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Differential
(Click to cross reference)
abdominal protrusion
acid maltase deficiency
acid maltase deficiency, adult
acridine orange-RNA fluorescence
areflexia
ataxia
brainstem, lesion of
bulbar palsy
bulbar palsy, progressive
calf hypertrophy
cardiomyopathy
CAT scan, abnormal
central nuclei, muscle
cerebral cortical atrophy
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
congenital myopathy
contractures, joint
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
denervation of muscle
denervation potentials
desmin
developmental disability
developmental milestones
developmental retardation
difficulty climbing stairs
disability, neurological
distal muscle weakness
dysphagia
dyspnea
dystrophin
electromyogram
electron microscopy
enzyme, defect
exercise intolerance
eye closure
face, elongated
facial appearance, abnormal
facial weakness
familial
fatigue
fetal movements, reduced
fetus
fibrillations
floppy infant
gait disorder
gene mutation
genetic counselling
genetic neurologic disorders
glycogen storage disease
Gowers maneuver
histochemistry
histochemistry of muscle
hypotonia
hypotonia, infants
intellectual deterioration
Kearns-Sayre syndrome
lactic acidemia
Leigh's disease
lid closure, weakness of
mental retardation
merosin
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal gammopathy
MRI
multicore myopathy
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle biopsy, needle
muscle cramp
muscle pain
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker, carrier
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, critically ill
myopathy, desmin
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, proximal
myopathy, quadriceps
myopathy, vacuolar
myotonia dystrophica
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neurogenic atrophy
neurogenic vs.myopathic atrophy
nucleotidase-5 activity
nystagmus
oculopharyngeal muscular dystrophy
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
pain
paraspinal muscle
paraspinal muscle weakness
poliomyelitis
polymyositis
polymyositis, infantile
polyneuropathy, critically ill
post polio syndrome
prognosis
progressive neurologic disorder
ptosis
ptosis, bilateral
ragged-red fibers
respiratory failure
review article
scoliosis
single-fiber electromyography
standing difficulty
stem cell transplantation
Stephens syndrome
stooped posture
suck, poor
treatment of neurologic disorder
type 1 muscle fiber
type 2 muscle fiber
undiagnosed
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weakness, proximal
wheelchair
winging of scapula
X-linked myopathy
Showing articles 800 to 850 of 3169 << Previous Next >>

Clinicopath Conf., Gliomatosis Cerebri
Neurol 69:600-606, Fleming,J.O.,et al, 2007

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

A Case of Spinal Cord Infarction Caused by Cervical Disc Herniation
Brain Nerve 59:997-1000, Arai, S.,et al, 2007

Migrainous Corpalgia: Body Pain and Allodynia Associated with Migraine Attacks
Cephalagia 28:87-91, Cuadrado,M.L.,et al, 2007

A Young Man with Rapidly Progressive Multifocal Disease Affecting the White matter
Pract Neurol 7:172-181, Hilton-Jones,D.,et al, 2007

Postpartum Headache: Is Your Work-Up Complete?
Am J Obstet Gynecol 196:318.e1-318.e7, Stella,C.L.,et al, 2007

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

Pediatric Encephalitis: What Is the Role of Mycoplasma Pneumoniae
Pediatrics 120:305-313, Christie,L.J., et al, 2007

HIV Infection Presenting with Motor Axonal Variant of Guillain-Barre Syndrome
J Clin Neuromusc Dis 9:303-305, Wagner, J.C. and Bromberg, M.B., 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Thromboembolic Adverse Events After Use of Recombinant Human Coagulation Factor VIIa
JAMA 295:293-298, OConnell,K.A.,et al, 2006

Myocardial Injury and Long-Term Mortality Following Moderate to Severe Carbon Monoxide Poisoning
JAMA 295:398-402, Henry,C.R.,et al, 2006

Human Botulism Immune Globulin for the Treatment of Infant Botulism
NEJM 354:462-471, Arnon,S.S.,et al, 2006

