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Differential
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abulia
adrenoleukodystrophy
adult-onset leukodystrophy, with neuroaxonal spheroids
alopecia
apraxia
areflexia
ataxia
ataxia, cerebellar
axonal degeneration
axonal spheroid
axonal transection
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
blindness
bradykinesia
bradyphrenia
brain biopsy
calcification, intracranial
calcifications, intracranial, punctate
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebral cortical atrophy
cerebral vasculature, calcification
cerebrovascular accident
chemotherapy, CNS treatment and complications with
children
Clinical Pathologic Conference(C.P.C.)
cognition
conjunctival biopsy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cranial nerves, toxins effecting
cranial neuropathy, multiple
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
dementia, familial
dementia, frontal lobe type
dementia, presenile
dental pulp biopsy
dentate nuclei
dentate nuclei, lesion of
depression
developmental milestones, loss of
developmental retardation
differential diagnosis
disability, neurological
dysarthria
dyscalculia
dysdiadochokinesia
dysphagia
electromyogram
electron microscopy
encephalopathy
exome sequencing
falling
familial
fatigue
frontal lobe, anatomy and physiology
frontal lobe, lesion of
gait disorder
gait, spastic
gangliosidosis GM1
gangliosidosis, generalized
gaze palsy
gene mutation
genetic neurologic disorders
genetic testing
genu of corpus callosum
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
Hallervorden Spatz disease
handwriting
heavy metal intoxication
histochemistry
hyperreflexia
hypotonia
imbalance
incoordination
intellectual deficit
intellectual deterioration
intrathecal chemotherapy
iron, brain
jaundice
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
liver disease
lysosomal storage disease
memory, impairment of
metachromatic leukodystrophy
methotrexate
microangiopathy, brain
mimics
misdiagnosis
mortality
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, black holes on
MRI, demyelinating disease
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, gradient-echo
MRI, high signal foci on
MRI, magnetization transfer sequence
MRI, paramagnetic effect
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, disability status scale
multiple sclerosis, misdiagnosis
muscle biopsy
muscle weakness
myoclonus
myoclonus, epilepsy
N-acetyl-L-aspartic acid
nerve biopsy
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neuronal cell death
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neurotoxin
next-generation sequencing
Niemann-Pick disease
ophthalmoplegia, plus syndrome
optic atrophy
PANK2 mutation
personality change
posterior column disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyramidal tract
quadriplegia
remote effect of cancer on the nervous system
review article
seizure
skin, biopsy
spinal cord
spinal cord, lesion of
thallium poisoning
tremor
tremor, intention
urinary incontinence
vibratory sensation, abnormal
vision, failure of in childhood
visual evoked response
visual impairment
vitamin deficiency
vitamin E deficiency
Wallerian degeneration
weakness, proximal
white matter disease
writing
Showing articles 500 to 539 of 539 << Previous

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

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

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior
BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972

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

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

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

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

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

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

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

Biochemical Abnormalities of the Sarcoplasmic Reticulum in Muscular Dystrophy
NEJM 290:184, Samaha,F.,et al, 1969

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

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

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

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

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968

Nine Neuropathies
Med Ann of the Dist of Columbia 37:89, Stevens,H., 1968

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967

Mental Deficiency Associated with Muscular Dystrophy
Brain 89:769, Rosman,N.P.,et al, 1966

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

Seronegative Ocular Syphilis & Neurosyphilis, Neuro-Ophthalmology Symposium, U. of Miami
(Ed) , St. Louis:C. V. Mosby Co. , 1965, p. 1, Smith,J.L., 1965

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

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

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Causalgia of the Face, Two Cases Successfully Treated by Sympathectomy
BMJ 1:804-805, Bingham,J.A.W., 1947

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



Showing articles 500 to 539 of 539 << Previous