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Differential
(Click to cross reference)
abdominal distention
areflexia
ataxia
basal ganglia, lesion, bilateral
brainstem, lesion of
cachexia
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
consanguinity
corpus callosum, lesion of
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cyst, parenchymal
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deep gray nuclei
diarrhea
extraocular muscle lesion
eye movement, disorders of
familial
fever
gait disorder
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
hearing loss
hepatomegaly
heralding manifestation
intestinal pseudoobstruction
Kearns-Sayre syndrome
Leber's hereditary optic neuropathy
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
MELAS syndrome
MERRF syndrome
microangiopathy, brain
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
muscle biopsy
muscle weakness, proximal
myopathy
myopathy, mitochondrial
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic symptoms
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, peripheral
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, progressive external
pain, abdominal
pigmentary retinopathy
polyneuropathy
prognosis
progressive neurologic disorder
ptosis
ragged-red fibers
retina, abnormal
retinal degeneration
retinal lesion
review article
sensorineural hearing loss
short stature
succinate dehydrogenase deficiency
symmetric brain lesions
systemic illness
thalamus, lesion of-bilateral
treatment of neurologic disorder
upgaze, paralysis of
visceral neuropathy
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
white matter disease
white matter disease, pattern
Showing articles 950 to 1000 of 2497 << Previous Next >>

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

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

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

Parkinson Disease in Twins,An Etiologic Study
JAMA 281:341-346,376, Tanner,C.M.,et al, 1999

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
Muscle & Nerve 21:1533-1536, Gossett,J.G.&Change,P.F., 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
Neurol 51:1226-1227, Wasay,M.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

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

Unilateral Thalamic Deep Brain Stimulation for Refractory Essential Tremor and Parkinson's Disease Tremor
Neurol 51:1063-1069, Ondo,W.,et al, 1998

Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
Neurol 51:1769-1770, Kelly,P.J.,et al, 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

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

Familial Idiopathic Intracranial Hypertension with Spinal and Radicular Pain
Arch Neurol 55:854-856, Santinelli,R.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998

Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
Lancet 352:1892-1897, Labauge,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Sneddon's Syndrome:Neuro-Ophthalmologic Manifestations in a Possible Autosomal Recessive Pattern
Neurol 51:1185-1187, Rehany,U.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Transdural Spinal Cord Herniation:Imaging and Clinical Spectra
AJNR 19:1337-1344, 11851998., Watters,M.R.,et al, 1998

Epilepsies in Twins:Genetics of the Major Epilepsy Syndromes
Ann Neurol 43:435-445, Berovic,S.F.,et al, 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

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

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
JAMA 280:619-622, 6521998., Wu,W.S.,et al, 1998

Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
JAMA 280:614-618, 6521998., Rogaeva,E.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,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

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

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

Sporadic Incusion-Body Myositis and hereditary Inclusion-Body Myopathies
Arch Neurol 55:915-920, Askanas,V.&Engel,W.K., 1998



Showing articles 950 to 1000 of 2497 << Previous Next >>