

craniopharyngioma

creatine phosphokinase(CPK)elevated

critical illness

Cushing's syndrome

cystinosis

degenerative diseases of CNS

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

dropped head syndrome

dystrophic calcification

dystrophin

edema, pedal

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

encephalitis, brainstem

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

erythrocyte

evidence-based research

evoked potentials

exercise

exophthalmus

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

fibrillations

fine motor function, impaired

finger drop

finger flexor weakness

finger weakness

fingernails, abnormal

gag reflex, depressed

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guyon's canal

gynecomastia

hallucination

hallucination, auditory

hammertoes

hand deformity

hand weakness

Hand-Schuller-Christian disease

head injury

headache

heart block

heart block, complete

heavy metal intoxication

hemidiaphragm, paralysis of

hemoglobinuria

hepatitis

hepatomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

high arched feet

high arched palate

histochemistry

histochemistry of muscle

hoarseness

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

hypokalemic alkalosis

hypokalemic periodic paralysis

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxic encephalopathy

imbalance

immunohistochemistry

immunologic disease

immunosuppressive agents

inability to sit up

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

intermittent positive pressure breathing

intrinsic hand muscles, wasting of

islet cell tumor

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

leukopenia

level of consciousness, decreased

lid closure, weakness of

life expectancy

liver disease

liver function enzymes

middle cerebral artery, occlusion of

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, treatment of

myasthenic crisis

myelopathy

myelopathy, carcinomatous

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, neurogenic hypothesis of

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, systemic cancer

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal migration disorder

neuronopathy

neuropathy

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, toxic

newborn, evaluation of

next-generation sequencing

nusinersen

occipital lobe, infarction

occipital lobe, lesion of

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, total

Oppenheim muscular dystrophy

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

percussion induced muscle contraction

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

pes cavus

pheochromocytoma

phosphorylase b kinase deficiency

phrenic nerve pacemaker

plasmapheresis

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis-like illness

polymerase chain reaction

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

polyneuropathy, familial

porphyria

position sensation, abnormal

positive sharp waves

post polio syndrome

posterior interosseous neuropathy

pregnancy, neurologic complications in

primary aldosteronism

prognosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proximal muscle atrophy

remote effect of cancer on the nervous system

renal stones

repetitive nerve stimulation

respirator

respiratory depression

scoliosis, neurologic association with

screening

seizure

seizure, children

seizure, treatment of

serologic testing

severe acute respiratory syndrome

short stature

skin, lesions in neurologic disorders

sleep apnea

slit lamp examination

SMN1 gene

spinal cord, injury of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

standing difficulty

steppage gait

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

survival motor neuron gene

sweating, abnormality of

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tetany

thoracic outlet syndromes

tongue, fasciculations of

tongue, weakness

torticollis

treatment of neurologic disorder

trinucleotide repeats

Trousseau's sign

ulnar neuropathy

uremia

urine test in toxic screen

vasculitides

viral infection

viral infection, CNS

visual evoked response

vital capacity

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

wheelchair

whistle, inability to

winging of scapula

workup

X-linked bulbospinal neuronopathy

Showing articles 800 to 850 of 2033 << Previous Next >>

Symptomatic Intracranial Atherosclerosis
Neurol 55:490-497, 465, Thijs,V.N. & Albers,G.W., 2000

Amusement Park Stroke
, Burneo,J.G. et al, 2000

Neuromuscular Findings in Thyroid Dysfunction: A Prospective Clinical and Electrodiagnostic Study
JNNP 68:750-755, Duyff,R.F. et al, 2000

Incidence and Prevalence of Neurological Disorders Associated with HIV Since the Introduction of Highly Active Antiretroviral Therapy (HAART)
JNNP 69:376-380, Maschke,M. et al, 2000

Treatment of Acute Ischemic Stroke
NEJM 343:710-722, Brott, T. & Bogousslavsky, J., 2000

Prediction of Malignant Middle Cerebral Artery Infarction by Diffusion-Weighted Imaging
Stroke 31:2175-2181, Oppenheim,C. et al, 2000

Treatable Dropped Head Syndrome in Hypothyroidism
Neurol 55:896-897, Askmark,H. et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

