Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973
Treating Problem Children with Stimulant Drugs
NEJM 289:407, Sroufe,L.A.,et al, 1973
Hereditary Quadriceps Myopathy
JNNP 36:1041, Espir,M.L.E.,et al, 1973
The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973
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
Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972
Medical Treatment of Spasmodic Torticollis
Arch Neurol 27:503, Gilbert,G., 1972
Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972
Dysautonomia, Its Significance in Neurologic Disease (Specialty Conference)
Calif Med 117:28, Wichser,J.,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
Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972
Differential Diagnosis of Tremors
Med Clin North Am 56:1363, Fahn,S., 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
Familial Calcification of the Basal Ganglions A Metabolic & Genetic Study
NEJM 285:72, Moskowitz,M.,et al, 1971
Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971
Myasthenia Gravis & Hyperthyroidism Occurring in Two Sisters
Neurol 21:377, Namba,T.,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
Infantile Nystagmus:A Prospec. Study of Spasmus Nutans, Congen. Nystag, & Unclass. Nystagmus of Infancy
J Pediatr 77:177, Jayalakshuni,R.,et al, 1970
Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969
Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968
Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, 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
Orthopaedic Aspects of Intraspinal Tumors in Infants & Children
J Bone & Joint Surg 47A:223965., Tachdjian,M.&Matson,D., 1965
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
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
Hereditary Ataxias
Genetics & the Inheritance of Integrated Neurol & Psych. Patterns-Vol 33, Proceed. Assoc. for Resear, h in NerSchut, J., 1850
Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 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,