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Differential
(Click to cross reference)
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 1250 to 1293 of 1293 << Previous

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

Juvenile Cerebral Arteriosclerosis & other Cerebral Arteriopathies of Childhood (Six Autopsied cases)
Acta Neurol Scand 48:479, Harvey,F.H.,et al, 1972

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Specific Learning Disorders in Childhood
Psych Annals 2:, 1972 May., Gomez,M.R., 1972

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

Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972

Effects of Viral Infection on the Developing Nervous System
Seminars in Medicine of the Beth Israel Hosp, Boston NEJM 287:5991972., Johnson,R., 1972

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

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

The Relationship of Motility Problems to Reading Problems
MCV Quart 8:298, McNeer,K., 1972

Spinabifida & Hydrocephalus
BMJ 4:796, Cook,R., 1971

Myasthenia Gravis & Hyperthyroidism Occurring in Two Sisters
Neurol 21:377, Namba,T.,et al, 1971

The Nervous System & Diabetes
Joslin's Diabetes Mellitus, 1971, p. 562., Locke,S., 1971

Perinatal Risk Associated with Maternal Genital Herpes Simplex Virus Infection
Am J OB Gyn 110:825-837, Nahmias,A.J.,et al, 1971

Natural History of Acute Hemiplegia of Childhood
Brain 93:107, Soloman,G.E.,et al, 1970

Fetal & Newborn Virus Infections
J Pediatr 77:315, Overall,J.,et al, 1970

Infantile Nystagmus:A Prospec. Study of Spasmus Nutans, Congen. Nystag, & Unclass. Nystagmus of Infancy
J Pediatr 77:177, Jayalakshuni,R.,et al, 1970

Bilateral Posterior Fracture Dislocation of the Shoulder An Uncommon Complication of a Convulsive Seizure
NEJM 283:135-136, Pear,B.L., 1970

The Carotid-Cavernous Fistula:Spontaneous & Traumatic, In Clinical Neuro-Ophthalmology
3rd Ed, Williams & Wilkins, Baltimore, p. 1714, Walsh,F.B.&Hoyt,W.F., 1969

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

Neurologic Manifestations of Bacterial Endocarditis
Ann Int Med 71:21, Jones,H.,et al, 1969

Acute Hemiplegia in Infancy & Childhood
Develop Med Child Neurol 2:162, Aicardi,J.,et al, 1969

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Congenital Rubella
Am J Dis Child 118:32-34, Menser,M.A.,et al, 1969

Cerebral Dominance & Its Disturbances
Ped Clin North Am 15:759-769, Benson,D.F.,et al, 1968

Internal Carotid Aneurysm as a Cause of Raeder's Para-trigeminal Syndrome
Neurol 18:43-46, Law,W.R.,et al, 1968

Clinical & Pathological Findings in a Child with a Developmental Learning Disability
J Lear Dis 1:486, Drake,V.E., 1968

Congenital Word Blindness of Specific Developmental Dyslexia:A Review
Med J Aust 1:783, Hagger,T.D., 1968

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

Diagnostic Significance of Median Facial Anomalies for Holoprosencephaly
Pediatr 256, 1964 Aug., DeMeyer,W.,et al, 1964

Neuro CPC of MGH
Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963

Recognition, Prognosis, & Treatment of the Guillain-Barre Syndrome (Acute Idiopathic Polyneuritis)
Med Clin North Am 47:1371, Eiben,R.,et al, 1963

Intracranial Aneurysms Causing Ophthalmoplegia
Arch Ophthal 70:75l, Cogan,D.,et al, 1963

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Neuro CPC of MGH
Multiple Cerebral Abscesses & Infarcts, NEJM 266:610-61762., , 1962

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

Cerebrovascular Accidents in Patients with Congenital Heart Disease
Arch Neurol & Psychiat 77:483957., Tyler,H.R.,et al, 1957

Fractures Complicating Electro-Convulsive Therapy & Chronic Epilepsy
J Bone Joint Surg (Brit) , 36:70-7954., Kelly,J.P., 1954

Neurologic Syndromes Accompanying Developmental Anomalies of Occipital Bone, Atlas, & Axis
Arch Neurol Psych 45:577, List,C., 1941

The Marcus Gunn Phenomenon, Report of a Case With Suggestions As To Relief
Arch Neurol Psych 35:487-500, Grant,F.C., 1936

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

Minamata:A Living Death
Text by D. Johnson Maryknol Missions, , 1850

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

Investigating suspected subarachnoid hemorrhage in adults
, Brown, S.C., et al,



Showing articles 1250 to 1293 of 1293 << Previous