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acid maltase deficiency
acid maltase deficiency, adult
acyl CoA dehydrogenase deficiency
advances in neurology
adverse drug reaction
alcohol
alcohol, heart involvement with
alcohol, neurologic complications with
alcoholism
alpha glucosidase
amyloid
amyloidosis
ANA
ankle edema
anterior horn cell disease
antiphospholipid antibody syndrome
areflexia
arrhythmia, cardiac
aspartate aminotransferase
aspiration
asthma
asymptomatic
ataxia
atrioventricular block
autoimmune disease
bradycardia
brain biopsy
brainstem, lesion of
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency
carnitine deficiency myopathy
carpal tunnel syndrome
cerebral embolism
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, nonvascular territory
cerebrovascular accident, postpartum
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
chemosis
chest pain
chloroquine
chronic progressive external ophthalmoplegia
Churg-Strauss syndrome
Clinical Pathologic Conference(C.P.C.)
complications
congestive heart failure
conjunctivitis
contractures, joint
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
dementia
dementia, cerebrovascular disease causing
depression
dermatomyositis
desmin
developmental retardation
diabetes mellitus
differential diagnosis
distal muscle weakness
drug induced neurologic disorders
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dystroglycanopathies
dystrophic calcification
dystrophin
echocardiogram
edema, leg
edema, periorbital
electrocardiogram, abnormal
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
enzyme, muscle disease
eosinophilia
eosinophilic granulomatosis with polyangiitis
epidemiology of neurology
episcleritis
exercise intolerance
exercise-induced neurologic dysfunction
extraocular muscle enlargement
facial weakness
falling
familial
fatigue
fever
fibrillations
fluctuate
fluorescein angiography
fundus, abnormality of
gastrocnemius muscle weakness
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
glycogen storage disease
granular atrophy, cerebral cortex
hammertoes
headache
heart block
hemianopia
hepatomegaly
high arched feet
hip pain
hirsutism
histochemistry
histochemistry of muscle
hypoglycemia
hypotonia
iatrogenic neurologic disorders
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
intellectual deficit
intellectual deterioration
ipecac
Kearns-Sayre syndrome
lactic acidemia
leg swelling
Leigh's disease
life expectancy
lipid storage myopathy
lordosis
lung biopsy
lysosomal storage disease
lysosomes, abnoral
MELAS syndrome
metabolic acidosis
microinfarcts
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
molecular genetics
mortality
motor neuron disease
MRI, abnormal
MRI, muscle
MRI, orbit
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenic syndrome
myocardial biopsy
myocardial infarction
myocarditis
myocytolysis
myoglobinuria
myopathy
myopathy, alcoholic
myopathy, amyloid
myopathy, desmin
myopathy, drug-induced
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, painful
myopathy, proximal
myopathy, steroid induced
myopathy, toxic
myositis
myositis, bacterial
myotonic discharges
neck weakness
nerve biopsy
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuropathology
neuropathy
neuropathy, toxic
neurotoxin
nystagmus
occipital lobe, infarction, bilateral
old age, neurology of
ophthalmoplegia
optic atrophy
orthopnea
pacemaker, cardiac-transvenous
pain
pain, calf
pain, leg
periarteritis nodosa
pericardial effusion
perineuritis
perineuritis, optic
peripheral vascular disease
poison, neurologic problems with
polymyositis
Pompe's disease of glycogen storage
postpartum
postpartum cardiomyopathy
postpartum cortical blindness
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
psychiatric problems in neurologic disorders
ptosis
ptosis, unilateral
pulmonary edema
quadriplegia
quality of life
radionuclide imaging, heart
renal biopsy
renal failure
renal failure, acute
repetitive nerve stimulation
respirator
respiratory failure
retinal vasculitis
retinopathy
review article
rhabdomyolysis
rigid spine syndrome
sedimentation rate, elevated
seizure
shoulder, pain in
sick sinus syndrome
skin, biopsy
steroid
steroid therapy, CNS treatment and complications with
strokelike episodes
systemic illness
tachycardia
thrombophlebitis
thrombotic microangiopathy
tongue, enlarged
toxins, nervous system
transient ischemic attack
treatment of neurologic disorder
type 1 muscle fiber
uveitis
viral myopathy
visual field defect
visual loss
walking frame
walking, difficulty with
weakness
weakness, acute
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
winging of scapula
workup
Showing articles 0 to 50 of 1596 Next >>

