Neudle.com: myopathy distal Laing

Differential
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abdominal muscle paralysis

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

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

anemia

anesthesia, general

anosmia

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

arthrogryposis multiplex

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

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.)

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

hypokalemic periodic paralysis

hypoparathyroidism

hyporeflexia

hypothalamus

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

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

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, treatment of

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, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

nemaline rod myopathy

nemaline rod myopathy, adult onset

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

pleural effusion

poison, mercury

poison, neurologic problems with

poliomyelitis

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

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 1800 to 1838 of 1838 << Previous

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968

Dementia in Cerebral Vascular Disease
Cerebral Vascular Diseases, Grunne & Stratton, Inc. , pp 232-236 (Edited by Toole & others), Fisher,C.M., 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

Neuromuscular Disease in Patients with Steatorrhoea
Gut 8:605-611, Binder,H.J.,et al, 1967

A Critical Survey of Stiff-Man Syndrome
Am J Med 42:582-599, Gordon,E.E.,et al, 1967

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

Infarction of the Fusiform & Calcarine Regions:Agitated Delirium & Hemianopia
Trans Am Neuro Assoc 92:85, Horenstein,S.,et al, 1967

Carotid Arteritis & Cerebral Infarction Due to Scleroderma
Neurol 17:18, Lee,J.E.,et al, 1967

A Spectrum of Myopathy Associated with Alcoholism (I. Clinical & Laboratory Features)
Ann Int Med 67:481, Perkoff,G.T.,et al, 1967

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Involvement of CNS in Collagen Disease
Jap Cir Jour 30:1292, Mozai,T., 1966

Neurological Aspect of SLE
Keio J Med l5:l39, Honda,M., 1966

Color-Naming Defects in Association With Alexia
Arch Neurol 15:137-146, Geschwind,N.,et al, 1966

Neurological Manifestations of Sarcoidosis
Neurol 15:1147, Wiederholt,W.,et al, 1965

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

Bacterial Meningitis-A Review of Selected Aspects
NEJM 272:725, Swartz,M.&Dodge,P., 1965

Motor Neurone Disease as a Manifestation of Neoplasm
Brain 88:479, Brain,L.,et al, 1965

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

CVA as Initial Major Manifestation of SLE
NY State J Med:2942, 1963 Oct., Silverstein,A., 1963

Recognition, Prognosis, & Treatment of the Guillain-Barre Syndrome (Acute Idiopathic Polyneuritis)
Med Clin North Am 47:1371, Eiben,R.,et al, 1963

Diabetic Amyotrophy
Am J Med 34:775, Locke,S.,et al, 1963

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

Pathology of Cerebral Arterial Occlusion
Fields, Wm. , Pathogenesis & Treatment of CVD., Adams,R.,et al, 1961

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Bilateral Loss of Vision from Cerebral Infarction
Brain 80:28, Symonds,C.,et al, 1957

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

The Posterior Cerebral Artery 1) Gross & Radiology Anat II, 2) Neuro Ophthalmologic Considerations I, 3) , Pathology III
Chp 16 p. 161, Parts II, III, & I., Margolis,M.T.,et al, 1850

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

Showing articles 1800 to 1838 of 1838 << Previous