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acid maltase deficiency

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amyotrophic lateral sclerosis, differential diagnosis

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amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

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anterior horn cell disease

anterior tibial muscle weakness

apraxia of eye movements

arthrogryposis multiplex

ataxia telangiectasia

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ataxia, truncal

atlanto axial dislocation, congenital

benign congenital hypotonia

Brugada syndrome

bulbar palsy, progressive

calf hypertrophy

carcinoembryonic antigen

cavernous sinus, syndrome

central core disease

cerebellar ataxia, children

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cerebellar degeneration

Charcot-Marie-Tooth

choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

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denervation potentials

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developmental milestones

developmental milestones, loss of

developmental retardation

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diaphragmatic paralysis

differential diagnosis

distal muscle atrophy

distal muscle weakness

electrocardiogram, abnormal

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, muscle disease

epidemiology of neurology

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facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

Friedreich's ataxia

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genetic linkage

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growth retardation

Guillain Barre syndrome

heavy metal intoxication

history of neurology

Huntington's chorea

hypoglycemic coma

hypotonia, infants

hypoxic encephalopathy

immunodeficiency

immunosuppression

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

infant, evaluation of

infantile tremor syndrome

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

leg weakness, bilateral

leg weakness, unilateral

lid closure, weakness of

life expectancy

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

mental retardation

molecular genetics

motor neuron disease

motor neuron disease, juvenile form

movement disorder

movement disorder, extrapyramidal

MRI, spinal cord

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

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

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myasthenia gravis

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myasthenic crisis

myocardial injury

myopathy, carcinomatous

myopathy, centronuclear

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myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

nemaline rod myopathy

nerve conduction studies

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neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic evaluation

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, peripheral, treatment

newborn, evaluation of

ocular motility, disorders of

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

Oppenheim muscular dystrophy

paraparesis, familial spastic

Parkinson disease

patient information and support

periodic paralysis

periodic paralysis, thyrotoxic

poison, mercury

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polyneuropathy, chronic inflammatory demyelinating

post polio syndrome

pregnancy, neurologic complications in

primary lateral sclerosis

progressive muscular dystrophy

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proximal muscle atrophy

radiation hypersensitivity

respiratory failure

risk-benefit assessment

scoliosis, neurologic association with

seizure, children

seizure, treatment of

skin, lesions in neurologic disorders

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 myelo-opticoneuropathy(S.M.O.N.)complex

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

subarachnoid hemorrhage

survival motor neuron gene

Tolosa Hunt syndrome

tongue, fasciculations of

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

tuberous sclerosis

vitamin E deficiency

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

whistle, inability to

winging of scapula

X-linked bulbospinal neuronopathy

Showing articles 1400 to 1450 of 8383 << Previous Next >>

Hereditary Quadriceps Myopathy
JNNP 36:1041, Espir,M.L.E.,et al, 1973

Nitrofurantoin Polyneuropathy
Neurol 23:554-559, Toole,J.F.&Parrish,M.L., 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Trichinosis with Central Nervous System Involvement
Neurol 22:485-491, Kramer,M.D.,et al, 1972

Peripheral NR. Injuries & their Repairs
Surg Clin North Am Oct 1972., , 1972

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

Medical Approach to Ophthalmopathy of Graves'Disease
Mayo Clin Proc 47:980, Ivy,H., 1972

Neurosyphilis
JAMA 219:726, Hooshmand,H.,et al, 1972

Injuries to the Major Branches of Peripheral Nerves of the Forearm
W. B. Saunders Pub. Co72., Spinner,M., 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Lead Encephalopathy in Adults
Am J Med 52:289, Whitfield,C.L.,et al, 1972

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Dumbbell Anterolateral Spinocranial Neurofibroma with a Note on Thigh Muscle Atrophy & Fasciculation
Neurochir 4:143, Bartal,A.D.,et al, 1972

Thromboangiitis Obliterans Cerebri
Edited by, Vinken, E. , Handbook Clinical Neurol 12:3842., Bernsmeier,A.&Held,K., 1972

The Nervous System & Diabetes
Joslin's Diabetes Mellitus, 1971, p. 562., Locke,S., 1971

Brain Stem Arteriovenous Malformations
Arch Ophthalmol 86:255, Lessel,S.,et al, 1971

Neurological Involvement in SLE
Singapore Med J 12:18, Tay,C.H.,et al, 1971

Internuclear Ophthalmoplegia, Typical & Atypical
Arch Ophthal 84:583, Cogan,D.G., 1970

The Anterior Interosseous-Nerve Syndrome (with special attention to its variations)
J Bone & Joint Surg 52-A:84970., Spinner,M.J., 1970

The Nervous System in Sickle Cell Disease
Afr J Med Sci 1:33, Adelove,A.,et al, 1970

Surgical Anatomy of the Hand
Clinical Symposia,Ciba 21:66-109, Lampe,E.W., 1969

Foot Drop
G P 40:89, Goldner,J.,et al, 1969

Encephalitis with Myoclonus in Whipple's Disease
JNNP 32:338, Stoupel,N.,et al, 1969

Neurological Examination of the Comatose Patient
Acta Neurol Scan Suppl. 38, Vol45969., Fisher,C.M., 1969

Syndromes of Central Motor Disorder
in Vinken, P. J. , Bruyn, G. W. , ed. , Handbook of Clinical Neurology, Vol. 1, North-Holland Publ C, , Amsterdam, 19Rondot, P., 1969

Polymyositis Presenting as Distal Muscle Weakness
J Neurol Sci 8:479-484, Hollinrake,K., 1969

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 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

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

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

Pure Motor Hemiplegia of Vascular Origin
Arch Neurol 13:30, Fisher,C.M.,et al, 1965

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

Neuro CPC of MGH
Acute Necrotizing Hemorrhagic Encephalopathy, NEJM 265:34-401961., , 1961

Clinical Syndromes in Cerebral Arterial Occlusion
(Ed) , Fields, Wm. Pathogenesis & Treatment of CVD, Charles C. Thomas, Publisher, Fisher,C.M., 1961

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

Neuro CPC of MGH
Congenital Vascular Malfor. of Spinal Cord, NEJM 258:949-954958., , 1958

Cysticercosis Cerebri
NEJM 256:479-486, White,J.C.,et al, 1957

Neurologic Signs & Symptoms as Early Manifestations of SLE
Neurol 5:84, Siekert,R.,et al, 1955

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

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

Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 1850

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

Imaging Findings in Giant Cell Arteritis:Dont Turn a Blind Eye to the Obvious!
AJNR 46:457-464, Bathla,G.,et al, 2025

A 62-Year-Old Man with Symmetric Saddle Hypoesthesia and Sphincter Dysfunction
Neurol 104:e213712, Crausaz,L.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

Showing articles 1400 to 1450 of 8383 << Previous Next >>