Neudle.com: myopathy distal

Differential
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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 550 to 600 of 2033 << Previous Next >>

Congenital Muscular Dystrophy
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Whipples Disease
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Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
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The Role of Muscle Biopsy in Investigating Isolated Muscle Pain
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Ischemic and Hemorrhagic Complications After Intra-Arterial Fibrinolysis in Vertebrobasilar Occlusion
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Detection of Intracranial Atherosclerotic Steno-Occlusive Disease With 3D Time-Of-Flight Magnetic Resonance Angiography With Sensitivity Encoding at 3T
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Admission Facility Is Associated With Outcome of Basilar Artery Occlusion
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Mechanical Thrombectomy of Intracranial Internal Carotid Occlusion: Pooled Results of the MERCI and Multi MERCI Part I Trials
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Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
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A 46-Year-Old Woman With Severe Weakness Following Acute Respiratory Distress Syndrome
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Inclusion Body Mositis With Human Immunodeficiency Virus Infection: Four Cases with Clonal Expansion of Viral-Specific T Cells
Ann Neurol 61:466-475, Dalakas,M.,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

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
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Emerging Endovascular Therapies for Symptomatic Intracranial Atherosclerotic Disease
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Proximal Paresis of the Upper Extremity in Patients With Stroke
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Aggressive Behavior and Posterior Cerebral Artery Stroke
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Magnetic Resonance Imaging of Biceps Femoris Muscles in Benign Acute Childhood Myositis
Arch Neurol 64:1200-1201, Kawarai,T.,et al, 2007

Acute Ischemic Stroke
NEJM 357:572-529, Bart van der Worp,H. &van Gijn,J., 2007

Randomized Trial of Intraarterial Infusion of Urokinase Within 6 Hours of Middle Cerebral Artery Stroke: The Middle Cerebral Artery Embolism Local Fibrinolytic Intervention Trial (MELT) Japan
Stroke 38:2633-2639,2627, Ogawa,A.,et al, 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

Decompressive Surgery for the Treatment of Malignant Infarction of the Middle Cerebral Artery (DESTINY)
Stroke 38:2518-2525,2410, Jttler,E.,et al, 2007

Anterior Cerebral Artery Emboli in Combined Intravenous and Intra-arterial rtPA Treatment of Acute Ischemic Stroke in the IMS I and II Trials
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Epilepsy in Pregnancy
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Multifocal Motor Neuropathy: The Diagnostic Spectrum and Response to Treatment
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"Salt and Pepper" in the Eye and Face: A Prelude to Brainstem Ischemia
Am J Ophthalmol 144:322-325, Conforto, A.B.,et al, 2007

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Glycogen-Storage Disease Type II
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Metabolic Disease and Stroke: MELAS
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The Natural History of Primary Lateral Sclerosis
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Natural History of Homonymous Hemianopia
Neurol 66:901-905, Zhang,X.,et al, 2006

Homonymous Hemianopias
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Predictors for Malignant Middle Cerebral Artery infarctions
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Frontotemporal Lobar Degeneration with Motor Neuron Disease
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Orgasmic Headache and Middle Cerebral Artery Dissection
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Mycophenolate Mofetil in Dermatomyositis: Is It Safe?
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Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
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Clinicopath Conf, Acute Ischemic Stroke
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Intra-Arterial Thrombolysis Is the Treatment of Choice for Basilar Thrombosis: Pro
Stroke 37:2436-2437,2440, Schellinger,P.D. &Hacke,W., 2006

Intra-Arterial Thrombolysis Is the Treatment of Choice for Basilar Thrombosis: Con
Stroke 37:2438-2439,2440, Ford,G.A., 2006

Tandem Internal Carotid Artery/Middle Cerebral Artery Occlusion: An Independent Predictor of Poor Outcome After Systemic Thrombolysis
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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West Nile Virus Neuroinvasive Disease
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The Tuberous Sclerosis Complex
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Outcome of Acute Vertebrobasilar Occlusions Treated with Intra-Arterial Fibrinolysis in 180 Patients
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Case 35-2006: A Newborn Boy with Hypotonia
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The Association of Chronic Hepatitis B and Myopathy
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Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Frequently Missed Diagnosis?
Neurol 67:1519, Koppel,S.,et al, 2006

Mechanical Thrombolysis in Ischemic Stroke Attributable to Basilar Artery Occlusion as First-Line Treatment
Stroke 37:145-150, Bergui,M.,et al, 2006

Showing articles 550 to 600 of 2033 << Previous Next >>