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Differential
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abdominal protrusion
acanthocytosis
acetazolamide
acid maltase deficiency
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, infants and children
acquired immunodeficiency syndrome, medical precautions with
acquired immunodeficiency syndrome-related complex
acyl CoA dehydrogenase deficiency
adducted thumb
advances in neurology
adverse drug reaction
agenesis of corpus callosum
airway obstruction
alpha-fetoprotein
alveolar hypoventilation
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anesthesia, general
aneurysm, intracranial
ankle clonous
ankle, swelling of
anterior horn cell disease
anterior tibial muscle weakness
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
anticonvulsants, absorption
anticonvulsants, bioavailability
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, subtherapeutic
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
antihistamines
arbovirus
areflexia
arrhythmia, cardiac
arthralgia
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, paroxysmal
autoimmune disease
automatic implantable cardioverter-defibrillator
azidodeoxythymidine
bacterial infection
baldness
basal ganglia, calcification of
basal ganglia, infarction
Bassen-Kornzweig syndrome
benign congenital hypotonia
blindness
blindness, sudden
botulism
brainstem, lesion of
Brazil
breast feeding
bulbar palsy
bulbar palsy, progressive
calcification, intracranial
calcium antagonist
calcium channel dysfunction
camptocormia
carbamazepine
carcinoma
cardiac arrest
cardiomyopathy
caribbean
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
cataracts, congenital
Central America
central core disease
central nervous system, infection of
central nuclei, muscle
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
cholelithiasis
chromosomal abnormality
chromosome 1
chromosome 5
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
complications
conduction block
congenital birth defects
congenital deformities
congenital heart disease
congenital heart disease, CNS complications with
congenital malformation
congenital myasthenic syndromes
congenital myopathy
congenital myopathy, inflammatory
congestive heart failure
consanguinity
contractures, joint
cornea, abnormal
corpus callosum
corpus callosum, thinning
cortical blindness
counselling
creatine phosphokinase(CPK)elevated
cry, weak
cryptorchidism
deafmute
deafness
degenerative diseases of CNS
delivery, complicated
dementia
developmental abnormality of brain
developmental disability
developmental milestones
developmental retardation
differential diagnosis
difficulty climbing stairs
digits, abnormal
dilantin
disability, neurological
dislocated hip, congenital
distal muscle weakness
dropped head syndrome
drug induced neurologic disorders
dwarfism
dysmorphic
dysphagia
dyspnea
dystroglycanopathies
dystrophin
dystrophin associated proteins
ear, abnormal
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, induction
epidemic
epidemiology of neurology
episodic disorders
episodic neurologic deficits
exome sequencing
exostosis
eye closure
face, elongated
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
false negative
familial
familial hemiplegic migraine
fasciculation
fatigue
Fazio-Londe's disease
feeding disorder
fetal movements, reduced
fetus
fever
fibrillations
flavivirus
floppy infant
folic acid
foot drop
Friedreich's ataxia
frontal balding
gait disorder
gait, waddling
gargoylism
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
glycosyltransferase
gonadal dysgenesis
Gowers maneuver
Guillain Barre syndrome
hair, loss
Hallgren's syndrome
head circumference
headache
hearing loss
heart block
heavy metal intoxication
hemiparesis
hemorrhagic diathesis
hepatomegaly
hepatosplenomegaly
high arched feet
high arched palate
highly active antiretroviral therapy
histochemistry
histochemistry of muscle
human immunodeficiency virus type 1
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperkalemic periodic paralysis
hyperreflexia
hypertelorism
hypertrophic cardiomyopathy
hypokalemia
hypokalemic periodic paralysis
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
infection
intellectual deficit
intrauterine
intrauterine infection
intrauterine infection, viral
jaundice
joint hypermobility
kaliuresis
karyotyping
Kearns-Sayre syndrome
keratoconus
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lactic acidemia
laminopathies
lamotrigine
Laurence-Moon-Bardet-Biedl syndrome
leg weakness, bilateral
lenticular nucleus, lesion of, bilateral
leukodystrophy
levonorgestrel
lid closure, weakness of
life expectancy
lissencephaly
liver function enzymes
LMNA gene
lordosis
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
MELAS syndrome
Melkersson's syndrome
melphalan
mental retardation
merosin
mestinon
metabolic acidosis
mexiletine
microcephaly
microdactyly
micrognathia
migraine
migraine, hemiplegic
Miller-Dieker syndrome
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mortality
mosquito
motor neuron disease
MRI
MRI, abnormal
MRI, fetal
MRI, intrauterine
MRI, muscle
mucopolysaccharidoses
multicore myopathy
multiminicore disease
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, LAMA2
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, distal weakness
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, limb-girdle
myasthenia gravis, neuromuscular junction in
myasthenia gravis, treatment of
myasthenic syndrome
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, focal
myopathy, metabolic
myopathy, mitochondrial
myopathy, monomelic
myopia
myositis
myositis ossificans, progressive
myositis, bacterial
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia, treatment of
myotubularin
nasal bridge, wide
nasal speech
nausea and vomiting
neck extension
neck weakness
neck, webbed
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, metastatic to CNS
neoplasm, primary of CNS
nerve conduction studies
neuritis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuronal migration disorder
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, painful
neuropathy, peripheral
newborn, evaluation of
nifedipine
Noonan Syndrome
nusinersen
obesity
obstetric neurologic injuries
occipital lobe, infarction
occipital lobe, lesion of
ocular myopathy
oculopharyngeal muscular dystrophy
opened mouth
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
Oppenheim muscular dystrophy
opportunistic infection
oral contraceptives
orbicularis oculi muscle
pacemaker, cardiac-transvenous
paramyotonia congenita
paraparesis
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
paresthesias
paroxysmal neurologic deficits
patient information and support
pectus excavatum
percussion induced muscle contraction
periodic paralysis
poison, mercury
poison, neurologic problems with
polydactyly
polyhydramnios
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
polyneuropathy, chronic inflammatory demyelinating
positive sharp waves
potassium channel antibodies
potassium channel dysfunction
practice guidelines
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
procainamide
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
pseudohypertrophy
pseudoretinitis pigmentosa
psychiatric disorder
ptosis
ptosis, bilateral
pulmonary stenosis
pyloric stenosis
pyomyositis
quadriparesis
quadriparesis, progressive
quadriplegia, transient
quality of life
ragged-red fibers
rash
repetitive nerve stimulation
respirator
respiratory failure
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
riboflavin
rigid spine syndrome
schizophrenia
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, injury following
seizure, pregnancy
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
serum alanine aminotransferase
short stature
short thumb
skin, biopsy
skin, lesions in neurologic disorders
sloped shoulders
SMN1 gene
sodium channel dysfunction
South America
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinal muscular atrophy, classification
spinocerebellar ataxia
spinocerebellar ataxia type 6
standing difficulty
stem cell transplantation
steroid
stooped posture
suck, poor
sudden death
syncope
systemic illness
temporalis muscle wasting
term infant
tocainide
tongue, fasciculations of
transverse smile
trauma
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
type 1 muscle fiber
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
Usher's syndrome
valvulopathy
viral infection
viral infection, CNS
viral myopathy
visual field defect
visual fields, constricted
visual impairment
vital capacity
vitamin K
vitamin supplementation
vomiting, recurrent
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, episodic
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
workup
xerostomia
x-linked hydrocephalus
X-linked myopathy
Zika virus infection
Showing articles 50 to 100 of 1980 << Previous Next >>

