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Differential
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abdominal distention
abducens nerve paralysis
abiotrophy
acoustic nerve
agammaglobulinemia
alcohol intolerance
alkylating agents
alopecia
altered states of consciousness
alveolar hypoventilation
anesthesia, general
antimetabolite
aphasia
areflexia
arrhythmia, cardiac
arthralgia
asparginase
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
atonic bladder
autonomic dysfunction
baldness
blood dyscrasias, neurologic findings with
brainstem, dysfunction
cachexia
calcification, intracranial
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
central core disease
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chromosome 19
chronic progressive external ophthalmoplegia
cleft palate
Clinical Pathologic Conference(C.P.C.)
coma
congenital heart disease
congenital malformation
congenital myasthenic syndromes
congenital myopathy
consanguinity
cough
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
dementia
developmental retardation
diarrhea
diplopia
distal muscle weakness
Duane syndrome
dysphagia
dyspnea
dyspraxia
electrocardiogram, abnormal
electromyogram
encephalopathy
encephalopathy, progressive
exercise intolerance
extraocular muscle lesion
eye movement, disorders of
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fatigue
fever
fluorescein angiography
fluorouracil
flush syndrome
foot drop
gait disorder
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
granulomatosis with polyangiitis
granulomatous disease
hallucination
headache
hearing loss
heart block
hemianopia
hemiparesis
hepatic failure
hepatomegaly
heralding manifestation
high arched palate
Hirschprung's disease
Holt-Oram syndrome
hypercapnia
hypogonadism
hyponatremia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
intestinal pseudoobstruction
iris, abnormal
isoniazid
jaw pain
Kearns-Sayre syndrome
klippel feil syndrome
Korsakoff's psychosis
lactic acidemia
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
leukopenia
lymphoma involving CNS
lymphomatoid granulomatosis
MELAS syndrome
meningismus
meningoencephalopathy
mental retardation
methotrexate
methylhydrazine derivatives
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoamine oxidase inhibitors
movement disorder
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, familial incidence of
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, seronegative
myoclonus
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myotonia
myotonia dystrophica
nasal speech
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular blockade
neuromuscular junction
neuromuscular junction, abnormality of
neuroophthalmology
neuropathy
neuropathy, peripheral
neurotoxin
nitrogen mustard
normal
nystagmus
nystagmus, dissociated
nystagmus, vertical
ocular motility, disorders of
ocular myopathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
orthostatic hypotension
pain
pain, abdominal
paraparesis
paraparesis, spastic
paresthesias
Parkinsonism syndrome
percussion induced muscle contraction
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polyneuropathy
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
prostigmine
pseudomyasthenia
psychosis
ptosis
ptosis, bilateral
ptosis, classification of
ptosis, familial
ptosis, unilateral
pulmonary infiltrates
ragged-red fibers
rash
retina, abnormal
retinal degeneration
retinal lesion
review article
seizure
sensorineural hearing loss
seronegative
short stature
skin, lesions in neurologic disorders
slit lamp examination
spasticity
spina bifida
splenomegaly
steroid therapy, CNS treatment and complications with
strokelike episodes
syringomyelia
systemic illness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
testicular atrophy
thrombocytopenia
tinnitus
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
vertigo
vinblastine
vincristine neurotoxicity
vocal cord paralysis
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weaning from respirator, failure to
web sites
weight loss
wheelchair
white matter disease
wide based gait
Wildervanck's syndrome
wrist drop
Showing articles 1700 to 1750 of 1869 << Previous Next >>

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Familial Hypopituitarism with Large Sella Turcica
NEJM 298:698, Parks,J.S.,et al, 1978

Familial Occurrence of Meralgia Paresthetica
Arch Neurol 35:182, Massey,E.W., 1978

Meningiomas in Five Members of a Family Over Two Generations, in One Member Simultaneously with Acoustic Neurinomas
Neurol 28:567, Delleman,J.W.,et al, 1978

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
Ann Neurol 3:144, Nakano,K.K.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Familial Cavernous Angiomas
Arch Neurol 35:746-749, Bicknell,J.M.,et al, 1978

Monozygotic Twins With Presumed Metachromatic Leukodystrophy
Arch Neurol 35:689-691, Hashimoto,T.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Familial Incidence of Ruptured Intracranial Aneurysms
Arch Neurol 35:675-677, Acosta-Rua,G.J., 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Tics & Tourette's:A Continuum of Symptoms
Ann Neurol 4:145-148, Golden,G.S., 1978

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Obstructive Sleep Apnea in Family Members
NEJM 299:969-973, Strohl,K.P.,et al, 1978

Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
Ann Neurol 4:130-144, Roman,G.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Malignant Optic Gliomas in Adults
Arch Neurol 35:731-735, Harper,C.G.,et al, 1978

Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Clinical Pathological Conference, Reticulum Cell Sarcoma of Brain
NEJM 299:1349-1359, Case Record 49-1978,Mass.Gen.Hosp., 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Cervical Myelopathy Due to Ossification of the Posterior Longitudinal Ligament
Arch Neurol 35:33, Murakami,N., 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Familial Vascular Malformation or Chance Occurrence
Neurol 28:98, Barre,R.G.,et al, 1978

Supratentorial Leptomeningeal Hemangioblastoma
Neurol 28:727, Lee,K.R.,et al, 1978

Transient Spastic Paraparesis Following Abdominal Aortography:Management with Cerebrospinal Fluid Lavage
Ann Neurol 3:185, Morariu,M.A., 1978

Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
Ann Neurol 3:464, Waybright,E.A.,et al, 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Myasthenia, In Neuroophthalmology
1978, Harper & Row, P. 268., Glaser,J.S., 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Superior Branch Palsy of the Oculomotor Nerve with Spontaneous Recovery
Ann Neurol 4:478-479, Derakhshan,I., 1978

Adrenomyeloneuropathy:A Probable Variant of Adrenoleukodystrophy
Neurol 27:1107-1113, Griffin,J.W.,et al, 1977

Downbeating Nystagmus & Hereditary Cerebellar Degeneration, Levin DB, et al, In Neuro-ophthalmology Update
Masson Publishing USA, INC. 1977 P 337-338., Smith,J.L., 1977

The Central Nervous System in a Case of Neurolathyrism
Neurol 27:1176, Striefler,M.,et al, 1977

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Neuroectodermal Tumors in the Cerebellum in Two Sisters
JNNP 40:886, Thomas,M.,et al, 1977

Clinical Neurogenetics
Neurol 27:1057, Bird,T.D.,et al, 1977



Showing articles 1700 to 1750 of 1869 << Previous Next >>