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

A 63-Year-Old Woman Presenting with Bilateral Leg Pain
Neurol 96:343-348, Budhu, J.,et al, 2021

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Diagnostic Challenges in a Young Patient with Hypereosinophilia
Neurol 89:e159-e165, Ortiz, J.G.,et al, 2017

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

MELAS
MedLink.com, August, Klopstock, T., 2012

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Clinicopath Conference, Postpartum Renal Failure Due to Thrombotic Microangiopathy Associated With Antiphospholipid Antibodies
NEJM 358:275-289, Case 2-2008, 2008

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

Ipecac Myopathy and Cardiomyopathy
JNNP 56:560-562, Dresser,L.P.,et al, 1992

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
Am J Med 82:447-455, Estes,M.L.,et al, 1987

Progressive Dementia, Visual Deficits, Amyotrophy, & Microinfarcts
Neurol 35:789-796, Kaplan,J.G.,et al, 1985

Alcoholic Myopathy in Heart & Skeletal Muscle
NEJM 301:28-33, Rubin,E., 1979

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

Primary Central Nervous System Lymphoma:Clinical Features, Diagnosis, and Extent of Disease Evaluation
www.UptoDate.com, Jan, Nayak,L & Batchelor,T., 2024

Risk of Stroke and Myocardial Infarction Among Initiators of Triptans
JAMA Neurol 81:248-254, Petersen,C.L.,et al, 2024

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
Neurol 102:e209396, Yang,Y.,et al, 2024

Treatment Modalities and Outcomes in Brainstem Cavernous Malformations: A Large Multicenter Observational Cohort Study
Stroke 55:1151-1160, Lu,J.,et al, 2024

Clinicopathologic Conference, Reversible Cerebral Vasoconstriction Syndrome with Takotsubo Cardiomyopathy
NEJM 390:2108-2118, Case 18-2024, 2024

Giant Cell Arteritis With Optic Perineuritis
Neurol 103:e209707, Taga,A.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
JAMA Neurol 81:977-984, Hadad,R.,et al, 2024

Tumour-Like Mass Lesion Secondary to Primary CNS Vasculitis
Neurol 103:e209819, Roberts,J.I.,et al, 2024

Incidence and Outcomes of Cardiocerebral Infarction:A Cohort Study of 2 National Population-Based Registries
Stroke 55:2221-2130, Ho,J.S-Y.,et al, 2024

Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
Neurol 102:e209188, Bai,X.,et al, 2024

A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
Neurol 103:e209900, Jones,F.J.S.,et al, 2024

Perivascular Tumefactive Neurosarcoidosis of the Basal Ganglia
Neurol 103:e209899, Aboseif,A.,et al, 2024

An Unusual Etiology of Lumbosacral Plexopathy in a Patient with HIV
Neurol 103:e209930, Madduluri,B.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinicopathologic Conference, Brain Abscess Due to Infection with Listeria Monocytogeneses
NEJM 391:1529-1538, Case 33-2024, 2024

Progressive Peripheral Neuropathy in a 66-Year-Old Woman with Sezary Syndrome
Neurol 103:e209983, Fanouraki,S.,et al, 2024

Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

A 22-Year-Old Man with Multifocal Brain and Osseous Lesions
Neurol 101:1025-1031, Reddy,S.,et al, 2023

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,et al, 2023



Showing articles 0 to 50 of 1596 Next >>