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Myopathy in Human Immunodeficiency Virus-Infected Children Receiving Long-Term Zidovudine Therapy
J Pediatr 119:152-155, Walter,E.B.,et al, 1991

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Pyomyositis in a Child with Acquired Immunodeficiency Syndrome
Am J Dis Child 143:779-781, Raphael,S.A.,et al, 1989

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

Neuromuscular Diseases Associated with Human Immunodeficiency Virus Infection
Ann Neurol 23:S38-S48, Dalakas,M.C.&Pezeshkpour,G.H., 1988

Subacute Structural Myopathy Associated with Human Immunodeficiency Virus Infection
Arch Neurol 45:585-587, Gonzales,M.F.,et al, 1988

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

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

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

Treatment of Myotonia
Editorial, Lancet 1:1242-12441987., , 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

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

Acetazolamide-Responsive Myotonia Congenita
Neurol 37:488-491, Trudell,R.G.,et al, 1987

Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986

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

Abnormalities of Eyelid Closure
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, 2:967, Miller,M.R., 1985

Nemaline Myopathy with Associated Cardiomyopathy, Report of Clinical & Detailed Autopsy Findings
Arch Neurol 42:1084-1086, Stoessl,A.J.,et al, 1985

Tubular Aggregates, Their Association with Neuromuscular Diseases, Including the Syndrome of Myalgias/Cramps
Arch Neurol 42:973-976, Rosenberg,N.L.,et al, 1985

Nemaline Myopathy Appearing in Adults as Cardio-myopathy
Arch Neurol 41:443-445, Meier,C.,et al, 1984

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

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

Nemaline Myopathy in the Neonate
Neurol 33:351-356, Norton,P.,et al, 1983

Nemaline Myopathy Presenting as Cardiomyopathy
NEJM 308:1536-1537, Meier,C.,et al, 1983

Type I Fiber Atrophy & Internal Nuclei, A Form of Centronuclear Myopathy
Arch Neurol 39:520-524, Peyronnard,J-M.,et al, 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,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

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

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

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

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

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

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

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

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

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



Showing articles 50 to 100 of 1980 << Previous Next >>