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Differential
(Click to cross reference)
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
arthrogryposis multiplex
autonomic dysfunction
autonomic neuropathy
autonomic neuropathy, idiopathic
blindness
case studies
cataracts
cataracts, congenital
central core disease
Charcot-Marie-Tooth
clubfoot as related to neurologic disease
coloboma
degenerative diseases of CNS
diabetes mellitus
electroretinograph
epidemiology of neurology
face, numbness of
familial
Fazio-Londe's disease
genetic neurologic disorders
heavy metal intoxication
hyperthyroidism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
internuclear ophthalmoplegia
Kugelberg-Welander syndrome
Leber's congenital amaurosis
mental retardation
misdiagnosis
motor neuron disease
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, sensory loss with
myotonia dystrophica
neurofibrillary degeneration
neuropathy
neuropathy, hereditary peripheral
neuropathy, sensory
neuropathy, sensory, hereditary
nystagmus
nystagmus, dissociated
nystagmus, monocular
poison, mercury
poison, neurologic problems with
polyneuropathy, familial
pseudointernuclear ophthalmoplegia
sensory polyneuropathy
skin, lesions in neurologic disorders
tensilon test
thyrotoxicosis
tricresylphosphate
vision, failure of in childhood
visual acuity, decreased
visual loss, congenital
Werdnig-Hoffman disease
Showing articles 100 to 150 of 5999 << Previous Next >>

Scalloped Pupils in Familial Amyloidosis
NEJM 293:914, Lessell,S.,et al, 1975

Congenital Malfor & Embryonic Neuropathy
NEJM 293:98, McCredie,J., 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Polyneroupathies of Undetermined Cause
Acta Neurol Scand (Supp) :5970., Prineas,J., 1970

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Intracranial Aneurysms Causing Ophthalmoplegia
Arch Ophthal 70:75l, Cogan,D.,et al, 1963

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

Orbital Apex Syndrome Associated with Herpes Zoster Ophthalmicus
Neurol 104:e213387, Imamura,D.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 63-Year-Old Man With Progressive Multicranial Neuropathy and Leptomeningeal Enhancement
Neurol 103:e210100, Taga,A.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

Phase 2 Trial of Difelikefalin in Notalgia Paresthetica
NEJM 388:511-517, Kin,B.S.,et al, 2023

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

A Comprehensive Review of Cluneal Neuralgia as a Cause of Lower Back Pain
Orthopedic Reviews doi:10.52965/001c-35505, Anderson,D.,et al, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

An Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

The Tolosa-Hunt Syndrome
NJJP 71:577-582, Kline,L.B. & Hoyt,W.F., 2021

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

"Cortical" Wrist Drop due to a Cerebral Peduncle Infarct
Case Rep Neurol 12:207-211, Venketasubramanian, N.,et al, 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019



Showing articles 100 to 150 of 5999 << Previous Next >>