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

Weak and Numb Feet in a Man with Knobby Hands, Report of a Case
Arch Neurol 57:271, Kaplan,P.W.,et al, 2000

GCG Genetic Expansions in Italian Patients with Oculopharyngeal Muscular Dystrophy
Neurol 54:608-614, Mirabella,M.,et al, 2000

Short-Term Arteriographic and Clinical Outcome After Cerebral Angioplasty and Stenting for Intracranial Vertebrobasilar and Carotid ATherosclerotic Occlusive Disease
AJNR 21:249-254, Mori,T.,et al, 2000

Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
NEJM 342:770-780, Dalakas,M.C.,et al, 2000

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Intracranial Percutaneous Transluminal Angioplasty for Arteriosclerotic Stenosis
Arch Neurol 57:1625-1630, Alazzaz,A.,et al, 2000

Clinicopath Conf, Granulomatous and Lymphocytic Hypophysitis
NEJM 343:1399-1406, Case 34-2000, 2000

Visual Manifestations of Giant Cell Arteritis
Medicine 79:283-292, Gonzalez-Gay,M.A.,et al, 2000

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

Dilated Stomach and Weak Muscles
Lancet 356:1898, Rigby,S.P.,et al, 2000

Critical Illness Myopathy
Muscle Nerve 23:1785-1788, Lacomis,D.,et al, 2000

Posttraumatic Headache-A Myth?
Arch Neurol 57:1778-1780, Warner,J.S., 2000

Posttraumatic Headache
Arch Neurol 57:1776-1778,1780, Saper,J.R., 2000

Dermatomyositis
Lancet 355:53-57, Callen,J.P., 2000

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

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Weak at the Knees
Lancet 354:1696, Webster,G.&Beynon,H., 1999

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

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

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

The Intensive Care Management of Acute Ischemic Stroke
The Neurologist 5:313-325, Deibert,E.&Diringer,M.N., 1999

Intra-Arterial Prourokinase for Acute Ischemic Stroke, The PROACT II Study:A Randomized Controlled Trial
JAMA 282:2003-2011, Furlan,A.,et al, 1999

Intravenous Immunoglobulin in the Treatment of Autoimmune Neuromuscular Diseases:Present Status and Practical Therapeutic Guidelines
Muscle & Nerve 22:1479-1497, Dalakas,M.C., 1999

Clinicopath Conf,Hepatitis C,Type II Cryoglobulinemia,Vasculitis,B-cell Lymphoma,Mononeuritis Multiplex,Case 3-1999
NEJM 340:300-307, , 1999

Late-Onset Myasthenia Graivs,A Changing Scene
Arch Neurol 56:25-27, Aarli,J.A., 1999

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

CT Angiography and Doppler Sonography for Emergency Assessment in Acute Basilar Artery Ischemia
Stroke 30:606-612, Brandt,T.,et al, 1999

Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

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

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

Neurologic Manifestations of Compressive Radiculopathy of the First Thoracic Root
Neurol 53:1149-1151, Levin,K.H., 1999

Bilateral Intracranial Vertebral Artery Disease in the New England Medical Center Posterior Circulation Registry
Arch Neurol 56:1353-1358,1329, Shin,H-K.,et al, 1999

Intra-Arterial Cerebral Thrombolysis for Acutre Ischemic Stroke in a Community Hospital
AJNR 20:1682-1687,1580, Edwards,M.T.,et al, 1999

Balloon Angioplasty for Embolic Total Occlusion of the Middle Cerebral Artery and Ipsilateral Carotid Stenting in an Acute Stroke Stage
AJNR 20:1462-1464,1389, Mori,T.,et al, 1999

A Sartorial Challenge
Lancet 354:996, Reading,P.J.,et al, 1999

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

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

The Clinical Spectrum of Sarcoglycanopathies
Neurol 52:176-179, Angelini,C.,et al, 1999

Medical Complications in Long-Term Survivors with X-Linked Myotubular Myopathy
J Pediatr 134:206-214, Herman,G.E.,et al,, 1999

Showing articles 800 to 850 of 2033 << Previous Next >>