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acyl CoA dehydrogenase deficiency
adrenoleukodystrophy
advances in neurology
alveolar hypoventilation
amniocentesis
anesthesia, general
arrhythmia, cardiac
aspiration
asymptomatic
ataxia
ataxia, hereditary
atrial fibrillation
atrial paralysis
atrioventricular block
autoimmune disease
baldness
cachexia
calf atrophy
calf hypertrophy
carcinoma
cardiomyopathy
cataracts
central nervous system, infection of
cerebral embolism
cerebral embolism, carotid origin
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
children
chromosome 19
chromosome 3
Clinical Pathologic Conference(C.P.C.)
complications
confidentiality
congenital birth defects
congenital heart disease
contractures, joint
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
delay in diagnosis
descending paralysis
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
distal muscle weakness
DNA probes
dropped head syndrome
dystrophin
echocardiogram
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
enzyme, defect
enzyme, muscle disease
ethics in neurology
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
family planning
fine motor function, impaired
foot drop
fragile-X syndrome
frontal balding
gait disorder
gait, waddling
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gowers maneuver
heart block
high arched palate
Huntington's chorea
hypercapnia
implantable cardioverter defibrillator
inborn errors of metabolism
inborn errors of metabolism, screening
learning disability
learning disability, in children
lid closure, weakness of
liver function enzymes
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
mortality
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myoglobinuria
myopathy
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neck weakness
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuronal migration disorder
neuropathy, hereditary peripheral
pacemaker, cardiac-transvenous
percussion induced muscle contraction
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
proximal myotonic myopathy
ptosis
review article
rhabdomyolysis
screening
shoulder-girdle wasting
slit lamp examination
speech disorder, childhood
speech, delayed development of
spinocerebellar ataxia
spinocerebellar degeneration
systemic illness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
toe walking
treatment of neurologic disorder
trinucleotide repeats
tripping
ultrasonography
urine, dark
viral infection, CNS
weakness
weakness, progressive
weakness, proximal
wheelchair
whistle, inability to
winging of scapula
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
Showing articles 350 to 400 of 1780 << Previous Next >>

Myasthenia Gravis & Myotonic Dystrophy in a 13-year-old Girl
Neurol 27:546, Schoen,R.T., 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

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

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

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

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

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

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

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

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

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,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

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

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,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

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 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

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy
NEJM 391:1256-1258, Laugwitz,L.,et al, 2024

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

Seizures When Exiting a Bath, A Rare Type of Reflex Epilepsy
Neurol 103:e210025, Pascarella,A.,et al, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,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

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

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

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

A Woman with Progressive Painless Sequential Monocular Vision Loss
Neurol 101:e2197-e2201, Ditrapani,J.,et al, 2023



Showing articles 350 to 400 of 1780 << Previous Next >>