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Differential
(Click to cross reference)
abscess, intracerebral
Alzheimer's disease
Alzheimer's disease, familial
Alzheimer's disease, pathogenesis
angiofibroma, facial
antibiotic prophylaxis
areflexia
arteriovenous malformation, pulmonary
ash leaf spots
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
Babinski sign
cardiomyopathy
CAT scan, chest
cerebrovascular accident
chest x-ray, abnormal
chromosomal abnormality
chromosome 16
chromosome 9
clubbing of fingers
clubfoot as related to neurologic disease
consanguinity
contraindications
cyanosis
deep tendon reflexes
developmental retardation
diabetes mellitus
diagnostic criteria
distal muscle weakness
dizziness
DNA probes
dysarthria
dysmorphic
dystonia
dystonia musculorum deformens
echocardiogram
embolism, paradoxical
endocarditis, prophylaxis
familial
fibrinolytic agents, contraindications
fibroma, ungual
foot drop
frataxin
Friedreich's ataxia
gene
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
hamartin
hamartoma
hearing loss
hereditary hemorrhagic telangiectasia(HHT)
hyperreflexia
hypopigmentation of skin
hypoxia
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
intracerebral hemorrhage
leg weakness, bilateral
mental retardation
molecular genetics
MRI
MRI, abnormal
muscle weakness
myopathy
myopathy, distal
myopathy, distal, vacuolar
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, vacuolar
neurologic disease, diagnoses of
neuropathology
neuropathy
pes cavus
phakomatoses
platelet inhibiting drugs
prognosis
retinal hamartoma
retinal lesion
review article
RFLPs
scoliosis
screening
seizure
shagreen patch
skin, lesions in neurologic disorders
subependymal nodules
telangiectases
transient ischemic attack
treatment of neurologic disorder
trinucleotide repeats
tuberin
tuberous sclerosis
ubiquilin 1
weakness, progressive
wheelchair
workup
Showing articles 1300 to 1326 of 1326 << Previous

Use of L-Dopa in the Detection of Presymptomatic Huntington's Chorea
NEJM 286:1332, Klawans,H.,et al, 1972

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

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

Familiar Basilar Impression
Neurol 22:554, Paradis,R.,et al, 1972

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

Pediatric Neurology
Psych Annals 2:1, , 1972

Ethical & Social Issues in Screening for Genetic Disease-Screening for Genetic Disease-A Group Report
NEJM 286:1129, 1972, 286:1155972., , 1972

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

Presymptomatic Detection of Huntington's Chorea
BMJ 540, 1972 Sept., , 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

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

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

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

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both
NEJM 274:384, Renuart,A., 1966

Inherited Aminoacidopathies Demonstrating Vitamin Dependency
NEJM 281:145, Rosenberg,L., 1965

Morquio's Disease, A Radiologic & Morphologic Study
Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964

Familial and Conjugal Multiple Sclerosis
Brain 86:315-332, Schapira,K.,et al, 1963

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

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Microcephaly
Arch Dis Child 37:623-627, Davies,H.,et al, 1962

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,



Showing articles 1300 to 1326 of 1326 << Previous