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Differential
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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
alcohol
alcohol, neurologic complications with
anesthesia, general
anterior horn cell disease
anterior tibial muscle weakness
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
autoimmune disease
breech delivery
bulbar palsy
cardiac arrest
cardiomyopathy
central core disease
children
chromosome 5
clubfoot as related to neurologic disease
Coats syndrome
congenital heart disease
congenital malformation
congenital myasthenic syndromes
congenital myopathy
consanguinity
contractures, joint
creatine phosphokinase(CPK)elevated
developmental retardation
differential diagnosis
dislocated hip, congenital
distal muscle weakness
dysmorphic
dysphagia
electromyogram
epicanthal folds
exome sequencing
eye closure
face, elongated
facial anomalies
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
fatigue
fetal alcohol syndrome
fetus
foot drop
gait disorder
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
high arched palate
histochemistry of muscle
human immunodeficiency virus type 1
hyporeflexia
hypotonia
hypotonia, infants
immunohistochemistry
immunomodulation
immunosuppressive agents
intellectual deficit
kyphoscoliosis, neurologic causes of
lid closure, weakness of
lip, abnormal
lordosis
malignant hyperpyrexia
mental retardation
mestinon
microcephaly
misdiagnosis
mitral valve prolapse
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
motor neuron disease
multicore myopathy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, neuromuscular junction in
myasthenia gravis, treatment of
myasthenic syndrome
myopathy
myopathy, acquired
myopathy, amyloid
myopathy, glycogen storage
myopathy, scleromyxedema
nasal bridge, wide
nasal speech
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuropathy
nose, abnormal
nusinersen
old age, neurology of
opened mouth
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
palpebral fissure, short
philtrum, hypoplastic
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
ptosis
ptosis, bilateral
repetitive nerve stimulation
respiratory failure
review article
scoliosis
scoliosis, neurologic association with
screening
short stature
sloped shoulders
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, classification
stem cell transplantation
systemic illness
tongue, fasciculations of
transverse smile
treatment of neurologic disorder
type 1 muscle fiber
viral myopathy
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
winging of scapula
xerostomia
Showing articles 0 to 50 of 1293 Next >>

Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
Neurol 105:213101, Soontrapa,P.,et al, 2025

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

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

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

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Progressive Nemaline (Rod) Myopathy Associated with HIV Infection
NEJM 317:1602-1603, Dalakas,M.C.,et al, 1987

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients
Lancet 2:85-91, Streissguth,A.P.,et al, 1985

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

Iatrogenic Cerebral Amyloid Angiopathy after Cardiac Surgery, Two Case Reports
Neurol 106:e214819, Brunet de Courssou,J-B.,et al, 2026

A 52-Year Old Man with Acute-Onset Blindness
Neurol 106:e214827, Brown,A.M.,et al, 2026

Case Fatality of Subarachnoid hemorrhge by Aneurysm Location
Neurol 106:e214918, Asikinen,.,et al, 2026

Unruptured Intracranial Aneurysms
NEJM 392:2357-2366, Ogilvy,C.S., 2025

Infantile Epileptic Spasms Syndrome (West Syndrome)
Stat Pearls PMID:30725936, Smith,M.S.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
Neurol 105:e214173, Wold,K.J.,et al, 2025

A 62-Year-Old Man with Progressive Limb Weakness, Involuntary Movements, and HyperCKemia
JAMA Neurol 82L:1286-1287, Liu,Y.,et al, 2025

Spontaneous Calcified Cerebral Emboli from Bicuspid Aortic Valve in Young Patients: Case Series and Review
Stroke:Vasc Inter Neurol doi.org/10.1161/svi 270000.138, Sardana,S.,et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
Stroke 56:e359-362, deLima, M.M.,et al, 2025

A 24-Year-Old Man With Persistent Spontaneous Dizziness
Neurol 105:e214337, Isaza-Pierotti,D.F., 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

"Innumerable" lesion burden on brain MRI - a diagnostic approach
Diagnosis doi.org/10.1515/dx- 2025-2029, Finelli,P.F., 2025

Clinicopathologic Conference, Posterior Reversible Encephalopathy Syndrome Due to Sickle Cell Disease
NEJM 392:268-276, Case 2-2025, 2025

Functional Outcome in Patients with Carotid Artery Dissection Undergoing Thrombectomy or Standard Medical Treatment
Neurol 104:e213465, Sykora,M.,et al, 2025

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

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Congenital and Acquired Chiari Syndrome
NEJM 390:2191-2198, Friedlander,R.M., 2024

Infective Endocarditis
Lancet 404:377-392, Li,M.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Ptosis as Partial Oculomotor Nerve Palsy Due to Compression by Infundibular Dilatation of Posterior Communicating Artery, Visualized with Three-Dimensional Computer Graphics:Case Report
Neurol Med Chir (Tokyo) 54:214-218, Fukushima,Y.,et al, 2024

Cerebral and Retinal Infarction in Bicuspid Aortic Valve
J Am Heart Assoc 12:e028789, Huntley,G.D.,et al, 2023

Subarachnoid Hemmorhage During Pregnancy and Puerperium:A Population-Based Study
Stroke 54:198-207, Korhonen,A., et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

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

Tersons Syndrome
NEJM 388:e79, Sherman,S.V., 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

Patient with Prior Spinal Cord Injury Who Developed Altered Mental Status After a Fall
Neurol 99:1122-1127, Dessy,A.,et al, 2022



Showing articles 0 to 50 of 1293 Next >>