Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
afebrile
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
anti MAG antibodies
anticonvulsants
areflexia
asymptomatic
autism
autoimmune disease
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
central nervous system, infection of
cerebral cortical encephaliis
chewing, impaired
children
chromosome 17
Clinical Pathologic Conference(C.P.C.)
CLOVES syndrome
clubfoot as related to neurologic disease
complications
confusion
congenital malformation
congenital myopathy
congestive heart failure
contractures, joint
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cotton-wool spots
cranial nerve enhancement
cranial nerve enlargement
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
delay in diagnosis
denervation of muscle
developmental retardation
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
dysferlinopathy
dysplasia of C.N.S.
dyspnea
dystonia
dystonia, post traumatic
dystrophin
dystrophin associated proteins
echocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
empty sella
entrapment neuropathy
enzyme, defect
epidermal nevus syndrome
Epstein-Barr virus
exercise
exophthalmus
eye, pain in
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
falling
false positive
familial
fatigue
fever
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globe, flattened posteriorly
Gowers maneuver
headache
hearing loss
heart murmur
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
heterotopia
hirsutism
histochemistry
hoarseness
hypercalcemia
hypertension
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hypothyroidism
inability to sit up
infantile spasm
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
learning disability
learning disability, in children
leg swelling
leukocytosis
life expectancy
limb hypertrophy
lipodystrophy
liver function enzymes
lordosis
lymphadenopathy
lymphopenia
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
malignant optic glioma of adulthood
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuropathy
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
MRI, orbit
MRI, venography
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myelitis
myelitis, transverse
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
myostatin
myotonia
myotonia congenita
nausea and vomiting
neoplasm, hormone producing, ectopic
nerve conduction studies
nerve injury
neurocutaneous disease
neuroendocrinology
neuroinfectious diseases
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
night sweats
obesity
optic chiasm, lesion of
optic disc
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, neoplasm of
optic nerve, tortuosity
optic neuritis
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optical coherence tomography
orthopnea
pain
pain, leg
palpitations
percussion induced muscle contraction
perineuritis
phakomatoses
plasma cell dyscrasia
polyneuropathy
post polio syndrome
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
radiculopathy
Red flags
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
root lesion, nerve
sarcoglycan
sciatic neuropathy
scoliosis
scotoma, central
seizure
shoulder, elevation
skin, lesions in neurologic disorders
speech disorder, childhood
speech, delayed development of
spinal accessory nerve
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
splenomegaly
steppage gait
steroid
steroid therapy, CNS treatment and complications with
strokelike episodes
subarachnoid hemorrhage
subcutaneous nodules
survival motor neuron gene
syringomyelia
systemic illness
telangiectases, retinal
third nerve palsy
thirst
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
trauma
treatment of neurologic disorder
tripping
urinary frequency
urine, dark
visual acuity, decreased, monocular
visual loss
visual loss, progressive
visual loss, slow-unilateral
visual symptoms
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
winging of scapula
Showing articles 0 to 50 of 1598 Next >>

Calf Hypertrophy and Myoedema Unravel a Diagnosis of Severe Hypothyroidism
Neurol 102:e209138, Camargos, S.,et al, 2024

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

Disseminated Cysticercosis
NEJM 375:e52, Baden, L.R., 2016

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

A 61-year-old Woman with a Swollen Optic Nerve and Progressive Visual Loss
Neurol 82:e205-e209, Pecen, P.E. & Bharti, M.T., 2014

Teaching NeuroImages: Unilateral Upper Limb Muscular Hyperplasia
Neurol 80:e170-e171, Gilhuis, J.,et al, 2013

Pseudotumor Cerebri: Brief Review of Clinical Syndrome and Imaging Findings
AJNR 32:1986-1993, Degnan, A.J. and Levy L.M., 2011

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Amyloid Myopathy Presenting with Distal Atrophic Weakness
Muscle Nerve 29:605-609, Smestad, C.,et al, 2004

Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child
NEJM 350:2682-2688,2642, Schuelke,M.,et al, 2004

The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
Neurol 60:1246-1251,1230, Poppe,M.,et al, 2003

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,et al, 1999

Post-Traumatic Shoulder 'Dystonia':Persistent Abnormal Postures of the Shoulder After Minor Trauma
Neurol 51:1205-1207, Thyagarajan,D.,et al, 1998

MR Findings in Isolated Oculomotor Nerve Palsy Associated with Infectious Mononucleosis Caused by Epstein-Barr Virus Infection
J Comput Assist Tomogr 22:995-997, Ishibashi,A.,et al, 1998

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Acute Focal Neuropathy in Male Weight Lifters
Muscle & Nerve 19:897-899996., Bird,S.J.&Brown,M.J., 1996

Syringomyelia as a Cause of Body Hypertrophy
Lancet 347:1593-1595, Sudo,K.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Kobberling-Dunnigan Syndrome:A Rare Cause of Generalized Muscular Hypertrophy
Muscle & Nerve 19:843-847996., Wildermuth,S.,et al, 1996

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Facioscapulohumeral Muscular Dystrophy in Early Childhood
Arch Neurol 51:387-394, Brouwer,O.F.,et al, 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Isolated Muscle Hypertrophy as a Sign of Radicular or Peripheral Nerve Injury
JNNP 54:325-329, Mattle,H.P.,et al, 1991

Epidermal Nevus Synd:A Neurologic Variant with Hemimegalencephaly, Gyral Malf, Mental Retard, Seizures & Facial Hemihyper
Neurol 41:266-271, Pavone,L.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Hypertrophy of the Calf with S-1 Radiculopathy
Arch Neurol 45:660-664, Ricker,K.,et al, 1988

Proximal Weakness of the Extremities as Main Feature of Amyloid Myopathy
JNNP 50:1353-1358, Jennekens,F.G.I.&Wokke,J.H.J., 1987

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Muscular Hypertrophy after Chronic Radiculopathy
Arch Neurol 41:397-398, Montagna,P.,et al, 1984

Isaacs'Syndrome with Muscle Hypertrophy Reversed by Phenytoin Therapy
Arch Neurol 40:241-242, Zisfein,J.,et al, 1983

Unilateral Calf Enlargement Following S1 Radiculopathy
Muscle & Nerve 5:434-438982., Mielke,U.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Congenital Hemihypertrophy:Oncogenic Potential of the Hypertrophic Side
Ann Neurol 10:199-201, Furukawa,T.,et al, 1981

Neurological Aspects of Thyroid Dysfunction
Mayo Clin Proc 56:504-512, Swanson,J.W.,et al, 1981

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Congenital Hemihypertrophy with Aortic, Skeletal, & Ocular Abnormalities
BMJ 87, 1973 Jan., Henry,M.,et al, 1973

Addressing Systemic Complications of Acute Stroke: A Scientific Statement From the American Heart Association
Stroke 56:e15-e29, Kumar,S.,et al, 2025

Rocky Mountain Spotted Fever Encephalitis and "Starry Sky" Pattern on MRI, A Case Report
Neurologist 30:34-38, Mikhaiel,J.P.,et al, 2025

Multiple Contrast Enhancing Subdural Lesions
BMJ 387:e079362, Liu,J. & Sun,Z., 2024



Showing articles 0 to 50 of 1598 Next >>