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Differential
(Click to cross reference)
abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
acrochordon
acromegaly
adverse drug reaction
alpha glucosidase
amenorrhea
amyloid
amyloid angiopathy, cerebral
amyloidosis
amyloidosis, oculoleptomeningeal, familial
amyotrophic lateral sclerosis
anemia
anemia, megaloblastic
aneurysm
angioedema, tongue
angioneurotic edema
anorexia
anterior horn cell disease
arterial dissection
arterial dissection, carotid
arteritis, temporal
arthralgia
arylsulfatase B
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxic gait
B 12 deficiency
basal ganglia, calcification of
bromocriptine
burning hands
burning paresthesia
calcification, intracranial
calf hypertrophy
cardiomegaly
cardiomyopathy
carpal tunnel syndrome
CAT scan
CAT scan, abnormal
cerebrovascular accident
Clinical Pathologic Conference(C.P.C.)
coma
complications
compression neuropathy
concentration, impaired
congestive heart failure
Congo red stain
cornea, opacity of
cranial nerve palsies
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyanosis
deafness
delusion
dementia
developmental retardation
dexterity, impaired
diabetes mellitus
diaphragmatic paralysis
diarrhea
diplopia
disorientation
dissociated sensory loss
distal muscle weakness
dopamine agonist
dysarthria
dysmorphic
dyspnea
dyspraxia
electrocardiogram, abnormal
electromyogram
electron microscopy
entrapment neuropathy
enzyme treatment
enzyme, defect
facial weakness
familial
fatigue
fibrinolytic agents
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
glycogen storage disease
goiter
growth hormone
growth retardation
hallucination
hand weakness
hands, large
headache
headache, severe
headache, temporal
headache, thunderclap
headache, unilateral
headache, worst of life
hearing loss
hepatomegaly
hepatosplenomegaly
heralding manifestation
hoarseness
hormone replacement
Hunter's syndrome
hydrocephalus
hyperhidrosis
hypersegmented polys
hypersomnia
hypertension
hypocalcemia
hypoglossal nerve paralysis
hypoparathyroidism
hypoparathyroidism, idiopathic
hypothyroidism
hypothyroidism, congenital
hypotonia
iatrogenic neurologic disorders
immunoelectrophoresis, serum
impotence
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, familial
intrauterine
iodine deficiency
jaundice
jaw pain
lactic dehydrogenase(LDH)
leg weakness, bilateral
level of consciousness, decreased
lysosomal storage disease
lysosomes, abnoral
mania
marche a petits pas
memory, impairment of
mental retardation
mental status, abnormal
methylmalonic acid, serum
microcephaly
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, angiography
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle hypertrophy
muscle pain
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myelopathy
myopathy
myopathy, amyloid
myopathy, metabolic
myopathy, necrotizing
myopathy, vacuolar
myxedema, neurologic manifestations of
nausea and vomiting
neck weakness
nerve growth factor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
obesity
octreotide
old age, neurology of
orthopnea
pain, abdominal
papilledema
paranoia
paraspinal muscle
paraspinal muscle weakness
paresthesias
paresthesias, hands
peripheral blood smear, abnormal
pernicious anemia
pituitary
pituitary, adenoma
pituitary, apoplexy
pituitary, enlargement
pituitary, microadenoma
plasma cell dyscrasia
polyneuropathy
Pompe's disease of glycogen storage
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognathism
prognosis
proton beam therapy
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
psychiatric problems in neurologic disorders
psychosis
quadriparesis
radiation necrosis
radiation therapy, CNS treatment and complications with
respiratory failure
review article
Romberg's sign
Sanfilippo syndrome
scalp tenderness
seizure
short stature
skin, lesions in neurologic disorders
sleep apnea
somnolence
spasticity
spinal cord, compression of
steroid
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
testosterone
testosterone, serum, low
tetany
tissue plasminogen activator, intravenous
tongue deviation
tongue, enlarged
tongue, infarction
tongue, numbness of
tongue, pain
tongue, smooth
tongue, swelling
tongue, weakness
treatment of neurologic disorder
urine, dark
visual loss
vital capacity
vitreous opacities
weakness
weakness, progressive
weakness, proximal
weight loss
winging of scapula
Showing articles 0 to 18 of 18

A 41-year-old man with Thunderclap Headache
Neurol 91:e87-e91, Grossman, S.et al, 2018

Hemi Orolingual Angioedema after tPA Administration for Acute Ischemic Stroke
West J Emerg Med 16:175-177, Madden, B. & Chebl, R.B., 2015

An Unusual Headache
BMJ 349:g5602, Graham, U.M.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Cretinism and Neonatal Myxedema
Adams & Victors Principles of Neurology Chp 40, pg 1156, Ropper, A.H.,et al, 2014

Macroglossia in Amyotrophic Lateral Sclerosis
JAMA Neurol 70:1432-1435, McKee, H.R.,et al, 2013

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

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

Amyloid Myopathy:An Underdiagnosed Entity
Ann Neurol 43:719-728, Spuler,S.,et al, 1999

A Boy with Heart Failure, A Thick Tongue, and Double Vision
Lancet 349:1516, Karstein,J.,et al, 1997

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Acromegaly
NEJM 322:966-977, Melmed,S., 1990

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,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

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Lingual Infarction in Cranial Arteritis
JAMA 243:2422-2423, Sofferman,R.A., 1980

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971



Showing articles 0 to 18 of 18