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Differential
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abducens nerve paralysis, bilateral
acanthocytosis
adrenoleukodystrophy
adverse drug reaction
agammaglobulinemia
aminoacidopathies
ANA
arrhythmia, cardiac
ataxia
ataxia, cerebellar
atrial fibrillation
basal ganglia, calcification of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
blindness
botulism
brainstem, lesion of
brainstem, tuberculoma of
calcification, intracranial
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, dense artery sign
cataracts
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
children
chronic progressive external ophthalmoplegia
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10 deficiency
collagen vascular disease
congestive heart failure
conjunctival biopsy
consanguinity
cornea, abnormal
corpus callosum, lesion of
creatine phosphokinase(CPK)elevated
cyst, parenchymal
deafmute
deafness
deep gray nuclei
dementia
diabetes mellitus
diplopia
DNA probes
drug induced neurologic disorders
dwarfism
dysphagia
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalopathy
extraocular muscle atrophy
extraocular muscle lesion
eye closure
eye movement, disorders of
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
familial
fatigue
Friedreich's ataxia
fundus, abnormality of
gangliosidosis GM1
gangliosidosis, generalized
gargoylism
gaze palsy, horizontal
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
glaucoma
Hallervorden Spatz disease
Hallgren's syndrome
headache
hearing loss
heart block
heart murmur
histochemistry of muscle
Hurler's syndrome
hypocalcemia
hypoglycorrhachia
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypothyroidism
hypotonia
intestinal pseudoobstruction
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
lid closure, weakness of
macular degeneration
malformation, CNS, congenital
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
meningitis
mental retardation
MERRF syndrome
metabolic acidosis
metachromatic leukodystrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
MNGIE syndrome
molecular genetics
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
mucopolysaccharidoses
muscle biopsy
muscle biopsy, extraocular
muscle cramp
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, congenital
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, seronegative
myasthenic syndrome
myelopathy
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myopia
myotonia
myotonia dystrophica
neck weakness
neuritis
neuroaxonal dystrophy
neuroendocrinology
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, hereditary peripheral
Niemann-Pick disease
night blindness
obesity
ocular myopathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
optic nerve
optic neuropathy
orbicularis oculi muscle
pancytopenia
peroxisomal disease
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polydactyly
pons, lesion of
prognosis
prostigmine
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
ptosis
ptosis, bilateral
pulmonary infiltrates
pyruvate metabolism, abnormality of
radiculopathy
ragged-red fibers
Raynaud's phenomenon
refractive errors
Refsum's disease
renal tubular acidosis
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
schizophrenia
scleroderma
scleroderma, neurologic involvement with
sedimentation rate
seizure
sensorineural hearing loss
seronegative
short stature
skin, biopsy
skin, tight
Southern immunoblot test
Spielmeyer Vogt syndrome
spinocerebellar degeneration
spongy degeneration of brain
Stephens syndrome
succinate dehydrogenase deficiency
sudden death
symmetric brain lesions
tapetoretinal degeneration
tetany
thalamus, lesion of-bilateral
tongue, fasciculations of
treatment of neurologic disorder
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
Usher's syndrome
visual field defect
visual fields, constricted
visual loss
weakness
weakness, fatiguable
weakness, generalized
weight loss
white matter disease
white matter disease, pattern
Showing articles 200 to 250 of 2710 << Previous Next >>

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

Clemastine Fumarate as a Remyelinating Therapy for Multiple Sclerosis (ReBUILD): A Randomised, Controlled, Double-Blind, Crossover Trial
Lancet 390:2481-2489, Green, A.J.,et al, 2017

Durability of the Rituximab Response in Acetylcholine Receptor Autoantibody-Positive Myasthenia Gravis
JAMA Neurol 74:60-66, Robeson, K.R.,et al, 2017

A 74-year-old Woman with Bilateral Foot Pain and a Palmar Rash
Neurol 88:e44-e50, Wynn, D.P.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
Lancet 389:1367-1368, Vale, T.C.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

Pure Sensory Ganglionopathy as the First Sign of Relapse in Non-Hodgkin Lymphoma
Neurol 88:1976-1977, Hossack, M. & McClean, J., 2017

Dont Fall for Pseudo-INO
Neurol 88:e205-e206, Traber, G.L.et al, 2017

Neuropsychiatric Involvement of Behcets Disease
www.SMGEbooks.com Dec, Soyak, M., 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Neurological, Respiratory, Musculoskeletal, Cardiac and Ocular Side-Effects of Anti-PD-1 Therapy
Eur J Cancer 60:210-225, Zimmer, L.,et al, 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

Orthostatic Tremor
Neurol 86:458-464, Hassan, A.,et al, 2016

Statin-Associated Autoimmune Myopathy
NEJM 374:664-669, Mammen, A.L., 2016

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

National Characteristics and Predictors of Neurology 30-day Readmissions
Neurol 86:669-675, Guterman, E.L.,et al, 2016

Myasthenia Gravis Exacerbation after Discontinuing Mycophenolate
Neurol 86:1159-1163, Oskarsson, B.,et al, 2016

Diabetic Sensory and Motor Neuropathy
NEJM 374:1455-1464, Vinik, A.I.,et al, 2016

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016

Myasthenia Gravis Treated with Autologous Hematopoietic Stem Cell Transplantation
JAMA Neurol 73:652-658,624, Bryant, A.,et al, 2016

A Randomized Controlled Trial of Methotrexate for Patients with Generalized Myasthenia Gravis
Neurol 87:57-64, Pasnoor, M.,et al, 2016

Neurologic Signs and Symptoms Frequently Manifest in Acute HIV Infection
Neurol 87:148-154, Hellmuth, J.,et al, 2016

International Consensus Guidance for Management of Myasthenia Gravis
Neurol 87:419-425, Sanders, D.B.,et al, 2016

Mills Syndrome
Neurol 87:e54, Porto, F.H.G.,et al, 2016

Randomized Trial of Thymectomy in Myasthenia Gravis
NEJM 375:511-522,576, Wolfe, G.I.,et al, 2016

Long-Term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Juvenile Metachromatic Leukodystrophy Compared with Nontransplanted Control Patients
JAMA Neurol 73:1133-1140, Groeschel, S.,et al, 2016

Physician-Assisted Death
Neurol 87:1152-1160, Abrahao, A.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

An Unusual Cause of Hypokalemic Paralysis
Neurol 87:e174-e177, Shree, R.,et al, 2016

Clinical Manifestations of Myasthenia Gravis
UptoDate Aug 2016, Bird, S.J., 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

Myasthenia Gravis after Botulinum Toxin Type A Injection
Turk J Neurol 22:143-144, Tekce, H.D.,et al, 2016

Chronic Hepatitis C Virus Infection and Neurological and Psychiatric Disorders
World J Gastroenterol 21:2269-2280, Adinolfi, L.E.,et al, 2015

Acute Flaccid Myelitis of Unknown Etiology in California 2012-2015
JAMA 314:2663-2671, Van Haren, K.,et al, 2015

A Young Woman with Blurred Vision and Distal Paresthesias
JAMA Neurol 72:1519-1523, Kung, N.H.,et al, 2015

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015

Magnetic Resonance Neurography Detects Diabetic Neuropathy Early and with Proximal Predominance
Ann Neurol 78:939-948, Pham, M.,et al, 2015

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Two Uncommon Causes of Guillain-Barr� Syndrome: Hepatitis E and Japanese Encephalitis
Case Reports Neurol Med Art ID:759495, Bandyopadhyay, D.,et al, 2015



Showing articles 200 to 250 of 2710 << Previous Next >>