Neudle.com: "macroglossia"

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal muscle paralysis

acid maltase deficiency

acid maltase deficiency, adult

adverse drug reaction

alpha glucosidase

amyloid angiopathy, cerebral

amyloidosis, oculoleptomeningeal, familial

amyotrophic lateral sclerosis

anemia, megaloblastic

angioedema, tongue

angioneurotic edema

anterior horn cell disease

arterial dissection

arterial dissection, carotid

arteritis, temporal

arylsulfatase B

aspartate aminotransferase

ataxia, cerebellar

B 12 deficiency

basal ganglia, calcification of

burning paresthesia

calcification, intracranial

calf hypertrophy

carpal tunnel syndrome

CAT scan, abnormal

cerebrovascular accident

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

concentration, impaired

congestive heart failure

Congo red stain

cornea, opacity of

cranial nerve palsies

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

developmental retardation

dexterity, impaired

diabetes mellitus

diaphragmatic paralysis

dissociated sensory loss

distal muscle weakness

dopamine agonist

edema, periorbital

electrocardiogram, abnormal

electron microscopy

entrapment neuropathy

enzyme treatment

extraocular muscle enlargement

facial weakness

fibrinolytic agents

genetic diagnosis, prenatal

genetic neurologic disorders

glycogen storage disease

growth retardation

headache, severe

headache, temporal

headache, thunderclap

headache, unilateral

headache, worst of life

hepatosplenomegaly

heralding manifestation

hormone replacement

Hunter's syndrome

hypersegmented polys

hypoglossal nerve paralysis

hypoparathyroidism

hypoparathyroidism, idiopathic

hypothyroidism, congenital

iatrogenic neurologic disorders

immunoelectrophoresis, serum

intellectual deterioration

intracerebral hemorrhage

intracerebral hemorrhage, familial

iodine deficiency

lactic dehydrogenase(LDH)

leg weakness, bilateral

level of consciousness, decreased

lysosomal storage disease

lysosomes, abnoral

marche a petits pas

memory, impairment of

mental retardation

mental status, abnormal

methylmalonic acid, serum

motor neuron disease

MRI, angiography

mucopolysaccharidoses

muscle atrophy, progressive

muscle hypertrophy

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myopathy, amyloid

myopathy, metabolic

myopathy, necrotizing

myopathy, vacuolar

myxedema, neurologic manifestations of

nausea and vomiting

nerve growth factor

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

old age, neurology of

pain, abdominal

paraspinal muscle

paraspinal muscle weakness

paresthesias, hands

perineuritis, optic

peripheral blood smear, abnormal

pernicious anemia

pituitary, adenoma

pituitary, apoplexy

pituitary, enlargement

pituitary, microadenoma

plasma cell dyscrasia

Pompe's disease of glycogen storage

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

proton beam therapy

proximal muscle atrophy

pseudohypertrophy

psychiatric problems in neurologic disorders

ptosis, unilateral

radiation necrosis

radiation therapy, CNS treatment and complications with

respiratory failure

Sanfilippo syndrome

scalp tenderness

skin, lesions in neurologic disorders

spinal cord, compression of

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

systemic illness

testosterone, serum, low

tissue plasminogen activator, intravenous

tongue deviation

tongue, enlarged

tongue, infarction

tongue, numbness of

tongue, swelling

tongue, weakness

treatment of neurologic disorder

vitreous opacities

weakness, progressive

weakness, proximal

winging of scapula

Showing articles 0 to 19 of 19

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

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 19 of 19