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Differential
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abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
alpha glucosidase
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
calf hypertrophy
cardiomegaly
cardiomyopathy
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
facial weakness
falling
familial
fatigue
fibrillations
floppy infant
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
hepatomegaly
hip flexor weakness
histochemistry of muscle
hypoglycemia
hypotonia
hypotonia, infants
hypoxia
imbalance
inborn errors of metabolism, screening
ischemic exercise test
leg weakness, bilateral
low back pain
lysosomal storage disease
lysosomes, abnoral
McArdle's disease
misdiagnosis
mortality
MRI, muscle
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, genetic
myopathy, metabolic
myopathy, necrotizing
myopathy, vacuolar
myotonic discharges
neck weakness
neurologic disease
neurologic disease, diagnoses of
orthopnea
pain, back
paraspinal muscle
paraspinal muscle weakness
PAS positive
patient in waiting
phosphorylase b kinase deficiency
Pompe's disease of glycogen storage
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
pseudomyotonia
pulmonary function tests
pulmonary hypertension
renal failure
respiratory failure
review article
screening
second wind phenomena
short stature
subarachnoid hemorrhage
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
urine, dark
vital capacity
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
winging of scapula
Showing articles 800 to 850 of 1614 << Previous Next >>

Clinicopath Conf
Noncaseating Granulomas Consistent with Sarcoidosis, Case 37-1996, NEJM 335:1668-1674996., , 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Whipple Disease Confined to the Central Nervous System in Childhood
AJNR 17:1589-1591, Duprez,T.P.J.,et al, 1996

Antibiotic Treatment for Giant-Cell Arteritis
Lancet 348:1630, Fontana,P.E.,et al, 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

Nonsystemic Vasculitic Mononeuropathy Multiplex, Cryoglobulinemia, and Hepatitis C
Muscle & Nerve 19:1596-1602996., David,W.S.,et al, 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

A Man with Weight Loss, Ataxia, and Confusion for 3 Months
Lancet 347:448, Beversdorf,D.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
NEJM 334:821-827, 8571996., Reuss,M.L.,et al, 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Maternal Phenylketonuria:Magnetic Resonance Imaging of the Brain in Offspring
J Pediatr 128:770-775, Levy,H.L.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Intellectual Impairment in Children Exposed to Polychlorinated Biphenyls in Utero
NEJM 335:783-789, Jacobson,J.L.,et al, 1996

Mastocytosis-Induced Nyctalopia
J Neuro-Ophthalmol 16:115-119, Lesser,R.L.,et al, 1996

Frequency of Dementia in Parkinson Disease
Arch Neurol 42:428-431, Aarsland,D.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Intelligence and the X Chromosome
Lancet 347:1814-1815, Turner,G., 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

New Antiepileptic Drugs
NEJM 334:1583-1590, Dichter,M.A.&Brodie,M.J., 1996

Iron Deficiency Anaemia and Febrile Convulsions:Case-Control Study in Children Under 2 Years
BMJ 313:343, Pisacane,A.,et al, 1996

Reversible Parkinsonism and Cognitive Impairment with Chronic Valproate Use
Neurol 47:626-635, Armon,C.,et al, 1996

Startle Provoked Epileptic Seizures:Features in 19 Patients
JNNP 61:151-156, Manford,M.R.A.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996

Vitamin D Deficiency and Osteopenia in Hemiplegic Limbs of Stroke Patients
Stroke 27:2183-2187, Sato,Y.,et al, 1996

Neuropsychiatric Aspects of Progressive Supranuclear Palsy
Neurol 47:1184-1189, Litvan,I.,et al, 1996

Reversibility of Cerebral Ventricular Enlargement in Anorexia Nervosa, Demonstrated by Quant MR
J Pediatr 128:296-301, Golden,N.H.,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

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

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

Wernicke's Encephalopathy After Vertical Banded Gastroplasty for Morbid Obesity
BMJ 312:434, Seehra,H.,et al, 1996

Optic Neuropathy
Neurol 46:315-322, Newman,N.J., 1996

MRI of White Matter Changes in the Sjogren-Larsson Syndrome
Neuroradiology 37:576-577, Hussain,M.Z.&Aihara,M., 1996

Clinicopath Conf
Focal Cortical Dysplasia, Case 7-1996, NEJM 334:586-592996., , 1996

Cognitive Impairment & Mortality in a Cohort of Elderly People
BMJ 312:608-611, Gale,C.R.,et al, 1996

Leukoencephalopathy-Related Cerebral Amyloid Angiopathy with Cystatin C Deposition
Stroke 27:1417-1419, Shimode,K.,et al, 1996

Reduced Response to Activated Protein C is Associated with Increased Risk for Cerebrovascular Disease
Ann Int Med 125:265-269, van der Bom,J.G.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

Carotid Artery Thrombus Associated with Severe Iron-Deficiency Anemia and Thrombocytosis
Stroke 27:1002-1005, Akins,P.T.,et al, 1996

Neurologic Presentation of Wilson Disease without Kayser-Fleischer Rings
Neurol 46:1040-1043, Demirkiran,M.,et al, 1996

Antiepileptic Medication and Oral Contraceptive Interactions:A National Survey of Neurologists and Obstetricians
Neurol 46:1534-1539, Krauss,G.L.,et al, 1996

Leukoencephalopathy Associated with Cobalamin Deficiency
Neurol 46:832-834, Chatterjee,A.,et al, 1996

Effect of Malnutrition after Acute Stroke on Clinical Outcome
Stroke 27:1028-1032, Davalos,A.,et al, 1996



Showing articles 800 to 850 of 1614 << Previous Next >>