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Differential
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case studies
diabetes mellitus
face, numbness of
familial
hyperthyroidism
hyperthyroidism, familial incidence of
internuclear ophthalmoplegia
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, sensory loss with
nystagmus
nystagmus, dissociated
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pseudointernuclear ophthalmoplegia
tensilon test
thyrotoxicosis
Showing articles 1850 to 1896 of 1896 << Previous

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Medical Treatment of Spasmodic Torticollis
Arch Neurol 27:503, Gilbert,G., 1972

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Eye Changes of Graves s Disease
Mayo Clin Proc 47:969, Werner,S., 1972

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

A New Ptosis Classification
Arch Ophthalmol 88:590, Fox,S.A., 1972

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

Benign Essential Tremor
Lancet 471, 1972 Sept., , 1972

Lesions in Cerebrovascular Disease & their Clinical Implications
BMJ 89, Hutchinson,E.C., 1972

Neoplasms of the CNS
Neurol 22:40, Percy,A.,et al, 1972

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

Medical Approach to Ophthalmopathy of Graves'Disease
Mayo Clin Proc 47:980, Ivy,H., 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

Familial Calcification of the Basal Ganglions A Metabolic & Genetic Study
NEJM 285:72, Moskowitz,M.,et al, 1971

Neurocutaneous Disease
in Dermatology in General Medicine, Fitzpatrick, et al, eds, McGraw Hill, 1971, pp. 1379-1434., Adams,R., 1971

Polyneroupathies of Undetermined Cause
Acta Neurol Scand (Supp) :5970., Prineas,J., 1970

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

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

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

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

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

Myasthenic Pseudo-Internuclear Ophthalmoplegis
Arch Ophthalmol 75:363, Glaser,J.S., 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

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

Thyrotoxicosis & Vitamin B-12
Lancet Sept. 22, 1962, p. 616, George,W.K.,et al, 1962

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

Neuro CPC of MGH
Meningioma at Thoracic Cord, NEJM 264:824-8271961., , 1961

Compression of the Thoracic Spinal Cord in a Patient with Scleroderma
Bull Hosp Joint Dis 18:98, 1957, Kaplan,A.,et al, 1957

Tumors Involving the Brain-Stem
Quart J Med 21:265, Barnett,H.J.,et al, 1952

Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 1850

Hereditary Ataxias
Genetics & the Inheritance of Integrated Neurol & Psych. Patterns-Vol 33, Proceed. Assoc. for Resear, h in NerSchut, J., 1850

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

Clinical Pathological Conference, Scleroderma, Spastic Paraparesis & Chronic Myelogenous Leukemia
Prov. VAH, Dec. 12, 77., Finelli,P.F., 1850

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

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



Showing articles 1850 to 1896 of 1896 << Previous