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advances in neurology
adverse drug reaction
alcohol
alcohol, neurologic complications with
algorithm
aminoacidurias
amyloidosis
amyotrophic lateral sclerosis
anemia
anemia, hemolytic
anterocollis
anticholinergic drugs
aphonia
artane
arthrogryposis multiplex
athetosis
athetosis, causes of
attention deficit disorder with hyperactivity
Babinski sign
basal ganglia
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
biopterin deficiency
blepharospasm
botulinum toxin
bradykinesia
Brueghel's syndrome
camptocormia
carbamazepine
CAT scan
CAT scan, abnormal
CAT scan, muscle
catecholamine
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chorea, causes of
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 14
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clonazepam
cogwheel rigidty
complications
conversion reaction
creatine phosphokinase(CPK)elevated
dementia
depression
dermatomyositis
developmental retardation
diurnal variation
dopa responsive dystonia
dopamine
drug induced neurologic disorders
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphonia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, laryngeal
dystonia, painful
dystonia, post traumatic
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
efficacy
electromyogram
encephalitis, brainstem
epidemiology of neurology
equinovarus
familial
gait disorder
gamma amino butyric acid
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
Hallervorden Spatz disease
handwriting
head nodding
head tilt
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatitis
hepatolenticular degeneration(Wilson's disease)
homovanillic acid
Huntington's chorea
hyperekplexia
hyperreflexia
iron, brain
Kayser-Fleischer ring
klippel feil syndrome
kyphosis
laminectomy
laminectomy, lumbar
laterocollis
L-dopa
leg spasms
leg spasms, painful
low back pain
migraine
migraine, children
misdiagnosis
molecular genetics
monoamines
mononeuropathy
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
MRI, abnormal
MRI, eye of tiger sign
MRI, gradient-echo
MRI, paramagnetic effect
MRI, susceptibility weighted
multiple sclerosis
muscle biopsy
muscle diseases, characteristics of
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myopathy
myopathy, carcinomatous
myopathy, metabolic
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nerve conduction studies
neuritis, causes of
neurodegeneration with brain iron accumulation
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, diabetic
neurotransmitter
norepinephrine
obsessive-compulsive disorder
old age, neurology of
pain
pancytopenia
PANK2 mutation
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
Parkinson disease, juvenile
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
patient information and support
penicillamine
phenylketonuria
poliomyelitis
polymyositis
polyneuropathy
porphyria
postoperative neurologic complications
postural abnormality
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
radiculopathy
reflex sympathetic dystrophy
retrocollis
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
salivation, excessive
sarcoidosis
schizophrenia
scoliosis
seizure
seizure, stimulus sensitive
sensory tricks
sinemet
slit lamp examination
spastic dysphonia
speech disorder
speech disorder, non aphasic
splenomegaly
startle reaction
stiff man syndrome
stimulation, deep brain
stooped posture
tardive dyskinesia
tardive dystonia
tetrabenazine
tic
toe walking
tonic foot response
torticollis
torticollis, benign paroxysmal
torticollis, familial
torticollis, infants and children
torticollis, post traumatic
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, post traumatic
tremor, postural
tremor, treatment of
tremor, voice
uric acid, low
vasospasm, cerebral
walking, difficulty with
weakness, progressive
Werdnig-Hoffman disease
wheelchair
workup
writers cramp
Showing articles 1700 to 1744 of 1744 << Previous

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

Treating Problem Children with Stimulant Drugs
NEJM 289:407, Sroufe,L.A.,et al, 1973

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

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

Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
Neurol 22:49, Nakano,K.K.,et al, 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Medical Treatment of Spasmodic Torticollis
Arch Neurol 27:503, Gilbert,G., 1972

Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972

Dysautonomia, Its Significance in Neurologic Disease (Specialty Conference)
Calif Med 117:28, Wichser,J.,et al, 1972

A New Ptosis Classification
Arch Ophthalmol 88:590, Fox,S.A., 1972

Familiar Basilar Impression
Neurol 22:554, Paradis,R.,et al, 1972

Benign Essential Tremor
Lancet 471, 1972 Sept., , 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Differential Diagnosis of Tremors
Med Clin North Am 56:1363, Fahn,S., 1972

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Familial Calcification of the Basal Ganglions A Metabolic & Genetic Study
NEJM 285:72, Moskowitz,M.,et al, 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Myasthenia Gravis & Hyperthyroidism Occurring in Two Sisters
Neurol 21:377, Namba,T.,et al, 1971

Neurocutaneous Disease
in Dermatology in General Medicine, Fitzpatrick, et al, eds, McGraw Hill, 1971, pp. 1379-1434., Adams,R., 1971

Polyneroupathies of Undetermined Cause
Acta Neurol Scand (Supp) :5970., Prineas,J., 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Infantile Nystagmus:A Prospec. Study of Spasmus Nutans, Congen. Nystag, & Unclass. Nystagmus of Infancy
J Pediatr 77:177, Jayalakshuni,R.,et al, 1970

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

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

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

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

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

Orthopaedic Aspects of Intraspinal Tumors in Infants & Children
J Bone & Joint Surg 47A:223965., Tachdjian,M.&Matson,D., 1965

Inherited Aminoacidopathies Demonstrating Vitamin Dependency
NEJM 281:145, Rosenberg,L., 1965

Morquio's Disease, A Radiologic & Morphologic Study
Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964

Familial and Conjugal Multiple Sclerosis
Brain 86:315-332, Schapira,K.,et al, 1963

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Microcephaly
Arch Dis Child 37:623-627, Davies,H.,et al, 1962

Neuro CPC of MGH
Meningioma at Thoracic Cord, NEJM 264:824-8271961., , 1961

Compression of the Thoracic Spinal Cord in a Patient with Scleroderma
Bull Hosp Joint Dis 18:98, 1957, Kaplan,A.,et al, 1957

Hereditary Ataxias
Genetics & the Inheritance of Integrated Neurol & Psych. Patterns-Vol 33, Proceed. Assoc. for Resear, h in NerSchut, J., 1850

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

Clinical Pathological Conference, Scleroderma, Spastic Paraparesis & Chronic Myelogenous Leukemia
Prov. VAH, Dec. 12, 77., Finelli,P.F., 1850

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 1700 to 1744 of 1744 << Previous