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Differential
(Click to cross reference)
alcohol
alcohol intolerance
alternating rapid movement
anxiety
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
Babinski sign
bladder dysfunction
blindness
CAG repeats
cavernous hemangioma
cerebellar atrophy, primary
cerebellar degeneration
children
choking
chromosomal abnormality
chromosome 7
Clinical Pathologic Conference(C.P.C.)
clonus
cone-rod dystrophy
dementia
diplopia
dysarthria
dysmetria
dysphagia
dystonia
electroretinograph
epsilon sarcoglycan gene
exome sequencing
eye movement, disorders of
familial
fatigue
finger nose finger test
Friedreich's ataxia
fundus, abnormality of
gait disorder
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
handwriting
heel-knee-shin test
Hispanics
hot cross bun sign
hyperreflexia
imbalance
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
memory, impairment of
Mexican
Mexico
mortality
movement disorder
MRI
MRI, abnormal
multiple system atrophy
myoclonic dystonia
myoclonus
myoclonus, action
neurologic disease, diagnoses of
neuropathology
neuropathy
next-generation sequencing
optic atrophy
optical coherence tomography
orbit, tomograms of
paraparesis, familial spastic
paraparesis, spastic
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyramidal tract
pyramidal tract dysfunction
retina, abnormal
retinal degeneration
review article
Romberg's sign
spastic ataxia
spastic dysphonia
spastic paraplegia, type 7
spasticity
speech disorder
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
urinary urgency
visual acuity, decreased
visual loss
visual loss, progressive
visual loss, slow
walking, difficulty with
wheelchair
Showing articles 1300 to 1327 of 1327 << Previous

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

Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
Neurol 22:49, Nakano,K.K.,et al, 1972

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

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 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

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

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

Thoracic Outlet Syndromes
Ciba Symposium 23:1, Lord,J.W.,et al, 1971

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

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

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

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

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

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

Familial and Conjugal Multiple Sclerosis
Brain 86:315-332, Schapira,K.,et al, 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 1327 of 1327 << Previous