Neudle.com: spinal muscular atrophy type I

Differential
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acid maltase deficiency

advances in neurology

adverse drug reaction

alpha-fetoprotein

Alzheimer's disease

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anterior horn cell disease

anterior tibial muscle weakness

apraxia of eye movements

areflexia

arthrogryposis multiplex

asymptomatic

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, truncal

benign congenital hypotonia

Brugada syndrome

bulbar palsy, progressive

calf hypertrophy

carcinoembryonic antigen

carcinoma

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

chromosomal abnormality

chromosome 11

chromosome 5

chronic polyneuritis, children

Clinical Pathologic Conference(C.P.C.)

clinodactyly

coma

complications

congenital heart disease

congenital myopathy

congestive heart failure

constipation

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

Dejerine-Sottas syndrome

denervation of muscle

denervation potentials

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

distal muscle atrophy

distal muscle weakness

electrocardiogram, abnormal

electromyogram

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, muscle disease

epidemiology of neurology

eye movement, disorders of

facial weakness, bilateral

facioscapulohumeral syndrome

familial

fasciculation

Fazio-Londe's disease

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

growth retardation

Guillain Barre syndrome

gynecomastia

heavy metal intoxication

history of neurology

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

hypoxic encephalopathy

immunodeficiency

immunosuppression

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

infant, evaluation of

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

leg weakness, bilateral

leg weakness, unilateral

leukemia

lid closure, weakness of

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, spinal cord

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenic crisis

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, centronuclear

myopathy, mitochondrial

myopathy, thyroid disease causing

myositis

myotonia congenita

myotonia dystrophica

nemaline rod myopathy

nerve conduction studies

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic evaluation

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuropathology

neuropathy

neuropathy, diabetic

neuropathy, hereditary peripheral

newborn, evaluation of

nusinersen

ocular motility, disorders of

Onufrowicz nucleus

Oppenheim muscular dystrophy

paraparesis, familial spastic

Parkinson disease

pathology

patient information and support

peroneal muscle atrophy, causes of

phrenic nerve

placebo

poison, mercury

poison, neurologic problems with

pregnancy, neurologic complications in

primary lateral sclerosis

progeria

prognosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

radiation hypersensitivity

risk-benefit assessment

scoliosis, neurologic association with

screening

skin, lesions in neurologic disorders

SMN1 gene

spinal cord

spinal cord degeneration

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

stiff man syndrome

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

sudden death

survival motor neuron gene

telangiectases

term infant

tongue, fasciculations of

torticollis

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

walking, difficulty with

weakness

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

West disease

wheelchair

whistle, inability to

winging of scapula

workup

X-linked bulbospinal neuronopathy

Showing articles 1150 to 1200 of 7312 << Previous Next >>

Infections with Herpes Simplex Viruses
NEJM 314:686-691, 749-7571986., Corey,L.&Spear,P.G., 1986

CT Myelography in Spinal Cysticercosis
J Comput Assist Tomogr 10:195-198, Zee,C.,et al, 1986

Causalgia as a Complication of Meningococcal Meningitis
BMJ 292:1710, McLelland,J.&Ellis,S.J., 1986

Progressive Polyradiculopathy in Acquired Immune Deficiency Syndrome
Neurol 36:912-916, Eidelberg,D.,et al, 1986

Segmental Myoclonus Clinical and Pharmacologic Study
Arch Neurol 43:1025-1031, Jankovic,J.&Pardo,R., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Neurosyphilis
Arch Neurol 42:606-613, Simon,R.P., 1985

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Sarcoidosis & Its Neurological Manifestations
Arch Neurol 42:909-917, Stern,B.J.,et al, 1985

Cytomegalovirus & Herpes Simplex Virus Ascending Myelitis in a Patient with Acquired Immune Deficiency Syndrome
Ann Neurol 18:74-79, Tucker,T.,et al, 1985

Progressive Encephalopathy in Children with Acquired Immune Deficiency Syndrome
Ann Neurol 17:488-496, Epstein,L.G.,et al, 1985

Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985

A New Complication of AIDS:Thoracic Myelitis Caused by Herpes Simplex Virus
Neurol 35:1071-1074, Britton,C.B.,et al, 1985

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Isolation of HTLV-III from CSF & Neural Tissues of Patients with Neurologic Syndromes Related to AIDS
NEJM 313:1493-1497, 15381985., Ho,D.D.,et al, 1985

Focal Epilepsy with Mesial Temporal Sclerosis after Acute Meningitis
Arch Neurol 42:1058-1060, Ounsted,C.,et al, 1985

Neurocysticercosis:A New Classification Based on Active & Inactive Forms, A Study of 753 Cases
Arch Int Med 145:442-445, Sotelo,J.,et al, 1985

Spinal Cord Degeneration in AIDS
Neurol 35:103-106, Goldstick,L.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Iatrogenic Causalgia
Arch Neurol 41:821-824, Horowitz,S.H., 1984

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Autonomic Dysfunction & Sleep Apnea in Olivoponto Cerebellar Degeneration
Arch Neurol 41:926-931, Chokroverty,S.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Evoked Potentials in Olivopontocerebellar Atrophy
Arch Neurol 40:366-369, Hammond,E.J.,et al, 1983

Fungal Meningitis Manifesting as Hydrocephalus
Arch Int Med 143:728-731, Mangham,D.,et al, 1983

Reflex Sympathetic Dystrophy (Causalgia) Treatment with Guanethidine
Arch Neurol 40:430-432, Tabira,T.,et al, 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Acute Hydrocephalus in Tuberculous Meningitis in Adults
Sem Hop 59:1687-1688, Tasseau,F., 1983

Optic Neuropathy & Paratrigeminal Syndrome Due to Aspergillus Fumigatus
Arch Neurol 39:582-585, Weinstein,J.M.,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

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

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

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

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

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

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

Unusual Effects of Metrizamide Lumbar Myelography
Arch Neurol 37:588-589, Kelley,R.E.,et al, 1980

Clinical Aspects of CNS Cysticercosis
Arch Int Med 140:1309-1313, Shanley,J.D.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Horner Syndrome with Causalgia
Neurol 30:534-535, Bernad,P.G.,et al, 1980

Showing articles 1150 to 1200 of 7312 << Previous Next >>