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Differential
(Click to cross reference)
abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
adverse drug reaction
alpha glucosidase
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
bright tongue sign
calf hypertrophy
cardiomegaly
cardiomyopathy
CAT scan, abnormal
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
complications
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
distal muscle weakness
dysarthria
dysphagia
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
enzyme treatment
enzyme, defect
exercise intolerance
facial weakness
falling
familial
fatigue
fibrillations
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
Gowers maneuver
hepatomegaly
heralding manifestation
hip flexor weakness
histochemistry of muscle
hypotonia
hypoxia
imbalance
inborn errors of metabolism, screening
leg weakness, bilateral
limb-girdle weakness
low back pain
lysosomal storage disease
lysosomes, abnoral
mortality
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, progressive
muscle biopsy
muscle hypertrophy
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myopathy
myopathy, genetic
myopathy, metabolic
myopathy, vacuolar
myotonic discharges
neck weakness
nerve biopsy
neurologic disease
neurologic disease, diagnoses of
next-generation sequencing
orthopnea
pain, back
paraspinal muscle
paraspinal muscle weakness
patient in waiting
Pompe's disease of glycogen storage
Pompe's disease, infantile
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
pseudomyotonia
pulmonary function tests
pulmonary hypertension
respiratory failure
respiratory tract infection
review article
screening
storage disease of CNS
subarachnoid hemorrhage
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
vital capacity
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
winging of scapula
Showing articles 200 to 250 of 3304 << Previous Next >>

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

Pellagra, Endocronology System, Vol. 4
The Ciba Collection of Medical Illustrations, p. 254-255981., Netter,F.H., 1981

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Neonatal Polycythemia Causing Multiple Cerebral Infarcts
Arch Neurol 37:109-110, Amit,M.,et al, 1980

Cognitive Function in Patients With Multiple Sclerosis
Arch Neurol 37:577-579, Peyser,J.M.,et al, 1980

The Neuropsychiatry of Megaloblastic Anaemia
BMJ 281:1036-1038, Shorvon,S.D.,et al, 1980

Cerebral Infarcts with Arterial Occlusion in Neonates
Ann Neurol 6:495-502, Barmada,M.A.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

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

Polyneuropathy & Folate Deficiency
Arch Neurol 35:581-584, Botez,M.I.,et al, 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

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

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

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Vitamin B-6-Dependent Seizures:Pathology & Chemical Findings in Brain
Neurol 28:47, Lott,I.T.,et al, 1978

Folate Deficiency & Restless Legs Syndrome in Pregnancy
NEJM 297:670, Botex,M.I.,et al, 1977

Plasma Anticonvulsant Concentrations During Pregnancy
Neurol 27:128, Lander,C.M.,et al, 1977

Vitamin Homeostasis in the Central Nervous System
NEJM 296:1393, Spector,R.,et al, 1977

Unrecognized Adult Phenylketonuria
NEJM 289:395, 1973, 289:1040, 1973, 290:1084., Perry,T.,et al, 1974

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

Organic Disease Presenting as a Psychiatric Syndrome
Postgrad Med 54:78, , 1973

Megaloblastic Anemia After Anticonvulsive Therapy
Corres, NEJM 287:9901972., , 1972

Chinese-Restaurant Syndrome, Recurrence, (Letter)
NEJM 286:893, Upton,A.R.M.,et al, 1972

Basilar Impression of the Skull in Patients with Adult Coeliac Disease & After Gastric Surgery
JNNP 35:92-93, Hurwitz,L.J.,et al, 1972

Electroencephalogram in Anitconvulsant-Induce Folate Deficiency
BMJ 2:207, Dow,W., 1971

Neurological Disorders & Adult Coeliac Disease
Gut 11:549, Morris,J.S.,et al, 1970

Nonatherosclerotic Causes of Stroke
Ann Int Med 70:807, Levine,J.,et al, 1969

Folic Acid & the Nervous System
BMJ 722, 1968 Dec., , 1968

Idiopathic Thrombocytosis
Neurol 18:711-713, Levine,J.,et al, 1968

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

Dementia & Folate Deficiency
Quart J Med 36:, 1967 Apr., Strachan,R.,et al, 1967

Neurological Disorders Associated with Adult Celiac Disease
Brain 89:683, Cooke,W.T.,et al, 1966

Cerebrovascular Accidents in Patients with Congenital Heart Disease
Arch Neurol & Psychiat 77:483957., Tyler,H.R.,et al, 1957

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

A Randomized Trial of Tenecteplase in Acute Central Retinal Artery Occlusion
NEJM 394:442-450, Ryan,S.J.,et al, 2026

Restless Legs Syndrome, A Review
JAMA 335:703-714, Winkelmen,J.W. & Wipper, B., 2026

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Endovascular Therapy for Medium-Vessel Occlusion Stroke - Narrowing the Target Population
NEJM 394:1955-1957,1894, Ospel,J.M. & Hill, M.D., 2026

Creutzfeldt-Jakob-Like Presentation in Anti-AMPAR Encephalitis
Ann Neurol 99:1466-1467, Durbano,K.et al, 2026

Niemann-Pick Disease Type C
Gene Reviews www.genereview.org, Bremova-Ertl,T. & Patterson, M., 2025

Anti-NMDAR Encephalitis Triggered by EBV and HSV-1
Medicine 104:28, Zhan,X.,et al, 2025

Spontaneous Calcified Cerebral Emboli from Bicuspid Aortic Valve in Young Patients: Case Series and Review
Stroke:Vasc Inter Neurol doi.org/10.1161/svi 270000.138, Sardana,S.,et al, 2025

Trident Sign in GFAP-Associated Meningoencephalomyelitis
Neurol 106:e214566, Mallett,N.S.,et al, 2025

Outcomes of Patients with Embolic Stroke of Undetermined Source Treated with Antiplatelet Agents or Anticoagulation, A Multicenter Cohort Study
Neurol 105: e213876, Seigler,J.E.,et al, 2025

Acute and Progressive Cognitive Decline in a 38-Year-Old Man
Neurol 105: e213871, Wu,L.,et al, 2025

The Spectrum of Fragile X Disorders
NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025

Clinicopathologic conference, Malignant Mixed Germ-Cell Tumor and Anti-NMDA Receptor Encephalitis
NEJM 303:488-496, Case 22-2025, 2025



Showing articles 200 to 250 of 3304 << Previous Next >>