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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
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
intellectual deficit
kyphoscoliosis, neurologic causes of
lid closure, weakness of
lip, abnormal
lordosis
malignant hyperpyrexia
mental retardation
mestinon
microcephaly
misdiagnosis
mitral valve prolapse
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
nasal bridge, wide
nasal speech
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromuscular junction
nose, abnormal
nusinersen
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
tongue, fasciculations of
transverse smile
treatment of neurologic disorder
type 1 muscle fiber
viral myopathy
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
winging of scapula
xerostomia
Showing articles 0 to 50 of 1267 Next >>

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

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

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

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

New Onset Focal Tremor in Patient with Human Immunodeficienccy Virus
Clin Infect Dis 75:1861-1863, Finelli,P.F., 2022

Case Report of Lambl Excrescences in a Pediatric Patient with Multifocal Strokes
Neurol 99:73-76, Robertson, D.M.,et al, 2022

Spina Bifida
NEJM 387:444-450, Iskandar, B.J. & Finnell, R.H., 2022

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

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

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

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

A Rare Treatable and Under Recognized Cause of Recurrent Convexity Subarachnoid Hemorrhage:Lupus anticoagulant Hypoprothombinemia Syndrome
Ann Indian Acad Neurol 24:986-989, Jain, S.,et al, 2021

A 7-Year-Old Boy with Acute-Onset Altered Mental Status
Neurol 96:e2774-e2778, Wong, G.J.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Delayed Leukoencephalopathy: A Rare Complication after Coiling of Cerebral Aneurysms
AJNR 41:286-292, Ikemura, A.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

Functional Neurological Disorder
Stroke 51:1629-1635, Popkirov, S., et al, 2020

Ondine Curse Syndrome Cause by Dorsolateral Medullary Stroke
Neurol 94:e1557-e1558, Fiedler, E. & Gill, R., 2020

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020



Showing articles 0 to 50 of 1267 Next >>