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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 200 to 250 of 1780 << Previous Next >>

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Allopurinol Not Effective In Muscular Dystrophy
NEJM 301:785, Bakouche,P.,et al, 1979

5'-Nucleotidase Activity in Duchenne Muscular Dystrophy
NEJM 301:726, Scholte,H.R.,et al, 1979

Carrier Detection in Duchenne Muscular Dystrophy
Neurol 29:1423-1425, Tagliavini,J.,et al, 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

Deformed Erythrocytes in Muscular Dystrophies
Neurol 28:842-844, Grassi,E.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

Alteration in Erythrocyte Membrane Structure in Duchenne Muscular Dystrophy
Ann Neurol 4:253-256, Wakayama,Y.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Prenatal Diagnosis of Duchenne's Muscular Dystrophy
NEJM 297:968, Mahoney,M.J.,et al, 1977

X-linked Muscular Dystrophy
Ann Neurol 2:414, Furukawa,T.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Carrier Detection in Duchenne Muscular Dystrophy
NEJM 294:193, Roses,A.D.,et al, 1976

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

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

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Biochemical Abnormalities of the Sarcoplasmic Reticulum in Muscular Dystrophy
NEJM 290:184, Samaha,F.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

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

Mental Deficiency Associated with Muscular Dystrophy
Brain 89:769, Rosman,N.P.,et al, 1966

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

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

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

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

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

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,et al, 2018

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014



Showing articles 200 to 250 of 1780 << Previous Next >>