Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979
Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979
Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979
CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979
Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979
Fetal Alcohol Syndrome & Related CNS Problems
Neurol 29:1429-1430, Wisniewski,K.,et al, 1979
Familial Arteriovenous Malformation
Ann Neurol 5:585-587, Snead,O.C.III.,et al, 1979
Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979
Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979
Famillial Carpal Tunnel Syndrome
Arch Neurol 36:727, Massey,E.W., 1979
Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
NEJM 301:588-590, Askanas,V.,et al, 1979
Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979
Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
Neurol 29:1402, Book,R.H.,et al, 1979
Huntington's Disease:Abnormality of Lymphocyte Capping
Ann Neurol 6:447-450, Noronha,A.B.C.,et al, 1979
Reversal of an Afferent Pupillary Defect with Cold Water Drinking
Ann Neurol 6:456, Czarnecki,J.S., 1979
Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979
Marfan's Syndrome
NEJM 301:273, Barr,M., 1979
Paraparesis in Hereditary Multiple Exostoses:Case Report
Neurol 29:973-977, Ferrari,G.,et al, 1979
Hereditary-Multiple Exostoses With Myelopathy
Arch Neurol 36:714, Ho,S.U.,et al, 1979
Carrier Detection in Duchenne Muscular Dystrophy
Neurol 29:1423-1425, Tagliavini,J.,et al, 1979
A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979
Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979
Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979
Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979
Familial Kearns-Sayre syndrome
Neurol 29:1172-1174, Schnitzler,E.R.,et al, 1979
Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979
"Agenesis"of the Temporal Lobe
Arch Neurol 36:590-591, Kansu,T.,et al, 1979
Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979
Familial Lumbar Spinal Stenosis with Acute Disc Herniation, Case Reports of Four Brothers
J Neurosurg 51:234-236, Varughese,G.,et al, 1979
Reversible Mental Symptoms in Temporal Arteritis
J Nerv Ment Dis 166:446-447, Cochran,J.W.,et al, 1978
Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978
Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978
Autosomal Dominant Neurological Disorders
Ann Neurol 4:548-552, Brady,R.O.,et al, 1978
Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978
Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978
Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978
Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978
Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978
Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978
Familial Hypopituitarism with Large Sella Turcica
NEJM 298:698, Parks,J.S.,et al, 1978
Cerebrovascular Disease in Infants & Children:A Study of Incidence, Clinical Features, & Survival
Neurol 28:763-768, Schoenberg,B.S.,et al, 1978
Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978
The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978
Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978
Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978
Memory Impairment in Korsakoff's Psychosis:A Correlation with Brain Noradrenergic Activity
Science 202:905-907, McEntee,W.J.,et al, 1978
Hypersomnia-sleep Apnea Due to Macrognathia
Arch Neurol 35:392, Weitzman,E.D.,et al, 1978
Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978
Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978
Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978