Chronic Daily Headache
NEJM 354:158-165, Dodick,D.W., 2006

Left Insular Stroke is Associated with Adverse Cardiac Outcome
Neurol 66:477-483, Laowattana,S.,et al, 2006

The Natural History of Primary Lateral Sclerosis
Neurol 66:647-653, Gordon,P.H.,et al, 2006

Electrocardiogram in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients Without Any Clinical Evidence of Coronary Artery Disease
Stroke 37:1100-1102, Cumurciuc,R.,et al, 2006

Hanging Leg Syndrome: Combined Bilateral Femoral and Sciatic Neuropathies
Neurol 66:1124-1125, Scherer,K.,et al, 2006

ADHD Drugs and Cardiovascular Risk
NEJM 354:1445-1448, Nissen,S.E., 2006

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

Adult Onset Subacute Sclerosing Panencephalitis: Clinical Profile of 39 Patients From a Tertiary Care Centre
JNNP 77:630-633, Prashanth,L.K.,et al, 2006

Mycophenolate Mofetil in Dermatomyositis: Is It Safe?
Neurol 66:1245-1247, Rowin,J.,et al, 2006

The Insular Cortex and Cardiac Response to Stroke
Neurol 66:1296-1297, Cheshire,W.P. Jr., &Saper,C.B., 2006

Elevated Troponin Levels are Associated with Higher Mortality Following Intracerebral Hemorrhage
Neurol 66:1330-1334, Hays,A. &Diringer,M.N., 2006

Phrenic Neuropathy Due to Neuralgic Amyotrophy
Neurol 66:1582-1584, Tsao,B.E.,et al, 2006

Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
Neurol 66:1585-1587, Fernandez,C.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Finding the Causes of Inherited Neuropathies
Arch Neurol 63:812-816, Scherer,S.S., 2006

Migraine and Risk of Cardiovascular Disease in Women
JAMA 296:283-291,333, Kurth,T.,et al, 2006

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Plasma Exchange in Neuroimmunological Disorders: Part 2. Treatment of Neuromuscular Disorders
Arch Neurol 63:1066-1071, Lehmann,H.C.,et al, 2006

West Nile Virus Neuroinvasive Disease
Ann Neurol 60:286-300, Davis,L.E.,et al, 2006

Early Coronary Revascularization Diminishes the Risk of Ischemic Stroke with Acute Myocardial Infarction
Stroke 37:2546-2551, vanDeGraaff,E.,et al, 2006

Myocardial Injury in patients with Intracerebral Hemorrhage Treated with Recombinant Factor VIIa
Neurol 67:1053-1055, Sugg,R.M.,et al, 2006

Severe Botulism After Focal Injection of Botulinum Toxin
Neurol 67:1855-1856, Souayah,N.,et al, 2006

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Unrecognized Myocardial Infarction and the Risk of Stroke: The Rotterdam Study
Neurol 67:1635-1639, Ikram,M.A.,et al, 2006

The Association of Chronic Hepatitis B and Myopathy
Neurol 67:1467-1469, Capasso,M.,et al, 2006

Magnetic Resonance Neurography in Extraspinal Sciatica
Arch Neurol 63:1469-1472, Lewis,A.M.,et al, 2006

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

Detection of CSF 14-3-3 Protein in Guillain-Barr Syndrome
Neurol 67:2211-2216, Bersano,A.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Concomitant Chronic Inflammatory Demyelinating Polyneuropathy and Myasthenia Gravis Following Cytomegalovirus Infection
J Neurol Sci 240:103-106, Mori, M.,et al, 2006

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006

Spinal dural arteriovenous fistulas: a congestive myelopathy that initially mimics a peripheral nerve disorder
Brain 129:3150-3164, Jellema, K., et al, 2006

Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
JNS 243:35-38, Tatsumoto, M.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Polyarteritis Nodosa Presenting as Rhabdomyolysis
J Korean Rheum Assoc Mar13(1):76-81, Bae,Y.D.,et al, 2006



Showing articles 800 to 850 of 3169 << Previous Next >>