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Differential
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abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acyl CoA dehydrogenase deficiency
adverse drug reaction
algorithm
aneurysm
anterior tibial muscle weakness
arthralgia
arthritis
autoimmune disease
azathioprine
azidodeoxythymidine
brachial plexus neuropathy
brain biopsy
brain biopsy, stereotaxic
calf hypertrophy
carcinoma
cardiomegaly
CAT scan, abnormal
CD4 counts
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
children
chloroquine
chromosomal abnormality
chromosome 9
cranial neuropathy
creatine phosphokinase(CPK)elevated
cryptococcal meningitis
cyclic vomiting
cystinosis
cytomegalovirus infection
delay in diagnosis
dementia
dermatitis
dermatomyositis
diaphragmatic paralysis
diarrhea
diarrhea, bloody
differential diagnosis
difficulty climbing stairs
disability rating scale, neurological
distal muscle atrophy
distal muscle weakness
dropped head syndrome
dysarthria
dysphagia
dyspnea
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalitis
encephalitis, focal
encephalitis, human immunodeficiency virus type 1
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
exercise
exercise intolerance
facial nerve palsy
facial nerve palsy, recurrent
facial weakness
falling
familial
fatigue
fibrillations
foot drop
foot drop, bilateral
fracture, long bone
gait disorder
gene
gene mutation
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
Guillain Barre syndrome
hand weakness
headache
hearing loss
heart block
heart block, complete
hepatomegaly
heralding manifestation
histochemistry of muscle
human immunodeficiency virus type 1
human immunodeficiency virus type 1, pathogenesis
hyperreflexia
imbalance
immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
intrinsic hand muscles, wasting of
leg weakness, bilateral
limb-girdle weakness
lymphoma
lymphoma involving CNS
lysosomal storage disease
Melkersson's syndrome
memory, impairment of
methotrexate
misdiagnosis
mitochondrial disease
molecular genetics
mononeuritis multiplex
mononeuropathy multiplex
MRI
MRI, abnormal
MRI, brachial plexus
MRI, muscle
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, distal, Miyoshi
myasthenia gravis
myelopathy
myelopathy, chronic progressive
myelopathy, vacuolar
myopathy
myopathy, distal
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, genetic
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, metabolic
myopathy, necrotizing
myopathy, proximal
myopathy, toxic
myopathy, vacuolar
myositis
myositis, ocular
myotonic discharges
nausea and vomiting
neck weakness
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neurosyphilis
next-generation sequencing
optic neuritis
orthopnea
pain, abdominal
paraspinal muscle
paraspinal muscle weakness
phosphorylase b kinase deficiency
polymyositis
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
prenatal diagnosis by amniocentesis
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proximal muscle atrophy
pseudomyotonia
quality of life
regional enteritis
research
respiratory failure
review article
riboflavin
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
short stature
standing difficulty
steppage gait
subarachnoid hemorrhage
syphilis, neurologic complications with
tongue, enlarged
tongue, weakness
toxoplasmosis, CNS
transient ischemic attack
treatment of neurologic disorder
ulcerative colitis
vital capacity
weakness
weakness, progressive
weakness, proximal
weight loss
winging of scapula
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 350 to 400 of 1044 << Previous Next >>

Weak at the Knees
Lancet 354:1696, Webster,G.&Beynon,H., 1999

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

MR Findings in AIDS-Associated Myelopathy
AJNR 20:1412-1416,1387, Chong,J.,et al, 1999

Intravenous Immunoglobulin in the Treatment of Autoimmune Neuromuscular Diseases:Present Status and Practical Therapeutic Guidelines
Muscle & Nerve 22:1479-1497, Dalakas,M.C., 1999

Churg-Strauss Syndrome, Clinical Study and Long-Term Follow-Up of 96 Patients
Medicine 78:26-37, Guillevin,L.,et al, 1999

Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

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

Critical Illness Neuropathy and Myopathy
Arch Neurol 56:527-528, Gutmann,L.&Gutmann,L., 1999

Focal, Steroid Responsive Myositis Causing Dropped Head Syndrome
Muscle & Nerve 22:769-771, Biran,I.,et al, 1999

Intravenous Immunoglobulin Treatment in Neurologic Disorders
Arch Neurol 56:1025-1027,1032, Sorensen,P.S., 1999

Is the Routine Use of Intravenous Immunoglobulin Treatment in Neurologic Disorders Justified?
Arch Neurol 56:1028-1032, Karussis,D.&Abramsky,O., 1999

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

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

A Sartorial Challenge
Lancet 354:996, Reading,P.J.,et al, 1999

Late-Onset Myasthenia Graivs,A Changing Scene
Arch Neurol 56:25-27, Aarli,J.A., 1999

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

The Clinical Spectrum of Sarcoglycanopathies
Neurol 52:176-179, Angelini,C.,et al, 1999

Medical Complications in Long-Term Survivors with X-Linked Myotubular Myopathy
J Pediatr 134:206-214, Herman,G.E.,et al,, 1999

Clinicopath Conf,Hepatitis C,Type II Cryoglobulinemia,Vasculitis,B-cell Lymphoma,Mononeuritis Multiplex,Case 3-1999
NEJM 340:300-307, , 1999

Microscopic Polyangiitis: Clinical and Laboratory Findings in Eighty-five Patients
Arthritis Rheum 42:421--430, Guillevin, L.,et al, 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Mild Traumatic Brain Injury,Toward Understanding Manifestations and Treatment
Arch Int Med 158:90-97, Kushner,D., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Dropped Head Synd & Bent Spine Synd:Two Separate Clin Entities or Different Manifest of Axial Myopathy
JNNP 65:258-259, Oerlemans,W.G.H.&Visser,M., 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
Neurol 51:1039-1045, Seale,C.G.,et al, 1998

Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
Neurol 51:944-948, Rpt of the Quality Stnds Subcmte AAN, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
Neurol 50:764-767, Levin,M.I.,et al, 1998

Steroid-Responsive Myopathy with Deficient Chondroitin Sulfate C in Skeletal Muscle Conn Tissue
Neurol 50:526-529, Al-Lozi,M.T.,et al, 1998

Acute Myopathy After Liver Transplantation
Neurol 50:46-53, Campellone,J.V.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
Neurol 50:1441-1445, Antonini,G.,et al, 1998

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

Spinal MRI in Vacuolar Myelopathy, and Correlation with Histopathological Findings
et a, Neuroradiology 39:865-8691997., Sartoretti-Schefer,S., 1997

Diseases of the Spine and Spinal Cord
In AIDS and the Nervous System, Lippencott-Raven, Phila, Ch 13, p 3667., Whiteman,M.L.H.,et al, 1997

Painful Proximal Diabetic Neuropathy:Inflammatory Nerve Lesions and Spontaneous Favorable Outcome
Ann Neurol 41:762-770, Said,G.,et al, 1997

Clinicopath Conf
Skeletal-Muscle Infarction Associated with Diabetes Mellitus, Case 29-1997, NEJM 337:839-845997., , 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
Arch Neurol 54:1420-1422, Sun,D.Y.,et al, 1997



Showing articles 350 to 400 of 1044 << Previous Next >>