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anemia
antiendomysial antibodies
aphonia
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ataxia
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ataxia, sensory
ataxia, truncal
ataxic gait
autoantibodies
autoimmune disease
B 12 deficiency
Bergmann's gliosis
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cerebellum, disease of
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cerebrospinal fluid
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cerebrospinal fluid, elevated protein of
children
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
confusion
degenerative diseases of CNS
dementia
dementia, treatment of
demyelinating disease
depression
dermatitis herpetiformis
diarrhea
diet
eye movement, disorders of
folic acid deficiency
gait disorder
ganglionitis
gastrointestinal disease, neurologic complications
gliadin antibodies
gluten ataxia
gluten sensitivity
gluten-free diet
growth retardation
headache
headache, episodic
hemorrhagic diathesis
hepatitis
HLA
hyperpigmentation of skin
hypocalcemia
hypogonadism
hypomagnesemia
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hypoprothrombinemia
hypothalamus, damage to
imbalance
intestinal biopsy
leukodystrophy
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leukoencephalopathy, differential diagnosis
lymphadenopathy
malabsorption
malabsorption syndrome
misdiagnosis
mononeuropathy multiplex
MRI
MRI, abnormal
MRS
muscle weakness
myelopathy
myoclonic ataxia
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myoclonus, epilepsy
myopathy
neurologic disease
neurologic disease, diagnoses of
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, motor
neuropathy, peripheral
nystagmus
oral ulcerations
osteoporosis
palatal myoclonus
paresthesias
posterior column disease
psychiatric problems in neurologic disorders
puberty
puberty, delayed
Purkinje cell
Ramsay Hunt syndrome
reticulum cell sarcoma
review article
screening
seizure
serologic testing
short stature
skin, lesions in neurologic disorders
speech disorder
speech disorder, non aphasic
spinal cord, lesion of
spinocerebellar degeneration
sprue
steatorrhea
systemic illness
tetany
transglutaminase antibodies
treatment of neurologic disorder
vasculitides
vitamin deficiency
vitamin E
walking, difficulty with
weight loss
white matter disease
wide based gait
Showing articles 1050 to 1100 of 1241 << Previous Next >>

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Primary Cerebellopontine Progressive Multifocal Leukoencephalopathy Diagnosed Premortem by Cerebellar Biopsy
Ann Neurol 11:199-202, Jones,H.R.,et al, 1982

Pronounced Cerebellar Features in Legionnaires'Disease
BMJ 283:276, Maskill,M.R., 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Meningeal Carcinomatosis
Arch Neurol 38:696-699, Theodore,W.H.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

Ataxic Hemiparesis from a Midbrain Mass
Ann Neurol 9:405-407, Bendheim,P.E.,et al, 1981

Ataxic Hemiparesis with Trigeminal Weakness
Neurol 31:635-636, Sakai,T.,et al, 1981

Epstein-Barr-virus-carrying Lymphoma in a Patient with Ataxia-telangiectasia
BMJ 282:425-427, Saemundsen,A.K.,et al, 1981

Lecithin Treatment in Friedreich's Ataxia
BMJ 282:1197-1198, Pentland,B.,et al, 1981

Visual involvement in Friedreich's Ataxia & Hereditary Spastic Ataxia
Arch Neurol 38:75-79, Livingstone,I.R.,et al, 1981

Double-blind, Triple-crossover Trial of Low Doses of Oral Physostigmine in Inherited Ataxias
Neurol 31:288-292, Kark,R.A.P.,et al, 1981

Tick Paralysis With Persistent Weakness & Electromyographic Abnormalities
Arch Neurol 38:59-61, Donat,J.R., 1981

Neurologic Complications of Lymphomatoid Granulomatosis
Neurol 31:619-620, Hogan,P.J.,et al, 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Clin. Path. Conference
Fibrillary Astrocytoma of Medulla, with Invasion of Subarachnoid Space, Case Record 6-1981, NEJM 304, 3430,1981., 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Effect Of Thyrotropin-Releasing Hormone On Ataxia Of Spinocerebellar Degeneration
Lancet 1:418-419, Sobue,I.,et al, 1981

Computed Tomography in Ataxia-Telangiectasia
J Comput Assist Tomogr 5:660-661, Assencio-Ferreira,V.J.,et al, 1981

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

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Association Of Spinocerebellar Disorders With Cystic Fibrosis Or Chronic Childhood Cholestasis & Very Low Serum Vit. E
Lancet 2:1319-1321, Elias,E.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Temporal Arteritis Presenting as Ataxia and Dementia
Post Grad Med 69:246-249, Shenberger,K.N.,et al, 1981

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

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

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Progressive & Treatable Cerebellar Ataxia in Macroglobulinemia
Neurol 30:536-538, Spencer,S.S.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Acute Cerebellar Ataxia Associated With Epstein-Barr Virus Infection
JAMA 243:148-149, Cleary,T.G.,et al, 1980

Mycoplasma Antibody in Guillain-Barre Syndrome & Other Neurological Disorders
Ann Neurol 7:108-112, Goldschmidt,B.,et al, 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Remission of Cerebellar Dysfunction After Pneumonectomy For Bronchogenic Carcinoma
NEJM 302:156, Paone,J.F.,et al, 1980

The Acute Sensory Neuronopathy Syndrome:A Distinct Clinical Entity
Ann Neurol 7:354-358, Sterman,A.B.,et al, 1980

Cerebellar Degeneration Due to Chronic Phenytoin Therapy
Ann Neurol 7:18-23, McLain,L.W.,et al, 1980

Homolateral Ataxia & Crural Paresis:Case Report
Neurol 30:1013-1015, Perman,G.P.,et al, 1980

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

The Use of Choline Chloride in Ataxic Disorders
JNNP 43:452-454, Lawrence,C.M.,et al, 1980

Cerebral Thrombosis in Two Patients with Malabsorption Syndrome Treated with Vitamin K
BMJ 281:541, Florholmen,J.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980



Showing articles 1050 to 1100 of 1241 << Previous Next >>