Neudle.com: cortical muscular atrophy

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Differential
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airway obstruction

Alzheimer's disease

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

aphasia, progressive, primary

aqueduct of Sylvius, stenosis

aqueductal stenosis

atrioventricular block

basal ganglia, calcification of

behavioral disorder

bruit, supraclavicular

calcification, intracranial

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, false negative

cataracts, congenital

cerebellar hypoplasia

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical spine injury

cervical spondylosis

chronic progressive external ophthalmoplegia

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

contractures, joint

controversies in neurology

cornea, opacity of

corpus callosum

corpus callosum, thinning

cortical hand knob

cortical muscular atrophy

cost effectiveness

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

developmental disability

developmental milestones

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

Emery-Dreifuss muscular dystrophy

encephalopathy, progressive

episodic neurologic deficits

ethics in neurology

evidence-based research

evoked potentials

exercise intolerance

exercise-induced vascular symptoms

facial weakness, bilateral

fetal movements, reduced

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

genetic counselling

genetic neurologic disorders

genetic testing

granular atrophy, cerebral cortex

heart block, complete

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

high arched feet

histochemistry of muscle

hydrocephalus, congenital

hypotonia, infants

inborn errors of metabolism

inflexibility, mental

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Kearns-Sayre syndrome

lactic acidemia

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Lewy body disease, diffuse

life sustaining treatment

locked-in syndrome

lysosomal storage disease

malformation, CNS, congenital

medical-legal aspects of neurology

mental retardation

metabolic disorder, primary

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

molecular genetics

monomelic amyotrophy

motor neuron disease

movement disorder

MRI, functional

MRI, gradient-echo

MRI, susceptibility weighted

multiple sclerosis

multiple sclerosis, diagnosis of

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myocardial infarction

myopathy, distal

myopathy, mitochondrial

myotonia congenita

myotonia dystrophica

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neuroendocrinology

neurologic complications of, systemic cancer

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic symptoms

neurologic testing

neuroophthalmology

neuropathology, brain

neuropathy, motor, multifocal

ophthalmoplegia

optic neuropathy

pacemaker, cardiac-transvenous

pain, increased response

palliative care

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

peripheral vascular disease

peroxisomal disease

personality change

physician assisted suicide

pigmentary retinopathy

positive sharp waves

posterior interosseous neuropathy

practice guidelines

progressive neurologic disorder

proximal muscle atrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract

quality of life

ragged-red fibers

release phenomena

respiratory failure

retinal detachment

retinal dysplasia

sensorineural hearing loss

single photon emission computed tomography

skin, lesions in neurologic disorders

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech, loss of

spinal cord, compression of

spinal cord, injury of

stereotyped behavior

sternocleidomastoid muscle

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subclavian artery stenosis

symmetric brain lesions

temporal lobe, atrophy

temporalis muscle wasting

thoracic outlet syndromes

tongue, fasciculations of

treatment of neurologic disorder

trinucleotide repeats

ultrasonography

upgaze, paralysis of

urea-cycle enzymopathies

visual field defect

Walker-Warburg syndrome

walking, difficulty with

weakness, congenital

weakness, progressive

white matter disease

white matter disease, periventricular

winging of scapula

word-finding difficulty

Showing articles 1200 to 1250 of 9396 << Previous Next >>

Hydrocephalus as a Cause of Disturbances of Gait in the Elderly
Neurol 32:1358-1363, Fisher,C.M., 1982

A Surgical Approach To The Treatment Of Fetal Hydrocephalus
NEJM 306:1320-1325, Clewell,W.H.,et al, 1982

Visual Field Defects in Obstructive Hydrocephalus
JNNP 45:591-597, Humphrey,P.R.D.,et al, 1982

Eosinophilic Meningitis & Hydrocephalus in an Infant
Arch Neurol 39:380-381, Enzenauer,R.W.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Immediate & Delayed Neurotoxicity After Mechlorethamine Preparation for Bone Marrow Transplantation
Ann Int Med 97:182-189, Sullivan,K.M.,et al, 1982

Colloid Cysts of the Third Ventricle
Arch Neurol 39:640-643, Michels,L.G.,et al, 1982

Clin. Path. Conference
Subependymoma of Fourth Ventricle, Case Record 46-1982, NEJM 307:1328-1335982., , 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Clin. Path. Conference
Tuberculous Meningitis, Case Record 2-1982, NEJM 306:91-97982., , 1982

Computed Tomography in Pick's Disease:Findings in a Family Affected in Three Consecutive Generations
J Comput Assist Tomogr 6:907-911, Groen,J.J.,et al, 1982

Cysticercosis Cerebri, Review of 127 Cases
Arch Neurol 39:534-539, McCormick,G.F.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Computerized Tomographic Scan Changes In Manic-Depressive Illness
Lancet 2:470, Pearlson,G.D.,et al, 1981

Ventricular Enlargement After Closed Head Injury
Arch Neurol 38:623-629, Levin,H.S.,et al, 1981

Chronic Blastomycotic Meningitis
Am J Med 71:501-505, Kravitz,G.R.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
NEJM 305:955, Clewell,W.H.,et al, 1981

The Intelligence of Hydrocephalic Children
Arch Neurol 38:607-615, Dennis,M.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Downbeat Nystagmus-A False Localising Sign Due to Communicating Hydrocephalus
(Letter) JNNP 44:459981., MacDonald,A.F., 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Cerebral Atrophy & Functional Deficits In Alcoholics Without Clinically Apparent Liver Disease
Neurol 31:377-385, Carlen,P.L.,et al, 1981

Subcortical Arteriosclerotic Encephalopathy:A Clinical & Radiological Investigation
JNNP 44:294-304, Loizou,L.A.,et al, 1981

Visual involvement in Friedreich's Ataxia & Hereditary Spastic Ataxia
Arch Neurol 38:75-79, Livingstone,I.R.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Lipomembranous Polycystic Osteodysplasia with Progressive Dementia
J Comput Assist Tomogr 5:580-582, Laasonen,E.M.,et al, 1981

Use of Radiologic Modalities in Coccidioidal Meningitis
Arch Int Med 141:75-78, Stadalnik,R.C.,et al, 1981

Ventriculoatrial Shunting for Hydrocephalus Complicating Tuberculous Meningitis
Am J Med 70:895-898, Murray,H.W.,et al, 1981

Parainfectious Acute Obstructive Hydrocephalus
Ann Neurol 10:62-63, Yanofsky,C.S.,et al, 1981

Antenatal Treatments Of Hydrocephalus
NEJM 303:1021-1023, Birnholz,J.C.,et al, 1981

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Epidermoid Tumors Involving the Fourth Ventricle
Neurosurgery 9:9-13, Rosario,M.,et al, 1981

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Meningeal Gliomatosis:A Review of 12 Cases
Ann Neurol 8:605-608, Young,W-k.A.,et al, 1980

Cerebellar Softening
Ann Neurol 8:133-140, Scotti,G.,et al, 1980

Acetazolamide-Induced Improvement in Hydro-cephalus
Arch Neurol 37:376, Donat,J.F., 1980

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Leber's Optic Neuropathy
Editorial, BMJ 280:1097-10981980., , 1980

Computed tomography in Hallervorden-Spatz disease
Neurol 30:1128-1130, Dooling,E.C.,et al, 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Showing articles 1200 to 1250 of 9396 << Previous Next >>